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Hemicellulases and auxiliary enzymes for improved conversion of lignocellulosic biomass to monosaccharides
BACKGROUND: High enzyme loading is a major economic bottleneck for the commercial processing of pretreated lignocellulosic biomass to produce fermentable sugars. Optimizing the enzyme cocktail for specific types of pretreated biomass allows for a significant reduction in enzyme loading without sacri...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3056733/ https://www.ncbi.nlm.nih.gov/pubmed/21342516 http://dx.doi.org/10.1186/1754-6834-4-5 |
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author | Gao, Dahai Uppugundla, Nirmal Chundawat, Shishir PS Yu, Xiurong Hermanson, Spencer Gowda, Krishne Brumm, Phillip Mead, David Balan, Venkatesh Dale, Bruce E |
author_facet | Gao, Dahai Uppugundla, Nirmal Chundawat, Shishir PS Yu, Xiurong Hermanson, Spencer Gowda, Krishne Brumm, Phillip Mead, David Balan, Venkatesh Dale, Bruce E |
author_sort | Gao, Dahai |
collection | PubMed |
description | BACKGROUND: High enzyme loading is a major economic bottleneck for the commercial processing of pretreated lignocellulosic biomass to produce fermentable sugars. Optimizing the enzyme cocktail for specific types of pretreated biomass allows for a significant reduction in enzyme loading without sacrificing hydrolysis yield. This is especially important for alkaline pretreatments such as Ammonia fiber expansion (AFEX) pretreated corn stover. Hence, a diverse set of hemicellulases supplemented along with cellulases is necessary for high recovery of monosaccharides. RESULTS: The core fungal cellulases in the optimal cocktail include cellobiohydrolase I [CBH I; glycoside hydrolase (GH) family 7A], cellobiohydrolase II (CBH II; GH family 6A), endoglucanase I (EG I; GH family 7B) and β-glucosidase (βG; GH family 3). Hemicellulases tested along with the core cellulases include xylanases (LX1, GH family 10; LX2, GH family 10; LX3, GH family 10; LX4, GH family 11; LX5, GH family 10; LX6, GH family 10), β-xylosidase (LβX; GH family 52), α-arabinofuranosidase (LArb, GH family 51) and α-glucuronidase (LαGl, GH family 67) that were cloned, expressed and/or purified from different bacterial sources. Different combinations of these enzymes were tested using a high-throughput microplate based 24 h hydrolysis assay. Both family 10 (LX3) and family 11 (LX4) xylanases were found to most efficiently hydrolyze AFEX pretreated corn stover in a synergistic manner. The optimal mass ratio of xylanases (LX3 and LX4) to cellulases (CBH I, CBH II and EG I) is 25:75. LβX (0.6 mg/g glucan) is crucial to obtaining monomeric xylose (54% xylose yield), while LArb (0.6 mg/g glucan) and LαGl (0.8 mg/g glucan) can both further increase xylose yield by an additional 20%. Compared with Accellerase 1000, a purified cocktail of cellulases supplemented with accessory hemicellulases will not only increase both glucose and xylose yields but will also decrease the total enzyme loading needed for equivalent yields. CONCLUSIONS: A diverse set of accessory hemicellulases was found necessary to enhance the synergistic action of cellulases hydrolysing AFEX pretreated corn stover. High glucose (around 80%) and xylose (around 70%) yields were achieved with a moderate enzyme loading (~20 mg protein/g glucan) using an in-house developed cocktail compared to commercial enzymes. |
format | Text |
id | pubmed-3056733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30567332011-03-15 Hemicellulases and auxiliary enzymes for improved conversion of lignocellulosic biomass to monosaccharides Gao, Dahai Uppugundla, Nirmal Chundawat, Shishir PS Yu, Xiurong Hermanson, Spencer Gowda, Krishne Brumm, Phillip Mead, David Balan, Venkatesh Dale, Bruce E Biotechnol Biofuels Research BACKGROUND: High enzyme loading is a major economic bottleneck for the commercial processing of pretreated lignocellulosic biomass to produce fermentable sugars. Optimizing the enzyme cocktail for specific types of pretreated biomass allows for a significant reduction in enzyme loading without sacrificing hydrolysis yield. This is especially important for alkaline pretreatments such as Ammonia fiber expansion (AFEX) pretreated corn stover. Hence, a diverse set of hemicellulases supplemented along with cellulases is necessary for high recovery of monosaccharides. RESULTS: The core fungal cellulases in the optimal cocktail include cellobiohydrolase I [CBH I; glycoside hydrolase (GH) family 7A], cellobiohydrolase II (CBH II; GH family 6A), endoglucanase I (EG I; GH family 7B) and β-glucosidase (βG; GH family 3). Hemicellulases tested along with the core cellulases include xylanases (LX1, GH family 10; LX2, GH family 10; LX3, GH family 10; LX4, GH family 11; LX5, GH family 10; LX6, GH family 10), β-xylosidase (LβX; GH family 52), α-arabinofuranosidase (LArb, GH family 51) and α-glucuronidase (LαGl, GH family 67) that were cloned, expressed and/or purified from different bacterial sources. Different combinations of these enzymes were tested using a high-throughput microplate based 24 h hydrolysis assay. Both family 10 (LX3) and family 11 (LX4) xylanases were found to most efficiently hydrolyze AFEX pretreated corn stover in a synergistic manner. The optimal mass ratio of xylanases (LX3 and LX4) to cellulases (CBH I, CBH II and EG I) is 25:75. LβX (0.6 mg/g glucan) is crucial to obtaining monomeric xylose (54% xylose yield), while LArb (0.6 mg/g glucan) and LαGl (0.8 mg/g glucan) can both further increase xylose yield by an additional 20%. Compared with Accellerase 1000, a purified cocktail of cellulases supplemented with accessory hemicellulases will not only increase both glucose and xylose yields but will also decrease the total enzyme loading needed for equivalent yields. CONCLUSIONS: A diverse set of accessory hemicellulases was found necessary to enhance the synergistic action of cellulases hydrolysing AFEX pretreated corn stover. High glucose (around 80%) and xylose (around 70%) yields were achieved with a moderate enzyme loading (~20 mg protein/g glucan) using an in-house developed cocktail compared to commercial enzymes. BioMed Central 2011-02-22 /pmc/articles/PMC3056733/ /pubmed/21342516 http://dx.doi.org/10.1186/1754-6834-4-5 Text en Copyright ©2011 Gao et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Gao, Dahai Uppugundla, Nirmal Chundawat, Shishir PS Yu, Xiurong Hermanson, Spencer Gowda, Krishne Brumm, Phillip Mead, David Balan, Venkatesh Dale, Bruce E Hemicellulases and auxiliary enzymes for improved conversion of lignocellulosic biomass to monosaccharides |
title | Hemicellulases and auxiliary enzymes for improved conversion of lignocellulosic biomass to monosaccharides |
title_full | Hemicellulases and auxiliary enzymes for improved conversion of lignocellulosic biomass to monosaccharides |
title_fullStr | Hemicellulases and auxiliary enzymes for improved conversion of lignocellulosic biomass to monosaccharides |
title_full_unstemmed | Hemicellulases and auxiliary enzymes for improved conversion of lignocellulosic biomass to monosaccharides |
title_short | Hemicellulases and auxiliary enzymes for improved conversion of lignocellulosic biomass to monosaccharides |
title_sort | hemicellulases and auxiliary enzymes for improved conversion of lignocellulosic biomass to monosaccharides |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3056733/ https://www.ncbi.nlm.nih.gov/pubmed/21342516 http://dx.doi.org/10.1186/1754-6834-4-5 |
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