Rutberg B, Hoch J A
J Bacteriol. 1970 Nov;104(2):826-33. doi: 10.1128/jb.104.2.826-833.1970.
The genetic location of mutations affecting the citric acid cycle and the properties of mutants of Bacillus subtilis possessing these mutations have been examined. Genes coding for the component enzymes of the cycle were found to be unlinked to each other and thus do not form an operon. The mutational defect in a mutant lacking fumarase mapped between thr-5 and cysB3. Mutations causing inability to produce isocitrate dehydrogenase and succinate dehydrogenase were found to map between argA11 and leu-1. The alpha-ketoglutarate dehydrogenase mutations were mapped at the terminal end of the B. subtilis chromosome through a weak linkage in phage PBS-1 transduction of one class of these mutations of ilvA2 and metB4. A second class of alpha-ketoglutarate dehydrogenase mutations mapped closer to ilvA2 and metB4 but still terminal with respect to these markers. Aconitaseless mutants possessed mutations that could not be linked to any of the known transducing segments of the chromosome. An effect of mutation conferring loss of one enzyme of the cycle on the specific activity of the other enzymes in the cycle was observed.
已经对影响柠檬酸循环的突变的基因定位以及具有这些突变的枯草芽孢杆菌突变体的特性进行了研究。发现编码该循环组成酶的基因彼此不连锁,因此不形成操纵子。缺乏延胡索酸酶的突变体中的突变缺陷位于thr-5和cysB3之间。发现导致无法产生异柠檬酸脱氢酶和琥珀酸脱氢酶的突变位于argA11和leu-1之间。通过噬菌体PBS-1转导ilvA2和metB4的一类这些突变中的弱连锁,将α-酮戊二酸脱氢酶突变定位在枯草芽孢杆菌染色体的末端。第二类α-酮戊二酸脱氢酶突变定位得更靠近ilvA2和metB4,但相对于这些标记仍位于末端。无乌头酸酶突变体具有的突变无法与染色体的任何已知转导区段连锁。观察到赋予循环中一种酶缺失的突变对循环中其他酶的比活性的影响。