Armstrong G D, Yamazaki H
Can J Microbiol. 1977 Oct;23(10):1384-93. doi: 10.1139/m77-207.
A method has been developed for the isolation of Escherichia coli mutants which are resistant to catabolic repression. The method is based on the fact that a mixture of glucose and gluconate inhibits the development of chemotactic motility in the wild type, but not in the mutants. A motile E. coli strain was mutagenized and grown in glucose and gluconate. Mutants which were able to swim into a tube containing a chemotactic attractant (aspartic acid) were isolated. Most of these mutants were able to produce beta-galactosidase in the presence of glucose and gluconate and were normal in their ability to degrade adenosine 3',5-cyclic monophosphate. Some of these mutants were defective in the glucose phosphotransferase system.
已开发出一种用于分离对分解代谢阻遏具有抗性的大肠杆菌突变体的方法。该方法基于这样一个事实,即葡萄糖和葡萄糖酸盐的混合物会抑制野生型中趋化运动的发展,但不会抑制突变体中的趋化运动。将一株运动性大肠杆菌菌株诱变,并在葡萄糖和葡萄糖酸盐中培养。分离出能够游入含有趋化引诱剂(天冬氨酸)的试管中的突变体。这些突变体中的大多数能够在葡萄糖和葡萄糖酸盐存在的情况下产生β-半乳糖苷酶,并且在降解3',5-环磷酸腺苷的能力方面正常。其中一些突变体在葡萄糖磷酸转移酶系统中存在缺陷。