The effect of carbon sources and lactate dehydrogenase deletion on 1,2-propanediol production in Escherichia coli

被引:41
作者
Berríos-Rivera, SJ
San, KY [1 ]
Bennett, GN
机构
[1] Rice Univ, Dept Bioengn, Houston, TX 77251 USA
[2] Rice Univ, Dept Chem Engn, Houston, TX USA
[3] Rice Univ, Dept Biochem & Cell Biol, Houston, TX USA
关键词
1,2-propanediol; Escherichia coli; lactate dehydrogenase deletion;
D O I
10.1007/s10295-002-0006-0
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 previous studies, we showed that cofactor manipulations can potentially be used as a tool in metabolic engineering. In this study, sugars similar to glucose, that can feed into glycolysis and pyruvate production, but with different oxidation states, were used as substrates. This provided a simple way of testing the effect of manipulating the NADH/NAD+ ratio or the availability of NADH on the metabolic patterns of Escherichia coli under anaerobic conditions and on the production of 1,2-propanediol (1,2-PD), which requires NADH for its synthesis. Production of 1,2-PD was achieved by overexpressing the two enzymes methylglyoxal synthase from Clostridium acetobutylicum and glycerol dehydrogenase from E. coli. In addition, the effect of eliminating a pathway competing for NADH by using a ldh(-) strain (without lactate dehydrogenase activity) on the production of 1,2-PD was investigated. The oxidation state of the carbon source significantly affected the yield of metabolites, such as ethanol, acetate and lactate. However, feeding a more reduced carbon source did not increase the yield of 1,2-PD. The production of 1,2-PD with glucose as the carbon source was improved by the incorporation of a ldh- mutation. The results of these experiments indicate that our current 1,2-PD production system is not limited by NADH, but rather by the pathways following the formation of methylglyoxal.
引用
收藏
页码:34 / 40
页数:7
相关论文
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[21]   Redistribution of Metabolic Fluxes in Escherichia coli with Fermentative Lactate Dehydrogenase Overexpression and Deletion [J].
Yang, Yea-Tyng ;
San, Ka-Yiu .
METABOLIC ENGINEERING, 1999, 1 (02) :141-152