Methods for Improving By-Products from Fermentation Processes Using Xylanase

US2016333332A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016333332-A1
Application numberUS-201515112664-A
CountryUS
Kind codeA1
Filing dateJan 15, 2015
Priority dateJan 31, 2014
Publication dateNov 17, 2016
Grant date

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  5. First independent claim

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Abstract

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Provided are GH10 xylanases or a fragment thereof including modified xlyanase enzymes, all having xylanase activity, wherein the enzyme or fragment thereof provides increased oil recovery from a grain-based material compared with a control or parent GH10 xylanase enzyme, the parent GH10 xylanase having been modified at at least one or more of the following positions 7, 25, 33, 64, 79, 89, 217 and 298, wherein the numbering is based on the amino acid numbering of FveXyn4 (SEQ ID No. 1). Methods of using the GH10 xylanases, for example, for improved oil recovery are also provided.

First claim

Opening claim text (preview).

1 . A modified xylanase enzyme wherein said enzyme is a GH10 xylanase or a fragment thereof having xylanase activity, wherein said enzyme or fragment thereof provides increased oil recovery from a grain-based material compared with a parent GH10 xylanase enzyme, the parent GH10 xylanase having been modified at at least one or more of the following positions 7, 25, 33, 64, 79, 89, 217 and 298, wherein the numbering is based on the amino acid numbering of FveXyn4 (SEQ ID No. 1). 2 . The enzyme according to claim 1 wherein the increased oil recovery is measurable at end of fermentation oil recovery. 3 . The enzyme according to claim 1 wherein the parent GH10 xylanase has been modified at at least two or more of the positions 7, 25, 33, 64, 79, 89, 217 and 298, wherein the numbering is based on the amino acid numbering of FveXyn4 (SEQ ID No. 1). 4 . The enzyme according to claim 1 wherein the parent GH10 xylanase has been modified at at least three or more of the positions 7, 25, 33, 64, 79, 89, 217 and 298, wherein the numbering is based on the amino acid numbering of FveXyn4 (SEQ ID No. 1). 5 . The enzyme according to claim 1 wherein the modification is selected from the group consisting of N7D, N25P, T33V, G64T, K9Y, S89G, A217Q and T298Y. 6 . The enzyme according to claim 1 wherein the enzyme has further modifications at one or more of the following positions: 57, 62, 103, 115, 147, 181, 193, and 219. 7 . The enzyme according to claim 6 wherein the modification is selected from the group consisting of S57Q, N62T, T103M, V115L, N147Q, G181Q, S193Y, and G219P. 8 . The enzyme according claim 1 wherein the parent GH10 xylanase is: a) a xylanase enzyme comprising the amino acid sequence of SEQ ID No. 21; or b) a xylanase enzyme comprising an amino acid sequence having at least 70% identity (suitably at least 80%, suitably at least 90%, suitably at least 95%, suitably at least 98%, suitably at least 99% identity) with SEQ ID No. 21; or c) a xylanase enzyme encoded by a nucleotide sequence comprising the nucleotide sequence shown herein as SEQ ID No. 16; or d) a xylanase enzyme encoded by a nucleotide sequence comprising a nucleotide sequence having at least 70% identity (suitably at least 80%, suitably at least 90%, suitably at least 95%, suitably at least 98%, suitably at least 99% identity) with SEQ ID No. 16; or e) a xylanase enzyme encoded by a nucleotide sequence which can hybridize to SEQ ID No. 16 under high stringency conditions. 9 . A process of recovering oil, comprising (a) liquefying a grain-based material into dextrins with an alpha-amylase; (b) saccharifying the dextrins using a carbohydrate source generating enzyme to form a sugar; (c) fermenting the sugar in a fermentation medium into a fermentation product using a fermenting organism; (d) distilling the fermentation product to form a whole stillage; (e) separating the whole stillage into thin stillage and wet cake; and (f) recovering the oil from the thin stillage, wherein at least one or more of liquefying, saccharifying and fermenting comprise admixing a GH10 xylanase or a fragment thereof wherein the GH10 xylanase is: i. a xylanase enzyme comprising the amino acid sequence of SEQ ID No. 1; or ii.) a xylanase enzyme comprising an amino acid sequence having at least 70% identity (suitably at least 80%, suitably at least 90%, suitably at least 95%, suitably at least 98%, suitably at least 99% identity) with SEQ ID No. 1; or iii.) a xylanase enzyme encoded by a nucleotide sequence consisting of the nucleotide sequence shown herein as SEQ ID No. 2; or iv.) a xylanase enzyme encoded by a nucleotide sequence comprising a nucleotide sequence having at least 70% identity (suitably at least 80%, suitably at least 90%, suitably at least 95%, suitably at least 98%, suitably at least 99% identity) with SEQ ID No. 2; or v.) a xylanase enzyme encoded by a nucleotide sequence which can hybridize to SEQ ID No. 2 under high stringency conditions. 