NZ622442B2 - Method for the simultaneous production of ethanol and a fermented, solid product - Google Patents
Method for the simultaneous production of ethanol and a fermented, solid product Download PDFInfo
- Publication number
- NZ622442B2 NZ622442B2 NZ622442A NZ62244212A NZ622442B2 NZ 622442 B2 NZ622442 B2 NZ 622442B2 NZ 622442 A NZ622442 A NZ 622442A NZ 62244212 A NZ62244212 A NZ 62244212A NZ 622442 B2 NZ622442 B2 NZ 622442B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- fermented
- mixture
- biomass
- solid product
- yeast
- Prior art date
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims abstract description 157
- 238000000034 method Methods 0.000 title claims abstract description 95
- 239000012265 solid product Substances 0.000 title claims abstract description 30
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 18
- 239000000203 mixture Substances 0.000 claims abstract description 79
- 238000000855 fermentation Methods 0.000 claims abstract description 47
- 230000004151 fermentation Effects 0.000 claims abstract description 47
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 35
- 239000002028 Biomass Substances 0.000 claims abstract description 33
- 229920001282 polysaccharide Polymers 0.000 claims abstract description 30
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims abstract description 29
- 150000004676 glycans Chemical class 0.000 claims abstract description 28
- 239000005017 polysaccharide Substances 0.000 claims abstract description 28
- 150000002482 oligosaccharides Chemical class 0.000 claims abstract description 23
- 239000006057 Non-nutritive feed additive Substances 0.000 claims abstract description 21
- 229920001542 oligosaccharide Polymers 0.000 claims abstract description 19
- 238000002347 injection Methods 0.000 claims abstract description 8
- 239000007924 injection Substances 0.000 claims abstract description 8
- 239000000654 additive Substances 0.000 claims abstract description 4
- 239000000047 product Substances 0.000 claims description 36
- 102000004169 proteins and genes Human genes 0.000 claims description 29
- 108090000623 proteins and genes Proteins 0.000 claims description 29
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 claims description 28
- 150000001720 carbohydrates Chemical class 0.000 claims description 26
- 235000014633 carbohydrates Nutrition 0.000 claims description 26
- 239000002253 acid Substances 0.000 claims description 20
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- 229940088598 enzyme Drugs 0.000 claims description 15
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 15
- 241000196324 Embryophyta Species 0.000 claims description 12
- 238000012545 processing Methods 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 9
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- QPRQEDXDYOZYLA-UHFFFAOYSA-N 2-methylbutan-1-ol Chemical compound CCC(C)CO QPRQEDXDYOZYLA-UHFFFAOYSA-N 0.000 claims description 6
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- 239000007787 solid Substances 0.000 claims description 5
- ZIIUUSVHCHPIQD-UHFFFAOYSA-N 2,4,6-trimethyl-N-[3-(trifluoromethyl)phenyl]benzenesulfonamide Chemical compound CC1=CC(C)=CC(C)=C1S(=O)(=O)NC1=CC=CC(C(F)(F)F)=C1 ZIIUUSVHCHPIQD-UHFFFAOYSA-N 0.000 claims description 4
- 108010011619 6-Phytase Proteins 0.000 claims description 4
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- IWTBVKIGCDZRPL-LURJTMIESA-N 3-Methylbutanol Natural products CC[C@H](C)CCO IWTBVKIGCDZRPL-LURJTMIESA-N 0.000 claims description 3
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- AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
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- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
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- 238000010923 batch production Methods 0.000 description 2
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- LSDULPZJLTZEFD-UHFFFAOYSA-N lupulone Chemical compound CC(C)CC(=O)C1=C(O)C(CC=C(C)C)=C(O)C(CC=C(C)C)(CC=C(C)C)C1=O LSDULPZJLTZEFD-UHFFFAOYSA-N 0.000 description 2
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Classifications
-
- 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
- A23K10/12—Animal feeding-stuffs obtained by microbiological or biochemical processes by fermentation of natural products, e.g. of vegetable material, animal waste material or biomass
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K10/00—Animal feeding-stuffs
- A23K10/30—Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms
- A23K10/37—Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms from waste material
- A23K10/38—Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms from waste material from distillers' or brewers' waste
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, 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
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, 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
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/17—Amino acids, peptides or proteins
- A23L33/185—Vegetable proteins
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- 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
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/42—Proteins; Polypeptides; Degradation products thereof; Derivatives thereof, e.g. albumin, gelatin or zein
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/60—Sugars; Derivatives thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
- A61K8/645—Proteins of vegetable origin; Derivatives or degradation products thereof
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- C—CHEMISTRY; METALLURGY
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- C12P1/00—Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes
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- C12P19/14—Preparation of compounds containing saccharide radicals produced by the action of a carbohydrase (EC 3.2.x), e.g. by alpha-amylase, e.g. by cellulase, hemicellulase
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- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
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- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
- C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
- C12P7/06—Ethanol, i.e. non-beverage
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- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
- C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
- C12P7/06—Ethanol, i.e. non-beverage
- C12P7/08—Ethanol, i.e. non-beverage produced as by-product or from waste or cellulosic material substrate
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- 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)
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- C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
- C12Y302/01001—Alpha-amylase (3.2.1.1)
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- 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)
- C12Y302/01003—Glucan 1,4-alpha-glucosidase (3.2.1.3), i.e. glucoamylase
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- 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)
