US20150216203A1 - Feed additive composition - Google Patents

Feed additive composition Download PDF

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US20150216203A1
US20150216203A1 US14/609,911 US201314609911A US2015216203A1 US 20150216203 A1 US20150216203 A1 US 20150216203A1 US 201314609911 A US201314609911 A US 201314609911A US 2015216203 A1 US2015216203 A1 US 2015216203A1
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Prior art keywords
feed
dfm
xylanase
strain
enzyme
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Inventor
Mai Faurschou Isaksen
Marion Bernardeau
Luis Fernando Romero Millan
Elijah Gituanjah Kiarie
Susan Lund Arent
Piiivi Helena Nurminen
Sofia Forssten
Daniel Petri
Elizabeth Ann Galbraith
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DuPont Nutrition Biosciences ApS
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DuPont Nutrition Biosciences ApS
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/43—Enzymes; Proenzymes; Derivatives thereof
    • A61K38/46—Hydrolases (3)
    • A61K38/47—Hydrolases (3) acting on glycosyl compounds (3.2), e.g. cellulases, lactases
    • A23K1/009—
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23K—FODDER
    • A23K10/00—Animal feeding-stuffs
    • A23K10/10—Animal feeding-stuffs obtained by microbiological or biochemical processes
    • A23K10/16—Addition of microorganisms or extracts thereof, e.g. single-cell proteins, to feeding-stuff compositions
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23K—FODDER
    • A23K10/00—Animal feeding-stuffs
    • A23K10/10—Animal feeding-stuffs obtained by microbiological or biochemical processes
    • A23K10/16—Addition of microorganisms or extracts thereof, e.g. single-cell proteins, to feeding-stuff compositions
    • A23K10/18—Addition of microorganisms or extracts thereof, e.g. single-cell proteins, to feeding-stuff compositions of live microorganisms
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23K—FODDER
    • A23K20/00—Accessory food factors for animal feeding-stuffs
    • A23K20/10—Organic substances
    • A23K20/189—Enzymes
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23K—FODDER
    • A23K50/00—Feeding-stuffs specially adapted for particular animals
    • A23K50/30—Feeding-stuffs specially adapted for particular animals for swines
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23K—FODDER
    • A23K50/00—Feeding-stuffs specially adapted for particular animals
    • A23K50/60—Feeding-stuffs specially adapted for particular animals for weanlings
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23K—FODDER
    • A23K50/00—Feeding-stuffs specially adapted for particular animals
    • A23K50/70—Feeding-stuffs specially adapted for particular animals for birds
    • A23K50/75—Feeding-stuffs specially adapted for particular animals for birds for poultry
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66—Microorganisms or materials therefrom
    • A61K35/74—Bacteria
    • A61K35/741—Probiotics
    • A61K35/742—Spore-forming bacteria, e.g. Bacillus coagulans, Bacillus subtilis, clostridium or Lactobacillus sporogenes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66—Microorganisms or materials therefrom
    • A61K35/74—Bacteria
    • A61K35/741—Probiotics
    • A61K35/744—Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
    • A61K35/747—Lactobacilli, e.g. L. acidophilus or L. brevis
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/24—Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402—Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00—Lactic or propionic acid bacteria
    • A23V2400/11—Lactobacillus
    • A23Y2220/00—
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
    • C12Y302/01008—Endo-1,4-beta-xylanase (3.2.1.8)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
    • C12Y302/01021—Beta-glucosidase (3.2.1.21)

Definitions

  • the present invention relates to methods for improving feed compositions using a specific direct fed microbial in combination with a xylanase and a ⁇ -glucanase, and to a feed additive composition comprising a direct fed microbial in combination with a xylanase and a ⁇ -glucanase.
  • the present invention further relates to uses and kits.
  • Supplemental enzymes are used as additives to animal feed, particularly poultry and swine feeds, as a means to improve nutrient utilization and production performance characteristics.
  • Enzyme blends are available to improve the nutritional value of diets containing cereal grains, soybean meal, animal protein meals, or high fibre food and industrial by-products.
  • DFM direct fed microbials
  • the present invention relates to novel specific combinations which surprisingly significantly improve production performance characteristics of animals.
  • a seminal finding of the present invention is that the degradation of dietary material derived from plant cell wall particles which is high in non-starch polysaccharides (NSP) by xylanases can be optimized for improved animal performance when combining xylanase and a ⁇ -glucanase with one or more specific direct fed-microbials (DFMs) selected for their capacity to digest plant cell wall structural carbohydrates and/or their capacity of producing Short Chain Fatty Acids (SCFA) from pentoses (e.g. arabinoxylans) contained in the NSP fraction of ingredients in anaerobic conditions.
  • NSP non-starch polysaccharides
  • the energy value from plant products can be optimized by combining xylanase and a ⁇ -glucanase and specific DFMs that can either produce SCFAs from NSP fraction pentoses in anaerobic conditions or that can modulate the microbial populations in the GIT to increase SCFA production from the sugars released.
  • the DFMs may adapt their metabolism to synergistically increase the fibre hydrolysis in combination with xylanase and ⁇ -glucanase.
  • DFMs with fibrolytic enzymes can provide additional benefits and maximize the benefits of the carbohydrases.
  • Specific DFMs selected for their enzymatic activities can be considered as a glycan-driven bacterial food chain.
  • the specifically selected DFMs taught herein may preferentially utilize dietary fibres, a trait that allows them to carry out the initial glycan digestion steps to liberate shorter, more soluble polysaccharides for other bacteria, e.g. other endogenous GIT microflora.
  • the specific DFMs have been selected for their metabolism which adjusts according to the glycans released by enzymes (e.g. xylanase and ⁇ -glucanase) to improve the efficacy of the enzymes taught herein and the DFM(s) combination compared to use of a combination of enzymes alone or the use of DFM(s) alone.
  • dietary material derived from plant cell wall particles which is rich in source-specific glycans such as cellulose, hemicellulose and pectin (plant material) or glycosaminoglycans enter the distal gut in particulate forms that are attacked by the specific DFMs glycan degraders which are capable of directly binding to these insoluble particles and digesting their glycan components.
  • DFMs glycan degraders which are capable of directly binding to these insoluble particles and digesting their glycan components.
  • more-soluble glycan fragments can be digested by secondary glycan degraders present in the caecum, which contribute to the liberated pool of short-chain fatty acid (SOFA) fermentation products that is derived from both types of degraders.
  • SOFA short-chain fatty acid
  • SCFA concentration can be an index of the anaerobic-organism population.
  • SOFA may actually provide a number of benefits to the host animal, acting as metabolic fuel for intestine, muscle, kidney, heart, liver and brain tissue, and also affording bacteriostatic and bacteriocidal properties against organisms such as Salmonella and E. coli.
  • the nutritional value of fibre in non-ruminants can mainly be derived through short chain fatty acids (SCFA) production via fermentation of solubilized or degraded fibres by effective fibre degrading enzymes (e.g. a xylanase and a ⁇ -glucanase, suitably in combination with a further fibre degrading enzyme).
  • SCFA short chain fatty acids
  • effective fibre degrading enzymes e.g. a xylanase and a ⁇ -glucanase, suitably in combination with a further fibre degrading enzyme.
  • Feed xylanase alone is not enough to use fibrous ingredients in animal (especially non-ruminant) diets.
  • An enzyme application depends on the characteristics of the plant (feed) material.
  • SCFAs have different energy values and some can serve as precursors of glucose and some can contribute to the maintenance of intestinal integrity and health.
  • the inventors have found that the specific combinations taught herein preferentially move the fermentation process in an animal's GIT towards the production of more valuable/useful SCFA's such as butyric acid and/or propionic acids.
  • the present invention provides a feed additive composition
  • a feed additive composition comprising a direct fed microbial (DFM), in combination with a xylanase and a ⁇ -glucanase, wherein the DFM is selected from the group consisting of an enzyme producing strain; a C5 sugar-fermenting strain; a short-chain fatty acid-producing strain; a fibrolytic, endogenous microflora-promoting strain; or combinations thereof.
  • DFM direct fed microbial
  • the present invention further provides a method for:
  • the present invention yet further provides a premix comprising a feed additive composition according to the present invention or a direct fed microbial (DFM), a xylanase and a ⁇ -glucanase, wherein the DFM is selected from the group consisting of an enzyme producing strain; a C5 sugar-fermenting strain; a short-chain fatty acid-producing strain; a fibrolytic, endogenous microflora-promoting strain; or combinations thereof, and at least one vitamin and/or at least one mineral.
  • DFM direct fed microbial
  • the present invention provides a feed comprising a feed additive composition according to the present invention or a premix according to the present invention.
  • the present invention yet further provides a feed comprising a direct fed microbial (DFM), in combination with a xylanase and a ⁇ -glucanase, wherein the DFM is selected from the group consisting of an enzyme producing strain; a C5 sugar-fermenting strain; a short-chain fatty acid-producing strain; a fibrolytic, endogenous microflora-promoting strain; or combinations thereof.
  • DFM direct fed microbial
  • a method of preparing a feedstuff comprising admixing a feed component with a feed additive composition according to the present invention or a premix according to the present invention.
  • a further aspect of the present invention is a method of preparing a feedstuff comprising admixing a feed component with a direct fed microbial (DFM), in combination with a xylanase and a ⁇ -glucanase, wherein the DFM is selected from the group consisting of an enzyme producing strain; a C5 sugar-fermenting strain; a short-chain fatty acid-producing strain; a fibrolytic, endogenous microflora-promoting strain; or combinations thereof
  • DFM direct fed microbial
  • the present invention yet further provides use of a direct fed microbial (DFM), in combination with a xylanase and a ⁇ -glucanase, wherein the DFM is selected from the group consisting of an enzyme producing strain; a C5 sugar-fermenting strain; a short-chain fatty acid-producing strain; a fibrolytic, endogenous microflora-promoting strain; or combinations thereof:
  • DFM direct fed microbial
  • a further aspect relates to a kit comprising a direct fed microbial (DFM), a xylanase and a ⁇ -glucanase, wherein the DFM is selected from the group consisting of an enzyme producing strain; a C5 sugar-fermenting strain; a short-chain fatty acid-producing strain; a fibrolytic, endogenous microflora-promoting strain; or combinations thereof (and optionally at least one vitamin and/or optionally at least one mineral) and instructions for administration.
  • DFM direct fed microbial
  • FIG. 1 shows the effects of xylanase and ⁇ -glucanase without or with Bacillus direct fed microbial (DFM) on fecal lactobacillus and E. coli counts (log transformed colony forming unit/gram of feces, Log 10 cfu/g).
  • DFM Bacillus direct fed microbial
  • the enzyme(s) used in the present invention are exogenous to the DFM.
  • the enzyme(s) are preferably added to or admixed with the DFM.
  • Amino acids are referred to herein using the name of the amino acid, the three letter abbreviation or the single letter abbreviation.
  • protein includes proteins, polypeptides, and peptides.
  • amino acid sequence is synonymous with the term “polypeptide” and/or the term “protein”. In some instances, the term “amino acid sequence” is synonymous with the term “peptide”. In some instances, the term “amino acid sequence” is synonymous with the term “enzyme”.
  • polypeptide proteins and “polypeptide” are used interchangeably herein.
  • the conventional one-letter and three-letter codes for amino acid residues may be used.
  • the 3-letter code for amino acids as defined in conformity with the IUPACIUB Joint Commission on Biochemical Nomenclature (JCBN). It is also understood that a polypeptide may be coded for by more than one nucleotide sequence due to the degeneracy of the genetic code.
  • the enzymes for use in the present invention can be produced either by solid or submerged culture, including batch, fed-batch and continuous-flow processes. Culturing is accomplished in a growth medium comprising an aqueous mineral salts medium, organic growth factors, the carbon and energy source material, molecular oxygen, and, of course, a starting inoculum of one or more particular microorganism species to be employed.
  • the DFM for use in the present invention may be an enzyme producing strain.
  • the DFM for use in the present invention may be a C5 sugar-fermenting strain.
  • the DFM for use in the present invention may be a short-chain fatty acid-producing strain.
  • the DFM for use in the present invention may be a fibrolytic, endogenous microflora-promoting strain.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain according to the present invention may be selected from the group consisting of the following genera: Bacillus, Enterococcus, Lactobacillus, Propionibacterium and combinations thereof.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain according to the present invention may be at least one strain selected from the Bacillus genus, particularly Bacillus subtilis, B. licheniformis, B. amyloliquefaciens or B.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain according to the present invention may be at least one strain selected from the Enterococcus genus, particularly Enterococcus faecium.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain according to the present invention may be selected from the group consisting of: Bacillus subtilis AGTP BS3BP5, Bacillus subtilis AGTP BS442, B. subtilis AGTP BS521, B. subtilis AGTP BS918, Bacillus subtilis AGTP BS1013, B. subtilis AGTP BS1069, B.
  • subtilis AGTP 944 Bacillus subtilis BS 2084 (NRRL B-50013), Bacillus subtilis LSSAO1 (NRRL B-50104), Bacillus subtilis 3A-P4 (PTA-6506), Bacillus subtilis 22C-P1 (PTA-6508), Bacillus licheniformis BL21 (NRRL B-50134), Bacillus subtilis BS-27 (NRRL B-50105), Bacillus subtilis BS18 (NRRL B-50633), Bacillus subtilis 15A-P4 (PTA-6507), Bacillus subtilis BS278 (NRRL B-50634), Bacillus licheniformis BL842 (NRRL B-50516), B.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain for use in the present invention is preferably a viable bacterium.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain for use in the present invention may be in the form of an endospore.
  • the xylanase for use in the present invention is preferably an endo-1,4- ⁇ -d-xylanase (E.C. 3.2.1.8).
  • the xylanase and the ⁇ -glucanase are used in combination with at least one further fibre degrading enzyme.
  • the (further) fibre degrading enzyme may be selected from the group consisting of a cellobiohydrolase (E.C. 3.2.1.176 and E.C. 3.2.1.91), a ⁇ -glucosidase (E.C. 3.2.1.21), a ⁇ -xylosidase (E.C. 3.2.1.37), a feruloyl esterase (E.C. 3.1.1.73), an ⁇ -arabinofuranosidase (E.C. 3.2.1.55), a pectinase (e.g.
  • E.C. 3.2.1.15 an endopolygalacturonase
  • E.C. 3.2.1.67 an exopolygalacturonase
  • E.C. 4.2.2.2 a pectate lyase
  • fibre degrading enzyme suitably more than two, suitably more than three, suitably more than four, suitably more than five.
  • the feed additive composition according to the present invention or the composition comprising a DFM in combination with a xylanase, a ⁇ -glucanase and at least one further degrading enzyme move the fermentation process in the subject's gastrointestinal tract towards the production of butyric acid and/or propionic acid.
  • microorganism herein is used interchangeably with “microorganism”.
  • the DFM for use in the present invention may be any suitable DFM which is an “enzyme producing strain”—such as an enzyme producing Bacillus strain.
  • an enzyme producing Bacillus strain such as an enzyme producing Bacillus strain.
  • the DFM assay defined herein as “enzyme producing DFM assay” may be used.
  • a DFM is considered to be an enzyme producing DFM if it is classed as an enzyme producing DFM using the “enzyme producing DFM assay” taught herein.
  • the DFM for use in the present invention may be any suitable DFM which is a “C5 sugar-fermenting strain”.
  • a DFM is a “C5 sugar-fermenting strain”
  • the DFM assay defined herein as “C5 sugar-fermenting DFM assay” may be used.
  • a DFM is considered to be a C5 sugar-fermenting DFM if it is classed as C5 sugar fermenting using the “C5 sugar-fermenting DFM assay” taught herein.
  • the DFM for use in the present invention may be any suitable DFM which is a “short chain fatty acid (SCFA)-producing strain”.
  • SCFA short chain fatty acid
  • the DFM assay defined herein as “SCFA-producing DFM assay” may be used.
  • a DFM is considered to be a SCFA-producing DFM if it is classed as SCFA producing using the “SCFA-producing DFM assay” taught herein.
  • the DFM for use in the in present invention may be any suitable DFM which is a “fibrolytic, endogenous microflora-promoting strain”.
  • a DFM is a “fibrolytic, endogenous microflora-promoting strain”
  • the DFM assay defined herein as ““fibrolytic, endogenous microflora-promoting DFM assay” may be used.
  • a DFM is considered to be a fibrolytic, endogenous microflora-promoting DFM if it promotes or stimulates endogenous fibrolytic microflora using the assay taught herein.
  • the DFM for use in the present invention may be any suitable DFM which is an “enzyme producing strain”, a “C5 sugar-fermenting strain”, a “SCFA-producing strain”, a “fibrolytic, endogenous microflora-promoting strain” or combinations thereof.
  • the DFM for use in the present invention may be a DFM which is a strain that would be classified as being an “enzyme producing strain” and/or a “C5 sugar-fermenting strain” and/or a “SCFA-producing strain” and/or a “fibrolytic, endogenous microflora-promoting strain”.
  • the DFM may be a strain that is classified as having more than one type of activity, e.g. at least 2, suitably at least 3, suitably all 4 activities, e.g. enzyme producing activity, C5 sugar-fermenting activity, SCFA-producing activity and/or fibrolytic, endogenous microflora-promoting activity.
  • the DFMs according to the present invention provide benefits to animals fed high levels of high-fibre plant by-products, such as dried distillers grains with solubles (DDGS).
  • high-fibre plant by-products such as dried distillers grains with solubles (DDGS).
  • High-throughput screening of these test strains was performed by replicate spot plating of 2 microliters liquid culture onto 15.0 ml of various substrate media types of interest in 100 ⁇ 100 ⁇ 15 mm grid plates.
  • Cellulase, ⁇ -amylase, zeinase, soy protease, esterase, lipase and xylanase activities were determined based on specific substrate utilization by the individual strains.
  • Media components used to assay the substrate utilization properties from enzymatic activity of the environmentally derived strains are described in Table 1. Assay plates were left to dry for 30 minutes following culture application, and then incubated at 32° C. for 24 hours. Enzymatic activities for each strain were determined by measuring the zone of substrate degradation in millimeters, as indicated by clearing of the surrounding edge of colony growth. Mean values from replicate plates were recorded.
  • Yeast Extract 1.0% Polypeptone, 1.5% Agar, 0.75% Carboxymethyl Cellulose (CMC) Esterase/ 1.0% Polypeptone, 1.5% Agar, None; Measure Zone of Lipase 0.5% Yeast Extract, Clearing in opaque media 1.5% Tween 80, 1.5% Tributyrin, 0.01% Victoria Blue B Dye (filtered). Zeinase Nutrient Agar, 2% Purified Zein, None; Measure Zone of solubilized in 70% methanol Clearing in opaque media Xylanase Nutrient Agar, 2% Xylan None; Measure Zone of Clearing in opaque media
  • the enzyme producing strain produces one or more the following enzyme activities: cellulase activity, a-amylase activity, xylanase activity, esterase activity, lipase activity, ⁇ -mannanase activity, protease activity (e.g. zeinase or soy protease activity) and combinations thereof.
  • the enzyme producing strain produced one or more of the following enzyme activities: cellulose activity, xylanase activity ⁇ -mannanase activity, or combinations thereof.
  • the enzyme producing DFM is a strain selected from the group consisting of the species Bacillus subtilis, Bacillus pumilus, Bacillus licheniformis, Bacillus amyloliquefaciens or mixtures thereof.
  • the enzyme producing strain of DFM may be one or more of the strains taught in U.S. 61/527,371 and U.S. 61/526,881, both of which are incorporated herein by reference.
  • Bacillus strains are grown overnight on plates of Tryptic soy agar (Difco) at 32° C., and lactic acid bacteria are grown overnight on MRS agar (Difco) under anaerobic conditions at 37° C.
