WO2017174398A1 - Cyanophycin for slow feeding aquatic organisms - Google Patents

Cyanophycin for slow feeding aquatic organisms Download PDF

Info

Publication number
WO2017174398A1
WO2017174398A1 PCT/EP2017/057267 EP2017057267W WO2017174398A1 WO 2017174398 A1 WO2017174398 A1 WO 2017174398A1 EP 2017057267 W EP2017057267 W EP 2017057267W WO 2017174398 A1 WO2017174398 A1 WO 2017174398A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
amino acids
cgp
fish
slow
Prior art date
Application number
PCT/EP2017/057267
Other languages
French (fr)
Inventor
Ahmed Sallam
Martin KREHENBRINK
Original Assignee
Cysal Gmbh
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Cysal Gmbh filed Critical Cysal Gmbh
Priority to CN201780022465.9A priority Critical patent/CN108882728B/en
Publication of WO2017174398A1 publication Critical patent/WO2017174398A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/17Amino acids, peptides or proteins
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23KFODDER
    • A23K20/00Accessory food factors for animal feeding-stuffs
    • A23K20/10Organic substances
    • A23K20/142Amino acids; Derivatives thereof
    • A23K20/147Polymeric derivatives, e.g. peptides or proteins
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23KFODDER
    • A23K50/00Feeding-stuffs specially adapted for particular animals
    • A23K50/80Feeding-stuffs specially adapted for particular animals for aquatic animals, e.g. fish, crustaceans or molluscs
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/17Amino acids, peptides or proteins
    • A23L33/195Proteins from microorganisms

