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氨基酸饥饿期间大肠杆菌relA+和relA菌株中单个蛋白质的生物合成调控。

Biosynthetic regulation of individual proteins in relA+ and relA strains of Escherichia coli during amino acid starvation.

作者信息

Reeh S, Pedersen S, Friesen J D

出版信息

Mol Gen Genet. 1976 Dec 22;149(3):279-89. doi: 10.1007/BF00268529.

Abstract

An isogenic pair of Escherichia coli mutants (relA+ tufB valSts and relA1 tufB valSts) has been cultured at several temperatures to establish various degrees of limitation for valyl-tRNA synthetase. The biosynthetic rate of 16 identifiable proteins, most of which are components of the transcription and translation apparatus, was measured by pulse-labelling with [35S]-methionine, followed by protein separation using two-dimensional gel electrophoresis (O'Farrell, 1975). No single pattern of response to amino acid starvation of biosynthetic rate was observed. EF-Ts, L12 and S6 were found to be under strong stringent and relaxed regulation; EF-G, EF-Tu-A and S1 are under strong stringent, but weak relaxed regulation; EF-Tu-B, alpha, VRS, IRS and ARS are under week stringent and weak relaxed regulation; beta is under weak stringent regulation and does not respond at all to relaxed conditions; the biosynthetic rate of a protein called stringent starvation protein is strongly stimulated, relative to other proteins, in the starved stringent strain.

摘要

一对同基因的大肠杆菌突变体(relA⁺ tufB valSts 和 relA1 tufB valSts)在几个温度下培养,以建立对缬氨酰 - tRNA 合成酶的不同程度的限制。通过用[³⁵S] - 甲硫氨酸脉冲标记,然后使用二维凝胶电泳进行蛋白质分离(奥法雷尔,1975 年),测量了 16 种可识别蛋白质的生物合成速率,其中大多数是转录和翻译装置的组成部分。未观察到生物合成速率对氨基酸饥饿的单一响应模式。发现 EF - Ts、L12 和 S6 受到强烈的严谨型和松弛型调控;EF - G、EF - Tu - A 和 S1 受到强烈的严谨型,但松弛型调控较弱;EF - Tu - B、α、VRS、IRS 和 ARS 受到较弱的严谨型和较弱的松弛型调控;β 受到较弱的严谨型调控,在松弛条件下完全无反应;相对于其他蛋白质,一种称为严谨饥饿蛋白(stringent starvation protein)的蛋白质的生物合成速率在饥饿的严谨型菌株中受到强烈刺激。

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