  • API 50 CHB and API 50 CHL media bioMerieux, Marcy I′Etoile, France
  • Strips are incubated at 32° C. ( Bacillus ) or 37° C. under anaerobic conditions (lactic acid bacteria) and monitored at 24 and 48 hours for colorimetric changes.
  • C5 sugar as used herein means any sugar having 5 carbons. C5 sugars may be referred to herein as pentoses.
  • the C5 sugars include D-arabinose, L-arabinose, D-ribose, D-xylose and L-xylose.
  • the C5 sugar-fermenting strain of DFM is selected from the group consisting of:
  • a 1% vol/vol inoculum of a 48 hr culture of a DFM is used to inoculate 10 ml tubes of modified Sodium Lactate Broth (NLB) (1% sodium lactate; Sigma-Aldrich, St Louis, Mo.; 1% tryptone; Oxoid Ltd., Hampshire, England, 0.5% yeast extract; Oxoid Ltd. and 0.5% KH 2 PO 4 ) devoid of sodium lactate and supplemented with a commensurate amount (1% wt/vol) of one of nine different carbohydrates (lactate, glucose, galactose, arabinose, sucrose, starch, xylose, cellobiose, fructose; Sigma-Aldrich, St. Louis, Mo.).
  • NLB modified Sodium Lactate Broth
  • Cultures are grown under anaerobic conditions at 32° C., and after 0, 24, 48, and 72 hours of incubation, duplicate tubes are centrifuged at 5000 ⁇ g for 10 min and spent broth collected from each culture. Production of short chain fatty acids in the spent broth was measured via high performance liquid chromatography (HPLC). Duplicate 1 ml samples of spent culture broth are removed from each sampling tube and mixed with 10 ml 0.005M H 2 SO 4 . Three mls of each diluted sample are filtered through a 0.2 micron filter into HPLC vials and capped.
  • the short chain fatty acid (SCFA)-producing strain may be Propionibacterium acidipropionici P169.
  • the short chain fatty acid (SCFA)-producing strain may be Enterococcus faecium ID7.
  • short chain fatty acid as used herein includes volatile fatty acids as well as lactic acid.
  • the SCFA may be selected from the group consisting of: acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, 2-methylbutyric acids and lactic acid.
  • the SCFA may be butyric acid.
  • FIBROLYTIC, ENDOGENOUS MICROFLORA-PROMOTING DFM ASSAY A pen trial is conducted to determine the effects of a DFM on broiler chickens compared to a control without DFM. Samples are collected on days 11 and 42 of the trial. At each sampling date one bird is collected from each pen for a total of eight birds per treatment. Birds are euthanized and the total gastrointestinal tract (GIT) from below the gizzard to the ileal-cecal junction is collected from each bird.
  • GIT total gastrointestinal tract
  • Cecal samples from each bird are sliced open and digesta and cecal tissue are collected in a whirl-pak bag and masticated in 99 ml of 0.1% peptone at 7.0 strokes/s for 60 seconds to release mucosa-associated bacterial cells from the cecal tissue.
  • Aliquots of the masticated solution containing bacteria from the cecal mucosa and digesta are flash-frozen in liquid nitrogen and stored at ⁇ 20° C. until further analysis.
  • Genomic DNA is isolated from 250 ⁇ l of each sample by phenol chloroform extraction and purified using Roche Applied Science High Pure PCR Template Purification Kit (Roche Diagnostics Corp., Indianapolis, Ind.).
  • DNA from two birds per treatment is pooled in equal amounts and submitted for pyrosequencing as a single sample, resulting in four samples per treatment from each age.
  • Bacterial tag-encoded FLX amplicon pyrosequencing is performed as described previously (Dowd, et al BMC Microbiol. 2008 Jul. 24; 8:125).
  • the V1-V3 region of the 16S rRNA gene is amplified in each pooled sample using the primers 28 F (5′-GAGTTTGATCNTGGCTCAG) and 519R (5′-GTNTTACNGCGGCKGCTG).
  • Pyrosequencing data is processed and analysed using the Qiime v.1.4.0. software pipeline. Briefly, raw sequence data is screened and trimmed based on quality.
  • Sequences are trimmed to 350 bp. Sequences are binned by individual samples based on barcode sequences. Barcode tags and primers are removed from the sequences and non-bacterial ribosomal sequences are removed. Sequences are clustered into operational taxonomic units (OTUs) at 97% similarity using uclust. Representative sequences from each OTU are then aligned using PyNAST and taxonomy is assigned by sequence comparison to known bacterial 16S rRNA gene sequences in the SILVA database using the RDP classifier. A random subsampling of sequences is performed to normalize each sample so that the same number of sequences are analyzed. Analysis of Variance (ANOVA) analysis is used to determine if any fibrolytic microflora (taxa) are significantly affected by treatment.
  • OTUs operational taxonomic units
  • fibrolytic microflora as used herein means a group of microorganisms that are able to process complex plant polysaccharides due to their ability to synthesize cellulolytic and hemicellulolytic enzymes.
  • endogenous means present in (or originating in) the GIT of a subject (e.g. an animal).
  • a subject e.g. an animal
  • the fibrolytic, endogenous microflora is not a DFM.
  • the fibrolytic, endogenous microflora is not added to the subject's feed.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain for use in the present invention comprises a viable microorganism.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain comprises a viable bacterium or a viable yeast or a viable fungi.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain comprises a viable bacterium.
  • viable microorganism means a microorganism which is metabolically active or able to differentiate.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain may be a spore forming bacterium and hence the term DFM may be comprised of or contain spores, e.g. bacterial spores. Therefore in one embodiment the term “viable microorganism” as used herein may include microbial spores, such as endospores or conidia.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain in the feed additive composition according to the present invention is not comprised of or does not contain microbial spores, e.g. endospores or conidia.
  • the microorganism may be a naturally occurring microorganism or it may be a transformed microorganism.
  • the microorganism may also be a combination of suitable microorganisms.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain according to the present invention may be one or more of the following: a bacterium, a yeast or a fungi.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain according to the present invention is a probiotic microorganism.
  • direct fed microbial encompasses direct fed bacteria, direct fed yeast, direct fed fungi and combinations thereof.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain is a direct fed bacterium.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain may comprise a bacterium from one or more of the following genera: Bacillus, Lactobacillus, Propionibacterium and combinations thereof.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain may be a strain selected from the Bacillus genus.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain may be selected from the following Bacillus spp: Bacillus subtilis, Bacillus cereus, Bacillus licheniformis, B. pumilus, B. coagulans, B. amyloliquefaciens, B. stearothermophilus, B. brevis, B. alkalophilus, B. clausii, B. halodurans, B. megaterium, B. circulars, B. lautus, B. thuringiensis and B. lentus strains.
  • the B. subtilis strain(s) is (are) Bacillus subtilis AGTP BS3BP5, Bacillus subtilis AGTP BS442, B. subtilis AGTP BS521, B. subtilis AGTP BS918, Bacillus subtilis AGTP BS1013, B. subtilis AGTP BS1069, B. subtilis AGTP 944.
  • the B. subtilis strain(s) is (are) Bacillus subtilis 15A-P4 (PTA-6507), LSSAO1 (NRRL B-50104).
  • the B. pumilus strain is B. pumilus AGTP BS 1068 or B. pumilus KX11-1.
  • Strains 3A-P4 (PTA-6506), 15A-P4 (PTA-6507) and 22C-P1 (PTA-6508) are publically available from American Type Culture Collection (ATCC).
  • Strains 2084 (NRRL B-500130); LSSA01 (NRRL-B-50104); BS27 (NRRL B-50105) are publically available from the Agricultural Research Service Culture Collection (NRRL).
  • Strain Bacillus subtilis LSSA01 is sometimes referred to as B. subtilis 8. These strains are taught in U.S. Pat. No. 7,754,469 B2.
  • AgTech Products, Inc has authorised DuPont Nutrition Biosciences ApS of Langebrogade 1, PO Box 17, DK-1001, Copenhagen K, Denmark to refer to this deposited biological material in this patent application and has given unreserved and irrevocable consent to the deposited material being made available to the public.
  • ⁇ -mannanase is the name given to a class of enzymes which can hydrolyze 1,4- ⁇ -D-glycosidic bonds of ⁇ -mannan, galactomannan and glucomannan into mannan oligosaccharides and mannose, thus breaking down mannan containing hemicellulose, one of the major components of plant cell walls.
  • ⁇ -mannanase is endo-1,4- ⁇ -D-mannanase (E.C. 3.2.1.78).
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain for use in the present invention may be a strain selected from the Propionibacterium genus.
  • the DFM for use in the present invention may be selected from the species Propionibacterium acidipropionici.
  • the DFM for use in the present invention is Propionibacterium acidipropionici P169.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain for use in the present invention may be a strain from the Enterococcus genus.
  • the DFM for use in the present invention may be selected from the species Enterococcus faecium.
  • the DFM for use in the present invention may be Enterococcus faecium ID7.
  • Lactococcus lactis ID7 (which was later reclassified as Enterococcus faecium ID7) was deposited on 22 Jun. 2004 under the Budapest Treaty as Lactococcus lactis ID7 with the American Type Culture Collection (ATCC), Manassas, Va. 20110-2209, USA as Accession no. PTA-6103. Lactococcus lactis ID7 (which was later reclassified as Enterococcus faecium ID7) was referenced in granted patent U.S. Pat. No. 7,384,628 and is publically available from ATCC.
  • Enterococcus faecium ID7 When “ Enterococcus faecium ID7” is used herein it will be understood that this organism's name is interchangeable with “ Lactococcus lactis ID7” which was deposited as Accession no. PTA-6103. Enterococcus faecium ID7 is also publically available from Danisco Animal Nutrition, Denmark.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain for use in the present invention may be a strain from Lactobacillus genus.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strains and/or the fibrolytic, endogenous microflora-promoting strain may be selected from the following Lactobacillus spp: Lactobacillus buchneri, Lactobacillus acidophilus, Lactobacillus casei, Lactobacillus kefiri, Lactobacillus bifidus, Lactobacillus brevis, Lactobacillus helveticus, Lactobacillus paracasei, Lactobacillus rhamnosus, Lactobacillus salivarius, Lactobacillus curvatus, Lactobacillus bulgaricus, Lactobacillus sakei, Lactobacillus reuteri, Lactobacillus fermentum, Lactobacillus farciminis, Lactobacillus lactis, Lactobacillus delbreuckii, Lactobacillus plantarum, Lactobacillus
  • the DFM may be selected from one or more of the following strains: Lactobacillus rhamnosus CNCM-I-3698 and Lactobacillus farciminis CNCM-I-3699. These strains were deposited at the Collection Nationale de Cultures de Microorganims (CNCM) 25, Rue due Dondel Roux, F75724 Paris Cedex 15, France on 8 Dec. 2006 by Sorbial, Route de Spay 72700 Allonnes, France and all right, title and interest in the deposits were subsequently transferred to Danisco France SAS of 20, Rue de Brunel, 75017 Paris, France.
  • CNCM Collection Nationale de Cultures de Microorganims
  • the DFM may be selected from Lactobacillus lactis DJ6 (PTA 6102) and/or Lactococcus lactis ID7 (PTA 6103).
  • AgTech Products, Inc. has authorised DuPont Nutrition Biosciences ApS of Langebrogade 1, PO Box 17, DK-1001, Copenhagen K, Denmark to refer to these deposited biological materials in this patent application and has given unreserved and irrevocable consent to the deposited material being made available to the public.
  • more than one of the strain(s) described herein is (are) combined.
  • the enzyme producing strain and/or the C-5 sugar-fermenting strain and/or the short-chain fatty acid-producing strain and/or the fibrolytic, endogenous microflora-promoting strain used in the present invention may be a combination of at least two, suitably at least three, suitably at least four DFM strains described herein, e.g. DFM strains selected from the group consisting of Bacillus subtilis AGTP BS3BP5, Bacillus subtilis AGTP BS442, B. subtilis AGTP BS521, B. subtilis AGTP BS918, Bacillus subtilis AGTP BS1013, B. subtilis AGTP BS1069, B. subtilis AGTP 944, B. pumilus AGTP BS 1068, B. pumilus KX11-1, Propionibacterium P169, Lactobacillus rhamnosus CNCM-I-3698 or Lactobacillus farciminis CNCM-I-3699.
  • DFM strains selected from the group consisting of Bacill
  • the DFM may be one or more of the group consisting of Bacillus subtilis AGTP BS3BP5, Bacillus subtilis AGTP BS442, B. subtilis AGTP BS521, B. subtilis AGTP BS918, Bacillus subtilis AGTP BS1013, B. subtilis AGTP BS1069, B. subtilis AGTP 944, B. pumilus AGTP BS 1068, B. pumilus KX11-1 and a combination thereof.
  • Bacillus variant strains having all the characteristics of Bacillus subtilis AGTP BS3BP5, Bacillus subtilis AGTP BS442, B. subtilis AGTP BS521, B. subtilis AGTP BS918, Bacillus subtilis AGTP BS1013, B. subtilis AGTP BS1069, B. subtilis AGTP 944, B. pumilus AGTP BS 1068 or B. pumilus KX11-1 are also included and are useful in the methods described and claimed herein.
  • a “variant” has at least 80% identity of genetic sequences with the disclosed strains using random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) analysis.
  • the degree of identity of genetic sequences can vary.
  • the variant has at least 85%, 90%, 95%, 96%, 97%, 98% or 99% identity of genetic sequences with the disclosed strains using RAPD-PCR analysis.
  • RAPD analysis can be performed using Ready-to-GoTM RAPD Analysis Beads (Amersham Biosciences, Sweden), which are designed as pre-mixed, pre-dispensed reactions for performing RAPD analysis.
  • the direct fed bacterium used in the present invention may be of the same type (genus, species and strain) or may comprise a mixture of genera, species and/or strains.
  • the DFM to be used in accordance with the present invention is a microorganism which is generally recognised as safe and, which is preferably GRAS approved.
  • the DFM used in accordance with the present invention is one which is suitable for animal consumption.
  • the viable DFM should remain effective through the normal “sell-by” or “expiration” date of the product during which the feed or feed additive composition is offered for sale by the retailer.
  • the desired lengths of time and normal shelf life will vary from feedstuff to feedstuff and those of ordinary skill in the art will recognise that shelf-life times will vary upon the type of feedstuff, the size of the feedstuff, storage temperatures, processing conditions, packaging material and packaging equipment.
  • the DFM is tolerant to heat, i.e. is thermotolerant. This is particularly the case where the feed is pelleted. Therefore in one embodiment the DFM may be a thermotolerant microorganism, such as a thermotolerant bacteria, including for example Bacillus spp.
  • the DFM is a spore producing bacteria, such as Bacilli, e.g. Bacillus spp. Bacilli are able to from stable endospores when conditions for growth are unfavorable and are very resistant to heat, pH, moisture and disinfectants.
  • Bacilli e.g. Bacillus spp. Bacilli are able to from stable endospores when conditions for growth are unfavorable and are very resistant to heat, pH, moisture and disinfectants.
  • the DFM is not an inactivated microorganism.
  • the DFM may be a viable or inviable microorganism which is used in isolated or semi-isolated form.
  • the DFM may be used in combination with or without the growth medium in which it was cultured.
  • the DFM is capable of producing colony forming units when grown on an appropriate media.
  • the appropriate media may comprise (or consist of) a feed or a feed constituent.
  • the DFM is incapable of producing colony forming units when grown on an appropriate media.
  • the appropriate media may comprise (or consist of) a feed or a feed constituent.
  • the cells may be still metabolically active (e.g. even if they are unable to divide).
  • the DFM may be administered as inviable cells.
  • the DFM may be administered as a viable microorganism.
  • the DFM may be dosed appropriately.
  • dosages of DFM in the feed may be between about 1 ⁇ 10 3 CFU/g feed to about 1 ⁇ 10 9 CFU/g feed, suitably between about 1 ⁇ 10 4 CFU/g feed to about 1 ⁇ 10 3 CFU/g feed, suitably between about 7.5 ⁇ 10 4 CFU/g feed to about 1 ⁇ 10 7 CFU/g feed.
  • the DFM is dosed in the feedstuff at more than about 1 ⁇ 10 3 CFU/g feed, suitably more than about 1 ⁇ 10 4 CFU/g feed, suitably more than about 7.5 ⁇ 10 4 CFU/g feed.
  • dosages of DFM in the feed additive composition may be between about 1 ⁇ 10 5 CFU/g composition to about 1 ⁇ 10 13 CFU/g composition, suitably between about 1 ⁇ 10 6 CFU/g composition to about 1 ⁇ 10 12 CFU/g composition, suitably between about 3.75 ⁇ 10 7 CFU/g composition to about 1 ⁇ 10 11 CFU/g composition.
  • the DFM is dosed in the feed additive composition at more than about 1 ⁇ 10 5 CFU/g composition, suitably more than about 1 ⁇ 10 6 CFU/g composition, suitably more than about 3.75 ⁇ 10 7 CFU/g composition.
  • the DFM may be dosed in the feed additive composition at between about 5 ⁇ 10 7 to about 1 ⁇ 10 9 CFU/g, suitably at between about 1 ⁇ 10 8 to about 5 ⁇ 10 8 CFU/g composition.
  • the DFM may be dosed in the feed additive composition at between about 5 ⁇ 10 3 to about 5 ⁇ 10 5 U/g, suitably at between about 1 ⁇ 10 4 to about 1 ⁇ 10 5 CFU/g composition.
  • the DFM as taught herein may be used in combination with at least one xylanase and at least one ⁇ -glucanase (and optionally at least one further fibre degrading enzyme).
  • ⁇ -glucanase or endo-glucanase is the name given to a class of enzymes which can hydrolyze (1,3)- ⁇ -D-glycosidic and/or (1,4)- ⁇ -D-glycosidic bonds of (1,4)- ⁇ -glucan, (1,3;1,4)- ⁇ -glucan and cellulose into glucose oligosaccharides and glucose, thus breaking down cellulose and hemicellulose, the major components of plant cell walls.
  • the ⁇ -glucanase for use in the present invention may be any commercially available ⁇ -glucanase.
  • the ⁇ -glucanase is an endoglucanase, e.g. an endo-1,4- ⁇ -D-glucanase (classified as E.C. 3.2.1.4).
  • the ⁇ -glucanase for use in the present invention may be a ⁇ -glucanase from Bacillus, Trichoderma, Aspergillus, Thermomyces, Fusarium and Penicillium.
  • the fibre degrading enzyme may be a ⁇ -glucanase produced from one or more of the expression hosts selected from the group consisting of: Bacillus lentus, Aspergillus niger, Trichoderma reesel, Penicillium funiculosum, Trichoderma longibrachiatum, Humicola insolens, Bacillus amyloliquefaciens, Aspergillus aculeates, Aspergillus aculeates.
  • the fibre degrading enzyme may be one or more of the following commercial products which comprises at least a ⁇ -glucanase fibre degrading enzyme:
  • Econase® GT or Econase® BG available from AB Vista
  • Rovabio Excel® available from Adisseo
  • Endofeed® DC and Amylofeed® available from Andres Pintaluba S.A.
  • AveMix® XG10 from Aveve
  • Natugrain®, Natugrain®TS, or Natugrain® TS/L available from BASF
  • the ⁇ -glucanase may be obtained from Axtra®XB.
  • ⁇ -glucanase may be dosed in any suitable amount.
  • the ⁇ -glucanase for use in the present invention may be present in the feedstuff in a range of about 50 BGU/kg feed to about 50000 BGU/kg feed, suitably about 100 BGU/kg feed to about 1000 BGU/kg feed.
  • the ⁇ -glucanase for use in the present invention may be present in the feedstuff in a range of about 75 BGU/kg feed to about 400 BGU/kg feed, suitably about 150 BGU/kg feed to about 200 BGU/kg feed.
  • the ⁇ -glucanase is present in the feedstuff at less than 1000 BGU/kg feed, suitably less than about 500 BGU/kg feed, suitably less than 250 BGU/kg feed.