Definitions

  • the invention provides a composition for use in providing slow-feeding aquatic animals, with defined amino acids, said composition comprising the polymer cyanophycin (also abbreviated CGP, Cyanophycin Granule Peptide) that is essentially comprised of a poly(L-aspartic acid) backbone covalently bound to other amino acid residues, and has a molecular weight between 15 and 100 kDa. While these are mostly arginine residues, one or more structurally similar amino acids such as lysine, ornithine, glutamicacid, citrul line and canavanine, may partially replace the arginine residues of CGP depending on the bacterial strain and/or environmental/cultivation conditions.
  • CGP Cyanophycin Granule Peptide
  • the present invention provides a novel approach in the supplementation of certain amino acids in the form of the polypeptide cyanophycin, which can overcome the above mentioned limitations in the areas of food and feed.
  • the field of aquaculture was chosen for the experimental part of the present invention.
  • Shrimp were chosen as model organism due to the sensitivity to unbalanced amino acid content in their nutrition (limitation A) and due to their slow- feeding behavior, resulting in high levels of leaching of amino acids from feed (limitation B).
  • US20030099689 describes the use of synthetic peptides as growth-promoting feed additives for aquatic animals with a peptide proportion of 6-50% (wt/wt) of the total feed formulation .
  • the enantioselective synthesis of these synthetic oligo- and polypeptides is, however, very complicated, expensive, and difficult to scale up .
  • the efficacy of homopolypeptides consisting of one individual amino acid is disputed due to their very slow or even absent conversion to free amino acids under physiological conditions (Boebel and Baker, J . Nutr. 112 : 1130-1132 ( 1982)) .
  • WO2002088667 describes the enantioselective synthesis and use of oligomers of Methionine Hydroxy Analog (M HA) and amino acids, e .g . methionine, as feed additives. It is claimed that faster growth can be achieved as a result.
  • M HA Methionine Hydroxy Analog
  • the oligomers described are synthesized by an enzyme-catalyzed reaction and have a very wide distribution of chain lengths of the individual oligomers. As a consequence, the method, and thereby the product, is unselective, expensive, and complicated in execution and purification .
  • US20110295006 describes various known problems of the use of crystalline essential amino acids with certain species of fishes and crustaceans. It cites several previously published trials for the synthesis of chemically protected oligopeptides in the form of diketopiperazines (cyclo-dipeptides, dehydrodipeptides) as a solution, and also the disadvantages thereof.
  • the invention relates to feed additives containing synthetic chemically-protected diketopiperazines of essential limiting amino acids.
  • the dipeptide cyclo-DL-Met-DL-Met was preferably used .
  • WO2009150252 discloses the preparation of unprotected amino acids in the form of ⁇ -dipeptides, such as L-arginine-p-L-aspartic acid and L-lysine- ⁇ -L-aspartic acid by hydrolysis of CGP (see also Sallam and Steinbuchel, J. Appl. Microbiol 107:474-484 (2009); Sallam and Steinbuchel, Appl . Microbiol. Biotechnol . 87 :815-828 (2010)) .
  • the present invention provides a further solution towards better food and feed formulations.
  • the bioavailability of CGP can be explained either by the presence of CGP-degrading bacteria in gut flora which was previously shown during an in-vitro screening study on several mammalian, avian, and fish gut flora (Sallam and Steinbuchel, J . Appl. Microbiol. 107 :474-484 (2009)), or by the degradation of CGP via endogenous digestive enzymes. In both cases, the positive overall nutritional effect is most probably due to the absorption of the dipeptides resulting from CGP- degradation .
  • said composition can serve as a substitute for the widely applied free amino acids as a component/additive for food and animal feed formulations with very high biological value, and has good handling, storage, and stability properties in the usual conditions of mixed feed processing. Furthermore, it renders efforts and costs for protecting the respective free amino acids unnecessary. In this way, additional efficient sources of the essential amino acids constituting the biopolymer could be made available.
  • the use of the said composition in the present invention could solve or effectively participate in solving known problems of amino acids in the areas of food and feed.
  • the invention thus provides
  • compositions for use in providing human beings and animals with defined amino acids comprising the polymer CGP, wherein CGP comprises essentially a poly(L-aspartic acid) backbone covalently bound to other amino acid residues, and has a molecular weight between 15 and 100 kDa;
  • composition is for use in culturing aquatic animals, notably for culturing slow-feeding aquatic animals;
  • CGP is a reserve material for carbon and nitrogen which is mostly composed of the two amino acids aspartic acid and arginine and exhibits low solubility under physiological conditions.
  • One or more amino acids that are structurally similar to arginine, such as lysine, ornithine, glutamicacid, citrulline, and canavanine, may replace the arginine content of CGP depending on the bacterial strain and/or the environmental/cultivation conditions. The latter factors also determine the length, and thereby the molecular weight, of the polydisperse polymer which ranges from 15 to 100 kDa.
  • CGP is a polypeptidic structure essentially comprised of a poly(L-aspartic acid) backbone and covalently bound amino acid residues, preferably said residues are composed of the amino acids arginine, lysine, glutamic acid, citrulline, ornithine, canavanine, and the like.
  • the CGP is prepared by culturing a prokaryotic or eukaryotic cell line.
