Starch-derived clathrate-forming compositions
US-11959114-B2 · Apr 16, 2024 · US
US9458483B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9458483-B2 |
| Application number | US-201514713751-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 15, 2015 |
| Priority date | Aug 12, 2010 |
| Publication date | Oct 4, 2016 |
| Grant date | Oct 4, 2016 |
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The present invention relates to compositions comprising: a polypeptide having cellulolytic enhancing activity and a bicyclic compound. The present invention also relates to methods of using the compositions.
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What is claimed is: 1. A method for producing a fermentation product, comprising: (a) saccharifying a cellulosic material with an enzyme composition in the presence of a GH61 polypeptide having cellulolytic enhancing activity and a bicyclic compound; (b) fermenting the saccharified cellulosic material with one or more fermenting microorganisms to produce the fermentation product; and (c) recovering the fermentation product from the fermentation, wherein the bicyclic compound is of formula (I) or (II): GH 61 effect = % conversion ( + GH 61 ) % conversion ( no GH 61 ) . wherein the bond indicated with a dashed line can be single or double; R 1 and R 2 are independently hydrogen, —C(O)R 5 , —C(O)OR 6 , —C(O)NHR 7 , or an optionally substituted moiety selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkyl-alkyl, heterocycloalkyl, heterocycloalkyl-alkyl, aryl, aralkyl, heteroaryl, and heteroaralkyl; R 3 , R 4a , R 4b , and R 4c are independently hydrogen, halogen, —OH, —OR 8 , —CN, —NO 2 , —N(R 9 )(R 10 ), —C(O)R 5 , —C(O)OR 6 , —C(O)NHR 7 , —OC(O)R 11 , —NHC(O) R 12 , —OC(O)OR 13 , —NHC(O)OR 14 , —OC(O)NHR 15 , —NHC(O)NHR 16 , —SO 2 R 17 , —SO 2 N(R 18 )(R 19 ), —SR 20 , or an optionally substituted moiety selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkyl-alkyl, heterocycloalkyl, heterocycloalkyl-alkyl, aryl, aralkyl, heteroaryl, and heteroaralkyl; and wherein two of R 4a , R 4b , and R 4c may together form an optionally substituted fused ring; R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , R 18 , R 19 , and R 20 are independently hydrogen, or an optionally substituted moiety selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkyl-alkyl, heterocycloalkyl, heterocycloalkyl-alkyl, aryl, aralkyl, heteroaryl, and heteroaralkyl; and R 17 is an optionally substituted moiety selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkyl-alkyl, heterocycloalkyl, heterocycloalkyl-alkyl, aryl, aralkyl, heteroaryl, and heteroaralkyl; or a salt or solvate thereof; wherein the combination of the GH61 polypeptide having cellulolytic enhancing activity and the bicyclic compound enhances hydrolysis of a cellulosic material by the enzyme composition according to the following formula with a ratio greater than 1: GH 61 effect = % conversion ( + GH 61 ) % conversion ( no GH 61 ) . 2. The method of claim 1 , wherein the bicyclic compound is of the formula (I-A) or (II-A): or a salt or solvate thereof. 3. The method of claim 1 , wherein the bicyclic compound is of the formula (I-B) or (II-B): or a salt or solvate thereof. 4. The method of claim 1 , wherein the bicyclic compound is of the formula (I-C), (I-D), (I-E), or (I-F): or a salt or solvate thereof. 5. The method of claim 1 , wherein the bicyclic compound
Stabilising an enzyme by forming an adduct or a composition; Forming enzyme conjugates · CPC title
Cellulase (3.2.1.4), i.e. endo-1,4-beta-glucanase · CPC title
Pretreatment of cellulosic or lignocellulosic material for subsequent enzymatic treatment or hydrolysis · CPC title
Fermentation products obtained from optionally pretreated or hydrolyzed cellulosic or lignocellulosic material as the carbon source · CPC title
Alpha- or beta- amino acids {(other amino acids C12P13/005)} · CPC title
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