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细菌核糖体的肽基转移酶:对蛋白酶K的抗性

Peptidyl transferase of bacterial ribosome: resistance to proteinase K.

作者信息

Bernabeu C, Conde P, Vázquez D, Ballesta J P

出版信息

Eur J Biochem. 1979 Feb 1;93(3):527-33. doi: 10.1111/j.1432-1033.1979.tb12851.x.

Abstract

70-S ribosomes and 50-S ribosomal subunits from Escherichia coli D10 were treated with proteinase K for increasing periods of time. Peptidyl transferase activity and sparsomycin-induced binding of (U)C-A-C-C-A-[3H]Leu-Ac were tested in the treated particles, the binding of the substrate being more sensitive to the protease than peptide bond formation. Comparison of the amounts of proteins present in the treated particles with the residual activity indicates that only proteins L3 and L14 are released at a similar rate to that at which peptidyl transferase activity is lost. Proteins related to this ribosomal activity by other techniques are lost at a faster rate than the activity itself. In addition, the results indicate that sparsomycin stimulates the binding of the substrate by a different mechanism from that which inhibits peptide bond formation.

摘要

用蛋白酶K对来自大肠杆菌D10的70-S核糖体和50-S核糖体亚基进行不同时长的处理。在处理后的颗粒中检测肽基转移酶活性以及稀疏霉素诱导的(U)C-A-C-C-A-[3H]亮氨酰-乙酰的结合,底物的结合比肽键形成对蛋白酶更敏感。将处理后颗粒中存在的蛋白量与残余活性进行比较表明,只有蛋白质L3和L14以与肽基转移酶活性丧失相似的速率被释放。通过其他技术与这种核糖体活性相关的蛋白质比活性本身更快地丧失。此外,结果表明稀疏霉素通过与抑制肽键形成不同的机制刺激底物的结合。

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