  • the ⁇ -glucanase is present in the feedstuff at more than 75 BGU/kg feed, suitably more than 100 BGU/kg feed.
  • the ⁇ -glucanase is present in the feed additive composition in the range of about 150 BGU/g composition to about 3000 BGU/g composition, suitably in the range of about 300 BGU/g composition to about 1500 BGU/g composition.
  • the ⁇ -glucanase is present in the feed additive composition at less than 5000 BGU/g composition, suitably at less than 4000 BGU/g composition, suitably at less than 3000 BGU/g composition, suitably at less than 2000 BGU/g composition.
  • the ⁇ -glucanase is present in the feed additive composition at more than 50 BGU/g composition, suitably at more than 100 BGU/g composition, suitably at more than 125 BGU/g composition.
  • the activity of ⁇ -glucanase can be calculated using the “ ⁇ -glucanase Activity Assay (BGU)” as taught herein.
  • the ⁇ -glucanase for use in the present invention may have ⁇ -glucanase activity as determined using the “ ⁇ -glucanase Activity Assay (CMC U/g)” taught herein.
  • fibre degrading enzyme may include one or more of the following fibre degrading enzymes: a xylanase (e.g. an endo-1,4- ⁇ -D-xylanase (E.C. 3.2.1.8) or a 1,4 ⁇ -xylosidase (E.C. 3.2.1.37)), a ⁇ -glucanase (E.C. 3.2.1.4), a cellobiohydrolase (E.C. 3.2.1.176 and E.C. 3.2.1.91), a ⁇ -glucosidase (E.C. 3.2.1.21), a feruloyl esterase (E.C.
  • a xylanase e.g. an endo-1,4- ⁇ -D-xylanase (E.C. 3.2.1.8) or a 1,4 ⁇ -xylosidase (E.C. 3.2.1.37)
  • a ⁇ -glucanase E.C. 3.2
  • an ⁇ -arabinofuranosidase (E.C. 3.2.1.55), a pectinase (e.g. an endopolygalacturonase (E.C. 3.2.1.15), an exopolygalacturonase (E.C. 3.2.1.67) or a pectate lyase (E.C. 4.2.2.2)), or combinations thereof.
  • a pectinase e.g. an endopolygalacturonase (E.C. 3.2.1.15), an exopolygalacturonase (E.C. 3.2.1.67) or a pectate lyase (E.C. 4.2.2.2)
  • fibre degrading enzyme may include one or more of the following fibre degrading enzymes: a cellobiohydrolase (E.C. 3.2.1.176 and E.C. 3.2.1.91), a ⁇ -glucosidase (E.C. 3.2.1.21), a ⁇ -xylosidase (E.C. 3.2.1.37), a feruloyl esterase (E.C. 3.1.1.73), an ⁇ -arabinofuranosidase (E.C. 3.2.1.55), a pectinase (e.g. an endopolygalacturonase (E.C. 3.2.1.15), an exopolygalacturonase (E.C. 3.2.1.67) or a pectate lyase (E.C. 4.2.2.2)), or combinations thereof.
  • a cellobiohydrolase E.C. 3.2.1.176 and E.C. 3.2.1.91
  • a further fibre degrading enzyme may encompass multiple further fibre degrading enzymes.
  • the DFM as taught herein may be used in combination with at least one xylanase, at least one ⁇ -glucanase and at least one further fibre degrading enzyme.
  • the DFM as taught herein may be used in combination with at least one xylanase, at least one ⁇ -glucanase and two (or at least two) further fibre degrading enzymes.
  • the DFM as taught herein may be used in combination with at least one xylanase, at least one ⁇ -glucanase and three (or at least three) further fibre degrading enzymes.
  • the DFM as taught herein may be used in combination with at least one xylanase, at least one ⁇ -glucanase and four (or at least four) further fibre degrading enzymes.
  • the DFM as taught herein may be used in combination with a broth or a solid-state fermentation product containing measurable enzyme activity or activities of the present invention.
  • the DFM as taught herein may be used in combination with the enzymes of the present invention, which enzymes are in isolated or purified form.
  • the DFM as taught herein may be used in combination with the enzymes of the present invention, which enzymes are exogenous to the DFM in the composition (e.g. if the DFM is an enzyme producing strain).
  • the fibre degrading enzyme(s) is present in the feedstuff in the range of about 0.05 to 5 g of enzyme protein per metric ton (MT) of feed (or mg/kg).
  • each fibre degrading enzyme may be present in the feedstuff in the range of about 0.05 to 5 g of enzyme protein per metric ton (MT) of feed (or mg/kg).
  • the fibre degrading enzymes in total are present in the feedstuff in the range of about 0.05 to 5 g of enzyme protein per metric ton (MT) of feed (or mg/kg).
  • the fibre degrading enzyme(s) is present in the feed additive composition (or premix) in the range of about 0.05 to 100 mg protein/g of composition (e.g. at a total inclusion in the diet of 50 to 1000 g/MT).
  • each fibre degrading enzyme is present in the feed additive composition (or premix) in the range of about 0.05 to 100 mg protein/g of composition (e.g. at a total inclusion in the diet of 50 to 1000 g/MT).
  • the fibre degrading enzymes in total is present in the feed additive composition (or premix) in the range of about 0.05 to 100 mg protein/g of composition (e.g. at a total inclusion in the diet of 50 to 1000 g/MT).
  • the fibre degrading enzyme (e.g. each fibre degrading enzyme or the fibre degrading enzymes in total) may be in the feed additive composition (or premix) in the range of about 50 to about 700 g/MT of feed.
  • the fibre degrading enzyme (e.g. each fibre degrading enzyme or the fibre degrading enzymes in total) may be in the feed additive composition (or premix) at about 100 to about 500 g/MT of feed.
  • the further fibre degrading enzyme(s) for use in the present invention may comprise (or consist essentially of, or consist of) a cellobiohydrolase (E.C. 3.2.1.176 and E.C. 3.2.1.91).
  • the further fibre degrading enzyme(s) for use in the present invention may comprise (or consist essentially of, or consist of) a ⁇ -glucosidase (E.C. 3.2.1.21).
  • the further fibre degrading enzyme may comprise (or consist essentially of, or consist of) a cellobiohydrolase (E.C. 3.2.1.176 and E.C. 3.2.1.91), a ⁇ -glucosidase (E.C. 3.2.1.21) or combinations thereof.
  • a cellobiohydrolase E.C. 3.2.1.176 and E.C. 3.2.1.91
  • a ⁇ -glucosidase E.C. 3.2.1.21
  • the further fibre degrading enzyme(s) for use in the present invention may comprise (or consist essentially of, or consist of) a ⁇ -xylosidase (E.C. 3.2.1.37).
  • the fibre degrading enzyme(s) for use in the present invention may comprise (or consist essentially of, or consist of) a feruloyl esterase (E.C. 3.1.1.73).
  • the further fibre degrading enzyme for use in the present invention may comprise (or consist essentially of, or consist of) an ⁇ -arabinofuranosidase (E.C. 3.2.1.55).
  • the further fibre degrading enzyme(s) for use in the present invention may comprise (or consist essentially of, or consist of) a pectinase (e.g. an endopolygalacturonase (E.C. 3.2.1.15), an exopolygalacturonase (E.C. 3.2.1.67) or a pectate lyase (E.C. 4.2.2.2)).
  • a pectinase e.g. an endopolygalacturonase (E.C. 3.2.1.15), an exopolygalacturonase (E.C. 3.2.1.67) or a pectate lyase (E.C. 4.2.2.2)
  • the further fibre degrading enzyme(s) for use in the present invention may comprise (or consist essentially of, or consist of) one or more (suitably two or two or more, suitably three) pectinase(s) selected from the group consisting of: an endopolygalacturonase (E.C. 3.2.1.15), an exopolygalacturonase (E.C. 3.2.1.67) and a pectate lyase (E.C. 4.2.2.2).
  • pectinase(s) selected from the group consisting of: an endopolygalacturonase (E.C. 3.2.1.15), an exopolygalacturonase (E.C. 3.2.1.67) and a pectate lyase (E.C. 4.2.2.2).
  • the further fibre degrading enzyme(s) for use in the present invention may comprise (or consist essentially of, or consist of) a cellobiohydrolase (E.C. 3.2.1.176 and E.C. 3.2.1.91), a ⁇ -glucosidase (E.C. 3.2.1.21), a ⁇ -xylosidase (E.C. 3.2.1.37), a feruloyl esterase (E.C. 3.1.1.73), an ⁇ -arabinofuranosidase (E.C. 3.2.1.55), and/or a pectinase (e.g. an endopolygalacturonase (E.C. 3.2.1.15), an exopolygalacturonase (E.C. 3.2.1.67) or a pectate lyase (E.C. 4.2.2.2).
  • a cellobiohydrolase E.C. 3.2.1.176 and E.C. 3.2.1.91
  • the present invention relates to the combination of at least one xylanase, with at least one ⁇ -glucanase and at least one specific DFM as taught herein.
  • the at least one xylanase, the at least one ⁇ -glucanase and the at least one specific DFM as taught herein may be combined with a further fibre degrading enzyme as taught herein.
  • the present invention further relates to the combination of at least one xylanase and at least one ⁇ -glucanase, with at least two, such as at least three or at least four or at least five, further fibre degrading enzymes and at least one specific DFM as taught herein.
  • Xylanase is the name given to a class of enzymes which degrade the linear polysaccharide beta-1,4-xylan into xylose, thus breaking down hemicellulose, one of the major components of plant cell walls.
  • the xylanase for use in the present invention may be any commercially available xylanase.
  • the xylanase may be an endo-1,4- ⁇ -d-xylanase (classified as E.C. 3.2.1.8).
  • the xylanase is an endoxylanase, e.g. an endo-1,4- ⁇ -d-xylanase.
  • the classification for an endo-1,4- ⁇ -d-xylanase is E.C. 3.2.1.8.
  • the present invention relates to a DFM in combination with an endoxylanase, e.g. an endo-1,4- ⁇ -d-xylanase, and another enzyme.
  • an endoxylanase e.g. an endo-1,4- ⁇ -d-xylanase
  • the xylanase for use in the present invention may be a xylanase from Bacillus or Trichoderma.
  • the xylanase may be a xylanase comprising (or consisting of) an amino acid sequence shown herein as SEQ ID No. 1, a xylanase comprising (or consisting of) an amino acid sequence shown herein as SEQ ID No. 2 or a xylanase comprising (or consisting of) an amino acid sequence shown herein as SEQ ID No. 3 (FveXyn4), a xylanase from Trichoderma reesei , Econase XTTM or Rovabio ExcelTM.
  • the xylanase may be the xylanase in Axtra XAP® or Avizyme 1502® or AxtraXBTM, both commercially available products from Danisco A/S.
  • the xylanase may be a xylanase comprising (or consisting of) a polypeptide sequence shown herein as SEQ ID No. 1, SEQ ID No. 2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, SEQ ID No. 7, SEQ ID No. 8, SEQ ID No. 9, SEQ ID No. 10, SEQ ID No. 11, or SEQ ID No. 12; or a variant, homologue, fragment or derivative thereof having at least 75% identity (such as at least 80%, 85%, 90%, 95%, 98% or 99% identity) with SEQ ID No. 1 or SEQ ID No. 2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No.
  • the xylanase may comprise a polypeptide sequence shown herein as SEQ ID No. 1, SEQ ID No. 2 or SEQ ID No. 3, or a variant, homologue, fragment or derivative thereof having at least 98.5% (e.g. at least 98.8 or 99 or 99.1 or 99.5%) identity with SEQ ID No. 1 or SEQ ID No. 2 or SEQ ID No. 3
  • SEQ ID No. 1 mklssflytaslvaa QAADSINKLIKNKGKLYYGTITDPNLLGVAKDTAIIKADFGAVTPEN SGKWDATEPSQGKFNFGSFDQVVNFAQQNGLKVRGHTLVWHSQLPQWVKNINDKATLTK VIENHVTQVVGRYKGKIYAWDVVNEIFEWDGTLRKDSHFNNVFGNDDYVGIAFRAARKADP NAKLYINDYSLDSGSASKVTKGMVPSVKKWLSQGVPVDGIGSQTHLDPGAAGQIQGALTAL ANSGVKEVAITELDIRTAPANDYATVTKACLNVPKCIGITVWGVSDKNSWRKEHDSLLFDAN YNPKPAYTAVVNALR SEQ ID No.
  • the xylanase is present in the feedstuff in range of about 500XU/kg to about 16,000XU/kg feed, more preferably about 750XU/kg feed to about 8000XU/kg feed, and even more preferably about 1000XU/kg feed to about 4000XU/kg feed
  • the xylanase is present in the feedstuff at more than about 500XU/kg feed, suitably more than about 600XU/kg feed, suitably more than about 700XU/kg feed, suitably more than about 800XU/kg feed, suitably more than about 900XU/kg feed, suitably more than about 1000XU/kg feed.
  • the xylanase is present in the feedstuff at less than about 16,000XU/kg feed, suitably less than about 8000XU/kg feed, suitably less than about 7000XU/kg feed, suitably less than about 6000XU/kg feed, suitably less than about 5000XU/kg feed, suitably less than about 4000XU/kg feed.
  • the xylanase is present in the feed additive composition in range of about 100XU/g to about 320,000XU/g composition, more preferably about 300XU/g composition to about 160,000XU/g composition, and even more preferably about 500XU/g composition to about 50,000 XU/g composition, and even more preferably about 500XU/g composition to about 40,000 XU/g composition.
  • the xylanase is present in the feed additive composition at more than about 100XU/g composition, suitably more than about 200XU/g composition, suitably more than about 300XU/g composition, suitably more than about 400XU/g composition, suitably more than about 500XU/g composition.
  • the xylanase is present in the feed additive composition at less than about 320,000XU/g composition, suitably less than about 160,000XU/g composition, suitably less than about 50,000XU/g composition, suitably less than about 40,000XU/g composition, suitably less than about 30000XU/g composition.
  • xylanase activity can be expressed in xylanase units (XU) measured as taught in the “Xylanase Activity Assay (XU)” taught herein. See also Bailey, M. J. Biely, P. and Poutanen, K., Journal of Biotechnology, Volume 23, (3), May 1992, 257-270 the teaching of which is incorporated herein by reference.
  • the enzyme is classified using the E.C. classification above, and the E.C. classification designates an enzyme having that activity when tested in the “Xylanase Activity Assay (XU)” taught herein for determining 1 XU.
  • E.C. classification designates an enzyme having that activity when tested in the “Xylanase Activity Assay (XU)” taught herein for determining 1 XU.
  • the xylanase for use in the present invention may have xylanase activity as determined using the “Xylanase Activity Assay (ABX U/g)” taught herein.
  • the feed additive composition may comprise a DFM in combination with a xylanase and a ⁇ -glucanase.
  • xylanase activity may be calculated using the “Xylanase Activity Assay (XU)” taught herein.
  • ⁇ -glucanase activity may be calculated using the “ ⁇ -glucanase Activity Assay (BGU)” taught herein.
  • the DFM in combination with a xylanase and a ⁇ -glucanase may be dosed as set out in the table below:
  • Dosage of constituent per g or per kg of final feedstuff Xylanase (e.g. endo-1,4- 500-16000 XU/kg ⁇ -d-xylanase) activity (preferably 2500-4000 XU/kg) ⁇ -glucanase activity 50-5000 BGU/kg (preferably 200-400 BGU/kg)
  • DFM 1 ⁇ 10 4 -1 ⁇ 10 9 CFU/g preferably 5 ⁇ 10 4 -5 ⁇ 10 8 CFU/g
  • the enzyme activity presented in units may be calculated for each enzyme as taught in tne preceding sections.
  • the feed additive composition may comprise a DFM in combination with a xylanase, a ⁇ -glucanase and a further fibre degrading enzyme as taught herein.
  • DFM DFM
  • xylanase xylanase
  • ⁇ -glucanase ⁇ -glucanase
  • further fibre degrading enzyme may be dosed as set out in the table below:
  • Dosage of constituent per g or per kg of final feedstuff Xylanase e.g. endo-1,4- 500-16000 (preferably ⁇ -d-xylanase) activity 2500-4000 XU/kg) ⁇ -glucanase activity 100-2500 CMC U/kg (preferably 800-1000 CMC U/kg)
  • DFM 1 ⁇ 10 3 -1 ⁇ 10 9 CFU/g preferably 5 ⁇ 10 4 -5 ⁇ 10 8 CFU/g
  • Further fibre degrading enzymes >800 ABX U/kg preferably >1200 (e.g. of another xylanase and a ABX U/kg) beta-glucosidase) >500 pNPG U/kg (preferably >800 pNPG U/kg)
  • a xylanase at at least 1000 XU/kg to 5000 XU/kg (suitably at at least 2000 XU/kg to 4500 XU/kg) of feed; a ⁇ -glucanase at at least 100 BGU/kg to 4000 BGU/kg (suitably at at least 150 BGU/kg to 3000 BGU/kg); and a DFM as taught herein at at least 50,000 CFU/g to 200,000 CFU/g (suitably at at least 70,000 CFU/g to 175,000 CFU/g) of feed.
  • a xylanase at at least 1000 XU/kg to 5000 XU/kg (suitably at at least 2000 XU/kg to 4500 XU/kg) of feed; a ⁇ -glucanase at at least 100 BGU/kg to 4000 BGU/kg (suitably at at least 150 BGU/kg to 3000 BGU/kg); and a DFM as taught herein at at least 37,500 CFU/g to 100,000 CFU/g (suitably at at least 37,500 CFU/g to 75,000 CFU/g) of feed.
  • a xylanase at at least 1000 XU/kg to 5000 XU/kg (suitably at at least 2000 XU/kg to 4500 XU/kg) of feed; a ⁇ -glucanase at at least 200-2000 CMC U/kg (suitably at least 500-1500 CMC U/kg) of feed; a DFM as taught herein at at least 50,000 CFU/g to 200,000 CFU/g (suitably at at least 70,000 CFU/g to 175,000 CFU/g) of feed; and a further fibre degrading enzyme mix comprising at least 800-3500 ABX U/kg (suitably at least 1000-2750 ABX U/g) of feed and 500-3000 pNPG U/kg (suitably at least 600-2000 pNPG U/kg) of feed.
  • a xylanase at at least 1000 XU/kg to 5000 XU/kg (suitably at at least 2000 XU/kg to 4500 XU/kg) of feed; a ⁇ -glucanase at at least 200-2000 CMC U/kg (suitably at least 500-1500 CMC U/kg) of feed; a DFM as taught herein at at least 37,500 CFU/g to 100,000 CFU/g (suitably at at least 37,500 CFU/g to 75,000 CFU/g) of feed; and a further fibre degrading enzyme mix comprising at least 800-3500 ABX U/kg (suitably at least 1000-2750 ABX U/g) of feed and 500-3000 pNPG U/kg (suitably at least 600-2000 pNPG U/kg) of feed.
  • the DFM may be dosed in accordance with the number of units of xylanase present in the composition. In one embodiment the DFM may be dosed in the range from 6.25 ⁇ 10 1 CFU DFM: 1 XU enzyme to 2 ⁇ 10 9 CFU DFM: 1 XU enzyme; preferably in the range from 1.88 ⁇ 10 4 CFU DFM: 1 XU enzyme to 1.0 ⁇ 10 7 CFU DFM: 1 XU enzyme.
  • the DFM taught herein may be used in combination with a xylanase and a ⁇ -glucanase.
  • the DFM taught herein may be used in combination with a xylanase, a ⁇ -glucanase and a further fibre degrading enzyme.
  • the further fibre degrading enzyme may be a ⁇ -glucosidase.
  • the xylanase for use in the present invention may have xylanase activity as determined using the “Xylanase Activity Assay (ABX U/g)” taught herein.
  • the ⁇ -glucanase for use in the present invention may have ⁇ -glucanase activity as determined using the “ ⁇ -glucanase Activity Assay (CMC U/g)” taught herein.
