CA2888333C - Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars - Google Patents
Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars Download PDFInfo
- Publication number
- CA2888333C CA2888333C CA2888333A CA2888333A CA2888333C CA 2888333 C CA2888333 C CA 2888333C CA 2888333 A CA2888333 A CA 2888333A CA 2888333 A CA2888333 A CA 2888333A CA 2888333 C CA2888333 C CA 2888333C
- Authority
- CA
- Canada
- Prior art keywords
- enzyme
- oxygen
- hydrolysis
- process according
- enzymatic hydrolysis
- Prior art date
- Legal status (The legal status 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 status listed.)
- Active
Links
- 238000000034 method Methods 0.000 title claims abstract description 188
- 230000008569 process Effects 0.000 title claims abstract description 161
- 238000000855 fermentation Methods 0.000 title claims abstract description 107
- 230000004151 fermentation Effects 0.000 title claims abstract description 105
- 230000007071 enzymatic hydrolysis Effects 0.000 title claims abstract description 97
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 title claims abstract description 97
- 239000012978 lignocellulosic material Substances 0.000 title claims abstract description 84
- 235000000346 sugar Nutrition 0.000 title claims description 83
- 150000008163 sugars Chemical class 0.000 title description 44
- 102000004190 Enzymes Human genes 0.000 claims abstract description 323
- 108090000790 Enzymes Proteins 0.000 claims abstract description 323
- 239000001301 oxygen Substances 0.000 claims abstract description 181
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 181
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 180
- 239000000203 mixture Substances 0.000 claims abstract description 138
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 66
- 102000004169 proteins and genes Human genes 0.000 claims abstract description 62
- 229920001503 Glucan Polymers 0.000 claims abstract description 45
- 238000002203 pretreatment Methods 0.000 claims abstract description 13
- 238000005406 washing Methods 0.000 claims abstract description 12
- 238000002360 preparation method Methods 0.000 claims abstract description 10
- 238000011084 recovery Methods 0.000 claims abstract description 8
- 238000006460 hydrolysis reaction Methods 0.000 claims description 204
- 230000007062 hydrolysis Effects 0.000 claims description 180
- 230000000694 effects Effects 0.000 claims description 77
- 241000678519 Rasamsonia Species 0.000 claims description 30
- 239000000463 material Substances 0.000 claims description 28
- 244000005700 microbiome Species 0.000 claims description 27
- 241000233866 Fungi Species 0.000 claims description 24
- 239000007789 gas Substances 0.000 claims description 16
- 108010084185 Cellulases Proteins 0.000 claims description 15
- 102000005575 Cellulases Human genes 0.000 claims description 15
- 230000035484 reaction time Effects 0.000 claims description 13
- 230000002538 fungal effect Effects 0.000 claims description 12
- 229940088598 enzyme Drugs 0.000 abstract description 293
- 108010059892 Cellulase Proteins 0.000 abstract description 49
- 229940106157 cellulase Drugs 0.000 abstract description 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 167
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 57
- 239000008103 glucose Substances 0.000 description 57
- 235000019441 ethanol Nutrition 0.000 description 56
- 235000018102 proteins Nutrition 0.000 description 52
- 239000000047 product Substances 0.000 description 47
- 102000004196 processed proteins & peptides Human genes 0.000 description 46
- 108090000765 processed proteins & peptides Proteins 0.000 description 46
- 229920001184 polypeptide Polymers 0.000 description 45
- 238000005273 aeration Methods 0.000 description 40
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 38
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 35
- 229920002678 cellulose Polymers 0.000 description 32
- 239000001913 cellulose Substances 0.000 description 32
- 238000006243 chemical reaction Methods 0.000 description 30
- 229920001282 polysaccharide Polymers 0.000 description 30
- 239000005017 polysaccharide Substances 0.000 description 30
- 150000004804 polysaccharides Chemical class 0.000 description 30
- 238000004519 manufacturing process Methods 0.000 description 28
- 238000002474 experimental method Methods 0.000 description 26
- 239000000243 solution Substances 0.000 description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 25
- 230000001461 cytolytic effect Effects 0.000 description 23
- 230000002829 reductive effect Effects 0.000 description 23
- 239000002253 acid Substances 0.000 description 22
- 229920001277 pectin Polymers 0.000 description 21
- 108010059820 Polygalacturonase Proteins 0.000 description 19
- 210000004027 cell Anatomy 0.000 description 19
- 238000003756 stirring Methods 0.000 description 19
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 240000008042 Zea mays Species 0.000 description 18
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 18
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 18
- 235000005822 corn Nutrition 0.000 description 18
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 18
- 239000001814 pectin Substances 0.000 description 17
- 235000010987 pectin Nutrition 0.000 description 17
- 239000000758 substrate Substances 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- 239000002028 Biomass Substances 0.000 description 16
- 108010093305 exopolygalacturonase Proteins 0.000 description 16
- 238000002156 mixing Methods 0.000 description 16
- 229920002488 Hemicellulose Polymers 0.000 description 15
- 241000228341 Talaromyces Species 0.000 description 15
- 230000009229 glucose formation Effects 0.000 description 15
- 239000007791 liquid phase Substances 0.000 description 15
- 241000196324 Embryophyta Species 0.000 description 14
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 14
- 108010002430 hemicellulase Proteins 0.000 description 14
- 229920001542 oligosaccharide Polymers 0.000 description 14
- 229940059442 hemicellulase Drugs 0.000 description 13
- SRBFZHDQGSBBOR-SOOFDHNKSA-N D-ribopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@@H]1O SRBFZHDQGSBBOR-SOOFDHNKSA-N 0.000 description 12
- 241000959173 Rasamsonia emersonii Species 0.000 description 12
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 12
- 230000008901 benefit Effects 0.000 description 12
- 150000002482 oligosaccharides Chemical class 0.000 description 12
- 229920001221 xylan Polymers 0.000 description 12
- 108090000856 Lyases Proteins 0.000 description 11
- 102000004317 Lyases Human genes 0.000 description 11
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 11
- -1 carbon sugars Chemical class 0.000 description 11
- 239000000523 sample Substances 0.000 description 11
- 239000010907 stover Substances 0.000 description 11
- 229920002230 Pectic acid Polymers 0.000 description 10
- 230000003301 hydrolyzing effect Effects 0.000 description 10
- 230000009467 reduction Effects 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 10
- 229960004319 trichloroacetic acid Drugs 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 108010029182 Pectin lyase Proteins 0.000 description 9
- 241000209140 Triticum Species 0.000 description 9
- 235000021307 Triticum Nutrition 0.000 description 9
