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Enhanced xylose fermentation and hydrolysate inhibitor tolerance of Scheffersomyces shehatae for efficient ethanol production from non-detoxified lignocellulosic hydrolysate

Effective conversion of xylose into ethanol is important for lignocellulosic ethanol production. In the present study, UV-C mutagenesis was used to improve the efficiency of xylose fermentation. The mutated Scheffersomyces shehatae strain TTC79 fermented glucose as efficiently and xylose more effici...

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Autores principales: Senatham, Srisuda, Chamduang, Thada, Kaewchingduang, Yotin, Thammasittirong, Anon, Srisodsuk, Malee, Elliston, Adam, Roberts, Ian N., Waldron, Keith W., Thammasittirong, Sutticha Na-Ranong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940357/
https://www.ncbi.nlm.nih.gov/pubmed/27462488
http://dx.doi.org/10.1186/s40064-016-2713-4
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author Senatham, Srisuda
Chamduang, Thada
Kaewchingduang, Yotin
Thammasittirong, Anon
Srisodsuk, Malee
Elliston, Adam
Roberts, Ian N.
Waldron, Keith W.
Thammasittirong, Sutticha Na-Ranong
author_facet Senatham, Srisuda
Chamduang, Thada
Kaewchingduang, Yotin
Thammasittirong, Anon
Srisodsuk, Malee
Elliston, Adam
Roberts, Ian N.
Waldron, Keith W.
Thammasittirong, Sutticha Na-Ranong
author_sort Senatham, Srisuda
collection PubMed
description Effective conversion of xylose into ethanol is important for lignocellulosic ethanol production. In the present study, UV-C mutagenesis was used to improve the efficiency of xylose fermentation. The mutated Scheffersomyces shehatae strain TTC79 fermented glucose as efficiently and xylose more efficiently, producing a higher ethanol concentration than the wild-type. A maximum ethanol concentration of 29.04 g/L was produced from 71.31 g/L xylose, which was 58.95 % higher than that of the wild-type. This mutant also displayed significantly improved hydrolysate inhibitors tolerance and increased ethanol production from non-detoxified lignocellulosic hydrolysates. The ethanol yield, productivity and theoretical yield by TTC79 from sugarcane bagasse hydrolysate were 0.46 g/g, 0.20 g/L/h and 90.61 %, respectively, while the corresponding values for the wild-type were 0.20 g/g, 0.04 g/L/h and 39.20 %, respectively. These results demonstrate that S. shehatae TTC79 is a useful non-recombinant strain, combining efficient xylose consumption and high inhibitor tolerance, with potential for application in ethanol production from lignocellulose hydrolysates.
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spelling pubmed-49403572016-07-26 Enhanced xylose fermentation and hydrolysate inhibitor tolerance of Scheffersomyces shehatae for efficient ethanol production from non-detoxified lignocellulosic hydrolysate Senatham, Srisuda Chamduang, Thada Kaewchingduang, Yotin Thammasittirong, Anon Srisodsuk, Malee Elliston, Adam Roberts, Ian N. Waldron, Keith W. Thammasittirong, Sutticha Na-Ranong Springerplus Research Effective conversion of xylose into ethanol is important for lignocellulosic ethanol production. In the present study, UV-C mutagenesis was used to improve the efficiency of xylose fermentation. The mutated Scheffersomyces shehatae strain TTC79 fermented glucose as efficiently and xylose more efficiently, producing a higher ethanol concentration than the wild-type. A maximum ethanol concentration of 29.04 g/L was produced from 71.31 g/L xylose, which was 58.95 % higher than that of the wild-type. This mutant also displayed significantly improved hydrolysate inhibitors tolerance and increased ethanol production from non-detoxified lignocellulosic hydrolysates. The ethanol yield, productivity and theoretical yield by TTC79 from sugarcane bagasse hydrolysate were 0.46 g/g, 0.20 g/L/h and 90.61 %, respectively, while the corresponding values for the wild-type were 0.20 g/g, 0.04 g/L/h and 39.20 %, respectively. These results demonstrate that S. shehatae TTC79 is a useful non-recombinant strain, combining efficient xylose consumption and high inhibitor tolerance, with potential for application in ethanol production from lignocellulose hydrolysates. Springer International Publishing 2016-07-11 /pmc/articles/PMC4940357/ /pubmed/27462488 http://dx.doi.org/10.1186/s40064-016-2713-4 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Senatham, Srisuda
Chamduang, Thada
Kaewchingduang, Yotin
Thammasittirong, Anon
Srisodsuk, Malee
Elliston, Adam
Roberts, Ian N.
Waldron, Keith W.
Thammasittirong, Sutticha Na-Ranong
Enhanced xylose fermentation and hydrolysate inhibitor tolerance of Scheffersomyces shehatae for efficient ethanol production from non-detoxified lignocellulosic hydrolysate
title Enhanced xylose fermentation and hydrolysate inhibitor tolerance of Scheffersomyces shehatae for efficient ethanol production from non-detoxified lignocellulosic hydrolysate
title_full Enhanced xylose fermentation and hydrolysate inhibitor tolerance of Scheffersomyces shehatae for efficient ethanol production from non-detoxified lignocellulosic hydrolysate
title_fullStr Enhanced xylose fermentation and hydrolysate inhibitor tolerance of Scheffersomyces shehatae for efficient ethanol production from non-detoxified lignocellulosic hydrolysate
title_full_unstemmed Enhanced xylose fermentation and hydrolysate inhibitor tolerance of Scheffersomyces shehatae for efficient ethanol production from non-detoxified lignocellulosic hydrolysate
title_short Enhanced xylose fermentation and hydrolysate inhibitor tolerance of Scheffersomyces shehatae for efficient ethanol production from non-detoxified lignocellulosic hydrolysate
title_sort enhanced xylose fermentation and hydrolysate inhibitor tolerance of scheffersomyces shehatae for efficient ethanol production from non-detoxified lignocellulosic hydrolysate
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940357/
https://www.ncbi.nlm.nih.gov/pubmed/27462488
http://dx.doi.org/10.1186/s40064-016-2713-4
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