  • the producing cell line may be any cell line capable of producing CGP. It is preferred that the producing cell line is selected from Escherichia coli, Ralstonia eutropha, Acinetobacter bayiyi, Corynebacterium giutamicum, Pseudomonas putida, yeast strains, and plant biomass. Particularly preferred producing cell lines are Ralstonia eutropha H 16-PHB " 4-Aec/a (pBBRlMCS-2 : cphA 63 w/ edaH 16) and E. coli DH 1 (pMa/c5-914: : c Mpcc6803) .
  • the above process may further comprise the steps of isolating, purifying and/or chemically or enzymatically modifying the CGP product obtained by cultivating the producing cell line.
  • isolation, purification, modification and separation may be applied by methods well established in the art.
  • compositions issued in the present invention are natural and stereospecific substances that are produced from biomass in a biotechnological and environmentally-friendly way. Their production furthermore requires much less technological expense and effort, very little time, and significantly less financial effort.
  • one or more of said polymeric structures comprise a reduced content of amino acid residues or are furtherly modified . Such modification includes phosphorylation, farnesylation, ubiquitination, glycosylation, acetylation, formylation, amidation, sumoylation, biotinylation, N-acylation, esterification, and cyclization .
  • the composition of aspect ( 1) comprises from 0.01 to 50 wt.% of the said polymeric structures, most preferably from 0.01 to 5 wt.% .
  • the composition of aspect ( 1) may further comprise one or more free amino acids or salts thereof. These free amino acids are preferably selected from arginine, lysine, and methionine. The content of free amino acids in the composition is preferably from 0.01 to 10 wt.%.
  • the polymeric products described above are highly stable under several conditions, and are suitable for being admixed with conventional food or feed components, e.g . cereals, vegetables, legumes, fishmeal, but also in combination with supplemented free amino acids, proteins, peptides, dipeptides, carbohydrates, vitamins, minerals, fats and/or oils.
  • the composition may also include active ingredients such as plant extracts, prebiotic compounds, probiotics, yeast extracts, short chain fatty acids, medium chain fatty acids, unsaturated long chain fatty acids, vitamins, and toxin absorbing compounds.
  • compositions of aspect (1) are basal diets that are supplemented with the said polymeric products to a concentration of 0.01 to 50 wt.% of said polymeric products, preferably from 0.01 to 5 wt.%.
  • basal diets can be formulated from individual components in common use.
  • composition of aspect (1) displays good pressing, pelletizing, and extrusion stability.
  • the composition of aspect (1) is preferred for use as food or feed or food/feed additive where it may serve as a growth promoter and/or enhancer for vitality, survival rates, and immune response for animals and human beings.
  • Animals that use said composition comprise omnivorous, carnivorous, and herbivorous mammals, birds and aquatic animals (including fish and crustaceans (shellfish)) .
  • the fish and crustaceans according to the invention include fry, juvenile fish and adult fish and larvae, postlarvae, juvenile and adult shellfish, respectively. Particularly preferred in the culture of slow-feeding aquatic animals such as fry and juvenile fish, and larvae, post larvae, juvenile and adult shellfish and fish and shellfish with feed uptake from the bottom (bottom feeders) .
  • composition (1) in supplementing the above mentioned animals with defined amino acids, namely those constituting the CGP, in the bound (polymeric) form including aspartic acid, arginine, lysine, ornithine, glutamic acid, citrulline, canavanine and the like.
  • CGP A recombinant strain of Ralstonia eutropha H 16-PHB " 4-Aec/a (pBBRlMCS-2 : :cphA 63 o 8 /eda 16) was used for the production of CGP in a 500L fermentation. CGP was then extracted from the produced biomass, purified, and analyzed for purity via HPLC, and finally dried to a powder (WO2009150252 and Sallam et al., AEM 75 :29-38(2009)). The pure CGP powder was added to the feed formulations for the supplementation experiments.
  • Example 1 and 2 Two experiments (examples 1 and 2) were conducted using CGP consisting of arginine and aspartic acid and different basal diets. Basal diets were formulated from individual components in common use in the aquaculture feed industry. For this, the published amino acid requirements of the species were considered to ensure arginine limitation in the diet for Example 2. Each basal diet was supplemented with the CGP to a concentration of 2.5 % (wt/wt), or with corresponding isonitrogenous concentrations of an amino acid mixture to determine the effect of free amino acids alone.
  • the used commercial diet contained wheat & Wheat bran, Soybean meal from husked seed (toasted), hemoglobin, fishmeal, fish oil, wheat gluten, sun flower meal, soybean oil, and had the following analysis values: crude protein 41%, crude fat 12 %, carbohydrates 29 %, crude ash 8 %, crude fiber 2.5 %, Lysine 2.5 %, phosphorus 1.4 %, energy 17.6 MJ/kg, Vitamin A 9.000 I.E./kg, vitamin E 150 mg/kg.
  • Kuruma shrimps responded well to the addition of the CGP product to the diet which increased the average final weight to around 157 % of the average weight showed by the test group fed on free amino acid.
  • the arginine-limited basal diets used in this experiment contained a calculated arginine content of about 1.5% (of diet), which is also lower than the minimum requirements of Kuruma shrimps : Corn 40 %, soybean meal 21 %, rice polishings 14 %, gluten 11 %, wheat bran 5 %, herring meal 5 %, monocalcium phosphate 0.8 %, limestone 0.7 %, L-lysine HCI 0.7 %, fish oil 0.5 %, vitamin mineral premix 0.3 %, sodium bicarbonate 0.15 %, salt 0.15 %, pellet binder 0.05 %.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Food Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Mycology (AREA)
  • Zoology (AREA)
  • Animal Husbandry (AREA)
  • Health & Medical Sciences (AREA)
  • Nutrition Science (AREA)
  • Birds (AREA)
  • Microbiology (AREA)
  • Marine Sciences & Fisheries (AREA)
  • Insects & Arthropods (AREA)
  • Fodder In General (AREA)
  • Feed For Specific Animals (AREA)

