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Methodology for enabling high-throughput simultaneous saccharification and fermentation screening of yeast using solid biomass as a substrate
BACKGROUND: High-throughput (HTP) screening is becoming an increasingly useful tool for collating biological data which would otherwise require the employment of excessive resources. Second generation biofuel production is one such process. HTP screening allows the investigation of large sample sets...
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/PMC4314751/ https://www.ncbi.nlm.nih.gov/pubmed/25648300 http://dx.doi.org/10.1186/s13068-014-0181-z |
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author | Elliston, Adam Wood, Ian P Soucouri, Marie J Tantale, Rachelle J Dicks, Jo Roberts, Ian N Waldron, Keith W |
author_facet | Elliston, Adam Wood, Ian P Soucouri, Marie J Tantale, Rachelle J Dicks, Jo Roberts, Ian N Waldron, Keith W |
author_sort | Elliston, Adam |
collection | PubMed |
description | BACKGROUND: High-throughput (HTP) screening is becoming an increasingly useful tool for collating biological data which would otherwise require the employment of excessive resources. Second generation biofuel production is one such process. HTP screening allows the investigation of large sample sets to be undertaken with increased speed and cost effectiveness. This paper outlines a methodology that will enable solid lignocellulosic substrates to be hydrolyzed and fermented at a 96-well plate scale, facilitating HTP screening of ethanol production, whilst maintaining repeatability similar to that achieved at a larger scale. RESULTS: The results showed that utilizing sheets of biomass of consistent density (handbills), for paper, and slurries of pretreated biomass that could be pipetted allowed standardized and accurate transfers to 96-well plates to be achieved (±3.1 and 1.7%, respectively). Processing these substrates by simultaneous saccharification and fermentation (SSF) at various volumes showed no significant difference on final ethanol yields, either at standard shake flask (200 mL), universal bottle (10 mL) or 96-well plate (1 mL) scales. Substrate concentrations of up to 10% (w/v) were trialed successfully for SSFs at 1 mL volume. The methodology was successfully tested by showing the effects of steam explosion pretreatment on both oilseed rape and wheat straws. CONCLUSIONS: This methodology could be used to replace large shake flask reactions with comparatively fast 96-well plate SSF assays allowing for HTP experimentation. Additionally this method is compatible with a number of standardized assay techniques such as simple colorimetric, High-performance liquid chromatography (HPLC) and Nuclear magnetic resonance (NMR) spectroscopy. Furthermore this research has practical uses in the biorefining of biomass substrates for second generation biofuels and novel biobased chemicals by allowing HTP SSF screening, which should allow selected samples to be scaled up or studied in more detail. |
format | Online Article Text |
id | pubmed-4314751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43147512015-02-04 Methodology for enabling high-throughput simultaneous saccharification and fermentation screening of yeast using solid biomass as a substrate Elliston, Adam Wood, Ian P Soucouri, Marie J Tantale, Rachelle J Dicks, Jo Roberts, Ian N Waldron, Keith W Biotechnol Biofuels Methodology BACKGROUND: High-throughput (HTP) screening is becoming an increasingly useful tool for collating biological data which would otherwise require the employment of excessive resources. Second generation biofuel production is one such process. HTP screening allows the investigation of large sample sets to be undertaken with increased speed and cost effectiveness. This paper outlines a methodology that will enable solid lignocellulosic substrates to be hydrolyzed and fermented at a 96-well plate scale, facilitating HTP screening of ethanol production, whilst maintaining repeatability similar to that achieved at a larger scale. RESULTS: The results showed that utilizing sheets of biomass of consistent density (handbills), for paper, and slurries of pretreated biomass that could be pipetted allowed standardized and accurate transfers to 96-well plates to be achieved (±3.1 and 1.7%, respectively). Processing these substrates by simultaneous saccharification and fermentation (SSF) at various volumes showed no significant difference on final ethanol yields, either at standard shake flask (200 mL), universal bottle (10 mL) or 96-well plate (1 mL) scales. Substrate concentrations of up to 10% (w/v) were trialed successfully for SSFs at 1 mL volume. The methodology was successfully tested by showing the effects of steam explosion pretreatment on both oilseed rape and wheat straws. CONCLUSIONS: This methodology could be used to replace large shake flask reactions with comparatively fast 96-well plate SSF assays allowing for HTP experimentation. Additionally this method is compatible with a number of standardized assay techniques such as simple colorimetric, High-performance liquid chromatography (HPLC) and Nuclear magnetic resonance (NMR) spectroscopy. Furthermore this research has practical uses in the biorefining of biomass substrates for second generation biofuels and novel biobased chemicals by allowing HTP SSF screening, which should allow selected samples to be scaled up or studied in more detail. BioMed Central 2015-01-22 /pmc/articles/PMC4314751/ /pubmed/25648300 http://dx.doi.org/10.1186/s13068-014-0181-z Text en © Elliston 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 | Methodology Elliston, Adam Wood, Ian P Soucouri, Marie J Tantale, Rachelle J Dicks, Jo Roberts, Ian N Waldron, Keith W Methodology for enabling high-throughput simultaneous saccharification and fermentation screening of yeast using solid biomass as a substrate |
title | Methodology for enabling high-throughput simultaneous saccharification and fermentation screening of yeast using solid biomass as a substrate |
title_full | Methodology for enabling high-throughput simultaneous saccharification and fermentation screening of yeast using solid biomass as a substrate |
title_fullStr | Methodology for enabling high-throughput simultaneous saccharification and fermentation screening of yeast using solid biomass as a substrate |
title_full_unstemmed | Methodology for enabling high-throughput simultaneous saccharification and fermentation screening of yeast using solid biomass as a substrate |
title_short | Methodology for enabling high-throughput simultaneous saccharification and fermentation screening of yeast using solid biomass as a substrate |
title_sort | methodology for enabling high-throughput simultaneous saccharification and fermentation screening of yeast using solid biomass as a substrate |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314751/ https://www.ncbi.nlm.nih.gov/pubmed/25648300 http://dx.doi.org/10.1186/s13068-014-0181-z |
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