Biohydrogen by Rhodobacter sphaeroides during photo-fermentation: Mixed vs. sole carbon sources enhance bacterial growth and H2 production

被引:27
|
作者
Hakobyan, Lilit [1 ]
Gabrielyan, Lilit [1 ,2 ]
Trchounian, Armen [1 ,2 ]
机构
[1] Yerevan State Univ, Res Inst Biol, Biol Fac, 1 A Manoukian Str, Yerevan 0025, Armenia
[2] Yerevan State Univ, Biol Fac, Dept Biochem Microbiol & Biotechnol, 1 A Manoukian Str, Yerevan 0025, Armenia
关键词
Biohydrogen; Carbon sources; Photo-fermentation; ATPase activity; Rhodobacter sphaeroides; BIO-HYDROGEN PRODUCTION; DARK;
D O I
10.1016/j.ijhydene.2018.11.082
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Mixed carbon sources fermentation by bacteria is a promising approach for biohydrogen (H-2) production biotechnology. In the present study, growth and H-2 production by purple bacteria Rhodobacter sphaeroides MDC6521 during mixed carbon sources (succinate + acetate, succinate + malate, and malate + acetate) photo-fermentation was investigated. The growth rate of bacteria in mixed carbon sources containing medium was of similar to 0.33 h(-1) which was considerably higher (1.3-1.7-fold) compared with sole carbon substrate containing one. Moreover, the H-2 production during photo-fermentation of succinate and acetate mixture was of similar to 6.5 mmol H(2)g(-1) (dry weight of biomass) and significantly more (similar to 2-3-fold) than that with appropriate sole sources and higher (1.5-fold) than that with succinate and malate mixture. Probably, supplementation of the mixed carbon sources into bacterial culture alters the mode of metabolism, resulting in enhanced H-2 production, thus they can be preferable compared to the sole carbon source. The changed FOF1-ATPase activity of membrane vesicles suggested its important role in the increase of H-2 production efficiency. The results showed that mixed carbon sources provide more H-2 than the sole carbon substrates and succinate with acetate mixture is better than succinate with malate. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:674 / 679
页数:6
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