Abstract

The invention relates to a composition for use in providing slow-feeding aquatic animals, with defined amino acids, wherein the composition comprises the polymer cyanophycin (also abbreviated CGP, Cyanophycin Granule Peptide) that is essentially comprised of a poly(L-aspartic acid) backbone covalently bound to other amino acid residues and has a molecular weight between 15 and 100 kDa. The invention further relates to use of said composition as food, feed or feed additive and in a method for providing slow-feeding aquatic animals with defined amino acids.

Description

Cyanophycin for Slow Feeding Aquatic Organisms
The invention provides a composition for use in providing slow-feeding aquatic animals, with defined amino acids, said composition comprising the polymer cyanophycin (also abbreviated CGP, Cyanophycin Granule Peptide) that is essentially comprised of a poly(L-aspartic acid) backbone covalently bound to other amino acid residues, and has a molecular weight between 15 and 100 kDa. While these are mostly arginine residues, one or more structurally similar amino acids such as lysine, ornithine, glutamicacid, citrul line and canavanine, may partially replace the arginine residues of CGP depending on the bacterial strain and/or environmental/cultivation conditions.
Background of the Invention
Global amino acids market demand was around 6.5 million tons in 2014 and is expected to exceed 10 million tons by 2022 (Global Amino Acids Market. July 2015. Online summary, ISBN : 978-1-68038-453-6. Grand View Research, CA, USA). The forecasted market growth is due to increasing application in various end-use segments such as dietary supplements, health food and sports nutrition, cosmetics, artificial sweeteners, but is mainly driven by the increasing demand in the area of animal feed.
Numerous studies have investigated the physiological roles of amino acids in humans and animals, and thereby laid the basis for many scientifically proven applications in nutrition and therapy. However, the importance of each amino acid varies among living organisms, for example : L-arginine is considered essential in most poultry and fish species, and varies among mammals from being semi- essential as for human adults, over being regarded as nutritionally critical as in the case of swine, to being essential for human infants and cats. Since natural sources of protein such as soy, corn, and wheat are usually deficient in certain essential amino acids, targeted supplementation with these amino acids, such as lysine, arginine, or methionine, contributes to balancing and/or improving the nutritional value of food and animal feed. On the other hand, and after being familiar with factors limiting the application of the free form of amino acids, an increasing demand for related but superior forms of amino acids emerged. Among these limiting factors, the following two are considered to be major:
A) Physiological limitation : absorption capacity, which is - in the case of several amino acids - largely influenced by the competition for shared transporters, and
B) Physical limitation : through the properties of the free amino acid itself where, for example, the pH value or the solubility of the free amino acid can be limiting in a certain formulation/application or advantageous in another.
Both kinds of limitations are relevant for human and animal nutrition. Besides numerous studies; however, their impact is most clear in the feed area due to the decisive role amino acids play in means of productivity. While often only the physiological limitation is relevant, for example in the field of poultry farming, where the amino acids L-lysine, L-arginine and L-methionine are known to strongly interact (Chamruspollert et al., Br. J. Nutr. 88(6) :655-60(2002)), both kinds of limitation coexist for example in the area of aquaculture, where a high solubility of the amino acid leads to disadvantageous leaching in the aquatic milieu.
The present invention provides a novel approach in the supplementation of certain amino acids in the form of the polypeptide cyanophycin, which can overcome the above mentioned limitations in the areas of food and feed. In order to best demonstrate the effectiveness of this approach in overcoming both limitations at the same time, the field of aquaculture was chosen for the experimental part of the present invention. Shrimp were chosen as model organism due to the sensitivity to unbalanced amino acid content in their nutrition (limitation A) and due to their slow- feeding behavior, resulting in high levels of leaching of amino acids from feed (limitation B).
Intensive efforts have been made in the past to avoid or overcome known problems of supplementing amino acids in the free form, including the above mentioned two limitations. For example, the effective feeding of fish and crustaceans in aquaculture often requires a suitable chemical or physical protection to render them sufficiently stable during feeding in the aqueous environment and prevent them from leaching out of the feed pellet. On the other hand, the formulation must allow the amino acid product to be taken up by the animal . Thus, many attempts have been conducted to develop suitable or optimized forms of amino acids, e.g. :
US20030099689 describes the use of synthetic peptides as growth-promoting feed additives for aquatic animals with a peptide proportion of 6-50% (wt/wt) of the total feed formulation . The enantioselective synthesis of these synthetic oligo- and polypeptides is, however, very complicated, expensive, and difficult to scale up . Moreover, the efficacy of homopolypeptides consisting of one individual amino acid is disputed due to their very slow or even absent conversion to free amino acids under physiological conditions (Boebel and Baker, J . Nutr. 112 : 1130-1132 ( 1982)) . WO2002088667 describes the enantioselective synthesis and use of oligomers of Methionine Hydroxy Analog (M HA) and amino acids, e .g . methionine, as feed additives. It is claimed that faster growth can be achieved as a result. The oligomers described are synthesized by an enzyme-catalyzed reaction and have a very wide distribution of chain lengths of the individual oligomers. As a consequence, the method, and thereby the product, is unselective, expensive, and complicated in execution and purification .
US20110295006 describes various known problems of the use of crystalline essential amino acids with certain species of fishes and crustaceans. It cites several previously published trials for the synthesis of chemically protected oligopeptides in the form of diketopiperazines (cyclo-dipeptides, dehydrodipeptides) as a solution, and also the disadvantages thereof. The invention relates to feed additives containing synthetic chemically-protected diketopiperazines of essential limiting amino acids. The dipeptide cyclo-DL-Met-DL-Met was preferably used .
