Katze J R, Simonian M H, Mosteller R D
J Bacteriol. 1977 Oct;132(1):174-9. doi: 10.1128/jb.132.1.174-179.1977.
Previously, we reported that starvation of Rel Escherichia coli for methionine, but not leucine or histidine, results in chromatographically unique species of aspartyl-specific transfer ribonucleic acid (tRNAAsp) lacking the modified nucleoside Q. The present studies demonstrate that methionine starvation of Rel+ E. coli yields a qualitatively similar, but less pronounced, effect. Furthermore, during recovery from methionine starvation in Rel E. coli, the chromatographic elution pattern of tRNAAsp shifts towards that observed for unstarved cells after 1 h of recovery, and the shift appears complete after 2 h of recovery. This shift is inhibited by rifampin. Incorporation of [2-14C]methionine or [methyl-3H]methionine into growing cells of E. coli does not result in labeling of nucleoside Q. We interpret these findings to indicate that methionine has an indirect role in Q formation and that Q-deficient tRNA can be modified slowly to contain Q but that transcription is required. The chromatographic elution patterns of tRNAAsp from Rel E. coli starved for arginine, lysine, or glutamic acid indicate that these amino acids are not the source of the three- or five-carbon sequences in the modified portion of Q.
此前,我们报道过,使Rel⁺大肠杆菌缺乏蛋氨酸而非亮氨酸或组氨酸,会导致缺乏修饰核苷Q的天冬氨酰特异性转移核糖核酸(tRNA⁺Asp)出现色谱上独特的种类。目前的研究表明,Rel⁺大肠杆菌蛋氨酸饥饿会产生性质上相似但不太明显的效果。此外,在Rel⁻大肠杆菌从蛋氨酸饥饿中恢复的过程中,tRNA⁺Asp的色谱洗脱模式在恢复1小时后向未饥饿细胞的模式转变,恢复2小时后这种转变似乎完成。这种转变受到利福平的抑制。将[2-¹⁴C]蛋氨酸或[甲基-³H]蛋氨酸掺入大肠杆菌生长细胞中不会导致核苷Q被标记。我们对这些发现的解释是,蛋氨酸在Q形成中起间接作用,缺乏Q的tRNA可以缓慢修饰以包含Q,但这需要转录。来自Rel⁻大肠杆菌的tRNA⁺Asp在精氨酸、赖氨酸或谷氨酸饥饿时的色谱洗脱模式表明,这些氨基酸不是Q修饰部分中三碳或五碳序列的来源。