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Enhanced photo-fermentative H(2) production using Rhodobacter sphaeroides by ethanol addition and analysis of soluble microbial products
BACKGROUND: Biological fermentation routes can provide an environmentally friendly way of producing H(2) since they use renewable biomass as feedstock and proceed under ambient temperature and pressure. In particular, photo-fermentation has superior properties in terms of achieving high H(2) yield t...
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/PMC4038723/ https://www.ncbi.nlm.nih.gov/pubmed/24883103 http://dx.doi.org/10.1186/1754-6834-7-79 |
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author | Kim, Dong-Hoon Lee, Ji-Hye Kang, Seoktae Hallenbeck, Patrick C Kim, Eui-Jin Lee, Jeong K Kim, Mi-Sun |
author_facet | Kim, Dong-Hoon Lee, Ji-Hye Kang, Seoktae Hallenbeck, Patrick C Kim, Eui-Jin Lee, Jeong K Kim, Mi-Sun |
author_sort | Kim, Dong-Hoon |
collection | PubMed |
description | BACKGROUND: Biological fermentation routes can provide an environmentally friendly way of producing H(2) since they use renewable biomass as feedstock and proceed under ambient temperature and pressure. In particular, photo-fermentation has superior properties in terms of achieving high H(2) yield through complete degradation of substrates. However, long-term H(2) production data with stable performance is limited, and this data is essential for practical applications. In the present work, continuous photo-fermentative H(2) production from lactate was attempted using the purple non-sulfur bacterium, Rhodobacter sphaeroides KD131. As a gradual drop in H(2) production was observed, we attempted to add ethanol (0.2% v/v) to the medium. RESULTS: As continuous operation went on, H(2) production was not sustained and showed a negligible H(2) yield (< 0.5 mol H(2)/mol lactate(added)) within two weeks. Electron balance analysis showed that the reason for the gradual drop in H(2) production was ascribed to the increase in production of soluble microbial products (SMP(s)). To see the possible effect of ethanol addition, a batch test was first conducted. The presence of ethanol significantly increased the H(2) yield from 1.15 to 2.20 mol H(2)/mol lactate(added), by suppressing the production of SMPs. The analysis of SMPs by size exclusion chromatography showed that, in the later period of fermentation, more than half of the low molecular weight SMPs (< 1 kDa) were consumed and used for H(2) production when ethanol had been added, while the concentration of SMPs continuously increased in the absence of ethanol. It was found that the addition of ethanol facilitated the utilization of reducing power, resulting in an increase in the cellular levels of NAD(+) and NADP(+). In continuous operation, ethanol addition was effective, such that stable H(2) production was attained with an H(2) yield of 2.5 mol H(2)/mol lactate(added). Less than 15% of substrate electrons were used for SMP production, whereas 35% were used in the control. CONCLUSIONS: We have found that SMPs are the key factor in photo-fermentative H(2) production, and their production can be suppressed by ethanol addition. However, since external addition of ethanol to the medium represents an extra economic burden, ethanol should be prepared in a cost-effective way. |
format | Online Article Text |
id | pubmed-4038723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40387232014-05-31 Enhanced photo-fermentative H(2) production using Rhodobacter sphaeroides by ethanol addition and analysis of soluble microbial products Kim, Dong-Hoon Lee, Ji-Hye Kang, Seoktae Hallenbeck, Patrick C Kim, Eui-Jin Lee, Jeong K Kim, Mi-Sun Biotechnol Biofuels Research BACKGROUND: Biological fermentation routes can provide an environmentally friendly way of producing H(2) since they use renewable biomass as feedstock and proceed under ambient temperature and pressure. In particular, photo-fermentation has superior properties in terms of achieving high H(2) yield through complete degradation of substrates. However, long-term H(2) production data with stable performance is limited, and this data is essential for practical applications. In the present work, continuous photo-fermentative H(2) production from lactate was attempted using the purple non-sulfur bacterium, Rhodobacter sphaeroides KD131. As a gradual drop in H(2) production was observed, we attempted to add ethanol (0.2% v/v) to the medium. RESULTS: As continuous operation went on, H(2) production was not sustained and showed a negligible H(2) yield (< 0.5 mol H(2)/mol lactate(added)) within two weeks. Electron balance analysis showed that the reason for the gradual drop in H(2) production was ascribed to the increase in production of soluble microbial products (SMP(s)). To see the possible effect of ethanol addition, a batch test was first conducted. The presence of ethanol significantly increased the H(2) yield from 1.15 to 2.20 mol H(2)/mol lactate(added), by suppressing the production of SMPs. The analysis of SMPs by size exclusion chromatography showed that, in the later period of fermentation, more than half of the low molecular weight SMPs (< 1 kDa) were consumed and used for H(2) production when ethanol had been added, while the concentration of SMPs continuously increased in the absence of ethanol. It was found that the addition of ethanol facilitated the utilization of reducing power, resulting in an increase in the cellular levels of NAD(+) and NADP(+). In continuous operation, ethanol addition was effective, such that stable H(2) production was attained with an H(2) yield of 2.5 mol H(2)/mol lactate(added). Less than 15% of substrate electrons were used for SMP production, whereas 35% were used in the control. CONCLUSIONS: We have found that SMPs are the key factor in photo-fermentative H(2) production, and their production can be suppressed by ethanol addition. However, since external addition of ethanol to the medium represents an extra economic burden, ethanol should be prepared in a cost-effective way. BioMed Central 2014-05-27 /pmc/articles/PMC4038723/ /pubmed/24883103 http://dx.doi.org/10.1186/1754-6834-7-79 Text en Copyright © 2014 Kim 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 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 Kim, Dong-Hoon Lee, Ji-Hye Kang, Seoktae Hallenbeck, Patrick C Kim, Eui-Jin Lee, Jeong K Kim, Mi-Sun Enhanced photo-fermentative H(2) production using Rhodobacter sphaeroides by ethanol addition and analysis of soluble microbial products |
title | Enhanced photo-fermentative H(2) production using Rhodobacter sphaeroides by ethanol addition and analysis of soluble microbial products |
title_full | Enhanced photo-fermentative H(2) production using Rhodobacter sphaeroides by ethanol addition and analysis of soluble microbial products |
title_fullStr | Enhanced photo-fermentative H(2) production using Rhodobacter sphaeroides by ethanol addition and analysis of soluble microbial products |
title_full_unstemmed | Enhanced photo-fermentative H(2) production using Rhodobacter sphaeroides by ethanol addition and analysis of soluble microbial products |
title_short | Enhanced photo-fermentative H(2) production using Rhodobacter sphaeroides by ethanol addition and analysis of soluble microbial products |
title_sort | enhanced photo-fermentative h(2) production using rhodobacter sphaeroides by ethanol addition and analysis of soluble microbial products |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038723/ https://www.ncbi.nlm.nih.gov/pubmed/24883103 http://dx.doi.org/10.1186/1754-6834-7-79 |
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