- IAJILQKETJEXLJ-RSJOWCBRSA-N aldehydo-D-galacturonic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-RSJOWCBRSA-N 0.000 description 9
- 230000015556 catabolic process Effects 0.000 description 9
- 230000000593 degrading effect Effects 0.000 description 9
- 230000012010 growth Effects 0.000 description 9
- 239000004310 lactic acid Substances 0.000 description 9
- 235000014655 lactic acid Nutrition 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 239000000178 monomer Substances 0.000 description 9
- 150000004823 xylans Chemical class 0.000 description 9
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 8
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 8
- 108010047754 beta-Glucosidase Proteins 0.000 description 8
- 102000006995 beta-Glucosidase Human genes 0.000 description 8
- 210000002421 cell wall Anatomy 0.000 description 8
- 229920005610 lignin Polymers 0.000 description 8
- 230000000813 microbial effect Effects 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 229920000189 Arabinogalactan Polymers 0.000 description 7
- GUBGYTABKSRVRQ-CUHNMECISA-N D-Cellobiose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-CUHNMECISA-N 0.000 description 7
- 235000019312 arabinogalactan Nutrition 0.000 description 7
- 230000009286 beneficial effect Effects 0.000 description 7
- 229910052799 carbon Inorganic materials 0.000 description 7
- 238000011109 contamination Methods 0.000 description 7
- 238000006731 degradation reaction Methods 0.000 description 7
- 239000000499 gel Substances 0.000 description 7
- 238000011534 incubation Methods 0.000 description 7
- 238000004064 recycling Methods 0.000 description 7
- 101001065065 Aspergillus awamori Feruloyl esterase A Proteins 0.000 description 6
- 108010008885 Cellulose 1,4-beta-Cellobiosidase Proteins 0.000 description 6
- 101710121765 Endo-1,4-beta-xylanase Proteins 0.000 description 6
- 241000973882 Geosmithia Species 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 102000004157 Hydrolases Human genes 0.000 description 6
- 108090000604 Hydrolases Proteins 0.000 description 6
- 108091005804 Peptidases Proteins 0.000 description 6
- 102000035195 Peptidases Human genes 0.000 description 6
- 239000004365 Protease Substances 0.000 description 6
- 241000030452 Rasamsonia byssochlamydoides Species 0.000 description 6
- 235000011054 acetic acid Nutrition 0.000 description 6
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 6
- 150000001720 carbohydrates Chemical class 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 6
- 239000010318 polygalacturonic acid Substances 0.000 description 6
- 239000010902 straw Substances 0.000 description 6
- 239000006228 supernatant Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 description 5
- 108010060309 Glucuronidase Proteins 0.000 description 5
- 102000053187 Glucuronidase Human genes 0.000 description 5
- SHZGCJCMOBCMKK-JFNONXLTSA-N L-rhamnopyranose Chemical compound C[C@@H]1OC(O)[C@H](O)[C@H](O)[C@H]1O SHZGCJCMOBCMKK-JFNONXLTSA-N 0.000 description 5
- PNNNRSAQSRJVSB-UHFFFAOYSA-N L-rhamnose Natural products CC(O)C(O)C(O)C(O)C=O PNNNRSAQSRJVSB-UHFFFAOYSA-N 0.000 description 5
- 241000223257 Thermomyces Species 0.000 description 5
- AEMOLEFTQBMNLQ-BKBMJHBISA-N alpha-D-galacturonic acid Chemical compound O[C@H]1O[C@H](C(O)=O)[C@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-BKBMJHBISA-N 0.000 description 5
- 238000004364 calculation method Methods 0.000 description 5
- 235000013339 cereals Nutrition 0.000 description 5
- 238000010790 dilution Methods 0.000 description 5
- 239000012895 dilution Substances 0.000 description 5
- 230000002255 enzymatic effect Effects 0.000 description 5
- 239000000706 filtrate Substances 0.000 description 5
- 229930182830 galactose Natural products 0.000 description 5
- 238000011081 inoculation Methods 0.000 description 5
- 108010087558 pectate lyase Proteins 0.000 description 5
- 108020004410 pectinesterase Proteins 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 238000005292 vacuum distillation Methods 0.000 description 5
- ALRHLSYJTWAHJZ-UHFFFAOYSA-N 3-hydroxypropionic acid Chemical compound OCCC(O)=O ALRHLSYJTWAHJZ-UHFFFAOYSA-N 0.000 description 4
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 4
- 101710112457 Exoglucanase Proteins 0.000 description 4
- 229920002581 Glucomannan Polymers 0.000 description 4
- 229920000057 Mannan Polymers 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 4
- 229910004354 OF 20 W Inorganic materials 0.000 description 4
- ZRWPUFFVAOMMNM-UHFFFAOYSA-N Patulin Chemical compound OC1OCC=C2OC(=O)C=C12 ZRWPUFFVAOMMNM-UHFFFAOYSA-N 0.000 description 4
- 108010044725 Pectate disaccharide-lyase Proteins 0.000 description 4
- 241000959199 Rasamsonia cylindrospora Species 0.000 description 4
- 241001484137 Talaromyces leycettanus Species 0.000 description 4
- 108010093941 acetylxylan esterase Proteins 0.000 description 4
- 235000001014 amino acid Nutrition 0.000 description 4
- 229940024606 amino acid Drugs 0.000 description 4
- 150000001413 amino acids Chemical class 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- 239000001569 carbon dioxide Substances 0.000 description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 description 4
- 239000006052 feed supplement Substances 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 230000000670 limiting effect Effects 0.000 description 4
- 108010089202 trans-4-coumaroyl esterase Proteins 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- PKAUICCNAWQPAU-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)acetic acid;n-methylmethanamine Chemical compound CNC.CC1=CC(Cl)=CC=C1OCC(O)=O PKAUICCNAWQPAU-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- 108010065511 Amylases Proteins 0.000 description 3
- 102000013142 Amylases Human genes 0.000 description 3
- 102100026189 Beta-galactosidase Human genes 0.000 description 3
- 102100032487 Beta-mannosidase Human genes 0.000 description 3
- 108010001817 Endo-1,4-beta Xylanases Proteins 0.000 description 3
- 102000005744 Glycoside Hydrolases Human genes 0.000 description 3
- 108010031186 Glycoside Hydrolases Proteins 0.000 description 3
- 241000223198 Humicola Species 0.000 description 3
- 108010029541 Laccase Proteins 0.000 description 3
- 229920002097 Lichenin Polymers 0.000 description 3
- 108010054320 Lignin peroxidase Proteins 0.000 description 3
- 108090001060 Lipase Proteins 0.000 description 3
- 239000004367 Lipase Substances 0.000 description 3
- 102000004882 Lipase Human genes 0.000 description 3
- 108010059896 Manganese peroxidase Proteins 0.000 description 3
- 241000226677 Myceliophthora Species 0.000 description 3
- 241001236817 Paecilomyces <Clavicipitaceae> Species 0.000 description 3
- 241000228143 Penicillium Species 0.000 description 3
- 241000985315 Rasamsonia argillacea Species 0.000 description 3
- 241000235402 Rhizomucor Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 3
- 241000228178 Thermoascus Species 0.000 description 3
- 241000640178 Thermoascus thermophilus Species 0.000 description 3
- 239000000370 acceptor Substances 0.000 description 3
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 description 3
- 235000019418 amylase Nutrition 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 229920000617 arabinoxylan Polymers 0.000 description 3