  • the ⁇ -glucosidase for use in the present invention may have ⁇ -glucosidase activity as determined using the “ ⁇ -glucosidase Activity Assay (pNPG U/g)” taught herein.
  • the DFM taught herein may be used in combination with a xylanase and a ⁇ -glucanase, wherein the xylanase and ⁇ -glucanase have the activities set out in the tables below:
  • Range of activity in Units/g of each enzyme activity in the composition Xylanase e.g endo-1,4- 1500-6000 ABX U/g 1 ⁇ -d-xylanase activity ⁇ -glucanase activity 500-4000 CMC U/g 2 Xylanase (e.g.
  • endo-1,4- 2000-6000 ABX U/g 1 ⁇ -d-xylanase) activity (preferably >3000 ABX u/g) ⁇ -glucanase activity 1000-3500 CMC U/g 2 (preferably about 2000-2600) CMC u/g) 1
  • One ABX unit is defined as the amount of enzyme required to generate 1 ⁇ mol of xylose reducing sugar equivalents per minute at 50° C. and pH 5.3. 2
  • One CMC unit of activity liberates 1 ⁇ mol of reducing sugars (expressed as glucose equivalents) in one minute at 50° C. and pH 4.8.
  • the DFM taught herein may be used in combination with a xylanase, a ⁇ -glucanase and a ⁇ -glucosidase wherein the xylanase, ⁇ -glucanase and ⁇ -glucosidase have the activities set out in the tables below:
  • Xylanase e.g. endo-1,4- ⁇ -d-xylanase 1500-6000 ABX U/g 1 activity ⁇ -glucanase activity 500-4000 CMC U/g 2 ⁇ -glucosidase activity 200-3500 pNPG U/g 3 Xylanase (e.g.
  • ABX U/g 1 activity preferably >3000 ABX U/g) ⁇ -glucanase activity 1000-3500 CMC U/g 2 (preferably about 2000-2600) CMC U/g) ⁇ -glucosidase activity 300-3000 pNPG U/g 3 (preferably >2000 pNPG U/g) 1
  • One ABX unit is defined as the amount of enzyme required to generate 1 ⁇ mol of xylose reducing sugar equivalents per minute at 50° C. and pH 5.3. 2
  • One CMC unit of activity liberates 1 ⁇ mol of reducing sugars (expressed as glucose equivalents) in one minute at 50° C. and pH 4.8.
  • One pNPG unit denotes 1 ⁇ mol of nitro-phenol liberated from para-nitrophenyl-B-D-glucopyranoside per minute at 50° C.and pH 4.8.
  • the xylanase and ⁇ -glucanase for use in the present invention may comprise (or consist essentially of, or consist of) more than about 3000 ABX u/g of xylanase activity and about 2000-2600 CMC u/g of ⁇ -glucanase activity, respectively.
  • the xylanase, ⁇ -glucanase and ⁇ -glucosidase for use in the present invention may comprise (or consist essentially of, or consist of) more than about 3000 ABX u/g of xylanase activity, about 2000-2600 CMC u/g of 3-glucanase activity and more than about 2000 pNPG u/g of ⁇ -glucosidase activity, respectively.
  • the xylanase for use in the present invention may comprise (or consist essentially of, or consist of) at least 2000 ABX u/g xylanase activity (suitably at least 2500 ABX u/g activity, suitably at least 3000 ABX u/g activity) as determined using the “Xylanase Activity Assay (ABX U/g)”.
  • the xylanase for use in the present invention may comprise (or consist essentially of, or consist of) about 2000 to about 5000 ABX u/g xylanase activity (suitably at least about 2500 to about 4000 ABX u/g activity, suitably at least about 3000 to about 4000 ABX u/g activity) as determined using the “Xylanase Activity Assay (ABX U/g)”.
  • the ⁇ -glucanase for use in the present invention may comprise (or consist essentially of, or consist of) at least 1000 CMC u/g ⁇ -glucanase activity (suitably at least 1500 CMC u/g activity, suitably at least 2000 CMC u/g activity) as determined using the “ ⁇ -glucanase Activity Assay (CMC U/g)”.
  • the ⁇ -glucanase for use in the present invention may comprise (or consist essentially of, or consist of) about 600 to about 4000 CMC u/g ⁇ -glucanase activity (suitably at least about 1000 to about 3000 CMC u/g activity, suitably at least about 1500 to about 2600 CMC u/g activity) as determined using the “ ⁇ -glucanase Activity Assay (CMC U/g)”.
  • the ⁇ -glucosidase for use in the present invention may comprise (or consist essentially of or consist of) at least 300 pNPG u/g ⁇ -glucosidase activity (suitably at least 500 pNPG u/g activity, suitably at least 1000 pNPG u/g activity or suitably at least 2000 pNPG u/g activity) as determined using the “ ⁇ -glucosidase Activity Assay(pNPG U/g)”.
  • the ⁇ -glucosidase for use in the present invention may comprise (or consist essentially of, or consist of) about 200 to about 4000 pNPG u/g ⁇ -glucosidase activity (suitably at least about 300 to about 3000 pNPG u/g activity, suitably at least about 1000 to about 3000 pNPG u/g activity or suitably at least about 2000 to about 3000 pNPG u/g activity) as determined using the “ ⁇ -glucosidase Activity Assay (pNPG U/g)”.
  • the DFM taught herein may be used in combination with a xylanase and a ⁇ -glucanase comprising (or consisting essentially of or consisting of) at least 2000 ABX u/g xylanase activity (suitably at least 2500 ABX u/g activity, suitably at least 3000 ABX u/g activity) as determined using the “Xylanase Activity Assay (ABX U/g)”; and at least 1000 CMC u/g ⁇ -glucanase activity (suitably at least 1500 CMC u/g activity, suitably at least 2000 CMC u/g activity) as determined using the “3-glucanase Activity Assay (CMC U/g)”.
  • the DFM taught herein may be used in combination with a xylanase, a ⁇ -glucanase and a ⁇ -glucosidase comprising (or consisting essentially of, or consisting of) at least 2000 ABX u/g xylanase activity (suitably at least 2500 ABX u/g activity, suitably at least 3000 ABX u/g activity) as determined using the “Xylanase Activity Assay (ABX U/g)”; and at least 1000 CMC u/g ⁇ -glucanase activity (suitably at least 1500 CMC u/g activity, suitably at least 2000 CMC u/g activity) as determined using the “ ⁇ -glucanase Activity Assay (CMC U/g)”; and at least 300 pNPG u/g ⁇ -glucosidase activity (suitably at least 500 pNPG u/g activity, suitably at least 1000 pNPG u///
  • the DFM taught herein may be used in combination with a xylanase and a ⁇ -glucanase comprising (or consisting essentially of, or consisting of) about 2000 to about 5000 ABX u/g xylanase activity (suitably at least about 2500 to about 4000 ABX u/g activity, suitably at least about 3000 to about 4000 ABX u/g activity) as determined using the “Xylanase Activity Assay (ABX U/g)”; and about 600 to about 4000 CMC u/g ⁇ -glucanase activity (suitably at least about 1000 to about 3000 CMC u/g activity, suitably at least about 1500 to about 2600 CMC u/g activity) as determined using the “ ⁇ -glucanase Activity Assay (CMC U/g)”.
  • the DFM taught herein may be used in combination with a xylanase, a ⁇ -glucanase and a ⁇ -glucosidase comprising (or consisting essentially of, or consisting of) about 2000 to about 5000 ABX u/g xylanase activity (suitably at least about 2500 to about 4000 ABX u/g activity, suitably at least about 3000 to about 4000 ABX u/g activity) as determined using the “Xylanase Activity Assay (ABX U/g)”; about 600 to about 4000 CMC u/g ⁇ -glucanase activity (suitably at least about 1000 to about 3000 CMC u/g activity, suitably at least about 1500 to about 2600 CMC u/g activity) as determined using the “ ⁇ -glucanase Activity Assay (CMC U/g)”; and about 200 to about 4000 pNPG u/g ⁇ -glucosidase activity
  • the xylanase activity can be expressed in xylanase units (XU) measured at pH 5.0 with AZCL-arabinoxylan (azurine-crosslinked wheat arabinoxylan, Xylazyme 100 mg tablets, Megazyme) as substrate. Hydrolysis by endo-(1-4)- ⁇ -D-xylanase (xylanase) produces water soluble dyed fragments, and the rate of release of these (increase in absorbance at 590 nm) can be related directly to enzyme activity.
  • XU xylanase units
  • xylanase units are determined relatively to an enzyme standard (Danisco Xylanase, available from Danisco Animal Nutrition) at standard reaction conditions, which are 40° C., 10 min reaction time in Mcllvaine buffer, pH 5.0.
  • the xylanase activity of the standard enzyme is determined as amount of released reducing sugar end groups from an oat-spelt-xylan substrate per min at pH 5.3 and 50° C.
  • the reducing sugar end groups react with 3, 5-Dinitrosalicylic acid and formation of the reaction product can be measured as increase in absorbance at 540 nm.
  • the enzyme activity is quantified relative to a xylose standard curve (reducing sugar equivalents).
  • One xylanase unit (XU) is the amount of standard enzyme that releases 0.5 ⁇ mol of reducing sugar equivalents per min at pH 5.3 and 50° C.
  • the xylanase activity can be expressed in acid birchwood xylanase units (ABX U) measured at pH 5.3 with birchwood 4-O methyl glucuronoxylan as substrate.
  • Pipette 1.8 ml of 1% birchwood 4-O methyl glucuronoxylan substrate solution into each test tube. Incubate for 10-15 minutes, allowing to equilibrate at 50° C. Pipette 0.2 ml of enzyme dilution using positive displacement pipettes or equivalent. Vortex to mix. Incubate each sample at 50° C. for exactly 5 minutes. Add 3 ml of 1% 3,5 nitrosalicylic acid sodium salt (DNS) solution and mix.
  • DNS 3,5 nitrosalicylic acid sodium salt
  • test tubes Cover the tops of the test tubes with caps to prevent evaporation. Place test tubes in a boiling bath for exactly 5 minutes. Cool test tubes for 10 minutes in ice/water bath. Incubate test tube for 10 minutes at room temperature. Transfer test tube contents to cuvettes and measure at 540 nm against deionised water. Correct the absorbance for background colour by subtracting the corresponding enzyme blank. The enzyme activity is quantified relative to a xylose standard curve (reducing sugar equivalents).
  • One ABX unit is defined as the amount of enzyme required to generate 1 ⁇ mol of xylose reducing sugar equivalents per minute at 50° C. and pH 5.3.
  • the ⁇ -glucanase activity can be expressed in CMC units measured at pH 4.8 with carboxylmethyl cellulose sodium salt (CMC) as substrate.
  • CMC carboxylmethyl cellulose sodium salt
  • Pipette 1 ml of 1% carboxylmethyl cellulose sodium salt (CMC) solution prepared with 0.05M sodium acetate buffer
  • CMC carboxylmethyl cellulose sodium salt
  • After 10 minute add 3 ml of 1% 3,5 dinitrosalicylic acid sodium salt (DNS) in the same order and timing as the enzyme addition to the sample tubes. Add 3 ml of DNS to the sample blank tubes.
  • DNS 3,5 dinitrosalicylic acid sodium salt
  • One CMC unit of activity liberates 1 ⁇ mol of reducing sugars (expressed as glucose equivalents) in one minute at 50° C. and pH 4.8.
  • the beta-glucanase activity can be expressed in beta-glucanase units (BGU) measured at pH 5.0 with AZCL-glucan (azurine-cross linked barley ⁇ -glucan, Glucazyme 100 mg tablets, Megazyme) as substrate. Hydrolysis by beta-glucanase produces soluble dyed fragments, and the rate of release of these (increase in absorbance at 590 nm) can be related directly to enzyme activity.
  • the beta-glucanase units (BGU) are determined relatively to an enzyme standard (Multifect BGL, available from Danisco Animal Nutrition) at standard reaction conditions, which are 50° C., 10 min reaction time in 0.1 M acetate buffer, pH 5.0.
  • the beta-glucanase activity of the standard enzyme is determined as amount of released reducing sugar end groups from a barley glucan substrate per min at pH 5.0 and 50° C.
  • the reducing sugar end groups react with 3,5-Dinitrosalicylic acid and formation of the reaction product can be measured as an increase in absorbance at 540 nm.
  • the enzyme activity is quantified relative to a glucose standard curve (reducing sugar equivalents).
  • One beta-glucanase unit (BGU) is the amount of standard enzyme that releases 2.4 ⁇ mol of reducing sugar equivalents per min at pH 5.0 and 50° C.
  • the ⁇ -glucosidase activity can be expressed in pNPG units measured at pH 4.8 with para-nitrophenyl-B-D-glucopyranoside (pNPG) as substrate.
  • Pipette 1 ml of 3% nitrophenyl-beta-D-glucopyranoside (pNPG) solution (prepared with 0.05M sodium acetate buffer) into duplicate test tubes for each sample and control. Place into 50° C. water bath for 5 minutes. Add 200 ⁇ l of control or sample to their respective duplicate tubes at intervals of 15-30 seconds. To the reagent blank tube, add 200 ⁇ l of sodium acetate buffer. Vortex each tube after addition of sample. Let the tubes incubate for exactly 10 minutes.
  • One pNPG unit denotes 1 ⁇ mol of nitro-phenol liberated from para-nitrophenyl-B-D-glucopyranoside per minute at 50° C. and pH 4.8.
  • feedstuffs comprising substantial quantities (sometimes 30-60%) of fibrous by-products (having a high content of non-starch polysaccharides, e.g. fibre) can be significantly improved, as can the performance and weight gain of a subject fed such feedstuffs.
  • One advantage of the present invention is the improvement of feed conversion ratio (FCR) observed by using the combination of the present invention.
  • the degradation of dietary material derived from plant cell wall particles which is high in non-starch polysaccharides (NSP) by xylanases can be optimized for improved animal performance when combining xylanase (e.g. endo-1,4- ⁇ -d-xylanase) with one or more ⁇ -glucanase (and optionally in combination with one or more further fibre degrading enzymes (e.g. a cellobiohydrolase (E.C. 3.2.1.176 and E.C. 3.2.1.91), a ⁇ -glucosidase (E.C. 3.2.1.21), a ⁇ -xylosidase (E.C.
  • xylanase e.g. endo-1,4- ⁇ -d-xylanase
  • ⁇ -glucanase e.g. a cellobiohydrolase (E.C. 3.2.1.176 and E.C. 3.2.1.91)
  • feruloyl esterase E.C. 3.1.1.73
  • ⁇ -arabinofuranosidase E.C. 3.2.1.55
  • pectinase e.g. an endopolygalacturonase (E.C. 3.2.1.15), an exopolygalacturonase (E.C. 3.2.1.67) or a pectate lyase (E.C.
  • DFMs specific direct fed-microbials selected for their capacity to produce enzymes and/or their capacity of producing Short Chain Fatty Acids (SCFA) from NSP fraction pentoses in anaerobic conditions and/or their capacity to promote endogenous populations of fibrolytic microflora in a subject's GIT and/or their capacity to degrade C5-sugars.
  • SCFA Short Chain Fatty Acids
  • the energy value from plant products can be optimized by combining xylanase (e.g. endo-1,4- ⁇ -d-xylanase) and ⁇ -glucanase (and optionally at least one other fibre degrading enzyme (including but not limited to a cellobiohydrolase (E.C. 3.2.1.176 and E.C. 3.2.1.91), a ⁇ -glucosidase (E.C. 3.2.1.21), a ⁇ -xylosidase (E.C.
  • DFMs that can produce SCFAs from NSP fraction pentoses in anaerobic conditions and/or that can modulate the microbial populations in the GIT to increase SCFA production from the sugars released and/or that can utilise C-5 sugars.
  • the DFMs may adapt their metabolism to synergistically increase the fibre hydrolysis in combination with xylanase and ⁇ -glucanase (and optionally at least one further fibre degrading enzyme).
  • DFMs that can produce (fibrolytic) enzymes can provide additional benefits and maximize the benefits of the added enzymes.
  • Specific DFMs selected for their enzymatic activities can be considered as a glycan-driven bacterial food chain.
  • the specifically selected DFMs taught herein may preferentially utilize dietary fibres, a trait that allows them to carry out the initial glycan digestion steps to liberate shorter, more soluble polysaccharides for other bacteria, e.g. other endogenous GIT microflora.
  • the specific DFMs have been selected for their metabolism which adjusts according to the glycans released by enzymes (e.g.
  • xylanase and ⁇ -glucanase (and optionally at least one further fibre degrading enzyme)) to improve the efficacy of the enzymes taught herein and the DFM(s) combination compared to use of a combination of enzymes alone or the use of DFM(s) alone.
  • dietary material derived from plant cell wall particles which is rich in source-specific glycans such as cellulose, hemicellulose and pectin (plant material) or glycosaminoglycans enter the distal gut in particulate forms that are attacked by the specific DFMs glycan degraders which are capable of directly binding to these insoluble particles and digesting their glycan components.
  • DFMs glycan degraders which are capable of directly binding to these insoluble particles and digesting their glycan components.
  • more-soluble glycan fragments can be digested by secondary glycan degraders present in the caecum, which contribute to the liberated pool of short-chain fatty acid (SCFA) fermentation products that is derived from both types of degraders.
  • SCFA short-chain fatty acid
  • SCFA concentration can be an index of the anaerobic-organism population.
  • SCFA may actually provide a number of benefits to the host animal, acting as metabolic fuel for intestine, muscle, kidney, heart, liver and brain tissue, and also affording bacteriostatic and bacteriocidal properties against organisms such as Salmonella and E. coli.
  • the nutritional value of fibre in non-ruminants can mainly be derived through short chain fatty acids (SCFA) production via fermentation of solubilized or degraded fibres by effective fibre degrading enzymes (e.g. xylanases and ⁇ -glucanase and/or a further fibre degrading enzyme as taught herein).
  • SCFA short chain fatty acids
  • Feed xylanase alone is not enough to use fibrous ingredients in animal (especially non-ruminant) diets.
  • a large array of chemical characteristics exists among plant-based feed ingredients. Enzyme application depends on the characteristics of the plant (feed) material.
  • SCFAs have different energy values and some can serve as precursors of glucose and some can contribute to the maintenance of intestinal integrity and health.
  • the inventors have found that the specific combinations taught herein preferentially move the fermentation process in an animal's GIT towards the production of more valuable/useful SCFA.
  • NSPs can be effectively degraded by a combination of a DFM according to the present invention and a xylanase and a ⁇ -glucanase (and optionally at least one further fibre degrading enzyme).
  • this specific combination releases C-5 sugars which usually have only marginal nutritional value to the animal.
  • microorganisms in the GIT either the DFM of the present invention
  • endogenous fibrolytic microflora which are stimulated by the combinations (of DFM) of the present invention
  • These short chain fatty acids can be utilised by the animal.
  • the system improves the nutritional value of a feedstuff for an animal.
  • the combination of a direct fed microbial, a xylanase and a ⁇ -glucanase increases fibre degradation in a feed additive composition, premix, feed or feedstuff, which leads to improved performance of a subject.
  • the combination of the present invention improves digestibility of a raw material in a feed resulting in an increase in nutrient bioavailability (e.g. nutrient digestibility) and metabolizable energy therein.
  • the DFM of the present invention and the enzymes may be formulated in any suitable way to ensure that the formulation comprises viable DFMs and active enzymes.
  • the DFM and enzymes may be formulated as a dry powder or a granule.
  • the dry powder or granules may be prepared by means known to those skilled in the art, such as in a microingredients mixer.
  • the DFM and/or the enzyme(s) may be coated, for example encapsulated.
  • the DFM and enzymes may be formulated within the same coating or encapsulated within the same capsule.
  • one or two or three or four of the enzymes may be formulated within the same coating or encapsulated within the same capsule and the DFM could be formulated in a coating separate to the one or more or all of the enzymes.
