Institute of Biochemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.
Appl Microbiol Biotechnol. 2010 Mar;86(1):255-62. doi: 10.1007/s00253-009-2274-3. Epub 2009 Oct 15.
The NAD+-dependent formate dehydrogenase FDH1 gene (fdh1), cloned from Candida boidinii, was expressed in the ldh-deleted mutant of Enterobacter aerogenes IAM1183 strain. The plasmid of pCom10 driven by the PalkB promoter was used to construct the fdh1 expression system and thus introduce a new dihydronicotinamide adenine dinucleotide (NADH) regeneration pathway from formate in the ldh-deleted mutant. The knockout of NADH-consuming lactate pathway affected the whole cellular metabolism, and the hydrogen yield increased by 11.4% compared with the wild strain. Expression of fdh1 in the ldh-deleted mutant caused lower final cell concentration and final pH after 16 h cultivation, and finally resulted in 86.8% of increase in hydrogen yield per mole consumed glucose. The analysis of cellular metabolites and estimated redox state balance in the fdhl-expressed strain showed that more excess of reducing power was formed by the rewired NADH regeneration pathway, changing the metabolic distribution and promoting the hydrogen production.
从毕赤酵母中克隆的依赖 NAD+的甲酸脱氢酶 FDH1 基因(fdh1)在缺失 ldh 的肠杆菌 Aerogenes IAM1183 突变株中表达。使用由 PalkB 启动子驱动的质粒 pCom10 构建了 fdh1 表达系统,从而在缺失 ldh 的突变株中引入了一种新的二氢烟酰胺腺嘌呤二核苷酸(NADH)再生途径从甲酸。NADH 消耗乳酸途径的敲除影响整个细胞代谢,与野生型菌株相比,氢气产量增加了 11.4%。在 ldh 缺失突变体中表达 fdh1 导致培养 16 小时后最终细胞浓度和最终 pH 值降低,最终每摩尔消耗葡萄糖的氢气产量增加了 86.8%。对表达 fdhl 的菌株中细胞代谢物的分析和估计的氧化还原状态平衡表明,通过重新布线的 NADH 再生途径形成了更多的多余还原力,改变了代谢分布并促进了氢气生成。