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首页> 外文期刊>Applied and Environmental Microbiology >Improved Succinic Acid Production in the Anaerobic Culture of an Escherichia coli pflB ldhA Double Mutant as a Result of Enhanced Anaplerotic Activities in the Preceding Aerobic Culture
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Improved Succinic Acid Production in the Anaerobic Culture of an Escherichia coli pflB ldhA Double Mutant as a Result of Enhanced Anaplerotic Activities in the Preceding Aerobic Culture

机译:在之前的好氧培养中增强的抗动脉粥样硬化活性导致大肠埃希菌pflB ldhA双突变体厌氧培养中琥珀酸产量的提高。

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摘要

Escherichia coli NZN111 is a pflB ldhA double mutant which loses its ability to ferment glucose anaerobically due to redox imbalance. In this study, two-stage culture of NZN111 was carried out for succinic acid production. It was found that when NZN111 was aerobically cultured on acetate, it regained the ability to ferment glucose with succinic acid as the major product in subsequent anaerobic culture. In two-stage culture carried out in flasks, succinic acid was produced at a level of 11.26 g/liter from 13.4 g/liter of glucose with a succinic acid yield of 1.28 mol/mol glucose and a productivity of 1.13 g/liter·h in the anaerobic stage. Analyses of key enzyme activities revealed that the activities of isocitrate lyase, malate dehydrogenase, malic enzyme, and phosphoenolpyruvate (PEP) carboxykinase were greatly enhanced while those of pyruvate kinase and PEP carboxylase were reduced in the acetate-grown cells. The two-stage culture was also performed in a 5-liter fermentor without separating the acetate-grown NZN111 cells from spent medium. The overall yield and concentration of succinic acid reached 1.13 mol/mol glucose and 28.2 g/liter, respectively, but the productivity of succinic acid in the anaerobic stage dropped to 0.7 g/liter·h due to cell autolysis and reduced anaplerotic activities. The results indicate the great potential to take advantage of cellular regulation mechanisms for improvement of succinic acid production by a metabolically engineered E. coli strain.
机译:大肠杆菌NZN111是pflB ldhA双突变体,由于氧化还原失衡而丧失了厌氧发酵葡萄糖的能力。在这项研究中,NZN111的两阶段培养进行了琥珀酸生产。发现当将NZN111在乙酸盐上需氧培养时,它在随后的厌氧培养中恢复了以琥珀酸为主要产物发酵葡萄糖的能力。在烧瓶中进行的两阶段培养中,由13.4克/升葡萄糖以11.26克/升的水平生产琥珀酸,琥珀酸的产量为1.28摩尔/摩尔葡萄糖,生产率为1.13克/升·小时在厌氧阶段。对关键酶活性的分析表明,在乙酸生长的细胞中,异柠檬酸裂合酶,苹果酸脱氢酶,苹果酸酶和磷酸烯醇丙酮酸(PEP)羧激酶的活性大大增强,而丙酮酸激酶和PEP羧化酶的活性降低。还在5升发酵罐中进行两阶段培养,而没有从用过的培养基中分离乙酸盐生长的NZN111细胞。琥珀酸的总产量和浓度分别达到1.13 mol / mol葡萄糖和28.2 g / l,但是由于细胞自溶作用和降低的抗动脉粥样硬化活性,厌氧阶段的琥珀酸生产率下降到0.7 g / l·h。结果表明利用细胞调节机制改善通过代谢工程改造的大肠杆菌菌株产生琥珀酸的巨大潜力。

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