  • the DFM may be provided without any coating.
  • the DFM endospores may be simply admixed with one or two or three or four enzymes. In the latter case, the enzymes may be coated, e.g.
  • the enzymes may be coated, e.g. encapsulated.
  • the enzymes may be encapsulated as mixtures (i.e. comprising one or more, two or more, three or more or all) of enzymes or they may be encapsulated separately, e.g. as single enzymes. In one preferred embodiment all four enzymes may be coated, e.g. encapsulated, together.
  • the coating protects the enzymes from heat and may be considered a thermoprotectant.
  • the feed additive composition is formulated to a dry powder or granules as described in WO2007/044968 (referred to as TPT granules) incorporated herein by reference.
  • the DFM (e.g. DFM endospores for example) may be diluted using a diluent, such as starch powder, lime stone or the like.
  • the feed additive composition may be formulated by applying, e.g. spraying, the enzyme(s) onto a carrier substrate, such as ground wheat for example.
  • the feed additive composition according to the present invention may be formulated as a premix.
  • the premix may comprise one or more feed components, such as one or more minerals and/or one or more vitamins.
  • the DFM and/or enzymes for use in the present invention are formulated with at least one physiologically acceptable carrier selected from at least one of maltodextrin, limestone (calcium carbonate), cyclodextrin, wheat or a wheat component, sucrose, starch, Na 2 SO 4 , Talc, PVA, sorbitol, benzoate, sorbiate, glycerol, sucrose, propylene glycol, 1,3-propane diol, glucose, parabens, sodium chloride, citrate, acetate, phosphate, calcium, metabisulfite, formate and mixtures thereof.
  • at least one physiologically acceptable carrier selected from at least one of maltodextrin, limestone (calcium carbonate), cyclodextrin, wheat or a wheat component, sucrose, starch, Na 2 SO 4 , Talc, PVA, sorbitol, benzoate, sorbiate, glycerol, sucrose, propylene glycol, 1,3-propane di
  • the feed additive composition and/or premix and/or feed or feedstuff according to the present invention is packaged.
  • the feed additive composition and/or premix and/or feed or feedstuff is packaged in a bag, such as a paper bag.
  • the feed additive composition and/or premix and/or feed or feedstuff may be sealed in a container. Any suitable container may be used.
  • the animal feed industry has seen an increased feeding of by-products, e.g. from biofuel processing, to animals (raising this form of animal feed from 0-10% to the current extremes of 30-60%).
  • the by-products are often high fibre (e.g. at least approximately 40% fibre) products. Consequently the inclusion of high-fibre by-product (e.g. DDGS) can have negative impact on animal growth performance and carcass characteristics.
  • high-fibre by-product e.g. DDGS
  • alterations in nutrient digestibility have implications for manure (e.g. swine-manure) handling, storage and decomposition.
  • by-product means any fibrous plant material, e.g. one which comprises at least approximately 20% or 30% fibre).
  • by-product means any by-product of a high fibre feed material.
  • the by-product as referred to herein may be selected from one or more of the following products: corn germ meal, corn bran, Hominy feed, corn gluten feed, Distillers Dried Grain Solubles (DDGS), Distillers Dried Grain (DDG), gluten meal, wheat shorts, wheat middlings or combinations thereof.
  • DDGS Distillers Dried Grain Solubles
  • DDG Distillers Dried Grain
  • the feedstuff of the present invention comprises a fibrous by-product such as corn germ meal, corn bran, Hominy feed, corn gluten feed, Distillers Dried Grain Solubles (DDGS), Distillers Dried Grain (DDG), gluten meal, wheat shorts, wheat middlings or combinations thereof.
  • a fibrous by-product such as corn germ meal, corn bran, Hominy feed, corn gluten feed, Distillers Dried Grain Solubles (DDGS), Distillers Dried Grain (DDG), gluten meal, wheat shorts, wheat middlings or combinations thereof.
  • the subject to which the DFM, xylanase and ⁇ -glucanase (and optionally at least one further fibre degrading enzyme) combination of the present invention or feed additive composition of the present invention is administered is also fed a feedstuff comprising a fibrous by-product such as corn germ meal, corn bran, Hominy feed, corn gluten feed, Distillers Dried Grain Solubles (DDGS), Distillers Dried Grain (DDG), gluten meal, wheat shorts, wheat middlings or combinations thereof.
  • a feedstuff comprising a fibrous by-product such as corn germ meal, corn bran, Hominy feed, corn gluten feed, Distillers Dried Grain Solubles (DDGS), Distillers Dried Grain (DDG), gluten meal, wheat shorts, wheat middlings or combinations thereof.
  • the enzyme (or composition comprising the enzyme) of the present invention or as disclosed herein may be used to breakdown (degrade) insoluble arabinoxylan (AXinsol) or soluble arabinoxylan (AXsol) or combinations thereof, or degradation products of AXinsol.
  • breakdown or “degrade” in synonymous with hydrolyses.
  • NSPs Non-Starch Polysaccharides
  • carbohydates A major part of common vegetable feed ingredients consists of carbohydrates, making carbohydates a crucial factor in animal production. Beside well digestible nutrients, such as starch and sugars, the carbohydrate fraction of vegetable origin includes indigestible (fibrous) components, such as cellulose, hemicellulose, pectins, beta-glucans and lignin.
  • indigestible (fibrous) components such as cellulose, hemicellulose, pectins, beta-glucans and lignin.
  • NSPs non-starch polysaccharides
  • fibre may be used interchangeably with the term NSPs.
  • hemicellulose itself is a heterogenous subgroup predominantly made up of xylans, arabinans, galatans, glucans and mannans.
  • Arabinoxylan is the principal NSP-fraction in several of the most important feed raw materials, including wheat and corn.
  • arabinoxylans as used herein means a polysaccharide consisting of a xylan backbone (1,4-linked xylose units) with L-arabinofuranose (L-arabinose in its 5-atom ring form) attached randomly by 1 ⁇ 2 and/or 1 ⁇ 3 linkages to the xylose units throughout the chain.
  • Arabinoxylan is a hemicellulose found in both the primary and secondary cell walls of plants. Arabinoxylan can be found in the bran of grains such as wheat, maize (corn), rye, and barley.
  • Arabinoxylan (AX) is found in close association with the plant cell wall, where it acts as a glue linking various building blocks of the plant cell wall and tissue, give it both structural strength and rigidity.
  • arabinoxylans are usually classified as pentosans.
  • AX is the principal Non Starch Polysaccharide (NSP)-fraction in several of the most important feed raw material, including wheat and corn.
  • AX an important anti-nutritional factor, reducing animal production efficiency.
  • AXs can also hold substantial amounts of water (which can be referred to as their water holding capacity)—this can cause soluble arabinoxylans to result in (high) viscosity—which is a disadvantage in many applications.
  • Water-insoluble arabinoxylan also known as water-unextractable arabinoxylan (WU-AX) constitutes a significant proportion of the dry matter of plant material.
  • wheat AXinsol can account for 6.3% of the dry matter. In wheat bran and wheat DDGS AXinsol can account for about 20.8% or 13.4% of the dry matter (w/w).
  • corn AXinsol can account for 5.1% of the dry matter. In corn DDGS AXinsol can account for 12.6% of the dry matter.
  • AXinsol causes nutrient entrapment in feed. Large quantities of well digestible nutrients such as starch and proteins remain either enclosed in clusters of cell wall material or bound to side chains of the AX. These entrapped nutrients will not be available for digestion and subsequent absorption in the small intestine.
  • AXsol Water-soluble arabinoxylan
  • WE-AX water extractable arabinoxylan
  • feed AXsol can have an anti-nutritional effect particularly in monogastrics as they cause a considerable increase of the viscosity of the intestinal content, caused by the extraordinary water-binding capacity of AXsol.
  • the increase viscosity can affect feed digestion and nutrient use as it can prevent proper mixing of feed with digestive enzymes and bile salts and/or it slows down nutrient availability and absorption and/or it stimulates fermentation in the hindgut.
  • wheat AXsol can account for 1.8% of the dry matter. In wheat bran and wheat DDGS AXsol can account for about 1.1% or 4.9% of the dry matter (w/w).
  • corn AXsol can account for 0.1% of the dry matter. In corn DDGS AXinsol can account for 0.4% of the dry matter.
  • xylanases have the ability to both solubilise AXinsol as well as to rapidly and efficiently breakdown the solubilised oligomers and/or pentosans thus the enzymes are able to solubilise AXinsol without increasing viscosity and/or decreasing viscosity.
  • a breakdown of AXsol can decrease viscosity.
  • a breakdown of AXsol can release nutrients.
  • the present invention can be used to reduce viscosity in any process where the water-binding capacity of AXsol causes an undesirable increase in viscosity.
  • the present invention relates to reducing viscosity by breaking down (degrading) AXsol or by breaking down (degrading) the polymers and/or oligomers produced by solubilising AXinsol.
  • a reduction in viscosity can be calculated by comparing one sample comprising the xylanase of the present invention (or taught herein) compared with another comparable sample without the xylanase of the present invention (or taught herein).
  • the xylanases taught herein are viscosity reducers.
  • the enzyme or feed additive composition of the present invention may be used as—or in the preparation of—a feed.
  • feed is used synonymously herein with “feedstuff”.
  • the feedstuff of the present invention comprises high fibre feed material and/or at least one by-product of the at least one high fibre feed material such as corn germ meal, corn bran, Hominy feed, corn gluten feed, Distillers Dried Grain Solubles (DDGS), Distillers Dried Grain (DDG), gluten meal, wheat shorts, wheat middlings or combinations thereof.
  • high fibre feed material such as corn germ meal, corn bran, Hominy feed, corn gluten feed, Distillers Dried Grain Solubles (DDGS), Distillers Dried Grain (DDG), gluten meal, wheat shorts, wheat middlings or combinations thereof.
  • the subject to which the DFM, xylanase and ⁇ -glucanase combination (optionally in combination a further fibre degrading enzyme) of the present invention or feed additive composition of the present invention is administered is also fed a feedstuff comprising a high fibre feed material and/or at least one by-product of the at least one high fibre feed material such as corn germ meal, corn bran, Hominy feed, corn gluten feed, Distillers Dried Grain Solubles (DDGS), Distillers Dried Grain (DDG), gluten meal, wheat shorts, wheat middlings or combinations thereof.
  • DDGS Distillers Dried Grain Solubles
  • DDG Distillers Dried Grain
  • gluten meal wheat shorts, wheat middlings or combinations thereof.
  • the cereal component of a poultry subject's diet can be either wheat or barley with rye, wheat middlings, wheat bran, oats, oats hulls whilst vegetable components can be soybean meal with or without other protein ingredients such as canola, rape seed meal, etc. provided that the diet will contain wheat-barley as the main ingredients and formulated to meet the nutrient requirements of the birds being fed.
  • the feed according to the present invention may be in the form of a solution or as a solid—depending on the use and/or the mode of application and/or the mode of administration.
  • the enzyme or composition of the present invention may be used in conjunction with one or more of: a nutritionally acceptable carrier, a nutritionally acceptable diluent, a nutritionally acceptable excipient, a nutritionally acceptable adjuvant, a nutritionally active ingredient.
  • the enzyme or feed additive composition of the present invention is admixed with a feed component to form a feedstuff.
  • feed component means all or part of the feedstuff. Part of the feedstuff may mean one constituent of the feedstuff or more than one constituent of the feedstuff, e.g. 2 or 3 or 4. In one embodiment the term “feed component” encompasses a premix or premix constituents.
  • the feed may be a fodder, or a premix thereof, a compound feed, or a premix thereof.
  • the feed additive composition according to the present invention may be admixed with a compound feed, a compound feed component or to a premix of a compound feed or to a fodder, a fodder component, or a premix of a fodder.
  • fodder means any food which is provided to an animal (rather than the animal having to forage for it themselves). Fodder encompasses plants that have been cut.
  • fodder includes silage, compressed and pelleted feeds, oils and mixed rations, and also sprouted grains and legumes.
  • Fodder may be obtained from one or more of the plants selected from: corn (maize), alfalfa (Lucerne), barley, birdsfoot trefoil, brassicas, Chau moellier, kale, rapeseed (canola), rutabaga (swede), turnip, clover, alsike clover, red clover, subterranean clover, white clover, fescue, brome, millet, oats, sorghum, soybeans, trees (pollard tree shoots for tree-hay), wheat, and legumes.
  • compound feed means a commercial feed in the form of a meal, a pellet, nuts, cake or a crumble.
  • Compound feeds may be blended from various raw materials and additives. These blends are formulated according to the specific requirements of the target animal.
  • Compound feeds can be complete feeds that provide all the daily required nutrients, concentrates that provide a part of the ration (protein, energy) or supplements that only provide additional micronutrients, such as minerals and vitamins.
  • the main ingredients used in compound feed are the feed grains, which include corn, wheat, wheat bran, soybeans, sorghum, oats, and barley.
  • a premix as referred to herein may be a composition composed of microingredients such as vitamins, minerals, chemical preservatives, antibiotics, fermentation products, and other essential ingredients. Premixes are usually compositions suitable for blending into commercial rations.
  • Any feedstuff of the present invention may comprise one or more feed materials selected from the group comprising a) cereals, such as small grains (e.g., wheat, barley, rye, oats, triticale and combinations thereof) and/or large grains such as maize or sorghum; b) by products from cereals, such as corn germ meal, corn bran, Hominy feed, corn gluten feed, Distillers Dried Grain Solubles (DDGS), Distillers Dried Grain (DDG), gluten meal, wheat shorts, wheat middlings or combinations thereof; c) protein obtained from sources such as soya, sunflower, peanut, lupin, peas, fava beans, cotton, canola, fish meal, dried plasma protein, meat and bone meal, potato protein, whey, copra, sesame; d) oils and fats obtained from vegetable and animal sources; e) minerals and vitamins.
  • cereals such as small grains (e.g., wheat, barley, rye, oats,
  • the feedstuff comprises or consists of corn, DDGS (such as cDDGS), wheat, wheat bran or a combination thereof.
  • the feed component may be corn, DDGS (e.g. cDDGS), wheat, wheat bran or a combination thereof.
  • the feedstuff comprises or consists of corn, DDGS (such as cDDGS) or a combination thereof.
  • a feed component may be corn, DDGS (such as corn DDGS (cDDGS)) or a combination thereof.
  • a feedstuff of the present invention may contain at least 30%, at least 40%, at least 50% or at least 60% by weight corn and soybean meal or corn and full fat soy, or wheat meal or sunflower meal.
  • a feedstuff of the present invention may contain between about 5 to about 40% corn DDGS.
  • the feedstuff on average may contain between about 7 to 12% corn DDGS.
  • the feedstuff may contain on average 5 to 40% corn DDGS.
  • a feedstuff of the present invention may contain corn as a single grain, in which case the feedstuff may comprise between about 35% to about 85% corn.
  • the feedstuff may comprise at least 10% corn.
  • a feedstuff of the present invention may comprise at least one high fibre feed material and/or at least one by-product of the at least one high fibre feed material to provide a high fibre feedstuff.
  • high fibre feed materials include: wheat, barley, rye, oats, by products from cereals, such as corn gluten meal, wet-cake, Distillers Dried Grain (DDG), Distillers Dried Grain with Solubles (DDGS), wheat bran, wheat middlings, wheat shorts, rice bran, rice hulls, oat hulls, palm kernel, and citrus pulp.
  • Some protein sources may also be regarded as high fibre: protein obtained from sources such as sunflower, lupin, fava beans and cotton.
  • the feedstuff of the present invention comprises at least one high fibre material and/or at least one by-product of the at least one high fibre feed material selected from the group consisting of Distillers Dried Grain with Solubles (DDGS)—particularly corn DDGS (cDDGS), wet-cake, Distillers Dried Grain (DDG)—particularly corn DDG (cDDG), wheat bran, and wheat for example.
  • DDGS Distillers Dried Grain with Solubles
  • DDG Distillers Dried Grain
  • cDDG corn DDG
  • wheat bran a feedstuff of the present invention
  • the feedstuff of the present invention comprises at least one high fibre material and/or at least one by-product of the at least one high fibre feed material selected from the group consisting of Distillers Dried Grain Solubles (DDGS)—particularly cDDGS, wheat bran, and wheat for example.
  • DDGS Distillers Dried Grain Solubles
  • the feed may be one or more of the following: a compound feed and premix, including pellets, nuts or (cattle) cake; a crop or crop residue: corn, soybeans, sorghum, oats, barley, copra, chaff, sugar beet waste; fish meal; meat and bone meal; molasses; oil cake and press cake; oligosaccharides; conserved forage plants: silage; seaweed; seeds and grains, either whole or prepared by crushing, milling etc.; sprouted grains and legumes; yeast extract.
  • a compound feed and premix including pellets, nuts or (cattle) cake
  • a crop or crop residue corn, soybeans, sorghum, oats, barley, copra, chaff, sugar beet waste
  • fish meal meat and bone meal
  • molasses oil cake and press cake
  • oligosaccharides conserved forage plants: silage; seaweed; seeds and grains, either whole or prepared by crushing, milling etc.; sprouted grains and
  • a pet food is plant or animal material intended for consumption by pets, such as dog food or cat food.
  • Pet food such as dog and cat food, may be either in a dry form, such as kibble for dogs, or wet canned form.
  • Cat food may contain the amino acid taurine.
  • feed in the present invention also encompasses in some embodiments fish food.
  • a fish food normally contains macro nutrients, trace elements and vitamins necessary to keep captive fish in good health.
  • Fish food may be in the form of a flake, pellet or tablet. Pelleted forms, some of which sink rapidly, are often used for larger fish or bottom feeding species.
  • Some fish foods also contain additives, such as beta carotene or sex hormones, to artificially enhance the color of ornamental fish.
  • feed in the present invention also encompasses in some embodiment bird food.
  • Bird food includes food that is used both in birdfeeders and to feed pet birds.
  • bird food comprises of a variety of seeds, but may also encompass suet (beef or mutton fat).
  • the term “contacted” refers to the indirect or direct application of the enzyme (or composition comprising the enzyme) of the present invention to the product (e.g. the feed).
  • the application methods include, but are not limited to, treating the product in a material comprising the feed additive composition, direct application by mixing the feed additive composition with the product, spraying the feed additive composition onto the product surface or dipping the product into a preparation of the feed additive composition.
  • the feed additive composition of the present invention is preferably admixed with the product (e.g. feedstuff).
  • the feed additive composition may be included in the emulsion or raw ingredients of a feedstuff.
  • composition is made available on or to the surface of a product to be affected/treated. This allows the composition to impart one or more of the following favourable characteristics: performance benefits.
  • the enzyme (or composition comprising the enzyme) of the present invention may be applied to intersperse, coat and/or impregnate a product (e.g. feedstuff or raw ingredients of a feedstuff) with a controlled amount of said enzyme.
  • a product e.g. feedstuff or raw ingredients of a feedstuff
  • the feed additive composition may be simply administered to the subject at the same time as feeding the animal a feedstuff.
  • the enzyme (or composition comprising the enzyme) of the present invention will be thermally stable to heat treatment up to about 70° C.; up to about 85° C.; or up to about 95° C.
  • the heat treatment may be performed for up to about 1 minute; up to about 5 minutes; up to about 10 minutes; up to about 30 minutes; up to about 60 minutes.
  • thermally stable means that at least about 75% of the enzyme that was present/active in the additive before heating to the specified temperature is still present/active after it cools to room temperature.
  • at least about 80% of the enzyme that is present and active in the additive before heating to the specified temperature is still present and active after it cools to room temperature.
  • the enzyme (or composition comprising the enzyme) of the present invention is homogenized to produce a powder.
  • the enzyme (or composition comprising the enzyme) of the present invention is formulated to granules as described in WO2007/044968 (referred to as TPT granules) incorporated herein by reference.
