Li Mai, Ho Pei Yee, Yao Shanjing, Shimizu Kazuyuki
Department of Bioscience and Bioinformatics, Kyushu Institute of Technology, Iizuka, Fukuoka 820-8502, Japan.
J Biotechnol. 2006 Mar 23;122(2):254-66. doi: 10.1016/j.jbiotec.2005.09.016. Epub 2005 Nov 23.
The lipoamide dehydrogenase (LPD) encoded by lpdA gene is a component of the pyruvate dehydrogenase complex (PDHc), alpha-ketoglutarate dehydrogenase (AKGDH) and the glycine cleavage multi-enzyme (GCV) systems. In the present study, cell growth characteristics, enzyme activities and intracellular metabolite concentrations were compared between the parent strain Escherichia coli BW25113 and its lpdA knockout mutant in batch and continuous cultures. The lpdA knockout mutant produced significantly more pyruvate and L-glutamate under aerobiosis. Some D-lactate and succinate also accumulated in the culture broth. Based on the investigation of enzyme activities and intracellular metabolite concentrations, acetyl-CoA was considered to be formed by the combined reactions through pyruvate oxidase (PoxB), acetyl-CoA synthetase (Acs) and acetate kinase (Ack)-phosphoacetyltransferase (Pta) in the lpdA mutant. The effect of the lpdA gene knockout on the intracellular metabolic flux distributions was investigated based on 1H-13C NMR spectra and GC-MS signals obtained from 13C-labeling experiment using the mixture of [U-13C] glucose, [1-13C] glucose, and naturally labeled glucose. Flux analysis of the lpdA mutant indicated that the Entner-Doudoroff (ED) pathway and the glyoxylate shunt were activated. The fluxes through glycolysis and oxidative pentose phosphate (PP) pathway (except for the flux through glucose-6-phosphate dehydrogenase) were slightly downregulated. The TCA cycle was also downregulated in the mutant strain. On the other hand, the fluxes through the anaplerotic reactions of PEP carboxylase, PEP carboxykinase and malic enzyme were upregulated, which were consistent with the results of enzyme activities. Furthermore, the influence of the poxB gene knockout on the growth of E. coli was also studied because of its similar function to PDHc which connects the glycolysis to the TCA cycle. Under aerobiosis, a comparison of lpdA mutant and poxB mutant indicated that PDHc is the main enzyme which catalyzes the reaction from pyruvate to acetyl-CoA in the parent strain, while PoxB plays a very important role in the PDHc-deficient strain.
由lpdA基因编码的硫辛酰胺脱氢酶(LPD)是丙酮酸脱氢酶复合体(PDHc)、α-酮戊二酸脱氢酶(AKGDH)和甘氨酸裂解多酶(GCV)系统的一个组成部分。在本研究中,对亲本菌株大肠杆菌BW25113及其lpdA基因敲除突变体在分批培养和连续培养中的细胞生长特性、酶活性和细胞内代谢物浓度进行了比较。lpdA基因敲除突变体在需氧条件下产生的丙酮酸和L-谷氨酸显著增多。培养液中还积累了一些D-乳酸和琥珀酸。基于对酶活性和细胞内代谢物浓度的研究,认为在lpdA突变体中,乙酰辅酶A是通过丙酮酸氧化酶(PoxB)、乙酰辅酶A合成酶(Acs)和乙酸激酶(Ack)-磷酸乙酰转移酶(Pta)的联合反应形成的。基于使用[U-13C]葡萄糖、[1-13C]葡萄糖和天然标记葡萄糖的混合物进行13C标记实验获得的1H-13C NMR光谱和GC-MS信号,研究了lpdA基因敲除对细胞内代谢通量分布的影响。lpdA突变体的通量分析表明,Entner-Doudoroff(ED)途径和乙醛酸分流被激活。通过糖酵解和氧化戊糖磷酸(PP)途径(葡萄糖-6-磷酸脱氢酶的通量除外)的通量略有下调。突变菌株中的三羧酸循环也下调。另一方面,通过磷酸烯醇式丙酮酸羧化酶、磷酸烯醇式丙酮酸羧激酶和苹果酸酶的回补反应的通量上调,这与酶活性结果一致。此外,由于poxB基因与连接糖酵解和三羧酸循环的PDHc功能相似,还研究了其敲除对大肠杆菌生长的影响。在需氧条件下,lpdA突变体和poxB突变体的比较表明,在亲本菌株中,PDHc是催化丙酮酸转化为乙酰辅酶A反应的主要酶,而在缺乏PDHc的菌株中,PoxB起着非常重要的作用。