- C12Y302/01022—Alpha-galactosidase (3.2.1.22)
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- C13K—SACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
- C13K1/00—Glucose; Glucose-containing syrups
- C13K1/02—Glucose; Glucose-containing syrups obtained by saccharification of cellulosic materials
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- C13K—SACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
- C13K13/00—Sugars not otherwise provided for in this class
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P60/00—Technologies relating to agriculture, livestock or agroalimentary industries
- Y02P60/80—Food processing, e.g. use of renewable energies or variable speed drives in handling, conveying or stacking
- Y02P60/87—Re-use of by-products of food processing for fodder production
Abstract
Disclosed is a method for the simultaneous production of a fermented, solid product and ethanol comprising the following steps: 1) providing a mixture of milled or flaked or otherwise disintegrated biomass, comprising oligosaccharides and/or polysaccharides and live yeast in a dry matter ratio of from 2:1 to 100:1, and water; 2) fermenting the mixture resulting from step (1) under conditions where the water content in the initial mixture does not exceed 65 % by weight, for 1-36 hours at a temperature of about 25-60°C under anaerobic conditions; 3) incubating the fermented mixture resulting from step (2) for 0.5-240 minutes at a temperature of about 70-150°C; and 4) separating wet fermented, solid product from the fermented mixture resulting from step (3); further comprising either a) that the fermentation in step (2) is performed in one or more interconnected paddle worm or continuous worm conveyers with inlet means for the fermentation mixture and additives and outlet means for the ferment as well as control means for rotation speed, temperature and pH, or b) that one or more processing aids are added in any of steps (1), (2) and (3) and further comprising a step of 5) separating crude ethanol from the fermented mixture in step (2) by vacuum and/or in step (3) by vacuum or by injection of steam and condensing the surplus stripping steam. om 2:1 to 100:1, and water; 2) fermenting the mixture resulting from step (1) under conditions where the water content in the initial mixture does not exceed 65 % by weight, for 1-36 hours at a temperature of about 25-60°C under anaerobic conditions; 3) incubating the fermented mixture resulting from step (2) for 0.5-240 minutes at a temperature of about 70-150°C; and 4) separating wet fermented, solid product from the fermented mixture resulting from step (3); further comprising either a) that the fermentation in step (2) is performed in one or more interconnected paddle worm or continuous worm conveyers with inlet means for the fermentation mixture and additives and outlet means for the ferment as well as control means for rotation speed, temperature and pH, or b) that one or more processing aids are added in any of steps (1), (2) and (3) and further comprising a step of 5) separating crude ethanol from the fermented mixture in step (2) by vacuum and/or in step (3) by vacuum or by injection of steam and condensing the surplus stripping steam.
Description
Method for the simultaneous production of ethanol
and a fermented, solid product
Field of the invention
The present invention relates to a method for the simultaneous production of
a fermented, solid product and ethanol.
Furthermore it relates to the products obtainable by the method as well as
the use of the products obtained.
ound of the invention
There is a need for development of sustainable energy sources, and bio
ethanol is an attractive source as fuel for transportation. Therefore, there is a
need for a process that can e bio ethanol at a low cost. There is
r a need for providing alternative sources of protein for human food and
animal feed.
The ability of yeast to convert simple sugars into ethanol is well known.
The conversion process is frequently performed by milling a starch-
2O containing raw al and converting the starch into fermentable sugars by
enzymatic or acid hydrolysis. After this, yeast is added to ferment the sugars
to alcohol and carbon e.
This process is usually med at low dry matter content in a batch or fed-
batch or a continuous s with water content of 90% or more. In 2nd
generation production of bio ethanol the dry matter in the fermentation broth
is reported to be up to approx. 20%. After fermentation the alcohol is distilled
off.
WO 50456
From an economic point of view the high water content in the process is
rable for the following reasons: High processing costs and high
investment costs due to the large volume of the reaction vessels.
A2 discloses a s for producing a fermentation
product, such as l, from milled starch-containing material comprising
saccharifying the milled starch-containing material with a lly derived
glucoamylase without gelatinization of said starch-containing material and
ting using a fermenting microorganism.
A1 discloses a method of preparing a fermented protein
t derived from yeast and proteinaceous pulse parts by fermenting
under anaerobic conditions at water content not exceeding 80 % and
incubating the fermented mixture in a closed system.
A3 discloses a method for the directed, ive solid-
phase culturing of stable microbial mixed populations for the continuous
preparation of defined enzyme and metabolite mixtures and a suitable
bioreactor therefore.
WO2006/129320 A2 discloses a method of producing a n concentrate
from starch containing grain which method comprises fermentation, and
wherein the fermentation product can be ethanol.
A2 discloses a method for the production of ethanol and a
modified animal feed by saccharification and fermentation.
WO2006/056838 A1 discloses a process for liquefaction and saccharification
of polysaccharide containing ses having a dry matter content of above
20 %, which method comprises enzymatic hydrolysis combined with mixing
by a gravity based type of mixing providing mechanical processing. The
2012/069601
resulting processed biomass of the process may be further utilized for
ethanol production in a subsequent fermentation s.
A1 discloses a process for production of fermentation
products, including bioethanol by pretreatment and enzymatic hydrolysis
fermentation of waste fractions containing mono- and/or polysaccharides,
having a dry matter t of above 20 % using free fall mixing for the
mechanical processing of the waste on and uent tation.
A fermentor for processing a raw material and an operational method
therefore is disclosed in EP 1 355 533 B1; the fermentor disclosed is for
continuous processing of a product mixture, particularly dough, or a mixture
of water and ground cereal products. A vertical reactor for continuous
fermentation utilizing an Archimedean screw is disclosed in GB 2 049 457 A.
The object of the present invention is to provide an improved method for the
production of bio ethanol allowing simultaneous production of a valuable
ted, solid product, where the water content during the process is low.
