Atherly A G
J Bacteriol. 1979 May;138(2):530-4. doi: 10.1128/jb.138.2.530-534.1979.
A mutant of Escherichia coli has been isolated that contains a large deletion (about 3 X 10(7) daltons of deoxyribonucleic acid) encompassing argA, fuc, and relA. This mutant strain (AA-787) is also cold sensitive for growth at 18 degrees C. Strain AA-787 was obtained fortuitously as a cold-sensitive pseudorevertant of a strain having a heat-sensitive peptidyl-transfer ribonucleic acid hydrolase. Genetic analysis, using transduction and interrupted mating, showed the cold sensitivity mutation to be located adjacent to relA. Further analysis demonstrated loss of relA, fuc, and argA gene functions but retention of eno and recB, closely linked genes adjacent to relA and argA, respectively. Unusually high cotransduction of flanking markers (cysC and thyA) indicated loss of approximately 1 min of the E. coli genetic map in strain AA-787. Guanosine 3'-diphosphate 5'-diphosphate (ppGpp) was synthetized in mutant strain AA-787 at basal levels, and ppGpp synthesis was stimulated by carbon-source downshift. No ppGpp synthesis could be obtained using ribosomes isolated from strain AA-787. These findings, taken together, show that deletion of relA in E. coli does not completely abolish ppGpp synthesis and suggests that another enzyme system must also be responsible for ppGpp synthesis.
已分离出一种大肠杆菌突变体,其含有一个大的缺失片段(约3×10⁷道尔顿的脱氧核糖核酸),该片段包含argA、fuc和relA。此突变菌株(AA - 787)在18℃下生长对温度敏感。菌株AA - 787是作为具有热敏感肽基转移核糖核酸水解酶的菌株的冷敏感假回复体偶然获得的。利用转导和中断杂交进行的遗传分析表明,冷敏感突变位于relA附近。进一步分析显示relA、fuc和argA基因功能丧失,但分别与relA和argA相邻的紧密连锁基因eno和recB得以保留。侧翼标记(cysC和thyA)的异常高共转导表明菌株AA - 787中大肠杆菌遗传图谱缺失了约1分钟。突变菌株AA - 787中鸟苷3'-二磷酸5'-二磷酸(ppGpp)以基础水平合成,并且ppGpp合成受碳源降档刺激。使用从菌株AA - 787分离的核糖体无法获得ppGpp合成。综合这些发现表明,大肠杆菌中relA的缺失并未完全消除ppGpp合成,这表明必定还有另一种酶系统负责ppGpp合成。