  • the feed additive composition when formulated into granules the granules comprise a hydrated barrier salt coated over the protein core.
  • the advantage of such salt coating is improved thermo-tolerance, improved storage stability and protection against other feed additives otherwise having adverse effect on the enzyme.
  • the salt used for the salt coating has a water activity greater than 0.25 or constant humidity greater than 60% at 20° C.
  • the salt coating comprises a Na 2 SO 4 .
  • the method of preparing an enzyme (or composition comprising the enzyme) of the present invention may also comprise the further step of pelleting the powder.
  • the powder may be mixed with other components known in the art.
  • the powder, or mixture comprising the powder may be forced through a die and the resulting strands are cut into suitable pellets of variable length.
  • the pelleting step may include a steam treatment, or conditioning stage, prior to formation of the pellets.
  • the mixture comprising the powder may be placed in a conditioner, e.g. a mixer with steam injection.
  • the mixture is heated in the conditioner up to a specified temperature, such as from 60-100° C., typical temperatures would be 70° C., 80° C., 85° C., 90° C. or 95° C.
  • the residence time can be variable from seconds to minutes and even hours. Such as 5 seconds, 10 seconds, 15 seconds, 30 seconds, 1 minutes 2 minutes., 5 minutes, 10 minutes, 15 minutes, 30 minutes and 1 hour.
  • the enzyme (or composition comprising the enzyme) of the present invention is suitable for addition to any appropriate feed material.
  • the feedstuff may also contain additional minerals such as, for example, calcium and/or additional vitamins.
  • the feedstuff is a corn soybean meal mix.
  • the feed is not pet food.
  • Feedstuff is typically produced in feed mills in which raw materials are first ground to a suitable particle size and then mixed with appropriate additives.
  • the feedstuff may then be produced as a mash or pellets; the later typically involves a method by which the temperature is raised to a target level and then the feed is passed through a die to produce pellets of a particular size. The pellets are allowed to cool. Subsequently liquid additives such as fat and enzyme may be added.
  • Production of feedstuff may also involve an additional step that includes extrusion or expansion prior to pelleting—in particular by suitable techniques that may include at least the use of steam.
  • the feedstuff may be a feedstuff for a monogastric animal, such as poultry (for example, broiler, layer, broiler breeders, turkey, duck, geese, water fowl), swine (all age categories), a pet (for example dogs, cats) or fish, preferably the feedstuff is for poultry.
  • poultry for example, broiler, layer, broiler breeders, turkey, duck, geese, water fowl
  • swine all age categories
  • a pet for example dogs, cats
  • fish preferably the feedstuff is for poultry.
  • the feedstuff may be a feedstuff for a monogastric animal, such as poultry (for example, broiler, layer, broiler breeders, turkey, duck, geese, water fowl), swine (all age categories), a pet (for example dogs, cats) or fish, preferably the feedstuff is for poultry.
  • poultry for example, broiler, layer, broiler breeders, turkey, duck, geese, water fowl
  • swine all age categories
  • a pet for example dogs, cats
  • fish preferably the feedstuff is for poultry.
  • the feedstuff is not for a layer.
  • a feedstuff for chickens e.g. broiler chickens may be comprises of one or more of the ingredients listed in the table below, for example in the % ages given in the table below:
  • a feedstuff laying hens may be comprises of one or more of the ingredients listed in the table below, for example in the % ages given in the table below:
  • a feedstuff for turkeys may be comprises of one or more of the ingredients listed in the table below, for example in the % ages given in the table below:
  • Phase 1 Phase 2 Phase 3 Phase 4 Ingredient (%) (%) (%) (%) (%) (%) (%) (%) (%) (%) (%) Wheat 33.6 42.3 52.4 61.6 Maize DDGS 7.0 7.0 7.0 Soyabean Meal 48% CP 44.6 36.6 27.2 19.2 Rapeseed Meal 4.0 4.0 4.0 4.0 Soyabean Oil 4.4 4.2 3.9 3.6 L-Lysine HCl 0.5 0.5 0.4 0.4 DL-methionine 0.4 0.4 0.3 0.2 L-threonine 0.2 0.2 0.1 0.1 Salt 0.3 0.3 0.3 0.3 0.3 Limestone 1.0 1.1 1.1 1.0 Dicalcium Phosphate 3.5 3.0 2.7 2.0 Poultry Vitamins and Micro- 0.4 0.4 0.4 0.4 minerals
  • a feedstuff for piglets may be comprises of one or more of the ingredients listed in the table below, for example in the % ages given in the table below:
  • a feedstuff for grower/finisher pigs may be comprises of one or more of the ingredients listed in the table below, for example in the % ages given in the table below:
  • Distillers Dried Grains and Distillers Dried Grains with Solubles are products obtained after the removal of ethyl alcohol by distillation from yeast fermentation of a grain or a grain mixture by methods employed in the grain distilling industry.
  • Stillage coming from the distillation (e.g. comprising water, remainings of the grain, yeast cells etc.) is separated into a “solid” part and a liquid part.
  • the solid part is called “wet-cake” and can be used as animal feed as such.
  • the liquid part is (partially) evaporated into a syrup (solubles).
  • Wet-cake may be used in dairy operations and beef cattle feedlots.
  • the dried DDGS may be used in livestock, e.g. dairy, beef and swine) feeds and poultry feeds.
  • Corn DDGS is a very good protein source for dairy cows.
  • the by-product of corn may be corn gluten meal (CGM).
  • CGM corn gluten meal
  • CGM is a powdery by-product of the corn milling inductry.
  • CGM has utility in, for example, animal feed. It can be used as an inexpensive protein source for feed such as pet food, livestock feed and poultry feed. It is an especially good source of the amino acid cysteine, but must be balanced with other proteins for lysine.
  • the feed additive composition of the present invention and/or the feedstuff comprising same may be used in any suitable form.
  • the feed additive composition of the present invention may be used in the form of solid or liquid preparations or alternatives thereof.
  • solid preparations include powders, pastes, boluses, capsules, pellets, tablets, dusts, and granules which may be wettable, spray-dried or freeze-dried.
  • liquid preparations include, but are not limited to, aqueous, organic or aqueous-organic solutions, suspensions and emulsions.
  • the feed additive compositions of the present invention may be mixed with feed or administered in the drinking water.
  • the present invention relates to a method of preparing a feed additive composition, comprising admixing a xylanase, a ⁇ -glucanase (and optionally at least one further fibre degrading enzyme) and a DFM as taught herein with a feed acceptable carrier, diluent or excipient, and (optionally) packaging.
  • the feedstuff and/or feed additive composition may be combined with at least one mineral and/or at least one vitamin.
  • the compositions thus derived may be referred to herein as a premix.
  • the feed additive composition of the present invention and other components and/or the feedstuff comprising same may be used in any suitable form.
  • the feed additive composition of the present invention may be used in the form of solid or liquid preparations or alternatives thereof.
  • solid preparations include powders, pastes, boluses, capsules, pellets, tablets, dusts, and granules which may be wettable, spray-dried or freeze-dried.
  • liquid preparations include, but are not limited to, aqueous, organic or aqueous-organic solutions, suspensions and emulsions.
  • DFM or feed additive compositions of the present invention may be mixed with feed or administered in the drinking water.
  • the dosage range for inclusion into water is about 1 ⁇ 10 3 CFU/animal/day to about 1 ⁇ 10 10 CFU/animal/day, and more preferably about 1 ⁇ 10 7 CFU/animal/day.
  • Suitable examples of forms include one or more of: powders, pastes, boluses, pellets, tablets, pills, capsules, ovules, solutions or suspensions, which may contain flavouring or colouring agents, for immediate-, delayed-, modified-, sustained-, pulsed- or controlled-release applications.
  • composition of the present invention may also contain one or more of: excipients such as microcrystalline cellulose, lactose, sodium citrate, calcium carbonate, dibasic calcium phosphate and glycine; disintegrants such as starch (preferably corn, potato or tapioca starch), sodium starch glycollate, croscarmellose sodium and certain complex silicates; granulation binders such as polyvinylpyrrolidone, hydroxypropylmethylcellulose (HPMC), hydroxypropylcellulose (HPC), sucrose, gelatin and acacia; lubricating agents such as magnesium stearate, stearic acid, glyceryl behenate and talc may be included.
  • excipients such as microcrystalline cellulose, lactose, sodium citrate, calcium carbonate, dibasic calcium phosphate and glycine
  • disintegrants such as starch (preferably corn, potato or tapioca starch), sodium starch glycollate, croscarmellose sodium and certain complex si
  • Examples of nutritionally acceptable carriers for use in preparing the forms include, for example, water, salt solutions, alcohol, silicone, waxes, petroleum jelly, vegetable oils, polyethylene glycols, propylene glycol, liposomes, sugars, gelatin, lactose, amylose, magnesium stearate, talc, surfactants, silicic acid, viscous paraffin, perfume oil, fatty acid monoglycerides and diglycerides, petroethral fatty acid esters, hydroxymethyl-cellulose, polyvinylpyrrolidone, and the like.
  • Preferred excipients for the forms include lactose, starch, a cellulose, milk sugar or high molecular weight polyethylene glycols.
  • composition of the present invention may be combined with various sweetening or flavouring agents, colouring matter or dyes, with emulsifying and/or suspending agents and with diluents such as water, propylene glycol and glycerin, and combinations thereof.
  • Non-hydroscopic whey is often used as a carrier for DFMs (particularly bacterial DFMs) and is a good medium to initiate growth.
  • Bacterial DFM containing pastes may be formulated with vegetable oil and inert gelling ingredients.
  • Fungal products may be formulated with grain by-products as carriers.
  • the feed additive composition according to the present invention is not in the form of a microparticle system, such as the microparticle system taught in WO2005/123034.
  • the DFM and/or feed additive composition according to the present invention may be designed for one-time dosing or may be designed for feeding on a daily basis.
  • the optimum amount of the composition (and each component therein) to be used in the combination of the present invention will depend on the product to be treated and/or the method of contacting the product with the composition and/or the intended use for the same.
  • the amount of DFM and enzymes used in the compositions should be a sufficient amount to be effective and to remain sufficiently effective in improving the performance of the animal fed feed products containing said composition. This length of time for effectiveness should extend up to at least the time of utilisation of the product (e.g. feed additive composition or feed containing same).
  • the DFM and enzyme(s) for use in the present invention may be used in combination with other components.
  • the present invention also relates to combinations.
  • the DFM in combination with the xylanase and a ⁇ -glucanase (and optionally at least one further fibre degrading enzyme) may be referred to herein as the feed additive composition of the present invention”.
  • the feed additive composition of the present invention may comprise (or consist essentially of, or consist of) DFM in combination with the xylanase and a ⁇ -glucanase and a further fibre degrading enzyme as taught herein (e.g. suitably at least two, suitably at least three further fibre degrading enzymes).
  • the feed additive composition of the present invention may comprise (or consist essentially of, or consist of) DFM in combination with the xylanase and a ⁇ -glucanase and a further fibre degrading enzyme as taught herein (e.g. suitably at least four, suitably at least five further fibre degrading enzymes).
  • the combination of the present invention comprises the feed additive composition of the present invention (or one or more of the constituents thereof) and another component which is suitable for animal consumption and is capable of providing a medical or physiological benefit to the consumer.
  • the “another component” is not a further enzyme or a further DFM.
  • the components may be prebiotics.
  • Prebiotics are typically non-digestible carbohydrate (oligo- or polysaccharides) or a sugar alcohol which is not degraded or absorbed in the upper digestive tract.
  • Known prebiotics used in commercial products and useful in accordance with the present invention include inulin (fructo-oligosaccharide, or FOS) and transgalacto-oligosaccharides (GOS or TOS).
  • Suitable prebiotics include palatinoseoligosaccharide, soybean oligosaccharide, alginate, xanthan, pectin, locust bean gum (LBG), inulin, guar gum, galacto-oligosaccharide (GOS), fructo-oligosaccharide (FOS), non-degradable starch, lactosaccharose, lactulose, lactitol, maltitol, maltodextrin, polydextrose (i.e.
  • the present invention relates to the combination of the feed additive composition according to the present invention (or one or more of the constituents thereof) with a prebiotic.
  • a feed additive composition comprising (or consisting essentially of or consisting of) a DFM in combination with a xylanase, a ⁇ -glucanase, an amylase, a phytase, a protease and a prebiotic.
  • the prebiotic may be administered simultaneously with (e.g. in admixture together with or delivered simultaneously by the same or different routes) or sequentially to (e.g. by the same or different routes) the feed additive composition (or constituents thereof) according to the present invention.
  • components of the combinations of the present invention include polydextrose, such as Litesse®, and/or a maltodextrin and/or lactitol. These other components may be optionally added to the feed additive composition to assist the drying process and help the survival of DFM.
  • suitable components include one or more of: thickeners, gelling agents, emulsifiers, binders, crystal modifiers, sweeteners (including artificial sweeteners), rheology modifiers, stabilisers, anti-oxidants, dyes, enzymes, carriers, vehicles, excipients, diluents, lubricating agents, flavouring agents, colouring matter, suspending agents, disintegrants, granulation binders etc.
  • sweeteners including artificial sweeteners
  • rheology modifiers stabilisers, anti-oxidants, dyes, enzymes, carriers, vehicles, excipients, diluents, lubricating agents, flavouring agents, colouring matter, suspending agents, disintegrants, granulation binders etc.
  • sweeteners including artificial sweeteners
  • rheology modifiers include one or more of: rheology modifiers, stabilisers, anti-oxidants, dyes, enzymes, carriers, vehicles, excipients, diluents, lubricating
  • the DFM and/or enzymes may be encapsulated.
  • the feed additive composition and/or DFM and/or enzymes is/are formulated as a dry powder or granule as described in WO2007/044968 (referred to as TPT granules)—reference incorporated herein by reference.
  • the DFM and/or enzymes for use in the present invention may be used in combination with one or more lipids.
  • the DFM and/or enzymes for use in the present invention may be used in combination with one or more lipid micelles.
  • the lipid micelle may be a simple lipid micelle or a complex lipid micelle.
  • the lipid micelle may be an aggregate of orientated molecules of amphipathic substances, such as a lipid and/or an oil.
  • thickener or gelling agent refers to a product that prevents separation by slowing or preventing the movement of particles, either droplets of immiscible liquids, air or insoluble solids. Thickening occurs when individual hydrated molecules cause an increase in viscosity, slowing the separation. Gelation occurs when the hydrated molecules link to form a three-dimensional network that traps the particles, thereby immobilising them.
  • stabiliser as used here is defined as an ingredient or combination of ingredients that keeps a product (e.g. a feed product) from changing over time.
  • Emulsifier refers to an ingredient (e.g. a feed ingredient) that prevents the separation of emulsions.
  • Emulsions are two immiscible substances, one present in droplet form, contained within the other.
  • Emulsions can consist of oil-in-water, where the droplet or dispersed phase is oil and the continuous phase is water; or water-in-oil, where the water becomes the dispersed phase and the continuous phase is oil.
  • Foams, which are gas-in-liquid, and suspensions, which are solid-in-liquid, can also be stabilised through the use of emulsifiers.
  • binder refers to an ingredient (e.g. a feed ingredient) that binds the product together through a physical or chemical reaction. During “gelation” for instance, water is absorbed, providing a binding effect. However, binders can absorb other liquids, such as oils, holding them within the product. In the context of the present invention binders would typically be used in solid or low-moisture products for instance baking products: pastries, doughnuts, bread and others.
  • Carriers or “vehicles” mean materials suitable for administration of the DFM and/or enzymes and include any such material known in the art such as, for example, any liquid, gel, solvent, liquid diluent, solubilizer, or the like, which is non-toxic and which does not interact with any components of the composition in a deleterious manner.
  • the feed additive composition, premix, feed or feedstuff of the present invention may be admixed with at least one physiologically acceptable carrier selected from at least one of maltodextrin, limestone (calcium carbonate), cyclodextrin, wheat or a wheat component, sucrose, starch, Na 2 SO 4 , Talc, PVA, sorbitol, benzoate, sorbiate, glycerol, sucrose, propylene glycol, 1,3-propane diol, glucose, parabens, sodium chloride, citrate, acetate, phosphate, calcium, metabisulfite, formate and mixtures thereof.
  • at least one physiologically acceptable carrier selected from at least one of maltodextrin, limestone (calcium carbonate), cyclodextrin, wheat or a wheat component, sucrose, starch, Na 2 SO 4 , Talc, PVA, sorbitol, benzoate, sorbiate, glycerol, sucrose, propylene glycol
  • excipients include one or more of: microcrystalline cellulose and other celluloses, lactose, sodium citrate, calcium carbonate, dibasic calcium phosphate, glycine, starch, milk sugar and high molecular weight polyethylene glycols.
  • disintegrants include one or more of: starch (preferably corn, potato or tapioca starch), sodium starch glycollate, croscarmellose sodium and certain complex silicates.
  • granulation binders include one or more of: polyvinylpyrrolidone, hydroxypropylmethylcellulose (HPMC), hydroxypropylcellulose (HPC), sucrose, maltose, gelatin and acacia.
  • lubricating agents include one or more of: magnesium stearate, stearic acid, glyceryl behenate and talc.
  • diluents include one or more of: water, ethanol, propylene glycol and glycerin, and combinations thereof.
  • the other components may be used simultaneously (e.g. when they are in admixture together or even when they are delivered by different routes) or sequentially (e.g. they may be delivered by different routes).
  • the DFM remains viable.
  • the feed additive according to the present invention does not contain sorbic acid.
  • the DFMs for use in the present invention may be in the form of concentrates. Typically these concentrates comprise a substantially high concentration of a DFM.
  • Feed additive compositions according to the present invention may have a content of viable cells (colony forming units, CFUs) which is in the range of at least 10 4 CFU/g (suitably including at least 10 5 CFU/g, such as at least 10 6 CFU/g, e.g. at least 10 7 CFU/g, at least 10 8 CFU/g, such as at least 10 9 CFU/g) to about 10 10 CFU/g (or even about 10 11 CFU/g or about 10 12 CFU/g).
  • viable cells colony forming units, CFUs
  • the feed additive compositions according to the present invention may have a content of viable cells in the range of at least 10 9 CFU/g to about 10 12 CFU/g, preferably at least 10 10 CFU/g to about 10 12 CFU/g.
  • Powders, granules and liquid compositions in the form of concentrates may be diluted with water or resuspended in water or other suitable diluents, for example, an appropriate growth medium such as milk or mineral or vegetable oils, to give compositions ready for use.
  • suitable diluents for example, an appropriate growth medium such as milk or mineral or vegetable oils
  • the DFM or feed additive composition of the present invention or the combinations of the present invention in the form of concentrates may be prepared according to methods known in the art.
  • the enzymes or feed is contacted by a composition in a concentrated form.
  • compositions of the present invention may be spray-dried or freeze-dried by methods known in the art.
  • Typical processes for making particles using a spray drying process involve a solid material which is dissolved in an appropriate solvent (e.g. a culture of a DFM in a fermentation medium).
  • an appropriate solvent e.g. a culture of a DFM in a fermentation medium.
  • the material can be suspended or emulsified in a non-solvent to form a suspension or emulsion.
  • Other ingredients (as discussed above) or components such as anti-microbial agents, stabilising agents, dyes and agents assisting with the drying process may optionally be added at this stage.
  • the solution then is atomised to form a fine mist of droplets.
  • the droplets immediately enter a drying chamber where they contact a drying gas.
  • the solvent is evaporated from the droplets into the drying gas to solidify the droplets, thereby forming particles.
  • the particles are then separated from the drying gas and collected.
  • subject means an animal that is to be or has been administered with a feed additive composition according to the present invention or a feedstuff comprising said feed additive composition according to the present invention.
  • subject means an animal.
  • the subject is a mammal, bird, fish or crustacean including for example livestock or a domesticated animal (e.g. a pet).
  • the “subject” is livestock.
  • livestock refers to any farmed animal.
