Enhancement of xylitol production by attenuation of intracellular xylitol dehydrogenase activity in Candida tropicalis

被引:16
作者
Ko, Byoung Sam [4 ]
Kim, Dong-Min [1 ]
Yoon, Byoung Hoon [2 ]
Bai, Suk [4 ]
Lee, Hyeon Yong [3 ]
Kim, Jung Hoe [2 ]
Kim, Il-Chul [4 ]
机构
[1] Chonnam Natl Univ, Coll Vet Med, Kwangju 500757, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
[3] Kangwon Natl Univ, Coll Biosci & Biotechnol, Chunchon 368701, South Korea
[4] Chonnam Natl Univ, Higher Educ Ctr Bioregulator Res, Kwangju 500757, South Korea
关键词
Candida tropicalis; Enzyme engineering; Fermentation; Xylitol; Xylitol dehydrogenase; GENE-DISRUPTED MUTANT; D-XYLOSE; YIELD;
D O I
10.1007/s10529-011-0558-z
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
To construct Candida tropicalis strains that produce a high yield of xylitol with no requirement for co-substrates, we engineered the yeast with an attenuated xylitol dehydrogenase (XDH) and then assessed the efficiency of xylitol production The mutants, strains XDH-5 (with only one copy of the XDH gene), and ARSdR-16 (with a mutated XDH gene) showed 70 and 40% of wild type (WT) XDH activity, respectively. Conversions of xylose to xylitol by WT, XDH-5, and ARSdR-16 were 62, 64, and 75%, respectively, with productivities of 0.52, 0.54, and 0.62 g l(-1) h(-1), respectively. The ARSdR-16 mutant strain produced xylitol with high yield and high productivity in a simple process that required no co-substrates, such as glycerol. This strain represents a promising alternative for efficient and cost-effective xylitol production.
引用
收藏
页码:1209 / 1213
页数:5
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