- 108010005774 beta-Galactosidase Proteins 0.000 description 3
- 108010055059 beta-Mannosidase Proteins 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 3
- 108010089934 carbohydrase Proteins 0.000 description 3
- 238000005119 centrifugation Methods 0.000 description 3
- 108010080434 cephalosporin-C deacetylase Proteins 0.000 description 3
- 238000003776 cleavage reaction Methods 0.000 description 3
- 239000000498 cooling water Substances 0.000 description 3
- 230000006196 deacetylation Effects 0.000 description 3
- 238000003381 deacetylation reaction Methods 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 239000012470 diluted sample Substances 0.000 description 3
- 238000010828 elution Methods 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 108010041969 feruloyl esterase Proteins 0.000 description 3
- 238000011010 flushing procedure Methods 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 150000002402 hexoses Chemical class 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 230000010354 integration Effects 0.000 description 3
- 108010062085 ligninase Proteins 0.000 description 3
- 235000019421 lipase Nutrition 0.000 description 3
- 150000002632 lipids Chemical class 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 239000010813 municipal solid waste Substances 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 230000036284 oxygen consumption Effects 0.000 description 3
- 239000010893 paper waste Substances 0.000 description 3
- 230000036961 partial effect Effects 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 150000002972 pentoses Chemical class 0.000 description 3
- 238000011020 pilot scale process Methods 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 235000019419 proteases Nutrition 0.000 description 3
- 238000001448 refractive index detection Methods 0.000 description 3
- 239000009754 rhamnogalacturonan I Substances 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 238000011172 small scale experimental method Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 239000012086 standard solution Substances 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000011782 vitamin Substances 0.000 description 3
- 235000013343 vitamin Nutrition 0.000 description 3
- 229940088594 vitamin Drugs 0.000 description 3
- 229930003231 vitamin Natural products 0.000 description 3
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 229940035437 1,3-propanediol Drugs 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- SATHPVQTSSUFFW-UHFFFAOYSA-N 4-[6-[(3,5-dihydroxy-4-methoxyoxan-2-yl)oxymethyl]-3,5-dihydroxy-4-methoxyoxan-2-yl]oxy-2-(hydroxymethyl)-6-methyloxane-3,5-diol Chemical compound OC1C(OC)C(O)COC1OCC1C(O)C(OC)C(O)C(OC2C(C(CO)OC(C)C2O)O)O1 SATHPVQTSSUFFW-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 102100026277 Alpha-galactosidase A Human genes 0.000 description 2
- 239000004382 Amylase Substances 0.000 description 2
- 239000001904 Arabinogalactan Substances 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 101000709143 Aspergillus aculeatus Rhamnogalacturonate lyase A Proteins 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 229920002498 Beta-glucan Polymers 0.000 description 2
- 229920002299 Cellodextrin Polymers 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 2
- 229920000324 Cellulosome Polymers 0.000 description 2
- 229930186147 Cephalosporin Natural products 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 108090000371 Esterases Proteins 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 101710098247 Exoglucanase 1 Proteins 0.000 description 2
- 101710098246 Exoglucanase 2 Proteins 0.000 description 2
- 108050000194 Expansin Proteins 0.000 description 2
- 229930091371 Fructose Natural products 0.000 description 2
- 239000005715 Fructose Substances 0.000 description 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 229920000926 Galactomannan Polymers 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 108010059881 Lactase Proteins 0.000 description 2
- 101000728666 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) Putative rhamnogalacturonase Proteins 0.000 description 2
- 241001520808 Panicum virgatum Species 0.000 description 2
- 241000228150 Penicillium chrysogenum Species 0.000 description 2
- 241000209504 Poaceae Species 0.000 description 2
- LCTONWCANYUPML-UHFFFAOYSA-M Pyruvate Chemical compound CC(=O)C([O-])=O LCTONWCANYUPML-UHFFFAOYSA-M 0.000 description 2
- PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 description 2
- 241001489203 Talaromyces bacillisporus Species 0.000 description 2
- 241000228182 Thermoascus aurantiacus Species 0.000 description 2
- 241000228184 Thermoascus crustaceus Species 0.000 description 2
- 241001136490 Thermomyces dupontii Species 0.000 description 2
- 241001494489 Thielavia Species 0.000 description 2
- 241000223259 Trichoderma Species 0.000 description 2
- 229920002000 Xyloglucan Polymers 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000002730 additional effect Effects 0.000 description 2
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 description 2
- 108010030291 alpha-Galactosidase Proteins 0.000 description 2
- 108010084650 alpha-N-arabinofuranosidase Proteins 0.000 description 2
- 150000004783 arabinoxylans Chemical class 0.000 description 2
- 238000003556 assay Methods 0.000 description 2
- 239000002551 biofuel Substances 0.000 description 2
- OWMVSZAMULFTJU-UHFFFAOYSA-N bis-tris Chemical compound OCCN(CCO)C(CO)(CO)CO OWMVSZAMULFTJU-UHFFFAOYSA-N 0.000 description 2
- 238000012511 carbohydrate analysis Methods 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 210000000166 cellulosome Anatomy 0.000 description 2
- 229940124587 cephalosporin Drugs 0.000 description 2
- 150000001780 cephalosporins Chemical class 0.000 description 2
- 230000007073 chemical hydrolysis Effects 0.000 description 2
- 239000012295 chemical reaction liquid Substances 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000007857 degradation product Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229910001882 dioxygen Inorganic materials 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 108010091371 endoglucanase 1 Proteins 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- KSEBMYQBYZTDHS-HWKANZROSA-N ferulic acid Chemical compound COC1=CC(\C=C\C(O)=O)=CC=C1O KSEBMYQBYZTDHS-HWKANZROSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 230000034659 glycolysis Effects 0.000 description 2
- 239000010903 husk Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 229940116108 lactase Drugs 0.000 description 2
- 108010076363 licheninase Proteins 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 150000002772 monosaccharides Chemical class 0.000 description 2
- 238000005457 optimization Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000001139 pH measurement Methods 0.000 description 2
- LCLHHZYHLXDRQG-ZNKJPWOQSA-N pectic acid Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)O[C@H](C(O)=O)[C@@H]1OC1[C@H](O)[C@@H](O)[C@@H](OC2[C@@H]([C@@H](O)[C@@H](O)[C@H](O2)C(O)=O)O)[C@@H](C(O)=O)O1 LCLHHZYHLXDRQG-ZNKJPWOQSA-N 0.000 description 2
- 108010072638 pectinacetylesterase Proteins 0.000 description 2
- 102000004251 pectinacetylesterase Human genes 0.000 description 2
- 239000012465 retentate Substances 0.000 description 2
- 108010035322 rhamnogalacturonan acetylesterase Proteins 0.000 description 2
