Potential of a Saccharomyces cerevisiae recombinant strain lacking ethanol and glycerol biosynthesis pathways in efficient anaerobic bioproduction

被引:6
|
作者
Hirasawa, Takashi [1 ]
Ida, Yoshihiro [2 ]
Furusawa, Chikara [3 ]
Shimizu, Hiroshi [2 ]
机构
[1] Tokyo Inst Technol, Dept Bioengn, Yokohama, Kanagawa, Japan
[2] Osaka Univ, Grad Sch Informat Sci & Technol, Dept Bioinformat Engn, Osaka, Japan
[3] RIKEN, Quantitat Biol Ctr, Osaka, Japan
关键词
alcohol dehydrogenase; bioproduction; ethanol; glycerol; L-lactate; Saccharomyces cerevisiae; DIHYDROXYACETONE PHOSPHATE; PYRUVATE DECARBOXYLASE; LACTATE PRODUCTION; GENE; SYSTEMS; PDC1; DEHYDROGENASES; MUTANTS;
D O I
10.4161/bioe.26569
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
Saccharomyces cerevisiae shows high growth activity under low pH conditions and can be used for producing acidic chemicals such as organic acids as well as fuel ethanol. However, ethanol can also be a problematic by-product in the production of chemicals except for ethanol. We have reported that a stable low-ethanol production phenotype was achieved by disrupting 6 NADH-dependent alcohol dehydrogenase genes of S. cerevisiae. Moreover, the genes encoding the NADH-dependent glycerol biosynthesis enzymes were further disrupted because the ADH-disrupted recombinant strain showed high glycerol production to maintain intracellular redox balance. The recombinant strain incapable producing ethanol and glycerol could have the potential to be a host for producing metabolite(s) whose biosynthesis is coupled with NADH oxidation. Indeed, we successfully achieved almost 100% yield for L-lactate production using this recombinant strain as a host. In addition, the potential of our constructed recombinant strain for efficient bioproduction, particularly under anaerobic conditions, is also discussed.
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页码:123 / 128
页数:6
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