10 . The method of claim 9 further comprising a step of steeping and/or a post fermentation processing step wherein said modified xylanase enzyme is admixed. 11 . (canceled) 12 . A process of recovering oil in a simultaneous saccharification and fermentation (SSF) process, comprising (a) admixing an alpha-amylase, a carbohydrate source generating enzyme and a fermenting organism to a grain-based material in a fermentation medium; (b) performing SSF to form a sugar in the fermentation medium and further fermenting the sugar into a fermentation product using the fermenting organism; (c) distilling the fermentation product to form a whole stillage; (d) separating the whole stillage into thin stillage and wet cake; and (e) recovering the oil from the thin stillage, wherein performing SSF comprises admixing a GH10 xylanase or a fragment thereof wherein the GH10 xylanase is: i. a xylanase enzyme comprising the amino acid sequence of SEQ ID No. 1; or ii.) a xylanase enzyme comprising an amino acid sequence having at least 70% identity (suitably at least 80%, suitably at least 90%, suitably at least 95%, suitably at least 98%, suitably at least 99% identity) with SEQ ID No. 1; or iii.) a xylanase enzyme encoded by a nucleotide sequence consisting of the nucleotide sequence shown herein as SEQ ID No. 2; or iv.) a xylanase enzyme encoded by a nucleotide sequence comprising a nucleotide sequence having at least 70% identity (suitably at least 80%, suitably at least 90%, suitably at least 95%, suitably at least 98%, suitably at least 99% identity) with SEQ ID No. 2; or v.) a xylanase enzyme encoded by a nucleotide sequence which can hybridize to SEQ ID No. 2 under high stringency conditions. 13 . (canceled) 14 . A process of recovering oil in a granular starch hydrolyzing enzyme (GSHE) process, comprising (a) contacting a grain-based material comprising granular starch at a temperature at or below the gelatinization temperature of the granular starch with one or more GSHE enzyme and a GH10 xylanase or a fragment thereof wherein the GH10 xylanase is: i. a xylanase enzyme comprising the amino acid sequence of SEQ ID No. 1; or ii.) a xylanase enzyme comprising an amino acid sequence having at least 70% identity (suitably at least 80%, suitably at least 90%, suitably at least 95%, suitably at least 98%, suitably at least 99% identity) with SEQ ID No. 1; or iii.) a xylanase enzyme encoded by a nucleotide sequence consisting of the nucleotide sequence shown herein as SEQ ID No. 2; or iv.) a xylanase enzyme encoded by a nucleotide sequence comprising a nucleotide sequence having at least 70% identity (suitably at least 80%, suitably at least 90%, suitably at least 95%, suitably at least 98%, suitably at least 99% identity) with SEQ ID No. 2; or v.) a xylanase enzyme encoded by a nucleotide sequence which can hybridize to SEQ ID No. 2 under high stringency conditions; (b) allowing the alpha amylase, GSHE enzyme and xylanase to act for a period of time between 2 and 100 hours to obtain a fermentable sugar syrup; (c) fermenting the sugar syrup into a fermentation product using a fermenting organism; (c) distilling the fermentation product to form a whole stillage; (d) separating the whole stillage into thin stillage and wet cake; and (e) recovering the oil from the thin stillage. 15 . The method of claim 14 wherein said sugar syrup is selected from the group consisting of a disaccharide, oliogosaccharide, polysaccharide, glucose, and maltose. 16 . (canceled) 17 . The method of claim 9 wherein the grain-based material comprises grain and/

Assignees

Inventors

Classifications

  • Endo-1,4-beta-xylanase (3.2.1.8) · CPC title

  • Monosaccharides (2-ketogulonic acid C12P7/60) · CPC title

  • produced by the action of a carbohydrase {(EC 3.2.x)}, e.g. by alpha-amylase {, e.g. by cellulase, hemicellulase} · CPC title

  • C12N9/2482Primary

    Endo-1,4-beta-xylanase (3.2.1.8) · CPC title

  • Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats · CPC title

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What does patent US2016333332A1 cover?
Provided are GH10 xylanases or a fragment thereof including modified xlyanase enzymes, all having xylanase activity, wherein the enzyme or fragment thereof provides increased oil recovery from a grain-based material compared with a control or parent GH10 xylanase enzyme, the parent GH10 xylanase having been modified at at least one or more of the following positions 7, 25, 33, 64, 79, 89, 217 a…
Who is the assignee on this patent?
Danisco Us Inc
What technology area does this patent fall under?
Primary CPC classification C12N9/2482. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Nov 17 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).