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操纵子融合在热休克反应研究中的应用:σ32改变对大肠杆菌热休克启动子功能的影响。

The use of operon fusions in studies of the heat-shock response: effects of altered sigma 32 on heat-shock promoter function in Escherichia coli.

作者信息

Yano R, Imai M, Yura T

出版信息

Mol Gen Genet. 1987 Apr;207(1):24-8. doi: 10.1007/BF00331486.

Abstract

Derivatives of lambda pF13 phage in which lacZ expression (beta-galactosidase synthesis) is directed by transcription initiated at a heat-shock promoter (PrpoDhs or PgroE) were constructed and used for analysis of the heat-shock response in Escherichia coli. A wild-type strain (MC4100) lysogenic for either of these phages exhibited typical transient induction of beta-galactosidase synthesis upon a temperature shift from 30 degrees to 42 degrees C or after addition of ethanol to the medium (4% to 5%) at 30 degrees C. In contrast, most amber rpoH (htpR) mutants tested (in a Su- background) failed to respond to a temperature shift, though some mutants affected in the carboxy-terminal region exhibited a partial response. All rpoH mutants tested showed a weak but significant response to ethanol. F' plasmids carrying each of six known nonsense suppressors were then introduced into each of four rpoH amber mutants lysogenic for lambda pF13-(Phs-lacZ), creating a set of F' strains that produce sigma 32 protein with a specific amino acid substitution at a known site. Some of these strains showed an essentially normal heat-shock response while others showed little response with either or both of the promoters. In some instances, the response was significantly delayed. These results point to the usefulness of the lambda pF13-derivative phages for quantitative and systematic analysis of heat-shock response in E. coli.

摘要

构建了λpF13噬菌体的衍生物,其中lacZ表达(β-半乳糖苷酶合成)由在热休克启动子(PrpoDhs或PgroE)起始的转录所指导,并用于分析大肠杆菌中的热休克反应。对于这些噬菌体中的任何一种呈溶原状态的野生型菌株(MC4100),在温度从30℃转变为42℃时或在30℃向培养基中添加乙醇(4%至5%)后,表现出典型的β-半乳糖苷酶合成的瞬时诱导。相比之下,所测试的大多数琥珀型rpoH(htpR)突变体(在Su-背景下)对温度转变没有反应,尽管一些在羧基末端区域受影响的突变体表现出部分反应。所有测试的rpoH突变体对乙醇均表现出微弱但显著的反应。然后将携带六种已知无义抑制子中每一种的F'质粒引入到四个对λpF13-(Phs-lacZ)呈溶原状态的rpoH琥珀型突变体中,创建了一组F'菌株,这些菌株产生在已知位点具有特定氨基酸取代的σ32蛋白。其中一些菌株表现出基本正常的热休克反应,而其他菌株对其中一个或两个启动子几乎没有反应。在某些情况下,反应明显延迟。这些结果表明λpF13衍生噬菌体对于定量和系统分析大肠杆菌中的热休克反应是有用的。

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