- 239000012723 sample buffer Substances 0.000 description 2
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 2
- 238000000527 sonication Methods 0.000 description 2
- 230000009469 supplementation Effects 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- AUJXJFHANFIVKH-GQCTYLIASA-N trans-methylferulate Chemical compound COC(=O)\C=C\C1=CC=C(O)C(OC)=C1 AUJXJFHANFIVKH-GQCTYLIASA-N 0.000 description 2
- 150000003722 vitamin derivatives Chemical class 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 239000010925 yard waste Substances 0.000 description 2
- LGQKSQQRKHFMLI-SJYYZXOBSA-N (2s,3r,4s,5r)-2-[(3r,4r,5r,6r)-4,5,6-trihydroxyoxan-3-yl]oxyoxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@H](O)CO[C@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)OC1 LGQKSQQRKHFMLI-SJYYZXOBSA-N 0.000 description 1
- DBTMGCOVALSLOR-DEVYUCJPSA-N (2s,3r,4s,5r,6r)-4-[(2s,3r,4s,5r,6r)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)oxane-2,3,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](CO)O[C@H](O)[C@@H]2O)O)O[C@H](CO)[C@H]1O DBTMGCOVALSLOR-DEVYUCJPSA-N 0.000 description 1
- FYGDTMLNYKFZSV-WFYNLLPOSA-N (2s,3r,4s,5s,6r)-2-[(2r,4r,5r,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,3s,4r,5r,6s)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-WFYNLLPOSA-N 0.000 description 1
- LUEWUZLMQUOBSB-FSKGGBMCSA-N (2s,3s,4s,5s,6r)-2-[(2r,3s,4r,5r,6s)-6-[(2r,3s,4r,5s,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,4r,5s,6r)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@@H](OC3[C@H](O[C@@H](O)[C@@H](O)[C@H]3O)CO)[C@@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O LUEWUZLMQUOBSB-FSKGGBMCSA-N 0.000 description 1
- YBADLXQNJCMBKR-UHFFFAOYSA-M (4-nitrophenyl)acetate Chemical compound [O-]C(=O)CC1=CC=C([N+]([O-])=O)C=C1 YBADLXQNJCMBKR-UHFFFAOYSA-M 0.000 description 1
- KSEBMYQBYZTDHS-HWKANZROSA-M (E)-Ferulic acid Natural products COC1=CC(\C=C\C([O-])=O)=CC=C1O KSEBMYQBYZTDHS-HWKANZROSA-M 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- KIAPWMKFHIKQOZ-UHFFFAOYSA-N 2-[[(4-fluorophenyl)-oxomethyl]amino]benzoic acid methyl ester Chemical compound COC(=O)C1=CC=CC=C1NC(=O)C1=CC=C(F)C=C1 KIAPWMKFHIKQOZ-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- LGQKSQQRKHFMLI-UHFFFAOYSA-N 4-O-beta-D-xylopyranosyl-beta-D-xylopyranose Natural products OC1C(O)C(O)COC1OC1C(O)C(O)C(O)OC1 LGQKSQQRKHFMLI-UHFFFAOYSA-N 0.000 description 1
- QAUUDNIGJSLPSX-UHFFFAOYSA-N 4-nitrophenyl acetate Chemical compound CC(=O)OC1=CC=C([N+]([O-])=O)C=C1 QAUUDNIGJSLPSX-UHFFFAOYSA-N 0.000 description 1
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
- 101100220718 Acetivibrio thermocellus (strain ATCC 27405 / DSM 1237 / JCM 9322 / NBRC 103400 / NCIMB 10682 / NRRL B-4536 / VPI 7372) cipA gene Proteins 0.000 description 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 1
- 108010013043 Acetylesterase Proteins 0.000 description 1
- 241001019659 Acremonium <Plectosphaerellaceae> Species 0.000 description 1
- 241000228431 Acremonium chrysogenum Species 0.000 description 1
- 241000222518 Agaricus Species 0.000 description 1
- 241000609240 Ambelania acida Species 0.000 description 1
- 101710152845 Arabinogalactan endo-beta-1,4-galactanase Proteins 0.000 description 1
- 241000209134 Arundinaria Species 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 241000228245 Aspergillus niger Species 0.000 description 1
- 241001370055 Aspergillus niger CBS 513.88 Species 0.000 description 1
- 240000006439 Aspergillus oryzae Species 0.000 description 1
- 235000002247 Aspergillus oryzae Nutrition 0.000 description 1
- 241000131386 Aspergillus sojae Species 0.000 description 1
- 241000223651 Aureobasidium Species 0.000 description 1
- 101001016801 Bacillus mannanilyticus (strain DSM 16130 / JCM 10596 / AM-001) Mannan endo-1,4-beta-mannosidase A and B Proteins 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 description 1
- 235000006008 Brassica napus var napus Nutrition 0.000 description 1
- 240000000385 Brassica napus var. napus Species 0.000 description 1
- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 101000957803 Caldicellulosiruptor saccharolyticus Endo-1,4-beta-glucanase Proteins 0.000 description 1
- 102000005367 Carboxypeptidases Human genes 0.000 description 1
- 108010006303 Carboxypeptidases Proteins 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 241000123346 Chrysosporium Species 0.000 description 1
- 241001674013 Chrysosporium lucknowense Species 0.000 description 1
- 241000222511 Coprinus Species 0.000 description 1
- 241001337994 Cryptococcus <scale insect> Species 0.000 description 1
- VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical compound [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- 229920000832 Cutin Polymers 0.000 description 1
- 108010005843 Cysteine Proteases Proteins 0.000 description 1
- 102000005927 Cysteine Proteases Human genes 0.000 description 1
- AVGPOAXYRRIZMM-UHFFFAOYSA-N D-Apiose Natural products OCC(O)(CO)C(O)C=O AVGPOAXYRRIZMM-UHFFFAOYSA-N 0.000 description 1
- ASNHGEVAWNWCRQ-LJJLCWGRSA-N D-apiofuranose Chemical compound OC[C@@]1(O)COC(O)[C@@H]1O ASNHGEVAWNWCRQ-LJJLCWGRSA-N 0.000 description 1
- ASNHGEVAWNWCRQ-UHFFFAOYSA-N D-apiofuranose Natural products OCC1(O)COC(O)C1O ASNHGEVAWNWCRQ-UHFFFAOYSA-N 0.000 description 1
- AEMOLEFTQBMNLQ-AQKNRBDQSA-N D-glucopyranuronic acid Chemical compound OC1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-AQKNRBDQSA-N 0.000 description 1
- SQNRKWHRVIAKLP-UHFFFAOYSA-N D-xylobiose Natural products O=CC(O)C(O)C(CO)OC1OCC(O)C(O)C1O SQNRKWHRVIAKLP-UHFFFAOYSA-N 0.000 description 1
- 125000000214 D-xylosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)CO1)* 0.000 description 1
- 108010087427 Endo-1,3(4)-beta-Glucanase Proteins 0.000 description 1
- 108010061142 Endo-arabinase Proteins 0.000 description 1
- 101710147028 Endo-beta-1,4-galactanase Proteins 0.000 description 1
- 241000228427 Eurotiales Species 0.000 description 1
- 241000223218 Fusarium Species 0.000 description 1
- 108010093031 Galactosidases Proteins 0.000 description 1
- 102000002464 Galactosidases Human genes 0.000 description 1
- 108010033128 Glucan Endo-1,3-beta-D-Glucosidase Proteins 0.000 description 1
- 229920001706 Glucuronoxylan Polymers 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 241000223200 Humicola grisea var. thermoidea Species 0.000 description 1
- 101710156134 Hyaluronoglucuronidase Proteins 0.000 description 1
- 101000755708 Hypocrea jecorina Alpha-glucuronidase Proteins 0.000 description 1
- 101001035456 Hypocrea jecorina Endoglucanase-4 Proteins 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 1
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 1
- 229920001543 Laminarin Polymers 0.000 description 1
- 239000005717 Laminarin Substances 0.000 description 1
- 108090001030 Lipoproteins Proteins 0.000 description 1
- 102000004895 Lipoproteins Human genes 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 241001344133 Magnaporthe Species 0.000 description 1
- 102000003843 Metalloendopeptidases Human genes 0.000 description 1
- 108090000131 Metalloendopeptidases Proteins 0.000 description 1
- 240000003433 Miscanthus floridulus Species 0.000 description 1
- 108010074633 Mixed Function Oxygenases Proteins 0.000 description 1
- 102000008109 Mixed Function Oxygenases Human genes 0.000 description 1