2O Another object is to provide a process, which can be performed at low costs
due to the low water content and equipment of low investment and thereby
also provide the products at lower costs.
Yet r object is to provide a fermented, solid product of high
commercial value.
These objects are fulfilled with the process and the products of the t
invenflon.
Summary of the invention
Accordingly, in one aspect the present invention relates to a method for the
aneous production of a fermented, solid product and ethanol
comprising the following steps:
1) providing a mixture of milled or flaked or ise disintegrated
biomass, comprising oligosaccharides and/or polysaccharides and live
yeast in a dry matter ratio of from 2:1 to 100:1, and water;
2) fermenting the mixture resulting from step (1) under conditions where
the water content in the initial mixture does not exceed 65 % by
weight, for 1-36 hours at a temperature of about 25-60°C under
anaerobic conditions;
3) incubating the fermented mixture resulting from step (2) for 05-240
minutes at a temperature of about 70-150°C; and
4) separating wet fermented, solid product from the fermented mixture
resulting from step (3);
2O further comprising that the fermentation in step (2) is performed in one or
more interconnected paddle worm or continuous worm conveyers, ally
arranged non-vertically, with inlet means for the fermentation mixture and
additives and outlet means for the ferment as well as control means for
rotation speed, ature and pH, and further comprising a step of
) ting crude ethanol from the fermented mixture in step (2) by
vacuum and/or in step (3) by vacuum or by injection of steam and
condensing the s stripping steam.
In a second aspect the invention relates to a method for the simultaneous
production of a fermented, solid product and ethanol comprising the following
steps:
1) providing a mixture of milled or flaked or otherwise disintegrated
biomass, comprising oligosaccharides and/or polysaccharides and live
yeast in a dry matter ratio of from 2:1 to 100:1, and water;
2) fermenting the e resulting from step (1) under conditions where
the water content in the initial e does not exceed 65 % by
1 0 weight, for 1-36 hours at a ature of about 25-60°C under
anaerobic conditions;
3) incubating the fermented mixture resulting from step (2) for 05-240
minutes at a temperature of about 70-150°C; and
4) separating wet fermented, solid product from the fermented mixture
resulting from step (3);
further comprising that one or more processing aids are added in any of
steps (1 ), (2) and (3), and further comprising a step of
5) separating crude ethanol from the fermented mixture in step (2) by
vacuum and/or in step (3) by vacuum or by ion of steam and
condensing the surplus stripping steam.
It is sing that by the combination ing to the first aspect of the
invention of two special measures in the method, viz. firstly, ming the
fermentation step (2) in one or more interconnected paddle worm or
continuous worm conveyers and, secondly, separating the crude ethanol
from the fermentation mixture already in step (2) by vacuum and/or in step
(3) by vacuum or by injection of steam and condensing the surplus stripping
steam, it is possible to t the method for producing ethanol at a
substantially higher dry matter content than in the prior art methods and
simultaneously to produce a valuable fermented, solid biological product.
It is further surprising that by applying the second aspect of the invention of
y, adding one or more processing aids, such as one or more enzymes or
one or more plant based components, and, secondly, separating the crude
ethanol from the tation mixture already in step (2) by vacuum and/or in
step (3) by vacuum or by injection of steam and sing the surplus
stripping steam, it is likewise le to conduct the method for producing
ethanol at a substantially higher dry matter content than in the prior art
methods and simultaneously to produce a valuable ted, solid
biological product.
Normally, when the water content is reduced, and thereby the dry matter
content of the mixture to be fermented is high, a fermentation mixture tends
to compact so that the transportation behavior is affected negatively, and at
certain water content the mixture is compacted to an extent so that the
transportation is stopped.
2O The water content may be further reduced to 60%, 55%, 50% or 45% or even
to 40% without seriously affecting the sion of oligosaccharides to
fermentable sugars or the subsequent tation of those sugars. The
production of the same amount of l in a d amount of water leads
to a higher concentration of alcohol in the product.
The method of the invention in its first aspect makes use of a special
fermentor ucted so that besides transportation the conveyers also
provide mixing and lifting of the material. This makes it possible to perform
the fermentation in a mixture where the water content initially does not
exceed 65% by weight i.e. the fermentation mixture has a content of dry
matter of 35% by weight or more in the initial fermentation mixture at the
beginning of the process, whereas the dry matter content in similar prior art
s are about 20 % or lower. Due to the low water content and the
possibility of separating crude ethanol in an early stage of the process, the
process can be performed at lower costs than prior art methods. The method
of the invention in its second aspect in one ment also makes use of
said special fermentor.
In one embodiment of the invention said continuous worm conveyer is an
optionally modified type of a single bladed or multi bladed Archimedean
screw or intersected screw designed to transport the fermenting mixture and
at the same time g the material so that it is transported and agitated
without compacting it, and in one aspect is non-vertical.
In another embodiment of the invention said special fermentor is a al
screw mixer, e.g. a Nauta Mixer.
Normally more than 90% by weight of the ethanol produced can be extracted.
The yield of ethanol is dependent upon the content of carbohydrates in the
fermentation mixture and the conversion into fermentable sugars.
2O On the basis of defatted soy it is possible to te 4-5% by weight of
ethanol, whereas on wheat approx. 20% by weight can be obtained.
The invention further es a crude ethanol obtainable by a process
according to the invention and further comprising small amounts of
components resulting from the fermented biomass, e.g. 0.01-1 % of other
alcohols and ethers, such as ethyl acetate, 3-methylbutanol and/or 2-
methylbutanol, and a fermented, solid product obtainable by a s
ing to the invention comprising proteins, carbohydrates and optionally
dietary fibers and/or salts resulting from the fermented s, wherein
yeast protein is comprised in an amount of 1- 95 % by weight on dry matter
basis, and carbohydrate is comprised in an amount of 5-99% by weight on
dry matter basis.
