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在缺乏腺苷甲硫氨酸合成酶活性的大肠杆菌突变体中热休克蛋白的异常诱导。

Abnormal induction of heat shock proteins in an Escherichia coli mutant deficient in adenosylmethionine synthetase activity.

作者信息

Matthews R G, Neidhardt F C

机构信息

Department of Biological Chemistry, University of Michigan, Ann Arbor 48109-0620.

出版信息

J Bacteriol. 1988 Apr;170(4):1582-8. doi: 10.1128/jb.170.4.1582-1588.1988.

Abstract

Most prototrophic strains of Escherichia coli become restricted for methionine at 44 degrees C. A mutant strain (RG62 metK) in which the level of S-adenosylmethionine synthetase activity is only 10 to 20% of normal shows constitutive expression of one of the heat shock proteins, the lysU gene product, lysyl-tRNA synthetase form II, at 37 degrees C. These findings suggested a possible linkage between methionine metabolism and heat shock. We examined the induction of heat shock polypeptides in strain RG62 (metK) and in its parent, RG (metK+), from which it was derived by spontaneous mutation. Exponential-phase cultures of the two strains were pulse-labeled with [3H]leucine shortly after a shift from 37 to 44 degrees C, and the total cellular polypeptides were examined by two-dimensional electrophoresis. The results confirmed the constitutive production of the lysU gene product previously reported for strain RG62, but also revealed that the induction of 2 of the 17 heat shock polypeptides, C14.7 and G13.5, was markedly depressed. Otherwise the heat shock induction pattern was similar in timing and magnitude in the two strains. Transformation of the mutant strain with a plasmid, pK8, containing the metK coding sequence and promoter region as a 1.8-kilobase insert into pBR322 restored normal induction of C14.7 and G13.5, but did not prevent constitutive expression of the lysU gene product in the medium required for growth of this strain. The three heat shock polypeptides abnormally controlled in strain RG62 are the three polypeptides which are not induced when rapid synthesis of the htpR gene product is induced by isopropyl-beta-D-thiogalactopyranoside at 28 degree C (R. A. VanBogelen, M. A. Acton, and F. C. Neidhardt, Genes Dev. 1:525-531, 1987). We postulate that induction of these three polypeptides involves metabolic signals in addition to the synthesis of the htpR gene product and that strain RG62 (metK) fails to produce the signals involved in induction of C14.7 and G13.5 on a shift-up in temperature and produces the signal related to lysU induction even at 37 degree C.

摘要

大多数原养型大肠杆菌菌株在44℃时会受到甲硫氨酸限制。一种突变菌株(RG62 metK),其S-腺苷甲硫氨酸合成酶活性水平仅为正常水平的10%至20%,在37℃时显示出一种热休克蛋白(lysU基因产物,赖氨酸-tRNA合成酶II型)的组成型表达。这些发现提示甲硫氨酸代谢与热休克之间可能存在联系。我们研究了RG62(metK)菌株及其亲本RG(metK+)(由自发突变产生)中热休克多肽的诱导情况。在从37℃转移至44℃后不久,用[3H]亮氨酸对这两种菌株的指数生长期培养物进行脉冲标记,并用二维电泳检测总细胞多肽。结果证实了之前报道的RG62菌株中lysU基因产物的组成型产生,但也显示17种热休克多肽中的2种(C14.7和G13.5)的诱导明显受到抑制。除此之外,两种菌株中热休克诱导模式在时间和程度上相似。用质粒pK8(含有metK编码序列和启动子区域,作为1.8千碱基插入片段插入pBR322)转化突变菌株,恢复了C14.7和G13.5的正常诱导,但并未阻止lysU基因产物在该菌株生长所需培养基中的组成型表达。在RG62菌株中异常调控的三种热休克多肽,是在28℃时用异丙基-β-D-硫代半乳糖苷诱导htpR基因产物快速合成时不被诱导的三种多肽(R. A. VanBogelen、M. A. Acton和F. C. Neidhardt,《基因与发育》1:525 - 531,1987)。我们推测,这三种多肽的诱导除了涉及htpR基因产物的合成外,还涉及代谢信号,并且RG62(metK)菌株在温度升高时未能产生与C14.7和G13.5诱导相关的信号,甚至在37℃时也产生与lysU诱导相关的信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511d/211005/59af13929931/jbacter00182-0181-a.jpg

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