State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
J Appl Microbiol. 2014 Sep;117(3):690-8. doi: 10.1111/jam.12588. Epub 2014 Jul 9.
To utilize excess NADH for 1,3-propanediol production by 2,3-butanediol-deficient mutants, the effect of dhaT overexpression in two distinct 2,3-butanediol-deficient mutants was investigated.
Two 2,3-butanediol-deficient mutants, KG1-3 (blocking of the 2,3-butanediol pathway only) and KG1-5 (blocking of both of 2,3-butanediol and lactate pathways) were constructed. Our results showed that although the intracellular redox balance (NADH/NAD(+)) was extremely high at the end of fermentation for both mutants, the status of intracellular redox in KG1-5 was maintained at a normal level following the first stage of fermentation. Analysis of cell growth and metabolite formation confirmed the inhibition of excess lactate in 2,3-butanediol pathway-deficient mutants. Furthermore, dhaT was overexpressed in two 2,3-butanediol-deficient mutants (KG1-3T and KG1-5T). In KG1-5T, the intracellular redox balance was restored to normal and 1,3-propanediol production increased. The yield of 1,3-propanediol from glycerol in KG1-5T was also restored to a normal level of 0·6.
The excess NADH in both the 2,3-butanediol- and lactate-deficient mutants can be used by overexpresstion of dhaT.
The metabolic flux tended to increase lactate production by the abolishment of the 2,3-butanediol pathway in Klebsiella pneumoniae, and the high accumulation of lactate prevented the cell from using excess NADH, thereby inhibiting cell growth and 1,3-propanediol production.
利用过剩的 NADH 生产 1,3-丙二醇,本研究调查了 dhaT 在两个不同的 2,3-丁二醇缺陷突变体中的过表达效果。
构建了两个 2,3-丁二醇缺陷突变体,KG1-3(仅阻断 2,3-丁二醇途径)和 KG1-5(同时阻断 2,3-丁二醇和乳酸途径)。结果表明,尽管两个突变体在发酵结束时细胞内氧化还原平衡(NADH/NAD(+))极高,但在发酵的第一阶段之后,KG1-5 中的细胞内氧化还原状态保持在正常水平。细胞生长和代谢产物形成分析证实,2,3-丁二醇途径缺陷突变体中过量乳酸的生成受到抑制。此外,在两个 2,3-丁二醇缺陷突变体(KG1-3T 和 KG1-5T)中过表达了 dhaT。在 KG1-5T 中,细胞内氧化还原平衡恢复正常,1,3-丙二醇产量增加。KG1-5T 中甘油转化为 1,3-丙二醇的产率也恢复到正常水平的 0.6。
过量的 NADH 可被 dhaT 的过表达用于 2,3-丁二醇和乳酸缺陷突变体。
在肺炎克雷伯氏菌中,2,3-丁二醇途径的阻断使代谢通量趋于增加乳酸的生成,而乳酸的大量积累阻止了细胞利用过剩的 NADH,从而抑制了细胞生长和 1,3-丙二醇的生产。