Definitions
In the context of the current invention, the following terms are meant to
comprise the following, unless defined elsewhere in the description.
The terms “about”, “around”, “approximately”, or “ ”
~ are meant to indicate
e.g. the measuring uncertainty commonly experienced in the art, which can
be in the order of ude of e.g. +/- 1, 2, 5, 10, 20, or even 50%.
The term "comprising" is to be interpreted as specifying the presence of the
stated part(s), step(s), feature(s), composition(s), chemical(s), or
component(s), but does not exclude the presence of one or more additional
parts, steps, features, compositions, chemicals or components. E.g., a
composition comprising a chemical compound may thus comprise additional
chemical compounds, etc.
Biomass:
2O Comprises ical al that can be used for fuel or as a raw al in
industrial production.
In this context, biomass refers to plant matter in the form of stem, twig, leaf,
flower, fruit, seed, etc.
ise disintegrated:
Means disintegrated by acid or alkaline pressure-cooking or ultrasonic
treatment.
accharides and polysaccharides:
An oligosaccharide is a saccharide polymer containing a small number of
ent monomer sugars, also known as simple sugars.
Polysaccharides are saccharide polymers containing a large number of
component monomer sugars, also known as complex carbohydrates.
Examples include storage ccharides such as starch and structural
polysaccharides such as cellulose.
Carbohydrates:
Comprise mono-, di-, oligo- and polysaccharides.
Proteinaceous als:
Comprise organic compounds made of amino acids arranged in a linear
chain and joined together by a bond called a peptide bond. At a chain length
of up to approximately 50 amino acids the compound is called a peptide, at
higher molecular weight the organic compound is called a polypeptide or a
protein.
Fats:
Comprise esters n fatty acids and glycerol. One molecule of glycerol
can be esterified to one, two and tree fatty acid molecules resulting in a
monoglyceride, a diglyceride or a ceride respectively. Usually fats
2O consist of mainly triglycerides and minor amounts of lecithins, sterols, etc. If
the fat is liquid at room temperature it is normally called oil. With respect to
oils, fats and related products in this context, reference is made to “Physical
and al Characteristics of Oils, Fats and Waxes”, AOCS, 1996, as well
as “Lipid Glossary 2”, PD. Gunstone, The Oily Press, 2004.
Glycerides:
Comprise mono-, di- and triglycerides.
Processing aids:
1. Enzymes
Enzyme(s) is a very large class of protein substances that act as catalysts.
Commonly, they are divided in six classes, and the main classes falling within
the scope of this invention can be transferases that transfer functional groups
and the hydrolases that hydrolyze various bonds. Typical es can
comprise: protease(s), peptidase(s), (d—)galactosidase(s), e(s),
glucanase(s), ase(s), hemicellulase(s), phytase(s), “pase(s), phospholi-
pase(s) and oxido-reductase(s).
2. Plant components and organic sing agents
Some of the functional properties that are important in this context are:
Antioxidant, anti-bacterial action, wetting properties and stimulation of
enzymes.
The list of plant-based components is huge, but the most ant are the
following: Rosemary, thyme, oregano, flavonoids, ic acids, saponins
and d — and B — acids from hops for the modulation of e carbohydrates
,e.g. d-lupulic acid.
Furthermore organic acids e.g. -, propionic-, lactic-, - and ascorbic
acid and their salts for the adjustment of the pH-value, preservation and
2O chelating properties is part of this group of processing aids.
A further member in this group is lipids for the modulation of ethanol
tolerance of the yeast e.g. Cholesterol, oils and olein fractions of vegetable
fats that are high in C18—unsaturated fatty acids.
3. Inorganic processing agents
Comprise inorganic compositions that are able to preserve the fermenting
mixture against bacterial attack during processing e.g. Sodium bisulfite, etc.
Anticaking and flow improving agents in the final product e.g. Potassium
aluminum silicate, etc.
Processed food products:
Comprise dairy products, processed meat products, sweets, desserts, ice
cream desserts, canned products, freeze dried meals, dressings, soups,
convenience food, bread, cakes, etc.
Processed feed products:
Comprise ready-to-use feed for animals such as piglets, calves, poultry,
furred animals, sheep, cats, dogs, fish and crustaceans, etc.
Pharmaceutical products:
Comprise products, lly in the form of a tablet or in granulated form,
containing one or more biologically active ingredients intended for curing
and/or alleviating the symptoms of a disease or a condition. Pharmaceutical
products furthermore comprise pharmaceutically acceptable excipients
and/or carriers. The solid bio products herein disclosed are very well suited
for use as a pharmaceutically acceptable ingredient in a tablet or granulate.
Cosmetic ts:
Comprise products intended for personal hygiene as well as ed
2O ance such as conditioners and bath preparations.
ed description of the invention
In one embodiment of the method of the invention in its first aspect one or
more processing aids are added in any of the steps (1), (2) and (3).
In one embodiments of the method of the ions in its second aspect the
fermentation in step (2) is performed in one or more interconnected paddle
worm or continuous worm conveyers, optionally arranged vertically, with inlet
means for the fermentation mixture and ves and outlet means for the
3O ferment as well as control means for rotation speed, temperature and pH,
and/or further comprising a step (5) of separating crude ethanol from the
fermented mixture in step (2) by vacuum and/or in step (3) by vacuum or by
injection of steam and condensing the surplus stripping steam.