In addition to trials to develop and/or use chemical derivatives of amino acids for aquaculture, various possibilities for physical protection were also investigated, e.g. coatings. For example, Alam et al ., Aquaculture 248 : 13-19 (2005) showed that coated methionine and lysine, in comparison to their uncoated form, have a very positive influence on the growth of young kuruma shrimp. Although the use of a special coating prevented leaching of methionine and lysine from the feed pellet, there are some serious disadvantages. Coating of amino acids is generally a technically complicated process and is therefore expensive, and the protective layer can easily be damaged by mechanical stresses during feed processing. Furthermore, coating or related techniques reduce the content of amino acid and are therefore often uneconomical.
In general, a realistic practical use of a functional peptidic molecule depends largely on the complexity of its synthesis method and whether it can be successfully scaled up. These main factors determine the economic feasibility of the product itself and thereby the industrial applicability of the functional peptidic molecule. For the chemical synthesis, the overview article of Pattabiraman and Bode, Nature 480 :471-479 (2011) describes the development in this field, which largely did not change until today: "Improved methods for the synthesis of amide functionality, whether catalytic and waste-free or chemoselective and suitable for fragment coupling, are in great demand." The author also refers to the vote of the American Chemical Society Green Chemistry Institute (comprising members from major pharmaceutical industries worldwide) in 2007 on the "amide formation avoiding poor atom economy reagents" as a "top challenge for the organic chemistry". Furthermore, the chemical peptide synthesis as well as promising biotechnological approaches such as L-amino acid ligase remains particularly challenging when it comes to basic amino acids like arginine and lysine, due to their properties.
On the other hand, WO2009150252 discloses the preparation of unprotected amino acids in the form of β-dipeptides, such as L-arginine-p-L-aspartic acid and L-lysine- β-L-aspartic acid by hydrolysis of CGP (see also Sallam and Steinbuchel, J. Appl. Microbiol 107:474-484 (2009); Sallam and Steinbuchel, Appl . Microbiol. Biotechnol . 87 :815-828 (2010)) .
In applicant's copending PCT/EP2016/075432 it has been furthermore shown that these β-dipeptides are a suitable source for essential amino acids for several omnivorous, herbivorous, and carnivorous fish and crustacean species that live in salt water or freshwater. Although the β-dipeptide form showed superiority to the free form of amino acids even for the slow-feeding kuruma shrimp, its potential is thought to be not fully reached due to its high leaching rate in the aqueous milieu at feeding.
The present invention provides a further solution towards better food and feed formulations. The bioavailability of CGP can be explained either by the presence of CGP-degrading bacteria in gut flora which was previously shown during an in-vitro screening study on several mammalian, avian, and fish gut flora (Sallam and Steinbuchel, J . Appl. Microbiol. 107 :474-484 (2009)), or by the degradation of CGP via endogenous digestive enzymes. In both cases, the positive overall nutritional effect is most probably due to the absorption of the dipeptides resulting from CGP- degradation . Although the absorbed ratio of dipeptides might be - due to the necessary degradation step of the biopolymer - less than that in case if dipeptides were supplemented directly, the overall nutritional benefit appears to be better in such application due to bypassing the physiological and/or physical limitations known for free amino acids.
Thus, said composition can serve as a substitute for the widely applied free amino acids as a component/additive for food and animal feed formulations with very high biological value, and has good handling, storage, and stability properties in the usual conditions of mixed feed processing. Furthermore, it renders efforts and costs for protecting the respective free amino acids unnecessary. In this way, additional efficient sources of the essential amino acids constituting the biopolymer could be made available. The use of the said composition in the present invention could solve or effectively participate in solving known problems of amino acids in the areas of food and feed.
Short Description of the Invention
The invention thus provides
(1) a composition for use in providing human beings and animals with defined amino acids, said composition comprising the polymer CGP, wherein CGP comprises essentially a poly(L-aspartic acid) backbone covalently bound to other amino acid residues, and has a molecular weight between 15 and 100 kDa;
(2) a preferred embodiment of (1) above, wherein the composition is for use in culturing aquatic animals, notably for culturing slow-feeding aquatic animals;
(3) the use of the composition as described in (1) above as food or (animal) feed or as food/feed additive; and
(4) a method for providing human beings and animals with defined amino acids, said method comprising supplementing the human beings and animals with the composition as described in ( 1) above. Detailed Description of the Invention
In nature, and in addition to several heterotrophic bacteria, most cyanobacterial species (blue-green algae) accumulate the polymer CGP of the composition of aspect (1) of the present invention . CGP is a reserve material for carbon and nitrogen which is mostly composed of the two amino acids aspartic acid and arginine and exhibits low solubility under physiological conditions. One or more amino acids that are structurally similar to arginine, such as lysine, ornithine, glutamicacid, citrulline, and canavanine, may replace the arginine content of CGP depending on the bacterial strain and/or the environmental/cultivation conditions. The latter factors also determine the length, and thereby the molecular weight, of the polydisperse polymer which ranges from 15 to 100 kDa.
Thus, "CGP" according to the present invention is a polypeptidic structure essentially comprised of a poly(L-aspartic acid) backbone and covalently bound amino acid residues, preferably said residues are composed of the amino acids arginine, lysine, glutamic acid, citrulline, ornithine, canavanine, and the like.
CGP is prepared by culturing a prokaryotic or eukaryotic cell line. The producing cell line may be any cell line capable of producing CGP. It is preferred that the producing cell line is selected from Escherichia coli, Ralstonia eutropha, Acinetobacter bayiyi, Corynebacterium giutamicum, Pseudomonas putida, yeast strains, and plant biomass. Particularly preferred producing cell lines are Ralstonia eutropha H 16-PHB"4-Aec/a (pBBRlMCS-2 : cphA63w/ edaH 16) and E. coli DH 1 (pMa/c5-914: : c Mpcc6803) .
The above process may further comprise the steps of isolating, purifying and/or chemically or enzymatically modifying the CGP product obtained by cultivating the producing cell line. Such isolation, purification, modification and separation may be applied by methods well established in the art.