  • livestock is one or more of cows or bulls (including calves), poultry, pigs (including piglets), poultry (including broilers, chickens and turkeys), birds, fish (including freshwater fish, such as salmon, cod, trout and carp, e.g. koi carp, and marine fish, such as sea bass), crustaceans (such as shrimps, mussels and scallops), horses (including race horses), sheep (including lambs).
  • livestock and/or poultry and/or chickens does not include egg layers.
  • the “subject” is a domesticated animal or pet or an animal maintained in a zoological environment.
  • domesticated animal or pet or animal maintained in a zoological environment refers to any relevant animal including canines (e.g. dogs), felines (e.g. cats), rodents (e.g. guinea pigs, rats, mice), birds, fish (including freshwater fish and marine fish), and horses.
  • canines e.g. dogs
  • felines e.g. cats
  • rodents e.g. guinea pigs, rats, mice
  • birds including freshwater fish and marine fish
  • fish including freshwater fish and marine fish
  • SCFA short chain fatty acid
  • acetic acid propionic acid
  • butyric acid isobutyric acid
  • valeric acid isovaleric acid
  • 2-methylbutyric acids 2-methylbutyric acids
  • lactic acid preferably propionic acid and/or butyric acid.
  • the SCFA may be butyric acid and/or propionic acid.
  • Short chain fatty acids (particularly volatile fatty acids, e.g. propionic acid and butyric acid, and lactic acid) may be analysed using the following method:
  • animal performance may be determined by the feed efficiency and/or weight gain of the animal and/or by the feed conversion ratio and/or by the digestibility of a nutrient in a feed (e.g. amino acid digestibility) and/or digestible energy or metabolizable energy in a feed and/or by nitrogen retention.
  • a nutrient in a feed e.g. amino acid digestibility
  • digestible energy or metabolizable energy in a feed e.g. amino acid digestibility
  • animal performance is determined by feed efficiency and/or weight gain of the animal and/or by the feed conversion ratio.
  • improved animal performance it is meant that there is increased feed efficiency, and/or increased weight gain and/or reduced feed conversion ratio and/or improved digestibility of nutrients or energy in a feed and/or by improved nitrogen retention resulting from the use of feed additive composition of the present invention in feed in comparison to feed which does not comprise said feed additive composition.
  • improved animal performance it is meant that there is increased feed efficiency and/or increased weight gain and/or reduced feed conversion ratio.
  • feed efficiency refers to the amount of weight gain in an animal that occurs when the animal is fed ad-libitum or a specified amount of food during a period of time.
  • feed additive composition in feed results in an increased weight gain per unit of feed intake compared with an animal fed without said feed additive composition being present.
  • feed conversion ratio refers to the amount of feed fed to an animal to increase the weight of the animal by a specified amount.
  • An improved feed conversion ratio means a lower feed conversion ratio.
  • lower feed conversion ratio or “improved feed conversion ratio” it is meant that the use of a feed additive composition in feed results in a lower amount of feed being required to be fed to an animal to increase the weight of the animal by a specified amount compared to the amount of feed required to increase the weight of the animal by the same amount when the feed does not comprise said feed additive composition.
  • Nutrient digestibility as used herein means the fraction of a nutrient that disappears from the gastro-intestinal tract or a specified segment of the gastro-intestinal tract, e.g. the small intestine. Nutrient digestibility may be measured as the difference between what is administered to the subject and what comes out in the faeces of the subject, or between what is administered to the subject and what remains in the digesta on a specified segment of the gastro intestinal trace, e.g. the ileum.
  • Nutrient digestibility as used herein may be measured by the difference between the intake of a nutrient and the excreted nutrient by means of the total collection of excreta during a period of time; or with the use of an inert marker that is not absorbed by the animal, and allows the researcher calculating the amount of nutrient that disappeared in the entire gastro-intestinal tract or a segment of the gastro-intestinal tract.
  • an inert marker may be titanium dioxide, chromic oxide or acid insoluble ash.
  • Digestibility may be expressed as a percentage of the nutrient in the feed, or as mass units of digestible nutrient per mass units of nutrient in the feed.
  • Nutrient digestibility as used herein encompasses starch digestibility, fat digestibility, protein digestibility, and amino acid digestibility.
  • Energy digestibility means the gross energy of the feed consumed minus the gross energy of the faeces or the gross energy of the feed consumed minus the gross energy of the remaining digesta on a specified segment of the gastro-intestinal tract of the animal, e.g. the ileum.
  • Metabolizable energy refers to apparent metabolizable energy and means the gross energy of the feed consumed minus the gross energy contained in the faeces, urine, and gaseous products of digestion.
  • Energy digestibility and metabolizable energy may be measured as the difference between the intake of gross energy and the gross energy excreted in the faeces or the digesta present in specified segment of the gastro-intestinal tract using the same methods to measure the digestibility of nutrients, with appropriate corrections for nitrogen excretion to calculate metabolizable energy of feed.
  • Nitrogen retention means as subject's ability to retain nitrogen from the diet as body mass. A negative nitrogen balance occurs when the excretion of nitrogen exceeds the daily intake and is often seen when the muscle is being lost. A positive nitrogen balance is often associated with muscle growth, particularly in growing animals.
  • Nitrogen retention may be measured as the difference between the intake of nitrogen and the excreted nitrogen by means of the total collection of excreta and urine during a period of time. It is understood that excreted nitrogen includes undigested protein from the feed, endogenous proteinaceous secretions, microbial protein, and urinary nitrogen.
  • carcass yield means the amount of carcass as a proportion of the live body weight, after a commercial or experimental process of slaughter.
  • carcass means the body of an animal that has been slaughtered for food, with the head, entrails, part of the limbs, and feathers or skin removed.
  • meat yield as used herein means the amount of edible meat as a proportion of the live body weight, or the amount of a specified meat cut as a proportion of the live body weight.
  • the present invention further provides a method of increasing weight gain in a subject, e.g. poultry or swine, comprising feeding said subject a feedstuff comprising a feed additive composition according to the present invention.
  • An “increased weight gain” refers to an animal having increased body weight on being fed feed comprising a feed additive composition compared with an animal being fed a feed without said feed additive composition being present.
  • the feed additive composition, feed, feedstuff or method according to the present invention may not modulate (e.g. improve) the immune response of the subject.
  • the feed additive composition, feed, feedstuff or method according to the present invention may not improve survival (e.g. reduce mortality) of the subject.
  • the feed additive composition, feed, feedstuff or method according to the present invention may not modulate (e.g. improve) the immune response or improve survival (e.g. reduce mortality) of the subject.
  • the DFM in the composition of the present invention can exert a probiotic culture effect. It is also within the scope of the present invention to add to the composition of the present invention further probiotic and/or prebiotics.
  • a non-digestible food ingredient that beneficially affects the host by selectively stimulating the growth and/or the activity of one or a limited number of beneficial bacteria”.
  • probiotic culture defines live microorganisms (including bacteria or yeasts for example) which, when for example ingested or locally applied in sufficient numbers, beneficially affects the host organism, i.e. by conferring one or more demonstrable health benefits on the host organism.
  • Probiotics may improve the microbial balance in one or more mucosal surfaces.
  • the mucosal surface may be the intestine, the urinary tract, the respiratory tract or the skin.
  • at least 10 6 -10 12 preferably at least 10 6 -10 10 , preferably 10 6 -10 9 , cfu as a daily dose will be effective to achieve the beneficial health effects in a subject.
  • the enzyme used in the present invention is in an isolated form.
  • isolated means that the enzyme is at least substantially free from at least one other component with which the enzyme is naturally associated in nature and as found in nature.
  • the enzyme of the present invention may be provided in a form that is substantially free of one or more contaminants with which the substance might otherwise be associated. Thus, for example it may be substantially free of one or more potentially contaminating polypeptides and/or nucleic acid molecules.
  • the enzyme and/or DFM according to the present invention is in a purified form.
  • the term “purified” means that the enzyme and/or DFM is present at a high level.
  • the enzyme and/or DFM is desirably the predominant component present in a composition. Preferably, it is present at a level of at least about 90%, or at least about 95% or at least about 98%, said level being determined on a dry weight/dry weight basis with respect to the total composition under consideration.
  • amino acid sequence is synonymous with the term “polypeptide” and/or the term “protein”. In some instances, the term “amino acid sequence” is synonymous with the term “peptide”. In some instances, the term “amino acid sequence” is synonymous with the term “enzyme”.
  • amino acid sequence may be prepared/isolated from a suitable source, or it may be made synthetically or it may be prepared by use of recombinant DNA techniques.
  • amino acid sequence when relating to and when encompassed by the per se scope of the present invention is not a native enzyme.
  • native enzyme means an entire enzyme that is in its native environment and when it has been expressed by its native nucleotide sequence.
  • the present invention also encompasses the use of sequences having a degree of sequence identity or sequence homology with amino acid sequence(s) of a polypeptide having the specific properties defined herein or of any nucleotide sequence encoding such a polypeptide (hereinafter referred to as a “homologous sequence(s)”).
  • a polypeptide having the specific properties defined herein or of any nucleotide sequence encoding such a polypeptide hereinafter referred to as a “homologous sequence(s)”.
  • the term “homologue” means an entity having a certain homology with the subject amino acid sequences and the subject nucleotide sequences.
  • the term “homology” can be equated with “identity”.
  • the homologous amino acid sequence and/or nucleotide sequence should provide and/or encode a polypeptide which retains the functional activity and/or enhances the activity of the enzyme.
  • nucleotide sequence in relation to the present invention includes genomic DNA, cDNA, synthetic DNA, and RNA. Preferably it means DNA, more preferably cDNA sequence coding for the present invention.
  • a homologous sequence is taken to include an amino acid or a nucleotide sequence which may be at least 97% identical, preferably at least 98 or 99% identical to the subject sequence.
  • a homologous sequence is taken to include an amino acid or a nucleotide sequence which may be at least 85% identical, preferably at least 90 or 95% identical to the subject sequence.
  • the homologues will comprise the same active sites etc. as the subject amino acid sequence for instance.
  • homology can also be considered in terms of similarity (i.e. amino acid residues having similar chemical properties/functions), in the context of the present invention it is preferred to express homology in terms of sequence identity.
  • a homologous sequence is taken to include an amino acid sequence or nucleotide sequence which has one or several additions, deletions and/or substitutions compared with the subject sequence.
  • the present invention relates to a protein whose amino acid sequence is represented herein or a protein derived from this (parent) protein by substitution, deletion or addition of one or several amino acids, such as 2, 3, 4, 5, 6, 7, 8, 9 amino acids, or more amino acids, such as 10 or more than 10 amino acids in the amino acid sequence of the parent protein and having the activity of the parent protein.
  • the homologues will comprise the same sequences that code for the active sites etc. as the subject sequence.
  • homology can also be considered in terms of similarity (i.e. amino acid residues having similar chemical properties/functions), in the context of the present invention it is preferred to express homology in terms of sequence identity.
  • Homology comparisons can be conducted by eye, or more usually, with the aid of readily available sequence comparison programs. These commercially available computer programs can calculate % homology between two or more sequences.
  • % homology may be calculated over contiguous sequences, i.e. one sequence is aligned with the other sequence and each amino acid in one sequence is directly compared with the corresponding amino acid in the other sequence, one residue at a time. This is called an “ungapped” alignment. Typically, such ungapped alignments are performed only over a relatively short number of residues.
  • a suitable computer program for carrying out such an alignment is the Vector NTI (Invitrogen Corp.).
  • software that can perform sequence comparisons include, but are not limited to, the BLAST package (see Ausubel et al 1999 Short Protocols in Molecular Biology, 4th Ed—Chapter 18), BLAST 2 (see FEMS Microbiol Lett 1999 174(2): 247-50; FEMS Microbiol Lett 1999 177(1): 187-8 and tatiana@ncbi.nlm.nih.gov), FASTA (Altschul et al 1990 J. Mol. Biol. 403-410) and AlignX for example. At least BLAST, BLAST 2 and FASTA are available for offline and online searching (see Ausubel et al 1999, pages 7-58 to 7-60).
  • % homology can be measured in terms of identity
  • the alignment process itself is typically not based on an all-or-nothing pair comparison.
  • a scaled similarity score matrix is generally used that assigns scores to each pairwise comparison based on chemical similarity or evolutionary distance.
  • An example of such a matrix commonly used is the BLOSUM62 matrix—the default matrix for the BLAST suite of programs.
  • Vector NTI programs generally use either the public default values or a custom symbol comparison table if supplied (see user manual for further details). For some applications, it is preferred to use the default values for the Vector NTI package.
  • percentage homologies may be calculated using the multiple alignment feature in Vector NTI (Invitrogen Corp.), based on an algorithm, analogous to CLUSTAL (Higgins DG & Sharp P M (1988), Gene 73(1), 237-244).
  • % homology preferably % sequence identity.
  • the software typically does this as part of the sequence comparison and generates a numerical result.
  • CLUSTAL may be used with the gap penalty and gap extension set as defined above.
  • the degree of identity with regard to an amino acid sequence is determined over at least 20 contiguous amino acid residues, preferably over at least 30 contiguous residues, preferably over at least 40 contiguous residues, preferably over at least 50 contiguous residues, preferably over at least 60 contiguous residues, preferably over at least 100 contiguous residues.
  • the degree of identity with regard to amino acid sequence may be determined over the whole sequence taught herein.
  • sequences may also have deletions, insertions or substitutions of amino acid residues which produce a silent change and result in a functionally equivalent substance.
  • Deliberate amino acid substitutions may be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity, and/or the amphipathic nature of the residues as long as the secondary binding activity of the substance is retained.
  • negatively charged amino acids include aspartic acid and glutamic acid; positively charged amino acids include lysine and arginine; and amino acids with uncharged polar head groups having similar hydrophilicity values include leucine, isoleucine, valine, glycine, alanine, asparagine, glutamine, serine, threonine, phenylalanine, and tyrosine.
  • the present invention also encompasses homologous substitution (substitution and replacement are both used herein to mean the interchange of an existing amino acid residue, with an alternative residue) that may occur i.e. like-for-like substitution such as basic for basic, acidic for acidic, polar for polar etc.
  • Non-homologous substitution may also occur i.e.
  • Z ornithine
  • B diaminobutyric acid ornithine
  • 0 norleucine ornithine
  • pyriylalanine thienylalanine
  • naphthylalanine phenylglycine
  • Replacements may also be made by unnatural amino acids include; alpha* and alpha-disubstituted* amino acids, N-alkyl amino acids*, lactic acid*, halide derivatives of natural amino acids such as trifluorotyrosine*, p-Cl-phenylalanine*, p-Br-phenylalanine*, p-I-phenylalanine*, L-allyl-glycine*, ⁇ -alanine*, L- ⁇ -amino butyric acid*, L- ⁇ -amino butyric acid*, L- ⁇ -amino isobutyric acid*, L- ⁇ -amino caproic acid # , 7-amino heptanoic acid*, L-methionine sulfone # *, L-norleucine*, L-norvaline*, p-nitro-L-phenylalanine*, L-hydroxyproline # , L-thioproline*, methyl derivative
  • Variant amino acid sequences may include suitable spacer groups that may be inserted between any two amino acid residues of the sequence including alkyl groups such as methyl, ethyl or propyl groups in addition to amino acid spacers such as glycine or ⁇ -alanine residues.
  • alkyl groups such as methyl, ethyl or propyl groups
  • amino acid spacers such as glycine or ⁇ -alanine residues.
  • a further form of variation involves the presence of one or more amino acid residues in peptoid form, will be well understood by those skilled in the art.
  • the peptoid form is used to refer to variant amino acid residues wherein the ⁇ -carbon substituent group is on the residue's nitrogen atom rather than the ⁇ -carbon.
  • the xylanase for use in the present invention may comprise a polypeptide sequence herein with a conservative substitution of at least one of the amino acids.
  • At least 2 conservative substitutions such as at least 3 or at least 4 or at least 5.
  • the use of animals and experimental protocol was approved by the Institutional Animal Experiment Committee.
  • a diet was formulated to be balanced for energy and nutrients for young broiler chicks (0-21 days of life) (Table 1, Diet I).
  • the cereal component of the diet was either wheat, barley, rye, wheat middlings, wheat bran or combinations thereof whilst the protein component was soybean meal and the source of fat was rapeseed oil. No synthetic antimicrobials or anti-coccidial drugs were included, and the diet was supplied as a mash.
  • the basal diet was divided into portions and the respective enzymes and DFMs added to constitute experimental diets identified in Table 2.
  • Each supplement was provided in a premix and added to the mixer during diet preparation. Diets containing the DFM were mixed first and the mixer was flushed between each diet to prevent cross contamination. Samples were collected from each treatment diet from the beginning, middle, and end of each batch and blended together to confirm enzyme activities and DFM presence in feed before commencement of the animal trial. Additional samples from each treatment diet were retained and stored until required at ⁇ 20° C. ⁇ 2° C. for analysis.
  • Male broiler (Ross 308) chicks were obtained as day-olds from a commercial hatchery. The chicks were individually weighed and allocated to 32 brooder cages (8 chicks per cage) so that the average bird weight per cage was similar. The 4 dietary treatments (Table 2) were then randomly assigned to 8 cages each.
  • the birds were transferred to grower cages.
  • the space allocation per bird in brooder and grower cages was 530 and 640 cm 2 , respectively.
  • the brooder and grower cages were housed in environmentally controlled rooms. The temperature was maintained at 31° C. in the first week and then gradually reduced to 22° C. by the end of third week.
  • the birds received 20 hours fluorescent illumination and, allowed free access to the diets and water.
  • the diets were offered from d 0 to 21. Body weights were recorded at weekly intervals throughout the 21-d experimental period. Mortality was recorded daily.
  • the data were analyzed using the GLM procedure of SAS.
  • a wheat-barley based diet was formulated to be balanced for energy and nutrients for young broiler chicks (0-21 days of life) (Table 1, Diet II). Titanium dioxide was included at 0.30% to allow determination of dietary component retention. No synthetic antimicrobials or anti-coccidial drugs were included, and the diet was supplied as a mash. The basal diet was divided into portions and the respective enzymes and DFMs added to constitute experimental diets identified in Table 4. Each supplement was pre-mixed and the mixer was flushed to prevent cross contamination of treated diets.
  • Samples were collected from each treatment diet from the beginning, middle, and end of each batch and blended together to confirm enzyme activities and DFM presence in feed before commencement of the animal trial. Additional samples from each treatment diet are retained and stored until required at ⁇ 20° C. ⁇ 2° C. for analysis.
  • Day-old male broiler chicks (Ross 308) were obtained from a commercial hatchery. The chicks were individually weighed upon arrival and stratified by body weight and allocated to 30 cages (five chicks per cage) so that the average bird weight per cage was similar. The four dietary treatments were then randomly assigned to six replicate cages.
  • the trial was conducted from day 0 to 21 during which the birds had free access to their assigned dietary treatments and water.
  • Titanium (digestibility marker) was analyzed according to the procedures described by Lomer et al. (2000 , Analyst 125:2339-2343). Retention/Digestibility was calculated using the standard procedures (Adeola, O. 2001. Digestion and balance techniques in pigs. Pages 903-916 in Swine Nutrition, 2nd ed. A. J. Lewis, and L. L. Southern, ed. CRC Press, Washington, D.C.). Data were analyzed using the General Linear Models procedure of SAS (2004).
  • a combination of xylanase, ⁇ -glucanase and a bacillus based direct fed microbial improved utilization of dietary energy young broiler compared to either, the control or xylanase alone or a combination of xylanase and ⁇ -glucanase (Table 5). This could be linked increased retention of energy yielding nutrients such as fibre, fat and nitrogen (Table 5).
  • the enhanced fat retention due to the three way combinations is noteworthy and could be linked to enhanced digestion and absorption of dietary fat and also production and absorption of short chain fatty acids from fermentation.