In one ment the methods of the invention further comprise a step of
2a) fermenting the mixture resulting from step (2) for 1-36 hours at a
ature of about 25-60°C under aerobic conditions and optionally
separating crude ethanol from the fermented mixture in step (2a) by
Vacuum.
In another embodiment step (3) is carried out at a temperature of about 70-
120°C. lly, in the incubation step (3) a high temperature is used for
short time, and lower temperatures are used for longer incubation times.
The dry matter t may vary from 35 to 70 % by weight of the mixture of
step 1), e.g. from 40 to 65 % or from 45 to 60 % or from 50 to 55 %.
In embodiments of both aspects of the method of the invention the at least
one processing aids added in any of steps (1), (2), (2a) and (3) is one or
2O more enzymes, and an enzymatic saccharification process converting the
oligo- and/or polysaccharides into fermentable carbohydrates takes place
aneously with the yeast fermentation. The enzyme(s) may be ed
from the group consisting of protease(s), peptidase(s), galactosidase(s),
amylase(s), pectinase(s), cellulase(s), hemicellulase(s), glucanase(s),
glucosidase(s), phytase(s), |ipase(s), oxido-reductase(s) and
phospholipase(s).
This embodiment has been found to be most advantageous from an
investment point of view as well as with a view to shorten reaction time.
Thus, by continuously fermenting the liberated fermentable sugars, catabolite
repression is avoided and the mass balance equilibrium pushed to the right.
This is of particular importance when operating at the high dry matter content
according to the invention.
In other embodiments of both aspects of the method of the ion the at
least one processing aids is one or more plant-based ent, such as a
component selected from rosemary, thyme, oregano, flavonoids, phenolic
acids, saponins and d — and B — acids from hops for the modulation of
soluble carbohydrates, e.g. d—lupulic acid.
The yeast to be used in the method of the invention may e.g. be ed
among Saccharomyces cerevisiae strains, including spent brewer’s yeast
and spent distiller’s yeast and spent yeast from wine production, as well as
yeast strains ting C5 sugars. C5 sugars are pentose-based sugars,
such as xylose and arabinose.
In another embodiment biomass comprising oligosaccharides and/or
polysaccharides further comprises proteins originating from proteinaceous
plant parts, e.g. pulses, such as soy, pea, lupine, and/or cereals, such as
wheat. An example of a suitable biomass is ground or flaked, defatted
2O soybeans. A suitable biomass can also be ground or flaked s e.g.
wheat. Furthermore, mixtures of pulse parts and cereals are suitable biomass
for processing by the method.
The s sing oligosaccharides and/or polysaccharides and
ally proteins may further comprise oils and fats, e.g. from seeds of oil
bearing plants, e.g. rape seed. An example of a suitable biomass is ground
or , full fat soybeans or rapeseeds or their mixtures.
The separation of fermented product and ethanol in steps (4) and (5) may be
performed by standard unit operations comprising e.g. stripping with steam,
2012/069601
evaporation, condensation, distillation, filtration, centrifugation and
sedimentation.
In other embodiments separated compounds may be subject to special
treatments sing e.g. purification, drying, milling and admixture of other
ingredients. All the unit operations that can be used for this as well as for the
separation in steps (4) and (5) are well known to a person skilled in the art.
The separated fermented, solid product may subsequently be made more
water-soluble by hydrolysis, e.g. by enzymes.
The method of the invention may e.g. be performed as a batch, fed-batch or
continuous process.
y, the ethanol produced by the process of the invention may be used to
generate heat for the process e.g. by tic combustion and thus at the
same time get rid of polluting volatile organic compounds, e.g. hexane. In
this case the by-products generated will be carbon dioxide and water.
In one embodiment the fermented, solid product of the ion comprises
2O protein in an amount of 25—90% by weight on dry matter basis, and glyceride
in an amount of 0—30% by weight on dry matter basis. About 1—35% ve
of said n may be originating from yeast protein and about 65—99%
relative of said protein may be originating from proteinaceous plant parts, e.g.
from pulses and/or cereal, such as soybeans and/or wheat.
In another embodiment the fermented, solid product is derived from biomass
inantly comprising oligosaccharides and/or polysaccharides and
comprises yeast protein in an amount of 1 — 95% by weight on dry matter
basis and carbohydrate in an amount of 5 - 99% by weight on dry matter
basis.
The crude ethanol obtainable according to the invention can be used for the
generation of heat for the fermentation process.
The invention also relates to the use of a fermented, solid t according
to the invention in a processed food product for human and/or animal
consumption; as an ingredient to be used in a food or feed product; or as an
ient of a cosmetic or a pharmaceutical product or a nutritional
supplement.
Finally the invention relates to a food, feed, cosmetic or ceutical
product or a nutritional supplement containing from 1 to 99% by weight of a
fermented, solid product according to the invention.
Examples
Example 1
Fermentation in a continuous process of a biomass comprising
polysaccharides and proteins from pulses
In the following the fermentation of a s based on defatted soy is
illustrated.
100 kg per hour of dehulled and defatted, flash desolventised soy flakes were
continuously fed to a closed single bladed worm conveyer able to transport,
lift and mix the material (bioreactor). At the same time water and slurry of
spent ’s yeast (10% dry matter) where added in an amount to reach a
dry matter content of 40% by weight in the mixture.
In the bioreactor the resulting slurry was incubated for 8 hours at 34°C.
Next, the slurry was heated in a second tor (bioreactor) to 100°C with
injection of a s of life steam for approx. 30 min. The surplus steam
ning volatile organic compounds (VOC’s) comprising ethanol was
transferred to a cooling heat exchanger.