Compared to chemically-synthesized peptides, the compositions issued in the present invention are natural and stereospecific substances that are produced from biomass in a biotechnological and environmentally-friendly way. Their production furthermore requires much less technological expense and effort, very little time, and significantly less financial effort. In a further embodiment, one or more of said polymeric structures comprise a reduced content of amino acid residues or are furtherly modified . Such modification includes phosphorylation, farnesylation, ubiquitination, glycosylation, acetylation, formylation, amidation, sumoylation, biotinylation, N-acylation, esterification, and cyclization . In a preferred embodiment, the composition of aspect ( 1) comprises from 0.01 to 50 wt.% of the said polymeric structures, most preferably from 0.01 to 5 wt.% . The composition of aspect ( 1) may further comprise one or more free amino acids or salts thereof. These free amino acids are preferably selected from arginine, lysine, and methionine. The content of free amino acids in the composition is preferably from 0.01 to 10 wt.%.
The polymeric products described above are highly stable under several conditions, and are suitable for being admixed with conventional food or feed components, e.g . cereals, vegetables, legumes, fishmeal, but also in combination with supplemented free amino acids, proteins, peptides, dipeptides, carbohydrates, vitamins, minerals, fats and/or oils. The composition may also include active ingredients such as plant extracts, prebiotic compounds, probiotics, yeast extracts, short chain fatty acids, medium chain fatty acids, unsaturated long chain fatty acids, vitamins, and toxin absorbing compounds.
In particular, the compositions of aspect (1) are basal diets that are supplemented with the said polymeric products to a concentration of 0.01 to 50 wt.% of said polymeric products, preferably from 0.01 to 5 wt.%. These basal diets can be formulated from individual components in common use.
Furthermore, the composition of aspect (1) displays good pressing, pelletizing, and extrusion stability.
The composition of aspect (1) is preferred for use as food or feed or food/feed additive where it may serve as a growth promoter and/or enhancer for vitality, survival rates, and immune response for animals and human beings. Animals that use said composition comprise omnivorous, carnivorous, and herbivorous mammals, birds and aquatic animals (including fish and crustaceans (shellfish)) . The fish and crustaceans according to the invention include fry, juvenile fish and adult fish and larvae, postlarvae, juvenile and adult shellfish, respectively. Particularly preferred in the culture of slow-feeding aquatic animals such as fry and juvenile fish, and larvae, post larvae, juvenile and adult shellfish and fish and shellfish with feed uptake from the bottom (bottom feeders) . Aspects (3) and (4) of the invention pertain to the use of the composition (1) in supplementing the above mentioned animals with defined amino acids, namely those constituting the CGP, in the bound (polymeric) form including aspartic acid, arginine, lysine, ornithine, glutamic acid, citrulline, canavanine and the like.
The invention will be further described in the following Examples, which are not to be construed as limiting the invention .
Experimental examples
Materials and Methods
Production of CGP: A recombinant strain of Ralstonia eutropha H 16-PHB"4-Aec/a (pBBRlMCS-2 : :cphA63o8/eda 16) was used for the production of CGP in a 500L fermentation. CGP was then extracted from the produced biomass, purified, and analyzed for purity via HPLC, and finally dried to a powder (WO2009150252 and Sallam et al., AEM 75 :29-38(2009)). The pure CGP powder was added to the feed formulations for the supplementation experiments.
Aquaculture experiments: In order to best demonstrate the effectiveness of the novel approach of the present invention in overcoming the addressed limitations known for using free amino acids in food and feed, kuruma shrimps (Marsupenaeus japonicas) were chosen as an ideal test-model organism due to 1) the sensitivity of balancing the amino acid content in their ration, and 2) their slow-feeding behavior resulting in maximum leaching of amino acids from feed.
Two experiments (examples 1 and 2) were conducted using CGP consisting of arginine and aspartic acid and different basal diets. Basal diets were formulated from individual components in common use in the aquaculture feed industry. For this, the published amino acid requirements of the species were considered to ensure arginine limitation in the diet for Example 2. Each basal diet was supplemented with the CGP to a concentration of 2.5 % (wt/wt), or with corresponding isonitrogenous concentrations of an amino acid mixture to determine the effect of free amino acids alone.
Shrimp were maintained in seawater and the experiments started with postlarvae. Water quality (oxygen levels, nitrite, and nitrate) was monitored weekly. Partial water replacements were performed if the desired levels were exceeded. (< 3 mg 02/l, detectable nitrite, > 25 mg/l nitrate). At the end of the experiments, the individual weights were recorded and the data analyzed statistically.
Example 1 :
In this experiment, the used commercial diet contained wheat & Wheat bran, Soybean meal from husked seed (toasted), hemoglobin, fishmeal, fish oil, wheat gluten, sun flower meal, soybean oil, and had the following analysis values: crude protein 41%, crude fat 12 %, carbohydrates 29 %, crude ash 8 %, crude fiber 2.5 %, Lysine 2.5 %, phosphorus 1.4 %, energy 17.6 MJ/kg, Vitamin A 9.000 I.E./kg, vitamin E 150 mg/kg.
Results:
Figure imgf000010_0001
After two months of feeding. Start/test group: 15 postlarvae (120 days old) . Arg/Asp: free amino acids mixture; CGP: cyanophycin.
Kuruma shrimps responded well to the addition of the CGP product to the diet which increased the average final weight to around 157 % of the average weight showed by the test group fed on free amino acid.
Example 2 :
The arginine-limited basal diets used in this experiment contained a calculated arginine content of about 1.5% (of diet), which is also lower than the minimum requirements of Kuruma shrimps : Corn 40 %, soybean meal 21 %, rice polishings 14 %, gluten 11 %, wheat bran 5 %, herring meal 5 %, monocalcium phosphate 0.8 %, limestone 0.7 %, L-lysine HCI 0.7 %, fish oil 0.5 %, vitamin mineral premix 0.3 %, sodium bicarbonate 0.15 %, salt 0.15 %, pellet binder 0.05 %.
Results:
Figure imgf000010_0002
After six weeks of feeding. Start/test group: 48 postlarvae (75 days old) . Arg/Asp: free amino acids mixture; CGP: cyanophycin. Shrimps responded well to the addition of CGP to the basal diet in this experiment as well . The supplementation increased the average final weight to around 153 % of the average weight showed by the control test group fed on the basal diet alone. The supplementation with free amino acid mixture increased the average final weight to around 129 % of the average weight showed by the control test group fed on the basal diet alone.
Results of both experiments (1 and 2) provide clear evidence on the superiority of the polymer CGP issued in the present invention when compared to the free form of amino acids. Thus, the present invention provides a novel possibility for supplementing amino acids in a form which can overcome known limitations of using their free form.