  • a chicken caecum model was developed from an earlier described human colon in vitro system (Mäkivuokko et al. 2006 ; Nutrition and Cancer 52:94-104, Switzerlandkeläinen et al. 2009 ; international Dairy Journal 19:675-683).
  • This caecum in vitro model is comprised of four connected vessels inoculated with fresh caecal microbes.
  • a wheat-wheat bran based basal diet was formulated to be balanced for energy and nutrients for young broiler chicks (Table 1, Diet III). No synthetic antimicrobials or anti-coccidial drugs were included in the basal diet.
  • the basal diet was divided into portions and the respective enzymes and DFMs added to constitute experimental diets identified in Table 6.
  • the different feeds underwent a simulated digestion of the upper gastrointestinal tract before they were fed to the in vitro caecum system during a 5-hour simulation.
  • the vessels model the caecum compartments of the chicken, each having the same pH (6.25).
  • Chromatographic analysis of lactic acid from the caecal simulation samples was performed with pivalic acid as internal standard in a similar matter as previously described (Ouwehand et al. 2009 ; The British Journal of Nutrition 101:367-375).
  • Lactic acid is produced by lactic acid bacteria, in which lactobacilli and streptococci predominate; these bacteria are known to have health-promoting properties in the gut (Walter, 2008 ; Applied and Environmental Microbiology 74: 4985-4996). Lactic acid has antibacterial effects on pathogens such as E. coli and Salmonella species (Nout et al. 1989 ; International Journal of Food Microbiology 8, 351-361), and lactobacilli can inhibit adhesion of E. coli to the intestines (Hillman et al.
  • Broiler chickens are assigned to pens based on initial body weight and experimental diets randomly allocated using a recognized experimental design. The birds are allowed free access to experimental diets for a period between day 0 to 21.
  • Excreta samples are collected daily from day d18 to d20 and stored at ⁇ 20° C. On d 21, the birds are euthanized by cervical dislocation, and contents of caeca obtained and stored frozen at ⁇ 20° C. for determination of caecal VFA.
  • DNA extraction 0.2 g of caecal digesta suspended in PBS, and then further isolated by a bead beating step and then automatically with MagMax using a commercial kit, MagMAXTM Total Nucleic Acid Isolation Kit (Applied biosystems).
  • MagMAXTM Total Nucleic Acid Isolation Kit Applied biosystems.
  • the amount of isolated DNA was determined by using a Nanodrop ND-1000 Full-spectrum UVNis Spectrophotometer (Wilmington, Del., USA). Flow cytometry utilised as previously described (Apajalahti et al. 2002, Appl Environ Microbiol 68(10): 4986-4995) for enumeration of total or specific bacteria from the samples.
  • PCR procedures Isolated DNA is analysed by qPCR (quantitative polymerase chain reaction) using a applied biosystem. Specific primers are used to detect specifically interesting microbial genus as described in 3.
  • xylanase+(mannanase or ⁇ -Glucanase)+DFMs induces a shift in caecal microbial population in favour of Lactobacillus and/or other specific groups known as fibrolytic bacteria: Ruminococcus, Bacteroides, Roseburia.
  • the basal diet, as fed, is formulated to be balanced for energy and protein, and to match the requirements for growing birds of this age and genotype (Table 9).
  • the cereal component of the diet is corn, and protein component can be soybean meal with or without other protein ingredients such as canola, rape seed meal, etc.
  • Corn co-products such as DDGS or corn gem meal or corn gluten feed can be included either singly or in combination provided that the diet is formulated to meet the nutrient requirements of the birds being fed. No synthetic antimicrobials or anti-coccidial drugs are included, and the diet is supplied as a mash.
  • a common digestibility marker (Titanium dioxide, chromic oxide or celite) is included at 3 g/kg to allow determination of digestibility of dietary components.
  • the basal diet is divided into portions and the respective enzymes and DFMs added to constitute experimental diets identified in Table 10. Each supplement is pre-mixed and the mixer is flushed to prevent cross contamination of treated diets. Samples are collected from each treatment diet from the beginning, middle, and end of each batch and blended together to confirm enzyme activities and DFM presence in feed before commencement of the animal trial. Additional samples from each treatment diet are retained and stored until required at ⁇ 20° C. ⁇ 2° C. for analysis.
  • endo-1,4- ⁇ -D-xylanase (E.C. 3.2.1.8) from two different origin organisms 2 Bacillus DFM selected as an enzyme producing strain 3 Lactobacillus DFM known to be a C5 sugar-fermenting strain; a short-chain fatty acid-producing strain; a fibrolytic, endogenous microflora-promoting strain; or combinations thereof 4 FDE mix: Combination of fibre degrading enzyme activities including beta-glucanase, beta-glucosidase, beta-xylosidase and/or alpha-arabinofuranosidase
  • Broiler chickens are assigned to pens based on initial body weight and experimental diets randomly allocated using a recognized experimental design. The birds are allowed free access to experimental diets for a period between day 0 to 21.
  • the body weight (BW), feed intake (FI) and mortalities are recorded to calculate body weight gain (BWG), feed conversion ratio (FCR) and feed conversion efficiency (FCE).
  • Excreta samples are collected daily from day d18 to d20 and stored at ⁇ 20° C. for determination of nutrients and fibre retention, and AME and AMEn contents.
  • the birds are euthanized by cervical dislocation, and contents of ileum (from Meckel's diverticulum to approximately 1 cm above the ileal-cecal junction) and ceca obtained and stored frozen at ⁇ 20° C. for determination of ileal digestibility of components and cecal VFA.
  • Coefficient of ileal apparent digestibility and coefficient of apparent retention of components are calculated according to Adeola et al., 2010 (Poult Sci. 2010 September; 89(9):1947-54).
  • the cage (pen) is the experimental unit.
  • ANOVA is conducted using the General Linear Models of SAS (SAS Inst. Inc., Cary, N.C.). When F-ratios indicate significance, treatment means are separated.
  • BWG g/bird/day
  • FCR g BW gain/g feed intake
  • the 9 dietary treatments (Table 11) were then randomly assigned to 8 cages each.
  • the cages were housed in environmentally controlled rooms.
  • the temperature was maintained at 31° C. in the first week and then gradually reduced to 22° C. by the end of third week.
  • the birds received 20 hours fluorescent illumination and, allowed free access to the diets and water for the duration of the study.
  • Body weights and feed intake were recorded the beginning and end of the 21-d experimental period. Mortality was recorded daily.
  • Feed conversion ratios were calculated by dividing total feed intake by weight gain of live plus dead birds. Data was analysed using the General Linear Models of SAS (SAS Inst. Inc., Cary, N.C.). When F-ratios indicate significance, treatment means are separated.
  • ⁇ -glucanase (Axtra ® XB)) are commercial products supplied by Danisco Animal nutrition b Enterococcus based DFM ( Enterococcus faecium ID7 (referred to as Lactococcus lactis ID7 in granted US Patent No. 7,384,628 and deposited at the ATCC depository as PTA-6103 and later reclassified as Enterococcus faecium ID7)), c FveXyn4 xylanase (an endo-1,4- ⁇ -D-xylanase (E.G. 3.2.1.8)) shown as SEQ ID No. 3 herein (also described in PCT/CN2012/079650 which is incorporated herein by reference), Danisco Animal Nutrition
  • the 9 dietary treatments (Table 13) were then randomly assigned to 8 cages each.
  • the cages were housed in environmentally controlled rooms.
  • the temperature was maintained at 31° C. in the first week and then gradually reduced to 22° C. by the end of third week.
  • the birds received 20 hours fluorescent illumination and, allowed free access to the diets and water for the duration of the study.
  • Body weights were recorded the beginning and end of the 21-d experimental period. Mortality was recorded daily.
  • the data were analyzed using the GLM procedure of SAS.
  • a corn-soybean meal-rapeseed meal based basal diet was formulated to be balanced for energy and nutrients for young broiler chicks (Table 9, Diet II). No synthetic antimicrobials or anti-coccidial drugs were included in the basal diet.
  • the basal diet was divided into portions and the respective enzymes and DFMs added to constitute experimental diets identified in Table 15. Subsequent procedures were similar to the ones described for Example 1, part III. followed. Chromatographic analysis of volatile fatty acids from simulation samples (see Example 1, part III) was performed with pivalic acid as internal standard in a similar matter as previously described (Ouwehand et al. 2009 ; The British Journal of Nutrition 101: 367-375 the teaching of which is incorporated herein by reference). Concentrations of acetic, propionic, butyric, isobutyric, valeric, isovaleric, and 2-methylbutyric acids were determined.
  • xylanase (Danisco Xylanase an endo-1,4- ⁇ -D-xylanase (E.G. 3.2.1.8)
  • ⁇ -glucanase (Axtra ® XB)
  • the basal diet as fed, is formulated to be balanced for energy and protein, and to match the requirements for growing pigs of this age and genotype (Table 17).
  • the major ingredients composition (type and inclusion levels) in the basal diet can vary as shown in table 17 provided that the diet is formulated to meet the nutrient requirements of the pigs being fed.
  • a common digestibility marker Tianium dioxide, chromic oxide or celite
  • No synthetic antimicrobials or anti-coccidial drugs are included, and the diet is supplied as a mash.
  • the basal diet is divided into portions which are then treated with the enzymes and DFMs identified in Table 18.
  • samples are collected from each treatment diet from the beginning, middle, and end of each batch and blended together to confirm enzyme activities and DFM presence in feed. Samples from each treatment diet are retained during mixing and stored at ⁇ 20° C. until required.
  • the experiment is planned and conducted to correspond to growing phase ( ⁇ 25 to ⁇ 60 kg body weight).
  • the experimental diets are fed for 42 days of 6 weeks.
  • a group of female and male pigs close to the target initial body are procured from the same herd (genetics).
  • Upon arrival pigs are weighed and allotted to the dietary treatments using a recognised experimental design such that each treatment has a minimum of 8 replicate pens.
  • the body weight and feed intake are monitored weekly for calculation of feed conversion efficiency of gain efficiency corrected for mortalities.
  • Fresh grab fecal samples are collected in week 3 and 6 to allow for calculation of dietary component digestibility.
  • Pig weights are recorded at the beginning and at the end of each period and the amount of feed supplied each day are recorded. Experimental period lasts for 15 d. The initial 10 days of each period are considered an adaptation period to the diet. Fresh grab fecal samples are collected on d 11 to 13 and Heal digesta are collected for 8 h on d 14 and 15 using standard operating procedures. For Heal digesta collection, a plastic bag is attached to the cannula barrel and digesta flowing into the bag collected. Bags are removed whenever they are filled with digesta—or at least once every 30 min and immediately frozen at ⁇ 20° C.
  • Fecal and Heal samples are thawed, mixed within animal and diet, and a sub-sample collected for chemical analysis. A sample of basal diet is also collected and analyzed. Digesta samples were lyophilized and finely ground prior to chemical analysis. Fecal samples are dried in an oven and finely ground for analysis. All samples were analyzed for dry matter, digestibility marker, gross energy, crude protein, fat and neutral detergent fibre according to standard procedures (AOAC, 2005).
  • xylanase plus a secondary fibre degrading enzyme ⁇ -Glucanase or FDE-mix
  • DFM Bacillus based direct fed microbial
  • a wheat-barley based diet was formulated to be balanced for energy and nutrients for young broiler chicks (0-21 days of life) (Table 19). Titanium dioxide was included at 0.30% to allow determination of dietary component retention. No synthetic antimicrobials or anti-coccidial drugs were included, and the diet was supplied as a mash. The basal diet was divided into portions and the respective enzymes and DFMs added to constitute experimental diets identified in Table 20. Each supplement was pre-mixed and the mixer was flushed to prevent cross contamination of treated diets.
  • Samples were collected from each treatment diet from the beginning, middle, and end of each batch and blended together to confirm enzyme activities and DFM presence in feed before commencement of the animal trial. Additional samples from each treatment diet are retained and stored until required at ⁇ 20° C. ⁇ 2° C. for analysis.
  • xylanase (Danisco Xylanase an endo-1,4- ⁇ -D-xylanase (E.C. 3.2.1.8)
  • ⁇ -glucanase (Axtra ® XB)
  • Day-old male broiler chicks (Ross 308) were obtained from a commercial hatchery. The chicks were individually weighed upon arrival and stratified by body weight and allocated to 30 cages (five chicks per cage) so that the average bird weight per cage was similar. The four dietary treatments were then randomly assigned to six replicate cages.
  • the trial was conducted from day 0 to 21 during which the birds had free access to their assigned dietary treatments and water.
  • Titanium (digestibility marker) was analyzed according to the procedures described by Lomer et al. (2000, Analyst 125:2339-2343), which is incorporated herein by reference. Retention/Digestibility was calculated using the standard procedures (Adeola, O. 2001. Digestion and balance techniques in pigs. Pages 903-916 in Swine Nutrition, 2nd ed. A. J. Lewis, and L. L. Southern, ed. CRC Press, Washington, D.C. which is incorporated herein by reference). Data were analyzed using the General Linear Models procedure of SAS (2004).
  • the enhanced fat retention due to the three way combinations is noteworthy and could be linked to enhanced digestion and absorption of dietary fat and also production and absorption of short chain fatty acids from fermentation.
  • Respective basal diets were formulated to meet the NRC nutrient recommendations for swine (NRC, 1998 Table 25 diet I for experiment 1 and diet II for experiment 2). In each experiment, one batch of the basal diet is manufactured and split into two portions and each portion subsequently mixed with additives identified in Table 26.
  • xylanase (Danisco Xylanase an endo-1,4- ⁇ -D-xylanase (E.C. 3.2.1.8)
  • ⁇ -glucanase (Axtra ® XB)
  • the treatments identified in table 26, were allocated to 7 and 8 replicate pens in experiment 1 and 2, respectively. Pen allocation to the treatments was randomized based on pig body weight at the start of the experiment. Body weight and Feed intake were recorded on a weekly basis and used to calculate feed conversion ratio. Pigs were offered the experimental diets for 42 days in both experiments. Feed and water were freely available at all times during experimentation. In experiment 2, fresh fecal samples were collected on days, 38, 39 and 40 for determination of nutrients, energy and fibre digestibility as well as fecal microbial counts. One gram of the composite fecal sample from each pen was diluted with 9 mL of 1% peptone broth (Becton, Dickinson and Co., Franklin Lakes, N.J.) and then homogenized.
  • peptone broth Becton, Dickinson and Co., Franklin Lakes, N.J.
  • Viable counts of bacteria in the fecal samples were then conducted by plating serial 10-fold dilutions (in 1% peptone solution) onto MacConkey agar plates (Difco Laboratories, Detroit, Mich.) and lactobacilli medium III agar plates (Medium 638, DSMZ, Braunschweig, Germany) to isolate the E. coli and Lactobacillus , respectively.
  • the lactobacilli medium III agar plates were then incubated for 48 h at 39° C. under anaerobic conditions.
  • the MacConkey agar plates were incubated for 24 h at 37° C.
  • the E. coli and Lactobacillus colonies were counted immediately after removal from the incubator.
  • the growth performance data (BW, ADFI, ADG and FCR) were subjected to the GLM procedures of SAS with treatments, experiment and interactions as effects in the model. Initial analysis revealed interactions were not significant and as such dropped in further analysis, subsequently treatments main effects are presented.
  • the microbial count data were log transformed and along with digestibility subjected to one-way anova using the GLM procedures of SAS.
  • Swine hindgut simulation experiments were performed in duplicate runs, each with 1 control and 3 treatments (Table 30). Each treatment was tested in triplicate.
  • a total of 24 Pyrex bottles with simulated ileal effluent and one 15 mL conical with cecal content were used. Bottles were thawed overnight and 240 mL sterile 0.1 M phosphate buffer solution (pH 6) with 4 g/L mucin (Sigma-Aldrich) added to each bottle, similar to methods described in (Christensen et al.
  • Bacillus * enzyme and direct-fed microbial products were included at a rate similar to 500 g per metric ton in feed inclusion, each experiment was performed in duplicate runs, treatments were measured in triplicate in each run;
  • Basal diet is either corn control diet (CC) or wheat control diet (CW), as described in table 29;
  • ⁇ Xylanase is either Y5 (Danisco Xylanase an endo-1,4- ⁇ -D-xylanase (E.C. 3.2.1.8)) or NGX (FveXyn4 (an endo-1,4- ⁇ -D-xylanase (E.C. 3.2.1.8)) shown as SEQ ID No.
  • ⁇ Fibre degrading enzyme is either Accel. (Accelerase Trio, ACCELLERASE ® TRIO TM enzyme complex contains a combination of multiple enzyme activities including ⁇ -glucanases (200 CMC U/kg), xylanases (e.g. endoxylanases, endo-1,4- ⁇ -D-xylanase (E.C.
  • Direct-fed microbial is either Bacillus based (equal proportions of strains AGTP BS918 NRRL B-50508, AGTP BS1013 NRRL B-50509 and AGTP BS3BP5 NRRL B-50510) with a guaranteed activity of 3.0 ⁇ 10 8 cfu per gram of product, or Propionibacterium acidipropionici P169 PTA-5271 Omni-Bos ® P169 with a guaranteed activity of 2.1 ⁇ 10 8 cfu per gram of product.
  • Bottles were flushed with CO 2 gas for 30 seconds while 250 ⁇ L of cecal inoculant were added (based on Coles et al. 2005, Animal Feed Science and Technology 123: 421-444 the teaching of which is incorporated herein by reference) and a 10 mL baseline sample was collected, baseline pH determined and sample stored at ⁇ 20° C. Bottles were capped, gently mixed and placed into a shaking water bath at 39° C. and 160 rpm. After 12 h, another 10 mL sample was collected, pH determined and sample stored at ⁇ 20° C.
  • VFA volatile fatty acid
  • HPLC high-performance liquid chromatography
  • ileal effluents were generated and hindgut fermentation set up as described in example 7.
  • the wheat based diet (CW, see Table 32) was used as control without any treatment, as well as CW in addition with Y5 xylanase (Treatment 1), CW with Y5 and Accelerase Trio fibre degrading enzyme mix (Treatment 2), CW with Y5, Accelerase in combination with a three strain Bacillus direct-fed microbial (Treatment 3), details to enzyme and DFM treatments see Table 33.
  • ⁇ Fibre degrading enzyme is either Accel. (Accelerase Trio, ACCELLERASE ® TRIO TM enzyme complex contains a potent combination of multiple enzyme activities including ⁇ -glucanases (200 CMC U/kg), xylanases (e.g. endoxylanases, endo-1,4- ⁇ -D-xylanase (E.G.
  • Direct-fed microbial is either Bacillus based (equal proportions of strains AGTP BS918 NRRL B-50508, AGTP BS1013 NRRL B-50509 and AGTP BS3BP5 NRRL B-50510) with a guaranteed activity of 3.0 ⁇ 10 8 cfu per gram of product, or Propionibacterium acidipropionici P169 PTA-5271 Omni-Bos ® P169 with a guaranteed activity of 2.1 ⁇ 10 9 cfu per gram of product.

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US20150210993A1 (en) * 2012-08-03 2015-07-30 Dupont Nutrition Biosciences Aps Xylanases for Solubilising Arabinoxylan-Containing Material
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WO2017083196A1 (en) * 2015-11-09 2017-05-18 Dupont Nutrition Biosciences Aps Feed additive composition
US20180235191A1 (en) * 2015-08-20 2018-08-23 Api Holdings, Llc Formulations and methods for promoting honeybee health
CN109393148A (zh) * 2018-12-23 2019-03-01 福建傲农生物科技集团股份有限公司 降低畜禽腹泻、提高饲料利用率的预混剂及其制备方法
WO2019213243A1 (en) * 2018-05-01 2019-11-07 Microbial Discovery Group, Llc Microbials for feed
CN110679728A (zh) * 2019-10-30 2020-01-14 博益德（北京）生物科技有限公司 一种发酵米糠饲料的制备方法及其应用
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