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通过过表达大肠杆菌柠檬酸合酶基因增强荧光假单胞菌ATCC 13525中的柠檬酸生物合成。

Enhanced citric acid biosynthesis in Pseudomonas fluorescens ATCC 13525 by overexpression of the Escherichia coli citrate synthase gene.

作者信息

Buch Aditi D, Archana G, Kumar G Naresh

机构信息

Molecular Microbial Biochemistry Laboratory, Department of Biochemistry, Faculty of Science, M. S. University of Baroda, Vadodara 390 002, India.

Department of Microbiology and Biotechnology Center, Faculty of Science, M. S. University of Baroda, Vadodara 390 002, India.

出版信息

Microbiology (Reading). 2009 Aug;155(Pt 8):2620-2629. doi: 10.1099/mic.0.028878-0. Epub 2009 May 14.

Abstract

Citric acid secretion by fluorescent pseudomonads has a distinct significance in microbial phosphate solubilization. The role of citrate synthase in citric acid biosynthesis and glucose catabolism in pseudomonads was investigated by overexpressing the Escherichia coli citrate synthase (gltA) gene in Pseudomonas fluorescens ATCC 13525. The resultant approximately 2-fold increase in citrate synthase activity in the gltA-overexpressing strain Pf(pAB7) enhanced the intracellular and extracellular citric acid yields during the stationary phase, by about 2- and 26-fold, respectively, as compared to the control, without affecting the growth rate, glucose depletion rate or biomass yield. Decreased glucose consumption was paralleled by increased gluconic acid production due to an increase in glucose dehydrogenase activity. While the extracellular acetic acid yield increased in Pf(pAB7), pyruvic acid secretion decreased, correlating with an increase in pyruvate carboxylase activity and suggesting an increased demand for the anabolic precursor oxaloacetate. Activities of two other key enzymes, glucose-6-phosphate dehydrogenase and isocitrate dehydrogenase, remained unaltered, and the contribution of phosphoenolpyruvate carboxylase and isocitrate lyase to glucose catabolism was negligible. Strain Pf(pAB7) demonstrated an enhanced phosphate-solubilizing ability compared to the control. Co-expression of the Synechococcus elongatus PCC 6301 phosphoenolpyruvate carboxylase and E. coli gltA genes in P. fluorescens ATCC 13525, so as to supplement oxaloacetate for citrate biosynthesis, neither significantly affected citrate biosynthesis nor caused any change in the other physiological and biochemical parameters measured, despite approximately 1.3- and 5-fold increases in citrate synthase and phosphoenolpyruvate carboxylase activities, respectively. Thus, our results demonstrate that citrate synthase is rate-limiting in enhancing citrate biosynthesis in P. fluorescens ATCC 13525. Significantly low extracellular citrate levels as compared to the intracellular levels in Pf(pAB7) suggested a probable limitation of efficient citrate transport.

摘要

荧光假单胞菌分泌柠檬酸在微生物磷溶解中具有独特意义。通过在荧光假单胞菌ATCC 13525中过表达大肠杆菌柠檬酸合酶(gltA)基因,研究了柠檬酸合酶在假单胞菌柠檬酸生物合成和葡萄糖分解代谢中的作用。与对照相比,在过表达gltA的菌株Pf(pAB7)中,柠檬酸合酶活性增加了约2倍,这使得稳定期细胞内和细胞外柠檬酸产量分别提高了约2倍和26倍,且不影响生长速率、葡萄糖消耗速率或生物量产量。由于葡萄糖脱氢酶活性增加,葡萄糖消耗减少的同时葡萄糖酸产量增加。虽然Pf(pAB7)细胞外乙酸产量增加,但丙酮酸分泌减少,这与丙酮酸羧化酶活性增加相关,表明对合成代谢前体草酰乙酸的需求增加。另外两种关键酶葡萄糖-6-磷酸脱氢酶和异柠檬酸脱氢酶的活性保持不变,磷酸烯醇式丙酮酸羧化酶和异柠檬酸裂解酶对葡萄糖分解代谢的贡献可忽略不计。与对照相比,菌株Pf(pAB7)表现出增强的磷溶解能力。在荧光假单胞菌ATCC 13525中共表达聚球藻PCC 6301磷酸烯醇式丙酮酸羧化酶和大肠杆菌gltA基因,以便为柠檬酸生物合成补充草酰乙酸,尽管柠檬酸合酶和磷酸烯醇式丙酮酸羧化酶活性分别增加了约1.3倍和5倍,但既未显著影响柠檬酸生物合成,也未导致所测的其他生理生化参数发生任何变化。因此,我们的结果表明,柠檬酸合酶是提高荧光假单胞菌ATCC 13525中柠檬酸生物合成的限速因素。与Pf(pAB7)细胞内水平相比,细胞外柠檬酸水平显著较低,这表明可能存在有效柠檬酸转运的限制。

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