- 102100036617 Monoacylglycerol lipase ABHD2 Human genes 0.000 description 1
- 241000235395 Mucor Species 0.000 description 1
- 241000235388 Mucorales Species 0.000 description 1
- 102000002568 Multienzyme Complexes Human genes 0.000 description 1
- 108010093369 Multienzyme Complexes Proteins 0.000 description 1
- 229910017974 NH40H Inorganic materials 0.000 description 1
- 229920002274 Nalgene Polymers 0.000 description 1
- 241000233892 Neocallimastix Species 0.000 description 1
- 241000221960 Neurospora Species 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 108090000854 Oxidoreductases Proteins 0.000 description 1
- 102000004316 Oxidoreductases Human genes 0.000 description 1
- 108090000526 Papain Proteins 0.000 description 1
- 241000712655 Papulaspora Species 0.000 description 1
- 241000228153 Penicillium citrinum Species 0.000 description 1
- 108090000284 Pepsin A Proteins 0.000 description 1
- 102000057297 Pepsin A Human genes 0.000 description 1
- 102000000447 Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase Human genes 0.000 description 1
- 108010055817 Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase Proteins 0.000 description 1
- 241000235379 Piromyces Species 0.000 description 1
- 241000222350 Pleurotus Species 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241000678504 Rasamsonia brevistipitata Species 0.000 description 1
- 108020004511 Recombinant DNA Proteins 0.000 description 1
- 241000235403 Rhizomucor miehei Species 0.000 description 1
- 241000235070 Saccharomyces Species 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 241000222480 Schizophyllum Species 0.000 description 1
- 102000012479 Serine Proteases Human genes 0.000 description 1
- 108010022999 Serine Proteases Proteins 0.000 description 1
- 241000221926 Sordariales Species 0.000 description 1
- 244000138286 Sorghum saccharatum Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 229930183415 Suberin Natural products 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- 241000223258 Thermomyces lanuginosus Species 0.000 description 1
- 241001313536 Thermothelomyces thermophila Species 0.000 description 1
- 241001495429 Thielavia terrestris Species 0.000 description 1
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 1
- 239000004473 Threonine Substances 0.000 description 1
- 240000003243 Thuja occidentalis Species 0.000 description 1
- 241001149964 Tolypocladium Species 0.000 description 1
- 102000004357 Transferases Human genes 0.000 description 1
- 108090000992 Transferases Proteins 0.000 description 1
- 241001136486 Trichocomaceae Species 0.000 description 1
- 241000499912 Trichoderma reesei Species 0.000 description 1
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 1
- 108010027199 Xylosidases Proteins 0.000 description 1
- UGXQOOQUZRUVSS-ZZXKWVIFSA-N [5-[3,5-dihydroxy-2-(1,3,4-trihydroxy-5-oxopentan-2-yl)oxyoxan-4-yl]oxy-3,4-dihydroxyoxolan-2-yl]methyl (e)-3-(4-hydroxyphenyl)prop-2-enoate Chemical compound OC1C(OC(CO)C(O)C(O)C=O)OCC(O)C1OC1C(O)C(O)C(COC(=O)\C=C\C=2C=CC(O)=CC=2)O1 UGXQOOQUZRUVSS-ZZXKWVIFSA-N 0.000 description 1
- IAJILQKETJEXLJ-QTBDOELSSA-N aldehydo-D-glucuronic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-QTBDOELSSA-N 0.000 description 1
- PNNNRSAQSRJVSB-BXKVDMCESA-N aldehydo-L-rhamnose Chemical compound C[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)C=O PNNNRSAQSRJVSB-BXKVDMCESA-N 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- IGSYEZFZPOZFNC-MMGXBETBSA-N alpha-D-GalpA-(1->4)-alpha-D-GalpA Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)O[C@H](C(O)=O)[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](C(O)=O)O1 IGSYEZFZPOZFNC-MMGXBETBSA-N 0.000 description 1
- AEMOLEFTQBMNLQ-BKBMJHBISA-M alpha-D-galacturonate Chemical compound O[C@H]1O[C@H](C([O-])=O)[C@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-BKBMJHBISA-M 0.000 description 1
- 108010044879 alpha-L-rhamnosidase Proteins 0.000 description 1
- 108010061261 alpha-glucuronidase Proteins 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- LUEWUZLMQUOBSB-ZLBHSGTGSA-N alpha-maltotetraose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@H](O[C@H](O[C@@H]3[C@H](O[C@H](O)[C@H](O)[C@H]3O)CO)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O LUEWUZLMQUOBSB-ZLBHSGTGSA-N 0.000 description 1
- 229940025131 amylases Drugs 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 108010076955 arabinogalactan endo-1,4-beta-galactosidase Proteins 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 239000010905 bagasse Substances 0.000 description 1
- 239000003782 beta lactam antibiotic agent Substances 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 238000007068 beta-elimination reaction Methods 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000012888 bovine serum Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 210000004899 c-terminal region Anatomy 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 108010085318 carboxymethylcellulase Proteins 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000010261 cell growth Effects 0.000 description 1
- 239000013592 cell lysate Substances 0.000 description 1
- FYGDTMLNYKFZSV-ZWSAEMDYSA-N cellotriose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](OC(O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-ZWSAEMDYSA-N 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 108091036078 conserved sequence Proteins 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- WBCMGDNFDRNGGZ-ACNVUDSMSA-N coumarate Natural products COC(=O)C1=CO[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]3[C@@H]1C=C[C@]34OC(=O)C(=C4)[C@H](C)OC(=O)C=Cc5ccc(O)cc5 WBCMGDNFDRNGGZ-ACNVUDSMSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000001982 diacylglycerols Chemical class 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 150000002016 disaccharides Chemical class 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000009837 dry grinding Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 108010091384 endoglucanase 2 Proteins 0.000 description 1
- 108010092450 endoglucanase Z Proteins 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229940093470 ethylene Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 238000009313 farming Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 229940114123 ferulate Drugs 0.000 description 1
- 229940114124 ferulic acid Drugs 0.000 description 1
- 235000001785 ferulic acid Nutrition 0.000 description 1
- KSEBMYQBYZTDHS-UHFFFAOYSA-N ferulic acid Natural products COC1=CC(C=CC(O)=O)=CC=C1O KSEBMYQBYZTDHS-UHFFFAOYSA-N 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 238000012239 gene modification Methods 0.000 description 1
- 230000005017 genetic modification Effects 0.000 description 1
- 235000013617 genetically modified food Nutrition 0.000 description 1
- 235000003869 genetically modified organism Nutrition 0.000 description 1
- 229940046240 glucomannan Drugs 0.000 description 1
- 229940097043 glucuronic acid Drugs 0.000 description 1
- 125000002367 glucuronosyl group Chemical group 0.000 description 1
- 229960005150 glycerol Drugs 0.000 description 1
- 229940074774 glycyrrhizinate Drugs 0.000 description 1
- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000009396 hybridization Methods 0.000 description 1
