Yokota A, Terasawa Y, Takaoka N, Shimizu H, Tomita F
Department of Bioscience and Chemistry, Faculty of Agriculture, Hokkaido University, Sapporo, Japan.
Biosci Biotechnol Biochem. 1994 Dec;58(12):2164-7. doi: 10.1271/bbb.58.2164.
An F1-ATPase-defective mutant, TBLA-1, was constructed by the transduction of a defective gene for the alpha subunit of F1-ATPase, atpA401, into Escherichia coli W1485lip2, a lipoic acid-requiring pyruvic acid producer. The pyruvic acid production of the strain TBLA-1 was found to be improved markedly compared with that of strain W1485lip2. In cultures using a jar fermentor, the strain W1485lip2 consumed 50 g/liter of glucose and produced 25 g/liter of pyruvic acid after culture for 32h, while strain TBLA-1 consumed the same amount of glucose, and produced more than 30 g/liter of pyruvic acid in a 24-h culture. A revertant, No. 63-1, derived from the strain TBLA-1, had a normal level of F1-ATPase activity, and showed a similar pattern of pyruvic acid production to that of strain W1485lip2.
通过将F1 - ATP酶α亚基的缺陷基因atpA401导入需要硫辛酸的丙酮酸生产菌大肠杆菌W1485lip2中,构建了一个F1 - ATP酶缺陷型突变体TBLA - 1。结果发现,与W1485lip2菌株相比,TBLA - 1菌株的丙酮酸产量有显著提高。在使用罐式发酵罐的培养中,W1485lip2菌株在培养32小时后消耗了50克/升葡萄糖,产生了25克/升丙酮酸,而TBLA - 1菌株消耗相同量的葡萄糖,在24小时培养中产生了超过30克/升的丙酮酸。来自TBLA - 1菌株的回复突变体63 - 1具有正常水平的F1 - ATP酶活性,并且丙酮酸生产模式与W1485lip2菌株相似。