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Adaptation of Scheffersomyces stipitis to hardwood spent sulfite liquor by evolutionary engineering
BACKGROUND: Hardwood spent sulfite liquor (HSSL) is a by-product of acid sulfite pulping process that is rich in xylose, a monosaccharide that can be fermented to ethanol by Scheffersomyces stipitis. However, HSSL also contains acetic acid and lignosulfonates that are inhibitory compounds of yeast g...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379546/ https://www.ncbi.nlm.nih.gov/pubmed/25829945 http://dx.doi.org/10.1186/s13068-015-0234-y |
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author | Pereira, Susana R Sànchez i Nogué, Violeta Frazão, Cláudio J R Serafim, Luísa S Gorwa-Grauslund, Marie F Xavier, Ana M R B |
author_facet | Pereira, Susana R Sànchez i Nogué, Violeta Frazão, Cláudio J R Serafim, Luísa S Gorwa-Grauslund, Marie F Xavier, Ana M R B |
author_sort | Pereira, Susana R |
collection | PubMed |
description | BACKGROUND: Hardwood spent sulfite liquor (HSSL) is a by-product of acid sulfite pulping process that is rich in xylose, a monosaccharide that can be fermented to ethanol by Scheffersomyces stipitis. However, HSSL also contains acetic acid and lignosulfonates that are inhibitory compounds of yeast growth. The main objective of this study was the use of an evolutionary engineering strategy to obtain variants of S. stipitis with increased tolerance to HSSL inhibitors while maintaining the ability to ferment xylose to ethanol. RESULTS: A continuous reactor with gradually increasing HSSL concentrations, from 20% to 60% (v/v), was operated for 382 generations. From the final obtained population (POP), a stable clone (C(4)) was isolated and characterized in 60% undetoxified HSSL. C(4) isolate was then compared with both the parental strain (PAR) and POP. Both POP and C(4) were able to grow in 60% undetoxified HSSL, with a higher capability to withstand HSSL inhibitors than PAR. Higher substrate uptake rates, 7% higher ethanol efficiency and improved ethanol yield were obtained using C4. CONCLUSION: S. stipitis was successfully adapted to 60% (v/v) undetoxified eucalyptus HSSL. A stable isolate, C(4), with an improved performance in undetoxified HSSL compared to PAR was successfully obtained from POP. Owing to its improved tolerance to inhibitors, C(4) may represent a major advantage for the production of bioethanol using HSSL as substrate. |
format | Online Article Text |
id | pubmed-4379546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43795462015-04-01 Adaptation of Scheffersomyces stipitis to hardwood spent sulfite liquor by evolutionary engineering Pereira, Susana R Sànchez i Nogué, Violeta Frazão, Cláudio J R Serafim, Luísa S Gorwa-Grauslund, Marie F Xavier, Ana M R B Biotechnol Biofuels Research Article BACKGROUND: Hardwood spent sulfite liquor (HSSL) is a by-product of acid sulfite pulping process that is rich in xylose, a monosaccharide that can be fermented to ethanol by Scheffersomyces stipitis. However, HSSL also contains acetic acid and lignosulfonates that are inhibitory compounds of yeast growth. The main objective of this study was the use of an evolutionary engineering strategy to obtain variants of S. stipitis with increased tolerance to HSSL inhibitors while maintaining the ability to ferment xylose to ethanol. RESULTS: A continuous reactor with gradually increasing HSSL concentrations, from 20% to 60% (v/v), was operated for 382 generations. From the final obtained population (POP), a stable clone (C(4)) was isolated and characterized in 60% undetoxified HSSL. C(4) isolate was then compared with both the parental strain (PAR) and POP. Both POP and C(4) were able to grow in 60% undetoxified HSSL, with a higher capability to withstand HSSL inhibitors than PAR. Higher substrate uptake rates, 7% higher ethanol efficiency and improved ethanol yield were obtained using C4. CONCLUSION: S. stipitis was successfully adapted to 60% (v/v) undetoxified eucalyptus HSSL. A stable isolate, C(4), with an improved performance in undetoxified HSSL compared to PAR was successfully obtained from POP. Owing to its improved tolerance to inhibitors, C(4) may represent a major advantage for the production of bioethanol using HSSL as substrate. BioMed Central 2015-03-26 /pmc/articles/PMC4379546/ /pubmed/25829945 http://dx.doi.org/10.1186/s13068-015-0234-y Text en © Pereira et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Pereira, Susana R Sànchez i Nogué, Violeta Frazão, Cláudio J R Serafim, Luísa S Gorwa-Grauslund, Marie F Xavier, Ana M R B Adaptation of Scheffersomyces stipitis to hardwood spent sulfite liquor by evolutionary engineering |
title | Adaptation of Scheffersomyces stipitis to hardwood spent sulfite liquor by evolutionary engineering |
title_full | Adaptation of Scheffersomyces stipitis to hardwood spent sulfite liquor by evolutionary engineering |
title_fullStr | Adaptation of Scheffersomyces stipitis to hardwood spent sulfite liquor by evolutionary engineering |
title_full_unstemmed | Adaptation of Scheffersomyces stipitis to hardwood spent sulfite liquor by evolutionary engineering |
title_short | Adaptation of Scheffersomyces stipitis to hardwood spent sulfite liquor by evolutionary engineering |
title_sort | adaptation of scheffersomyces stipitis to hardwood spent sulfite liquor by evolutionary engineering |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379546/ https://www.ncbi.nlm.nih.gov/pubmed/25829945 http://dx.doi.org/10.1186/s13068-015-0234-y |
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