- 239000000413 hydrolysate Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- JTLOUXXZZFFBBW-UHFFFAOYSA-N isoferulic acid methyl ester Natural products COC(=O)C=CC1=CC=C(OC)C(O)=C1 JTLOUXXZZFFBBW-UHFFFAOYSA-N 0.000 description 1
- 238000011174 lab scale experimental method Methods 0.000 description 1
- 238000011173 large scale experimental method Methods 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 230000002646 lignocellulolytic effect Effects 0.000 description 1
- 239000002029 lignocellulosic biomass Substances 0.000 description 1
- 235000015250 liver sausages Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- LUEWUZLMQUOBSB-GFVSVBBRSA-N mannan Chemical class O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@@H](O[C@H]3[C@H](O[C@@H](O)[C@@H](O)[C@H]3O)CO)[C@@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O LUEWUZLMQUOBSB-GFVSVBBRSA-N 0.000 description 1
- 150000008146 mannosides Chemical class 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- AUJXJFHANFIVKH-UHFFFAOYSA-N methyl cis-ferulate Natural products COC(=O)C=CC1=CC=C(O)C(OC)=C1 AUJXJFHANFIVKH-UHFFFAOYSA-N 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 210000003739 neck Anatomy 0.000 description 1
- 230000012666 negative regulation of transcription by glucose Effects 0.000 description 1
- 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 description 1
- BOPGDPNILDQYTO-NNYOXOHSSA-N nicotinamide-adenine dinucleotide Chemical compound C1=CCC(C(=O)N)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC=NC(N)=C3N=C2)O)O1 BOPGDPNILDQYTO-NNYOXOHSSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000010815 organic waste Substances 0.000 description 1
- 230000004792 oxidative damage Effects 0.000 description 1
- 230000010627 oxidative phosphorylation Effects 0.000 description 1
- 229940055729 papain Drugs 0.000 description 1
- 235000019834 papain Nutrition 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 238000002264 polyacrylamide gel electrophoresis Methods 0.000 description 1
- 108091033319 polynucleotide Proteins 0.000 description 1
- 102000040430 polynucleotide Human genes 0.000 description 1
- 239000002157 polynucleotide Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000013587 production medium Substances 0.000 description 1
- 235000019833 protease Nutrition 0.000 description 1
- 230000006920 protein precipitation Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 239000003642 reactive oxygen metabolite Substances 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000010979 ruby Substances 0.000 description 1
- 229910001750 ruby Inorganic materials 0.000 description 1
- XYSQXZCMOLNHOI-UHFFFAOYSA-N s-[2-[[4-(acetylsulfamoyl)phenyl]carbamoyl]phenyl] 5-pyridin-1-ium-1-ylpentanethioate;bromide Chemical compound [Br-].C1=CC(S(=O)(=O)NC(=O)C)=CC=C1NC(=O)C1=CC=CC=C1SC(=O)CCCC[N+]1=CC=CC=C1 XYSQXZCMOLNHOI-UHFFFAOYSA-N 0.000 description 1
- 108010038196 saccharide-binding proteins Proteins 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000009997 thermal pre-treatment Methods 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- QURCVMIEKCOAJU-UHFFFAOYSA-N trans-isoferulic acid Natural products COC1=CC=C(C=CC(O)=O)C=C1O QURCVMIEKCOAJU-UHFFFAOYSA-N 0.000 description 1
- 238000005820 transferase reaction Methods 0.000 description 1
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000009105 vegetative growth Effects 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002916 wood waste Substances 0.000 description 1
- 125000000969 xylosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)CO1)* 0.000 description 1
- 210000005253 yeast cell Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- 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
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/10—Nitrogen as only ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/02—Monosaccharides
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P35/00—Preparation of compounds having a 5-thia-1-azabicyclo [4.2.0] octane ring system, e.g. cephalosporin
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P5/00—Preparation of hydrocarbons or halogenated hydrocarbons
- C12P5/02—Preparation of hydrocarbons or halogenated hydrocarbons acyclic
- C12P5/026—Unsaturated compounds, i.e. alkenes, alkynes or allenes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- 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
- C12P7/10—Ethanol, i.e. non-beverage produced as by-product or from waste or cellulosic material substrate substrate containing cellulosic material
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- 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
- C12P7/16—Butanols
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- 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
- C12P7/18—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic polyhydric
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- 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
- C12P7/18—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic polyhydric
- C12P7/20—Glycerol
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/42—Hydroxy-carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/44—Polycarboxylic acids
- C12P7/46—Dicarboxylic acids having four or less carbon atoms, e.g. fumaric acid, maleic acid
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/44—Polycarboxylic acids
- C12P7/48—Tricarboxylic acids, e.g. citric acid
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/54—Acetic acid
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/56—Lactic acid
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P2203/00—Fermentation products obtained from optionally pretreated or hydrolyzed cellulosic or lignocellulosic material as the carbon source
-
- 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
-
- 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
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Enzymes And Modification Thereof (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12191957.5 | 2012-11-09 | ||
| EP12191957 | 2012-11-09 | ||
| EP13174656.2 | 2013-07-02 | ||
| EP13174656 | 2013-07-02 | ||
| EP13176083 | 2013-07-11 | ||
| EP13176083.7 | 2013-07-11 | ||
| EP13176500.0 | 2013-07-15 | ||
| EP13176500 | 2013-07-15 | ||
| EP13184701 | 2013-09-17 | ||
| EP13184702.2 | 2013-09-17 | ||
| EP13184702 | 2013-09-17 | ||
| EP13184701.4 | 2013-09-17 | ||
| PCT/EP2013/073255 WO2014072395A1 (en) | 2012-11-09 | 2013-11-07 | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2888333A1 CA2888333A1 (en) | 2014-05-15 |
| CA2888333C true CA2888333C (en) | 2023-01-24 |
Family
ID=49554250
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2888333A Active CA2888333C (en) | 2012-11-09 | 2013-11-07 | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars |
| CA2888170A Active CA2888170C (en) | 2012-11-09 | 2013-11-07 | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2888170A Active CA2888170C (en) | 2012-11-09 | 2013-11-07 | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars |
Country Status (23)
| Country | Link |
|---|---|
| US (7) | US9982280B2 (OSRAM) |
| EP (4) | EP2917355B1 (OSRAM) |
| JP (3) | JP6396307B2 (OSRAM) |
| KR (2) | KR102104151B1 (OSRAM) |
| CN (3) | CN104769116A (OSRAM) |
| AU (4) | AU2013343597B2 (OSRAM) |
| BR (3) | BR112015004344A2 (OSRAM) |
| CA (2) | CA2888333C (OSRAM) |
