Enhancement of biohydrogen production in Clostridium acetobutylicum ATCC 824 by overexpression of glyceraldehyde-3-phosphate dehydrogenase gene

被引:11
作者
Kim, Sang Hyun [1 ]
Hwang, Jeong Hyeon [1 ]
Kim, Hyun Joong [1 ]
Oh, Suk Jin [1 ]
Kim, Hyun Jin [1 ]
Shin, Nara [1 ]
Kim, Sang-Hyoun [2 ]
Park, Jeong-Hoon [3 ]
Bhatia, Shashi Kant [1 ,4 ]
Yang, Yung-Hun [1 ,4 ]
机构
[1] Konkuk Univ, Coll Engn, Dept Biol Engn, 120 Neungdong Ro, Seoul 05029, South Korea
[2] Yonsei Univ, Sch Civil & Environm Engn, 50 Yonsei Ro, Seoul 03722, South Korea
[3] Korea Inst Ind Technol KITECH, Sustainable Technol & Wellness R&D Grp, Jeju Si 63243, South Korea
[4] Konkuk Univ, Inst Ubiquitous Informat Technol & Applicat, Seoul 05029, South Korea
基金
新加坡国家研究基金会;
关键词
Biohydrogen production; Clostridium acetobutylicum; Glyceraldehyde-3-phosphate dehydrogenase; HYDROGEN-PRODUCTION; CORYNEBACTERIUM-GLUTAMICUM; ISOBUTANOL PRODUCTION; LYSINE PRODUCTION; ESCHERICHIA-COLI; FERMENTATION; ENERGY; METABOLISM; BUTYRICUM; PATHWAY;
D O I
10.1016/j.enzmictec.2023.110244
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In the dark fermentation of hydrogen, development of production host is crucial as bacteria act on substrates and produce hydrogen. The present study aimed to improve hydrogen production through the development of Clostridium acetobutylicum as a superior biohydrogen producer. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which produces NADH/NADPH for metabolites and energy in primary pathways, was introduced to enhance hydrogen production. The strain CAC824-G containing gapC that encodes GAPDH showed a 66.3 % higher hydrogen production than the wild-type strain, with increased NADH and NADPH pools. Glucose consumption and other byproducts, such as acetone, butanol, and ethanol, were also high in CAC824-G. Overexpression of gapC resulted in increased hydrogen production with sugars obtained from different biomass, even in the presence of inhibitors such as vanillin, 5-hydroxymethylfufural, acetic acid, and formic acid. Our results imply that overexpression of gapC in Clostridium is possible to expand the production of the reported biochemicals to produce hydrogen.
引用
收藏
页数:10
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