The resulting condensate had an ethanol concentration of 15% by weight.
The ethanol yield was 4.8kg per 100kg of soy flakes.
Subsequently, the wet solid product was flash dried and milled at an Alpine
pin mill.
The dried product had the following analysis:
Crude Protein (N X 6.25) 58.3%
Carbohydrates 24.0%
Moisture 5.6%
Crude fat 0.9%
Crude fiber 4.2%
Ash 7.0%
Furthermore, utritional factors in the dried, fermented product were
significantly d vs. the raw al content:
2O ted Product Raw Material
Oligosaccharides 0.9 % 13.5%
Trypsin Inhibitor 2,900 TlU/g 62,000 TlU/g
B-conglycinin 8 ppm 90,000 ppm
The fermented product is highly nutritious and palatable and thus suitable as
an ingredient in a number of food and feed products.
Example 2
Composition of VOC’s in exhaust drying air of a fermented biomass
comprising ccharides and proteins
In the following the content of volatile organic compounds (VOC’s) in the
drying air from a fermented biomass based on defatted soy is illustrated.
An air amount of two liter was collected at a ature of 557°C and a
relative humidity of 67.1 % in a Tedlarbag.
Analytical methods:
GC/FID — refers to a method where the sample from the Tedlarbag was
analyzed by GC analysis and quantified vs. Ethanol using a FID detector.
GC/MS — refers to a method where the sample ents from the
Tedlarbag are first adsorbed in a tube containing an adsorbent material
followed by tion for GO analysis by heating, and quantified by the
recording of peak area vs. Toluen—de. The identification was done by
comparison of the mass spectra with a atabase.
The results are tabulated in the following:
ent Analytical method
Ethanol GC/FID
2-Methyl-pentane GC/MS
3-methyl-pentane GC/MS
Ethyl acetate GC/MS
Hexane 1103 0.109 GC/MS
2-Methylpropanol GC/MS
3-Methylbutanol GC/MS
2-Methylbutanol GC/MS
l GC/MS
The analytical values are mean values of two determinations
From the listed components it can be an option to use the bio ethanol
obtained by the process to generate heat for the process e.g. by catalytic
combustion, and at the same time get rid of polluting volatile organic
compounds e.g. hexane.
Example 3
Fermentation in a batch process of a biomass comprising
polysaccharides and proteins from a mixture of pulses and cereals
added various enzymes as processing aid
In the following the fermentation of a biomass based on a mixture of ed
soy and wheat is illustrated.
300 kg of a mixture containing 10% by weight of dry matter of crushed wheat
and 90% by weight of dry matter of dehulled and defatted, flash
desolventised soy flakes were fed to a closed single bladed worm conveyer
2O able to transport, lift and mix the material actor). At the same time water
and a slurry of spent brewer’s yeast (10% dry ) and enzymes where
2012/069601
added in an amount to reach a dry matter content of 45% by weight in the
mixture.
The fermenting mixture had a content of 3.5% by weight of yeast based on
total dry matter and 0.4% by weight based on dry matter of each of
Viscozyme Wheat, Spirizyme Fuel and Liquozyme from Novozymes, which
enzymes provide alfa-amylase, glucoamylase, beta-glucanase activities and
side activities in the form of xylanase and cellulase activities.
In the bioreactor the ing slurry was transported, mixed and incubated
for 18 hours at 34°C.
The ethanol content in the ferment was 73.1g/kg dry matter corresponding to
7.3kg per 100kg dry matter of the wheat/soy mixture.
The wet solid product was flash dried and milled at an Alpine pin mill.
The dried fermented product had a water t of 6.6% by weight and a
n content of 59.1% by weight.
2O Example 4
Fermentation in a laboratory scale process of a s comprising
polysaccharides and proteins from soy, added B-lupulic acid from hop
as processing aid
The fermentation was performed on a biomass based on a e of
defatted soy and 3.5% by weight of yeast and water added in an amount to
reach a dry matter content of 48% by weight in the mixture.
To the fermentation mixtures B-Iupulic acid from hop was added in various
concentrations.
The fermentation was performed in small glass ners at 34°C for 17
hours followed by heat treatment to stop the fermentation.
After the fermentation was terminated the content of soluble ydrates
was extracted by stirring a watery suspension slurry of 10% DM for 30 min
followed by centrifugation for 10 min at 3000 x g.
The watery extracts of the ferment was analyzed for carbohydrate content by
the phenol-sulphuric acid method (Carbohydrate analysis — A practical
ch; IRL Press, Oxford. Ed. M.F. n & J.F. , 1986).
The results obtained are tabulated in the following:
B-lupulic acid Soluble carbohydrates
Concentration in ppm mg/ml in extract
The crude ethanol was not isolated in this ment. However, the crude
ethanol might have been separated from the fermented mixture by
tional methods, and the concentration of ethanol in the resulting
condensate determined by conventional methods, e.g. as described in
example 1.
From the results it can be seen that the use of B-Iupulic acid as processing
aid reduce the content of water—soluble carbohydrates in the fermented
2O product i.e. it improve the fermentation process.
Example 5
Fermentation in a batch process of a biomass comprising
polysaccharides and proteins from soy, added various hop based
sing aids
250 kg of ed and defatted, flash desolventised soy flakes were fed to a
closed single bladed worm conveyer able to transport, lift and mix the
material (bioreactor). At the same time water and a slurry of spent brewer’s
yeast (10% dry matter) and hop based processing aids where added in an
amount to reach a dry matter t of 45% by weight in the mixture.
The fermenting mixture had a content of 3.5% by weight of yeast based on
total dry matter and 3000ppm of d—, or B- acids, or d + B acids, or acids
from hop.