Claims

Claims
1. A composition for use in providing slow-feeding aquatic animals with defined amino acids, said composition comprising the polymer cyanophycin (CGP), or salts thereof, wherein the CGP comprises essentially a poly(L-aspartic acid) backbone covalently bound to other amino acid residues, and has a molecular weight between 15 and 100 kDa.
2. The composition of claim 1, wherein
(i) the CGP comprises one kind (homomeric) or different kinds (heteromeric) of other amino acid residues that are covalently bound to the same poly(L-aspartic acid) backbone; and/or
(ii) the composition comprises a mixture of two or more different kinds of homomeric and/or heteromeric forms of the CGP.
3. The composition of claim 1 or 2, wherein the other amino acid residues are selected from arginine, lysine, ornithine, glutamic acid, citrulline, and canavanine, preferably the other amino acid residues are arginine and/or lysine.
4. The composition of any one of claims 1 to 3, wherein the CGP is chemically or enzymatically modified and/or partially hydrolyzed.
5. The composition of any one of claims 1 to 4, wherein the composition comprises from 0.01 to 50 wt.% of the CGP.
6. The composition of any one of claims 1 to 5, wherein the composition further comprises one or more free amino acids or salts thereof.
7. The composition of claim 6, wherein
(i) the free amino acids are selected from arginine, lysine, and methionine, and/or
(ii) the composition comprises from 0.01 to 10 wt.% of the free amino acids.
8. The composition of any one of claims 1 to 7, which is for use in culturing slow- feeding aquatic animals, most preferably for culturing fry and juvenile fish, lavae, postlavae, juvenile and adult shellfish.
9. The composition of any one of claims 1 to 7, which is for use in culturing fish and shellfish with feed uptake from the bottom.
10. Use of the composition of any one of claims 1 to 7 as food or feed or as feed additive for slow-feeding aquatic animals.
11. The use of claim 10, which is a feed additive for fish and shellfish, including fry, juvenile fish and adult fish and larvae, postlarvae, juvenile and adult shellfish .
12. A method for providing slow-feeding aquatic animals with defined amino acids, said method comprising supplementing the slow-feeding aquatic animals with the composition as described in any one of claims 1 to 7.
13. The method of claim 12, which comprises feeding of slow-feeding aquatic animals, namely fish and shellfish, including fry, juvenile fish and adult fish and larvae, postlarvae, juvenile and adult shellfish, respectively.
14. The method of claim 12, which comprises feeding of fish and shellfish with feed uptake from the bottom.
PCT/EP2017/057267 2016-04-07 2017-03-28 Cyanophycin for slow feeding aquatic organisms WO2017174398A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201780022465.9A CN108882728B (en) 2016-04-07 2017-03-28 Phycocyanin for slow feeding of aquatic organisms

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP16164309 2016-04-07
EP16164309.3 2016-04-07

Publications (1)

Publication Number Publication Date
WO2017174398A1 true WO2017174398A1 (en) 2017-10-12

Family

ID=55701817

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2017/057267 WO2017174398A1 (en) 2016-04-07 2017-03-28 Cyanophycin for slow feeding aquatic organisms

Country Status (2)

Country Link
CN (1) CN108882728B (en)
WO (1) WO2017174398A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020025656A1 (en) 2018-08-01 2020-02-06 Cysal Gmbh Combining beta-dipeptides and amino acids for optimal nutritional supplementation

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002088667A2 (en) 2001-05-02 2002-11-07 Novus International, Inc. ENANTIOSELECTIVE OLIGOMERIZATION OF α-HYDROXY CARBOXYLIC ACIDS AND α-AMINO ACIDS
US20030099689A1 (en) 2001-08-31 2003-05-29 Ohio State Research Foundation Dietary formulations including peptides
WO2006093411A1 (en) * 2005-03-04 2006-09-08 Wageningen University Cyanophycin production from nitrogen-containing chemicals obtained from biomass
WO2009150252A2 (en) 2008-06-13 2009-12-17 Westfälische Wilhelms-Universität Münster Biotechnological production of cyanophycin dipeptides
US20110295006A1 (en) 2010-05-27 2011-12-01 Evonik Degussa Gmbh Cyclic dipeptides as feed additives
WO2013167680A1 (en) * 2012-05-08 2013-11-14 Eberhard Karls Universität Tübingen Method for producing cyanophycin

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19709024A1 (en) * 1997-03-06 1998-09-10 Bayer Ag Polyaspartic acid homopolymers and copolymers, their biotechnological production and use
CN100581380C (en) * 2007-08-06 2010-01-20 江苏省农业科学院 Method for obtaining free amino acid by the hydrolyzation of water bloom blue algae

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002088667A2 (en) 2001-05-02 2002-11-07 Novus International, Inc. ENANTIOSELECTIVE OLIGOMERIZATION OF α-HYDROXY CARBOXYLIC ACIDS AND α-AMINO ACIDS
US20030099689A1 (en) 2001-08-31 2003-05-29 Ohio State Research Foundation Dietary formulations including peptides
WO2006093411A1 (en) * 2005-03-04 2006-09-08 Wageningen University Cyanophycin production from nitrogen-containing chemicals obtained from biomass
WO2009150252A2 (en) 2008-06-13 2009-12-17 Westfälische Wilhelms-Universität Münster Biotechnological production of cyanophycin dipeptides
US20110295006A1 (en) 2010-05-27 2011-12-01 Evonik Degussa Gmbh Cyclic dipeptides as feed additives
WO2013167680A1 (en) * 2012-05-08 2013-11-14 Eberhard Karls Universität Tübingen Method for producing cyanophycin

Non-Patent Citations (13)

