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Studying the rapid bioconversion of lignocellulosic sugars into ethanol using high cell density fermentations with cell recycle
BACKGROUND: The Rapid Bioconversion with Integrated recycle Technology (RaBIT) process reduces capital costs, processing times, and biocatalyst cost for biochemical conversion of cellulosic biomass to biofuels by reducing total bioprocessing time (enzymatic hydrolysis plus fermentation) to 48 h, inc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026590/ https://www.ncbi.nlm.nih.gov/pubmed/24847379 http://dx.doi.org/10.1186/1754-6834-7-73 |
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author | Sarks, Cory Jin, Mingjie Sato, Trey K Balan, Venkatesh Dale, Bruce E |
author_facet | Sarks, Cory Jin, Mingjie Sato, Trey K Balan, Venkatesh Dale, Bruce E |
author_sort | Sarks, Cory |
collection | PubMed |
description | BACKGROUND: The Rapid Bioconversion with Integrated recycle Technology (RaBIT) process reduces capital costs, processing times, and biocatalyst cost for biochemical conversion of cellulosic biomass to biofuels by reducing total bioprocessing time (enzymatic hydrolysis plus fermentation) to 48 h, increasing biofuel productivity (g/L/h) twofold, and recycling biocatalysts (enzymes and microbes) to the next cycle. To achieve these results, RaBIT utilizes 24-h high cell density fermentations along with cell recycling to solve the slow/incomplete xylose fermentation issue, which is critical for lignocellulosic biofuel fermentations. Previous studies utilizing similar fermentation conditions showed a decrease in xylose consumption when recycling cells into the next fermentation cycle. Eliminating this decrease is critical for RaBIT process effectiveness for high cycle counts. RESULTS: Nine different engineered microbial strains (including Saccharomyces cerevisiae strains, Scheffersomyces (Pichia) stipitis strains, Zymomonas mobilis 8b, and Escherichia coli KO11) were tested under RaBIT platform fermentations to determine their suitability for this platform. Fermentation conditions were then optimized for S. cerevisiae GLBRCY128. Three different nutrient sources (corn steep liquor, yeast extract, and wheat germ) were evaluated to improve xylose consumption by recycled cells. Capacitance readings were used to accurately measure viable cell mass profiles over five cycles. CONCLUSION: The results showed that not all strains are capable of effectively performing the RaBIT process. Acceptable performance is largely correlated to the specific xylose consumption rate. Corn steep liquor was found to reduce the deleterious impacts of cell recycle and improve specific xylose consumption rates. The viable cell mass profiles indicated that reduction in specific xylose consumption rate, not a drop in viable cell mass, was the main cause for decreasing xylose consumption. |
format | Online Article Text |
id | pubmed-4026590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40265902014-05-21 Studying the rapid bioconversion of lignocellulosic sugars into ethanol using high cell density fermentations with cell recycle Sarks, Cory Jin, Mingjie Sato, Trey K Balan, Venkatesh Dale, Bruce E Biotechnol Biofuels Research BACKGROUND: The Rapid Bioconversion with Integrated recycle Technology (RaBIT) process reduces capital costs, processing times, and biocatalyst cost for biochemical conversion of cellulosic biomass to biofuels by reducing total bioprocessing time (enzymatic hydrolysis plus fermentation) to 48 h, increasing biofuel productivity (g/L/h) twofold, and recycling biocatalysts (enzymes and microbes) to the next cycle. To achieve these results, RaBIT utilizes 24-h high cell density fermentations along with cell recycling to solve the slow/incomplete xylose fermentation issue, which is critical for lignocellulosic biofuel fermentations. Previous studies utilizing similar fermentation conditions showed a decrease in xylose consumption when recycling cells into the next fermentation cycle. Eliminating this decrease is critical for RaBIT process effectiveness for high cycle counts. RESULTS: Nine different engineered microbial strains (including Saccharomyces cerevisiae strains, Scheffersomyces (Pichia) stipitis strains, Zymomonas mobilis 8b, and Escherichia coli KO11) were tested under RaBIT platform fermentations to determine their suitability for this platform. Fermentation conditions were then optimized for S. cerevisiae GLBRCY128. Three different nutrient sources (corn steep liquor, yeast extract, and wheat germ) were evaluated to improve xylose consumption by recycled cells. Capacitance readings were used to accurately measure viable cell mass profiles over five cycles. CONCLUSION: The results showed that not all strains are capable of effectively performing the RaBIT process. Acceptable performance is largely correlated to the specific xylose consumption rate. Corn steep liquor was found to reduce the deleterious impacts of cell recycle and improve specific xylose consumption rates. The viable cell mass profiles indicated that reduction in specific xylose consumption rate, not a drop in viable cell mass, was the main cause for decreasing xylose consumption. BioMed Central 2014-05-15 /pmc/articles/PMC4026590/ /pubmed/24847379 http://dx.doi.org/10.1186/1754-6834-7-73 Text en Copyright © 2014 Sarks et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 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 Sarks, Cory Jin, Mingjie Sato, Trey K Balan, Venkatesh Dale, Bruce E Studying the rapid bioconversion of lignocellulosic sugars into ethanol using high cell density fermentations with cell recycle |
title | Studying the rapid bioconversion of lignocellulosic sugars into ethanol using high cell density fermentations with cell recycle |
title_full | Studying the rapid bioconversion of lignocellulosic sugars into ethanol using high cell density fermentations with cell recycle |
title_fullStr | Studying the rapid bioconversion of lignocellulosic sugars into ethanol using high cell density fermentations with cell recycle |
title_full_unstemmed | Studying the rapid bioconversion of lignocellulosic sugars into ethanol using high cell density fermentations with cell recycle |
title_short | Studying the rapid bioconversion of lignocellulosic sugars into ethanol using high cell density fermentations with cell recycle |
title_sort | studying the rapid bioconversion of lignocellulosic sugars into ethanol using high cell density fermentations with cell recycle |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026590/ https://www.ncbi.nlm.nih.gov/pubmed/24847379 http://dx.doi.org/10.1186/1754-6834-7-73 |
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