In the bioreactor the resulting slurry was transported, mixed and ted
for 16 hours at 34°C.
The wet solid product was flash dried and milled at an Alpine pin mill.
The dried fermented products had a water content of 4.5 — 5.3% by weight
and a protein content of 56.0 — 56.8% by weight.
Before and after the fermentation was terminated the content of soluble
2O carbohydrates was analyzed on watery extracts of the ferment and on the
dried product by the method described in Example 4.
As ned in example 4 the crude ethanol was not isolated in this
experiment either. However, the crude ethanol might have been ted
from the fermented mixture by conventional methods, and the concentration
of ethanol in the resulting condensate determined by conventional methods,
e.g. as described in example 1.
The results obtained are tabulated in the following:
Type of Main Soluble e Soluble Soluble
processing constituents carbohydrates carbohydrates carbohydrates carbohydrates
aid added Before After Reduction in In an extract of
fermentation fermentation mg/ml and in % the dried product
-—————
Hop 002- B - acids 13.4 5.5 7.9 — 59.0% 6.3
extract
III-I-Hop d + 6 -
13.6 7.4 6.2 — 45.6% 7.8
Hop or + B- 18.1 10.1 8.0—44.2% 9.3
EtOH- acids
eXtraCt I...-
Hop iso- Ksalt of 13.1 5.1 8.0—61.1% 5.2
extract iso-d-
acids
From the results it can be seen that by the use of various hop components
during fermentation it is possible to modulate the amount of e
carbohydrates.
The presence of a hop extract where the main constituent is B — acids as well
as an extract where the main constituent is iso-d-acids reduced the content
of soluble carbohydrates, whereas the combined presence of d- and 6 —
acids tend to preserve the content of soluble carbohydrates ve to the
reference t any addition of hop processing aids.
As mentioned in example 4 the crude ethanol was not isolated in this
experiment as well. However, the crude ethanol might have been separated
from the fermented mixture by tional methods, and the concentration
of l in the resulting condensate determined by conventional methods,
eg. as described in example 1.
Claims (42)
1. A method for the simultaneous production of a fermented, solid product and ethanol comprising the following steps: 1) providing a e of milled or flaked biomass or biomass disintegrated by means of acid or ne pressure cooking or ultrasonic treatment, comprising oligosaccharides and/or polysaccharides and live yeast in a dry matter ratio of from 2:1 to 10 100:1, and water; 2) fermenting the e resulting from step (1) under conditions where the water content in the initial e does not exceed 65 % by weight, for 1-36 hours at a temperature of about 25-60ºC under bic conditions; 15 3) incubating the fermented mixture resulting from step (2) for 0.5-240 minutes at a temperature of about ºC; and 4) separating wet fermented, solid product from the fermented mixture resulting from step (3); 20 further comprising that the fermentation in step (2) is performed in one or more interconnected paddle worm or continuous worm conveyers with inlet means for the fermentation mixture and additives and outlet means for the ferment as well as control means for rotation speed, temperature and pH, and further comprising a step of 5) separating crude ethanol from the ted mixture in step (2) by vacuum and/or in step (3) by vacuum or by injection of steam and condensing the surplus stripping steam.
2. Method according to claim 1, wherein one or more processing aids selected from enzymes, plant components and organic processing agents and inorganic processing agent, are added in any of steps (1), (2) and (3). 5
3. Method ing to claim 1 or 2, wherein said one or more interconnected paddle worm or continuous worm ers is arranged nonvertically.
4. Method according to claim 2 or 3, wherein at least one of said one or more 10 processing aids is an enzyme, and wherein an enzymatic saccharification process ting said oligo- and/or polysaccharides into fermentable carbohydrates takes place simultaneously with the yeast fermentation in step (2). 15
5. Method according to claim 4, wherein said enzyme is selected from a protease, peptidase, (α-) galactosidase, amylase, glucanase, pectinase, hemicellulase, phytase, lipase, phospholipase or oxido-reductase.
6. Method according to claim 2 or 3, wherein at least one of said one or more 20 processing aids is a component selected from rosemary, thyme, oregano, flavonoids, phenolic acids, ns and α – and β – acids from hops for the modulation of soluble carbohydrates.
7. Method according to claim 6, wherein said sing aid is α-lupulic acid.
8. Method according to any one of the preceding claims, further comprising a step of: 2a) ting the mixture resulting from step (2) for 1-36 hours at a 30 temperature of about C under aerobic conditions and optionally ting crude ethanol from the fermented mixture in step (2a) by vacuum.
9. Method according to claim 8, further comprising that one or more 5 processing aids are added in step (2a).
10. Method according to claim 9, wherein at least one of said one or more processing aids are an enzyme, and wherein an tic saccharification process ting said oligo- and/or polysaccharides into fermentable 10 carbohydrates takes place simultaneously with the yeast fermentation in step (2a).
11. Method ing to claim 10, wherein at said enzyme is selected from a protease, peptidase, (α-) galactosidase, amylase, glucanase, pectinase, 15 hemicellulase, phytase, lipase, phospholipase or oxido-reductase.
12. Method according to claim 9, wherein at least one of said one or more processing aids is a component ed from rosemary, thyme, oregano, flavonoids, phenolic acids, saponins and α – and β – acids from hops for the 20 modulation of soluble carbohydrates.
13. Method according to claim 12, wherein the processing aid is α-lupulic acid. 25
14. Method according to any one of the preceding claims, wherein step (3) is carried out at a temperature of about 70-120ºC.