* Cited by examiner, † Cited by third party
Title
ALAM ET AL., AQUACULTURE, vol. 248, 2005, pages 13 - 19
ALAM MD S ET AL: "Supplemental effects of coated methionine and/or lysine to soy protein isolate diet for juvenile kuruma shrimp, Marsupenaeus japonicus", AQUACULTURE, ELSEVIER, AMSTERDAM, NL, vol. 248, no. 1-4, 29 July 2005 (2005-07-29), pages 13 - 19, XP027614643, ISSN: 0044-8486, [retrieved on 20050729] *
BOEBEL; BAKER, J. NUTR, vol. 112, 1982, pages 1130 - 1132
CHAMRUSPOLLERT ET AL., BR. J. NUTR., vol. 88, no. 6, 2002, pages 655 - 60
GLOBAL AMINO ACIDS MARKET., July 2015 (2015-07-01)
L. WIEFEL ET AL: "Solubility Behavior of Cyanophycin Depending on Lysine Content", APPLIED AND ENVIRONMENTAL MICROBIOLOGY, vol. 80, no. 3, 22 November 2013 (2013-11-22), US, pages 1091 - 1096, XP055305839, ISSN: 0099-2240, DOI: 10.1128/AEM.03159-13 *
LARS WIEFEL ET AL: "Enzymatic Modification of Soluble Cyanophycin Using the Type II Peptidyl Arginine Deiminase from Oryctolagus cuniculus", MACROMOLECULAR BIOSCIENCE, vol. 16, no. 7, 8 March 2016 (2016-03-08), DE, pages 1064 - 1071, XP055305867, ISSN: 1616-5187, DOI: 10.1002/mabi.201500433 *
PATTABIRAMAN; BODE, NATURE, vol. 480, 2011, pages 471 - 479
SALLAM A ET AL: "Cyanophycin-degrading bacteria in digestive tracts of mammals, birds and fish and consequences for possible applications of cyanophycin and its dipeptides in nutrition and therapy", JOURNAL OF APPLIED MICROBIOLOGY, WILEY-BLACKWELL PUBLISHING LTD, GB, 21 January 2009 (2009-01-21), pages 1 - 11, XP002516931, ISSN: 1364-5072, DOI: 10.1111/J.1365-2672.2009.04221.X *
SALLAM ET AL., AEM, vol. 75, 2009, pages 29 - 38
SALLAM; STEINBUCHEL, APPL. MICROBIOL. BIOTECHNOL., vol. 87, 2010, pages 815 - 828
SALLAM; STEINBUCHEL, J. APPL. MICROBIOL, vol. 107, 2009, pages 474 - 484
WEN-LIANG LIAO ET AL: "PIGMENTATION OF CULTURED BLACK TIGER PRAWN BY FEEDING WITH A SPIRULINA-SUPPLEMENTED DIET", NIPPON SUISAN GAKKAISHI - BULLETIN OF THE JAPANESE SOCIETY OF SCIENTIFIC FISHERIES, NIPPON SUISAN GAKKAI, TOKYO, JP, vol. 59, no. 1, January 1993 (1993-01-01), pages 165 - 169, XP009080213, ISSN: 0021-5392 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020025656A1 (en) 2018-08-01 2020-02-06 Cysal Gmbh Combining beta-dipeptides and amino acids for optimal nutritional supplementation

Also Published As

Publication number Publication date
CN108882728B (en) 2023-04-04
CN108882728A (en) 2018-11-23

Similar Documents

Publication Publication Date Title
EP3364774B1 (en) Aspartyl-dipeptides for aquaculture
CA2650716C (en) Hydroxybutyrate and poly-hydroxybutyrate as components of animal feed or feed additives
Vinoj Kumar et al. Amino acids in the seaweeds as an alternate source of protein for animal feed
Fabrikov et al. Comparative study of growth performance and amino acid catabolism in Oncorhynchus mykiss, Tinca tinca and Sparus aurata and the catabolic changes in response to insect meal inclusion in the diet
US6958385B2 (en) Bioactive peptides, uses thereof and process for the production of same
CN108289478A (en) Include the feed addictive for aquatic animal of essential oil and lysozyme
JPH0928309A (en) Feed containing poly-gamma-glutamic acid
WO2017174398A1 (en) Cyanophycin for slow feeding aquatic organisms
RU2606284C1 (en) Quail fodder at early age
BRPI0608859A2 (en) isolated polypeptide, isolated nucleic acid sequence, nucleic acid construct, recombinant expression vector, recombinant bacillus host cell, use of polypeptide, methods of producing a polypeptide, to improve feed to animal conversion rate, and to modulate the animal intestinal microflora, animal feed additive, and, animal feed compound
Efendi et al. Profile of Amino Acids and Proximate on the Extraction of Red Ginger Protease Enzymes in Commercial Feed for Aquaculture
JP2011142857A (en) Bivalve rearing feed and method for rearing bivalve
RU2479215C1 (en) Protein fodder additive for young fishes feeding
Hee-Mock Effect of Spirulina platensis and probiotics as feed additives on growth of shrimp Fenneropenaeus chinensis
JPH09301807A (en) Agent for preventing and treating parasitic disease of aquatic animal
AU2002364540B2 (en) Feed additive and method for controlling large bowel fermentation in the horse and similar animals
AS Nutritional value and potential of freshwater fish in rivers and mining pools of Malaysia
Limpisophon et al. Valorization of chicken intestine: A process of protein hydrolysate for fish feed attractant using pilot plant scale system
Chinnakkannu et al. Fish protein hydrolysates in aquafeed
JP3201840B2 (en) Fish farm feed
CN112931701B (en) Nutritional composition containing enzymolysis fish peptide powder and preparation method and application thereof
JPH07506489A (en) How to improve feed absorption efficiency
US8062681B2 (en) Amino acid oligomer dietary supplement
Shaviklo et al. Properties and shelf-stability of co-dried common kilka (Clupeonella cultriventris) protein hydrolysate with agricultural residues as a new protein feed supplement
JPH1198963A (en) Raw materials for aquatic animal feed

Legal Events

Date Code Title Description
DPE1 Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101)
NENP Non-entry into the national phase

Ref country code: DE

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17713027

Country of ref document: EP

Kind code of ref document: A1

122 Ep: pct application non-entry in european phase

Ref document number: 17713027

Country of ref document: EP

Kind code of ref document: A1