Young F S, Neidhardt F C
J Bacteriol. 1978 Aug;135(2):675-86. doi: 10.1128/jb.135.2.675-686.1978.
By using inhibitors of elongation factor Tu (L-1-tosylamido-2-phenylethyl chloromethyl ketone [TPCK] and kirromycin), we determined the effect of elongation factor Tu inhibition on the synthesis of individual components of the translation machinery. The rates of synthesis of individual proteins were measured in double-label experiments using a two-dimensional gel system. TPCK inhibition produce a coordinate decrease in the differential synthesis rates of all components of the translation machinery examined in these experiments. On the other hand, kirromycin inhibition increased the differential synthesis rates of some translation components and decreased the differential synthesis rates of others. These results suggest that the metabolic regulation of synthesis of various translation proteins is not mediated through a common signal.
通过使用延伸因子Tu的抑制剂(L-1-甲苯磺酰胺基-2-苯乙基氯甲基酮[TPCK]和奇霉素),我们确定了延伸因子Tu抑制对翻译机制各个组分合成的影响。在使用二维凝胶系统的双标记实验中测量了各个蛋白质的合成速率。TPCK抑制使这些实验中所检测的翻译机制所有组分的差异合成速率协同下降。另一方面,奇霉素抑制增加了一些翻译组分的差异合成速率,而降低了其他组分的差异合成速率。这些结果表明,各种翻译蛋白质合成的代谢调节不是通过共同信号介导的。