15. Method according to any one of the preceding claims, where said uous worm conveyer is a modified type of a single bladed or multi 30 bladed Archimedean screw or intersected screw, designed to transport the fermenting mixture in a non-vertical direction and at the same time lifting the material so that it is transported and agitated without compacting it.
16. Method according to any one of the ing claims, wherein said live 5 yeast is selected among Saccharomyces cerevisiae strains, including spent brewer’s yeast and spent distiller’s yeast and spent yeast from wine production, as well as yeast strains fermenting C5 .
17. Method according to any one of the preceding claims where said 10 biomass comprising oligosaccharides and/or polysaccharides further comprises proteins originating from proteinaceous plant parts.
18. Method according to claim 17 where said biomass comprising oligosaccharides and/or polysaccharides r comprises proteins 15 originating from proteinaceous pulses parts.
19. Method according to claim 18 where said biomass comprising oligosaccharides and/or polysaccharides further comprises proteins ating from soy, pea, lupine.
20. Method according to claim 17 where said biomass comprising oligosaccharides and/or polysaccharides further comprises proteins originating from s. 25
21. Method according to claim 20 where said biomass comprising oligosaccharides and/or polysaccharides further comprises proteins originating from wheat.
22. Method according to any one of the preceding claims where said biomass 30 comprising oligosaccharides and/or ccharides and optionally ns further comprises oils and fats.
23. Method according to claim 22 where said biomass comprising oligosaccharides and/or polysaccharides and optionally proteins further comprises oils and fats from seeds of oil bearing plants.
24. Method ing to claim 23 where said biomass comprising oligosaccharides and/or polysaccharides and optionally proteins further comprises oils and fats from rape seed. 10
25. Method according to any one of the preceding claims, where said separated fermented, solid product subsequently is made more water soluble by hydrolysis.
26. Method according to claim 25, where said separated fermented, solid 15 product subsequently is made more water soluble by hydrolysis by enzymes.
27. Method according to any one of the preceding claims performed as a batch, fed-batch or continuous process. 20
28. Method according to any one of the preceding claims where said ethanol produced is used to te heat for the process and thus at the same time get rid of polluting volatile c compounds.
29. Method according to claim 28 where said ethanol produced is used to 25 generate heat for the process by tic combustion and thus at the same time get rid of polluting volatile organic compounds.
30. Method according to claim 29 where said ethanol ed is used to generate heat for the process by tic combustion and thus at the same 30 time get rid of polluting volatile organic compounds in form of hexane.
31. Method according to any one of the preceding claims, wherein the fermenting step (2) is performed under conditions where the water content in 5 the initial mixture does not exceed 60%
32. Method according to claim 31, n the fermenting step (2) is med under conditions where the water content in the initial mixture does not exceed 55 %.
33. Method according to claim 32, wherein the fermenting step (2) is performed under ions where the water content in the initial mixture does not exceed 50 %. 15
34. Method according to claim 33, wherein the fermenting step (2) is performed under ions where the water content in the initial mixture does not exceed 45 %.
35. A crude ethanol obtainable by a process according to any one of claims 20 1-34 and further comprising hexane and optionally 0.01-1% of other components resulting from the fermented biomass selected from ethyl acetate, 3-methylbutanol and/or 2-methylbutanol.
36. A fermented, solid product able from a biomass predominantly 25 comprising oligosaccharides and/or polysaccharides by a process ing to any one of claims 1 – 34, n yeast protein is comprised in an amount of 1 – 95% by weight on dry matter basis, and carbohydrate is comprised in an amount of 5 - 99% by weight on dry matter basis. 30
37. Fermented, solid product according to claim 36, which comprises protein in an amount of 25–90% by weight on dry matter basis, and glyceride in an amount of 0–30% by weight on dry matter basis and, n about 1–35% relative of said protein is originating from yeast protein and about 65–99% relative of said protein is originating from proteinaceous plant parts. 5
38. Fermented, solid product according to claim 37, which comprises n in an amount of 25–90% by weight on dry matter basis, and ide in an amount of 0–30% by weight on dry matter basis and, wherein about 1–35% relative of said protein is originating from yeast protein and about 65–99% relative of said protein is originating from proteinaceous pulses parts.
39. ted, solid product ing to claim 37, which comprises protein in an amount of 25–90% by weight on dry matter basis, and glyceride in an amount of 0–30% by weight on dry matter basis and, wherein about 1–35% relative of said protein is originating from yeast protein and about 65–99% 15 relative of said protein is originating from s.
40. Fermented, solid product according to claim 37, wherein said biomass comprises rapeseed. 20
41. Use of a fermented, solid product according to any one of claims 36-40 in a processed food product for human and/or animal consumption or as an ingredient to be used in a food or feed product or as an ingredient of a cosmetic or a pharmaceutical product or a nutritional supplement. 25
42. A food, feed, cosmetic or pharmaceutical product or a nutritional supplement containing from 1 to 99% by weight of a fermented, solid product according to any one of claims 36-40.
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161543907P | 2011-10-06 | 2011-10-06 | |
EP11184135.9 | 2011-10-06 | ||
EP11184135 | 2011-10-06 | ||
US61/543,907 | 2011-10-06 | ||
US201261638777P | 2012-04-26 | 2012-04-26 | |
US61/638,777 | 2012-04-26 | ||
PCT/EP2012/069601 WO2013050456A1 (en) | 2011-10-06 | 2012-10-04 | Method for the simultaneous production of ethanol and a fermented, solid product |
Publications (2)
Publication Number | Publication Date |
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NZ622442A NZ622442A (en) | 2015-06-26 |
NZ622442B2 true NZ622442B2 (en) | 2015-09-29 |
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