| DK (3) | DK2917354T3 (OSRAM) |
| EA (2) | EA028880B9 (OSRAM) |
| ES (3) | ES2773953T3 (OSRAM) |
| FI (1) | FI3613860T3 (OSRAM) |
| HR (3) | HRP20240339T1 (OSRAM) |
| HU (3) | HUE048887T2 (OSRAM) |
| IN (2) | IN2015DN03027A (OSRAM) |
| LT (1) | LT3613860T (OSRAM) |
| MX (3) | MX360283B (OSRAM) |
| MY (2) | MY176707A (OSRAM) |
| PL (2) | PL3613860T3 (OSRAM) |
| RS (1) | RS65279B1 (OSRAM) |
| SI (1) | SI3613860T1 (OSRAM) |
| UA (2) | UA116789C2 (OSRAM) |
| WO (2) | WO2014072395A1 (OSRAM) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IN2015DN03027A (OSRAM) | 2012-11-09 | 2015-10-02 | Dsm Ip Assets Bv | |
| BR112015004118B1 (pt) | 2012-11-09 | 2018-09-18 | Dsm Ip Assets Bv | processo para a preparação de um produto de açúcar a partir de material lignocelulósico |
| WO2014130812A1 (en) | 2013-02-21 | 2014-08-28 | Novozymes A/S | Methods of saccharifying and fermenting a cellulosic material |
| WO2015004098A1 (en) * | 2013-07-11 | 2015-01-15 | Dsm Ip Assets B.V. | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars |
| DK3063285T3 (da) | 2013-11-01 | 2019-05-13 | Novozymes As | Fremgangsmåder til forsukring og fermentering af et celluloseholdigt materiale |
| JP2017512467A (ja) | 2014-04-03 | 2017-05-25 | ディーエスエム アイピー アセッツ ビー.ブイ. | リグノセルロース系材料の酵素加水分解および糖発酵のための方法および装置 |
| CN106460020B (zh) | 2014-04-30 | 2020-12-29 | 帝斯曼知识产权资产管理有限公司 | 酶促水解木质纤维素材料和发酵糖的方法 |
| WO2015175308A1 (en) * | 2014-05-13 | 2015-11-19 | Danisco Us Inc. | Improved enzymatic hydrolysis of biomass |
| WO2016029107A1 (en) * | 2014-08-21 | 2016-02-25 | Novozymes A/S | Process for saccharifying cellulosic material under oxygen addition |
| WO2016096971A1 (en) | 2014-12-19 | 2016-06-23 | Dsm Ip Assets B.V. | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars |
| DK3640336T3 (da) * | 2015-01-28 | 2022-06-27 | Dsm Ip Assets Bv | Fremgangsmåde til enzymatisk hydrolyse af lignocellulosemateriale og fermentering af sukre |
| WO2016120296A1 (en) | 2015-01-28 | 2016-08-04 | Dsm Ip Assets B.V. | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars |
| WO2016207147A1 (en) * | 2015-06-22 | 2016-12-29 | Dsm Ip Assets B.V. | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars |
| CA3024902A1 (en) | 2016-05-20 | 2017-11-23 | Poet Research, Inc. | Methods of removing one or more compounds from a lignocellulosic hydrolysate via gas stripping, and related systems |
| EP3545100A1 (en) * | 2016-11-24 | 2019-10-02 | DSM IP Assets B.V. | Enzyme composition |
| BR112020005439A2 (pt) * | 2017-10-09 | 2020-09-24 | Dsm Ip Assets B.V. | processo para hidrólise enzimática de material lignocelulósico e fermentação de açúcares |
| EP3710573A1 (en) | 2017-11-16 | 2020-09-23 | POET Research, Inc. | Methods for propagating microorganisms for fermentation&related methods&systems |
| WO2019118476A1 (en) | 2017-12-11 | 2019-06-20 | University Of Louisville Research Foundation, Inc. | Processes for isolation and recovery of c5 sugars |
| EP3530743A1 (en) | 2018-02-21 | 2019-08-28 | Cambridge Glycoscience Ltd | Method of production |
| AU2019321182B2 (en) | 2018-08-15 | 2025-01-09 | Cambridge Glycoscience Ltd. | Novel compositions, their use, and methods for their formation |
| FR3087449B1 (fr) | 2018-10-19 | 2024-10-11 | Afyren | Procede de preparation de molecules organiques par fermentation anaerobie |
| WO2020165398A1 (en) | 2019-02-15 | 2020-08-20 | Borregaard As | Chemically modified lignin as reducing agent for enzymatic hydrolysis of lignocellulosic biomass |
| EP4013240A1 (en) | 2019-08-16 | 2022-06-22 | Cambridge Glycoscience Ltd | Methods of treating biomass to produce oligosaccharides and related compositions |
| CN115279208B (zh) | 2019-12-12 | 2024-12-17 | 剑桥糖质科学有限公司 | 低糖多相食品 |
| JP7662320B2 (ja) * | 2020-09-30 | 2025-04-15 | 株式会社ヤクルト本社 | ヘミセルロース糖化用酵素組成物 |
| JP2024512872A (ja) * | 2021-04-08 | 2024-03-21 | ベルサリス エッセ.ピー.アー. | 糖生成物及び発酵生成物を製造するプロセス |
Family Cites Families (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3105581C2 (de) | 1981-02-16 | 1985-05-15 | Otto Dr. 2300 Kiel Moebus | Verfahren zur Fermentation von Kohlenhydraten unter Erzeugung von Äthanol und Biomasse |
| BR9106680A (pt) | 1991-04-18 | 1993-06-22 | Union Camp Patent Holding | Processo para obter melhorada seletividade de deslignificacao de pasta de carga marrom durante a deslignificacao com oxigenio de pasta de elevada consistencia,e,processo para obter aumentada deslignificacao de pasta nao branqueada durante a deslignificacao com oxigenio de pasta de elevada consistencia |
| FR2694768B1 (fr) | 1992-07-30 | 1994-12-23 | Pasteur Institut | Séquences d'oligonucléotides pour la détection spécifique de mollicutes par amplication de gènes conservés. |
| US5865898A (en) * | 1992-08-06 | 1999-02-02 | The Texas A&M University System | Methods of biomass pretreatment |
| CN1190373C (zh) | 2000-02-17 | 2005-02-23 | 里索国家实验室 | 处理木质纤维素材料的方法 |
| CN1505682A (zh) | 2000-06-26 | 2004-06-16 | ��ѧ�о��� | 用于同时糖化发酵的方法和组合物 |
| EP1392624A2 (en) | 2001-05-25 | 2004-03-03 | Bp Exploration Operating Company Limited | Fischer-tropsch process |
| US8580541B2 (en) | 2003-03-19 | 2013-11-12 | The Trustees Of Dartmouth College | Lignin blockers and uses thereof |
| HUE051490T2 (hu) | 2004-03-25 | 2021-03-01 | Novozymes Inc | Eljárások növényi sejtfal-poliszacharidok lebontására vagy átalakítására |
| ES2369605T3 (es) | 2004-11-29 | 2011-12-02 | Inbicon A/S | Hidrólisis enzimática de biomasas que tienen un alto contenido de materia seca (ms). |
| KR20080069980A (ko) | 2005-09-30 | 2008-07-29 | 노보자임스 인코포레이티드 | 셀룰로오스성 물질의 분해 또는 전환을 증진하는 방법 |
| IES20060090A2 (en) | 2006-02-10 | 2007-06-13 | Nat Univ Ireland | Talaromyces emersonii enzyme systems |
| US8968515B2 (en) | 2006-05-01 | 2015-03-03 | Board Of Trustees Of Michigan State University | Methods for pretreating biomass |
| WO2008008793A2 (en) | 2006-07-10 | 2008-01-17 | Dyadic International Inc. | Methods and compositions for degradation of lignocellulosic material |
| WO2008041840A1 (en) | 2006-10-02 | 2008-04-10 | Dsm Ip Assets B.V. | Metabolic engineering of arabinose- fermenting yeast cells |
| AU2008259986C1 (en) | 2007-05-31 | 2012-07-26 | Novozymes, Inc. | Methods of increasing the cellulolytic enhancing activity of a polypeptide |
| EP2162545A4 (en) | 2007-06-27 | 2012-05-16 | Novozymes As | PROCESS FOR PRODUCING FERMENTATION PRODUCTS |
| US8980599B2 (en) | 2007-08-02 | 2015-03-17 | Iogen Energy Corporation | Method for the production of alcohol from a pretreated lignocellulosic feedstock |
| US20090098616A1 (en) | 2007-10-09 | 2009-04-16 | Murray Burke | Enzymatic treatment of lignocellulosic materials |
| EP2207888A1 (en) * | 2007-10-10 | 2010-07-21 | Sunopta Bioprocess Inc. | Enzymatic treatment under vacuum of lignocellulosic materials |
| CA2939565C (en) | 2007-10-25 | 2018-05-01 | Landmark Ip Holdings, Llc | System and method for anaerobic digestion of biomasses |
| BRPI0821230A2 (pt) | 2007-12-19 | 2019-09-24 | Novozymes As | "constructo de ácido nucleico, cédula microbiana hospedeira recombinante, métodos para priduzir um polipeptídeo tendo atividade intensificadora celulolítica, para produzir um mutante de uma cédula precursora, para inibir a expressão de um polipeptídeo com atividade de intensificação celulolítica em uma célula, para produzir uma proteína, para degradar ou converter um material celulósico, e, para fermentar um material celulósico" |
