Zhao J, Baba T, Mori H, Shimizu K
Metabolome Unit, Institute for Advanced Biosciences, Keio University, Tsuruoka, Japan.
Appl Microbiol Biotechnol. 2004 Mar;64(1):91-8. doi: 10.1007/s00253-003-1458-5. Epub 2003 Dec 6.
An integrated study on cell growth, enzyme activities and carbon flux redistribution was made to investigate how the central metabolism of Escherichia coli changes with the knockout of genes in the oxidative pentose phosphate pathway (PPP). Mutants deficient in glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase were constructed by disrupting the zwf and gnd genes and were grown in minimal media with two different carbon sources, such as glucose or pyruvate. It was shown that the knockout of either gnd or zwf gene did not affect the cell growth rate significantly, but the cellular metabolism was changed. While the specific substrate uptake rate and the specific carbon dioxide evolution rate for either mutant grown on glucose were higher than those obtained for the parent strain, these two rates were markedly decreased in mutants grown on pyruvate. The measurement of enzyme activities implied a significant change in metabolism, when alternative pathways such as the Entner-Doudoroff pathway (EDP) and the malic enzyme pathway were activated in the gnd mutant grown on glucose. As compared with the parent strain, the activities of phosphoglucose isomerase were increased in mutants grown on glucose but decreased in mutants grown on pyruvate. The metabolic flux redistribution obtained based on 13C-labeling experiments further indicated that the direction of the flux through the non-oxidative PPP was reversed in response to the gene knockout. Moreover, the knockout of genes caused an increased flux through the tricarboxlic acid cycle in mutants grown on glucose but caused a decrease in the case of using pyruvate. There was also a negative correlation between the fluxes through malic enzyme and isocitrate dehydrogenase in the mutants; and a positive correlation was found between the fluxes through malic enzyme and phosphoenolpyruvate carboxylase.
开展了一项关于细胞生长、酶活性和碳通量重新分配的综合研究,以探究大肠杆菌的中心代谢如何随着氧化戊糖磷酸途径(PPP)中基因敲除而发生变化。通过破坏zwf和gnd基因构建了缺乏葡萄糖-6-磷酸脱氢酶和6-磷酸葡萄糖酸脱氢酶的突变体,并在含有两种不同碳源(如葡萄糖或丙酮酸)的基本培养基中培养。结果表明,敲除gnd或zwf基因均未显著影响细胞生长速率,但细胞代谢发生了变化。虽然在葡萄糖上生长的任一突变体的比底物摄取速率和比二氧化碳释放速率均高于亲本菌株,但在丙酮酸上生长的突变体中这两个速率显著降低。酶活性的测定表明,当在葡萄糖上生长的gnd突变体中激活诸如Entner-Doudoroff途径(EDP)和苹果酸酶途径等替代途径时,代谢发生了显著变化。与亲本菌株相比,在葡萄糖上生长的突变体中磷酸葡萄糖异构酶的活性增加,但在丙酮酸上生长的突变体中该活性降低。基于13C标记实验获得的代谢通量重新分配进一步表明,响应基因敲除,通过非氧化PPP的通量方向发生了逆转。此外,基因敲除导致在葡萄糖上生长的突变体中通过三羧酸循环的通量增加,但在使用丙酮酸的情况下通量减少。突变体中通过苹果酸酶和异柠檬酸脱氢酶的通量之间也存在负相关;并且发现通过苹果酸酶和磷酸烯醇式丙酮酸羧化酶的通量之间存在正相关。