| US20110201084A1 (en) | 2008-07-25 | 2011-08-18 | The Regents Of The University Of California | Enzymatic hydrolysis of cellulosic biomass through enhanced removal of oligomers |
| CA2731983C (en) | 2008-08-11 | 2017-02-14 | Dsm Ip Assets B.V. | Degradation of lignocellulosic material |
| EP2379733A2 (en) * | 2008-12-19 | 2011-10-26 | Novozymes Inc. | Methods for increasing hydrolysis of cellulosic material |
| CN102459582B (zh) | 2009-05-29 | 2014-09-03 | 诺维信股份有限公司 | 用于增强纤维素材料降解或转化的方法 |
| CA2765691A1 (en) * | 2009-07-03 | 2011-01-06 | Dsm Ip Assets B.V. | Talaromyces strains and enzyme compositions |
| MX361395B (es) | 2009-10-08 | 2018-12-05 | Dsm Ip Assets Bv | Proceso para la hidrólisis enzimática de material lignocelulósico y fermentación de azúcares. |
| EA201201125A1 (ru) * | 2010-02-11 | 2013-03-29 | ДСМ АйПи АССЕТС Б.В. | Клетка-хозяин, способная продуцировать ферменты, пригодные для деградации лигноцеллюлозного материала |
| CN102191299A (zh) | 2010-03-10 | 2011-09-21 | 中国科学院青岛生物能源与过程研究所 | 多步酶解提高木质纤维素糖化得率的方法 |
| DK2601302T3 (da) | 2010-08-06 | 2021-01-04 | Novozymes Inc | Fremgangsmåder til nedbrydning eller hydrolyse af et polysaccharid |
| WO2012061517A1 (en) * | 2010-11-02 | 2012-05-10 | Novozymes, Inc. | Methods of pretreating cellulosic material with a gh61 polypeptide |
| EP3333258A3 (en) * | 2011-03-25 | 2018-07-25 | Novozymes A/S | Method for degrading or converting cellulosic material |
| MX2013012338A (es) | 2011-04-29 | 2013-11-01 | Danisco Us Inc | Uso de celulasa y glucoamilasa para mejorar los rendimientos de etanol a partir de la fermentacion. |
| BR112014004171A2 (pt) | 2011-08-22 | 2018-11-06 | Codexis Inc | variantes da proteína glicósideo hidrolase gh61 e cofatores que aumentam a atividade de gh61 |
| WO2014072392A1 (en) | 2012-11-09 | 2014-05-15 | Dsm Ip Assets B.V. | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars |
| BR112015004118B1 (pt) | 2012-11-09 | 2018-09-18 | Dsm Ip Assets Bv | processo para a preparação de um produto de açúcar a partir de material lignocelulósico |
| IN2015DN03027A (OSRAM) | 2012-11-09 | 2015-10-02 | Dsm Ip Assets Bv | |
| WO2014130812A1 (en) | 2013-02-21 | 2014-08-28 | Novozymes A/S | Methods of saccharifying and fermenting a cellulosic material |
| JP2017512467A (ja) | 2014-04-03 | 2017-05-25 | ディーエスエム アイピー アセッツ ビー.ブイ. | リグノセルロース系材料の酵素加水分解および糖発酵のための方法および装置 |
| CN106460020B (zh) | 2014-04-30 | 2020-12-29 | 帝斯曼知识产权资产管理有限公司 | 酶促水解木质纤维素材料和发酵糖的方法 |
| WO2016096971A1 (en) | 2014-12-19 | 2016-06-23 | Dsm Ip Assets B.V. | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars |
-
2013
- 2013-11-07 IN IN3027DEN2015 patent/IN2015DN03027A/en unknown
- 2013-11-07 HR HRP20240339TT patent/HRP20240339T1/hr unknown
- 2013-11-07 WO PCT/EP2013/073255 patent/WO2014072395A1/en not_active Ceased
- 2013-11-07 MX MX2015005631A patent/MX360283B/es active IP Right Grant
- 2013-11-07 US US14/440,662 patent/US9982280B2/en active Active
- 2013-11-07 IN IN3084DEN2015 patent/IN2015DN03084A/en unknown
- 2013-11-07 US US14/440,658 patent/US9957528B2/en active Active
- 2013-11-07 MX MX2015005628A patent/MX360067B/es active IP Right Grant
- 2013-11-07 UA UAA201505519A patent/UA116789C2/uk unknown
- 2013-11-07 BR BR112015004344A patent/BR112015004344A2/pt not_active Application Discontinuation
- 2013-11-07 CN CN201380058328.2A patent/CN104769116A/zh active Pending
- 2013-11-07 FI FIEP19197489.8T patent/FI3613860T3/fi active
- 2013-11-07 EP EP13789530.6A patent/EP2917355B1/en active Active
- 2013-11-07 HU HUE13789275A patent/HUE048887T2/hu unknown
- 2013-11-07 DK DK13789275.8T patent/DK2917354T3/da active
- 2013-11-07 EP EP19214822.9A patent/EP3656866A1/en active Pending
- 2013-11-07 KR KR1020157011650A patent/KR102104151B1/ko active Active
- 2013-11-07 HU HUE13789530A patent/HUE047092T2/hu unknown
- 2013-11-07 CN CN202110183124.8A patent/CN112813119A/zh active Pending
- 2013-11-07 MY MYPI2015701144A patent/MY176707A/en unknown
- 2013-11-07 KR KR1020157011651A patent/KR102104152B1/ko active Active
- 2013-11-07 EP EP19197489.8A patent/EP3613860B1/en active Active
- 2013-11-07 PL PL19197489.8T patent/PL3613860T3/pl unknown
- 2013-11-07 ES ES13789275T patent/ES2773953T3/es active Active
- 2013-11-07 RS RS20240288A patent/RS65279B1/sr unknown
- 2013-11-07 JP JP2015541128A patent/JP6396307B2/ja active Active
- 2013-11-07 CA CA2888333A patent/CA2888333C/en active Active
- 2013-11-07 WO PCT/EP2013/073253 patent/WO2014072393A1/en not_active Ceased
- 2013-11-07 DK DK19197489.8T patent/DK3613860T3/da active
- 2013-11-07 BR BR122016020119-8A patent/BR122016020119B1/pt active IP Right Grant
- 2013-11-07 EA EA201500510A patent/EA028880B9/ru not_active IP Right Cessation
- 2013-11-07 ES ES13789530T patent/ES2761448T3/es active Active
- 2013-11-07 CA CA2888170A patent/CA2888170C/en active Active
- 2013-11-07 HR HRP20200092TT patent/HRP20200092T1/hr unknown
- 2013-11-07 CN CN201380058360.0A patent/CN104769117A/zh active Pending
- 2013-11-07 AU AU2013343597A patent/AU2013343597B2/en active Active
- 2013-11-07 MY MYPI2015701143A patent/MY169456A/en unknown
- 2013-11-07 ES ES19197489T patent/ES2973866T3/es active Active
- 2013-11-07 AU AU2013343595A patent/AU2013343595B2/en active Active
- 2013-11-07 LT LTEP19197489.8T patent/LT3613860T/lt unknown
- 2013-11-07 UA UAA201505516A patent/UA117357C2/uk unknown
- 2013-11-07 DK DK13789530.6T patent/DK2917355T3/da active
- 2013-11-07 JP JP2015541127A patent/JP6429155B2/ja active Active
- 2013-11-07 EP EP13789275.8A patent/EP2917354B1/en not_active Revoked
- 2013-11-07 HR HRP20191960TT patent/HRP20191960T1/hr unknown
- 2013-11-07 PL PL13789530T patent/PL2917355T3/pl unknown
- 2013-11-07 SI SI201332073T patent/SI3613860T1/sl unknown
- 2013-11-07 BR BR112015004163A patent/BR112015004163A2/pt not_active Application Discontinuation
- 2013-11-07 EA EA201500516A patent/EA032496B1/ru not_active IP Right Cessation
- 2013-11-07 HU HUE19197489A patent/HUE064894T2/hu unknown
-
2015
- 2015-05-04 MX MX2018012714A patent/MX2018012714A/es unknown
-
2017
- 2017-07-20 AU AU2017206241A patent/AU2017206241A1/en not_active Abandoned
- 2017-07-21 AU AU2017206278A patent/AU2017206278A1/en not_active Abandoned
-
2018
- 2018-03-23 US US15/934,636 patent/US10724057B2/en active Active
- 2018-04-19 US US15/956,841 patent/US10131923B2/en active Active
- 2018-08-29 JP JP2018160816A patent/JP6690085B2/ja active Active
- 2018-10-04 US US16/152,197 patent/US10717995B2/en active Active
-
2020
- 2020-04-01 US US16/837,637 patent/US11434507B2/en active Active
- 2020-04-23 US US16/856,143 patent/US11434508B2/en active Active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US11434508B2 (en) | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars | |
| US11427844B2 (en) | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars | |
| WO2014072394A1 (en) | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars | |
| WO2014072389A1 (en) | Process for enzymatic hydrolysis of lignocellulosic material and fermentation of sugars |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |
Effective date: 20181018 |
|
| EEER | Examination request |
Effective date: 20181018 |
|
| EEER | Examination request |
Effective date: 20181018 |
|
| EEER | Examination request |
Effective date: 20181018 |
|
| EEER | Examination request |
Effective date: 20181018 |