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枯草芽孢杆菌RNA聚合酶α因子及核心相关多肽的肽图谱分析

Peptide mapping of Bacillus subtilis RNA polymerase alpha factors and core-associated polypeptides.

作者信息

Wong S L, Doi R H

出版信息

J Biol Chem. 1982 Oct 25;257(20):11932-6.

PMID:6811591
Abstract

An analysis of the peptide maps of the sigma factors and core-associated subunits of Bacillus subtilis RNA polymerase has revealed that all the sigma factors ad core-associated polypeptides are derived from separate genes and are not proteolytically modified products of the major 55,000-dalton sigma factor. A comparison of the peptide pattern of the major B. subtilis and Escherichia coli sigma factors revealed limited homology between them. Furthermore, antibody prepared against the 55,000-dalton B. subtilis sigma factor cross-reacted against the E. coli sigma factor, but not against any of the other B. subtilis sigma factors and core-associated polypeptides. These results unambiguously demonstrate the independently derived nature of the B. subtilis RNA polymerase core-associated subunits and the partial relationship between the major sigma factors of B. subtilis and E. coli.

摘要

对枯草芽孢杆菌RNA聚合酶的σ因子和核心相关亚基的肽图分析表明,所有的σ因子和核心相关多肽均来自不同的基因,并非主要的55,000道尔顿σ因子的蛋白水解修饰产物。对枯草芽孢杆菌和大肠杆菌主要σ因子的肽图进行比较,发现它们之间存在有限的同源性。此外,针对55,000道尔顿枯草芽孢杆菌σ因子制备的抗体与大肠杆菌σ因子发生交叉反应,但不与其他任何枯草芽孢杆菌σ因子和核心相关多肽发生反应。这些结果明确证明了枯草芽孢杆菌RNA聚合酶核心相关亚基的独立起源性质,以及枯草芽孢杆菌和大肠杆菌主要σ因子之间的部分关系。

相似文献

1
Peptide mapping of Bacillus subtilis RNA polymerase alpha factors and core-associated polypeptides.枯草芽孢杆菌RNA聚合酶α因子及核心相关多肽的肽图谱分析
J Biol Chem. 1982 Oct 25;257(20):11932-6.
2
The interaction of Escherichia coli core RNA polymerase with specificity-determining subunits derived from unmodified and SP82-modified Bacillus subtilis RNA polymerase.大肠杆菌核心RNA聚合酶与源自未修饰和SP82修饰的枯草芽孢杆菌RNA聚合酶的特异性决定亚基之间的相互作用。
J Biol Chem. 1980 Dec 25;255(24):11957-64.
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Interactions of Bacillus subtilis RNA polymerase with subunits determining the specificity of initiation. Sigma and delta peptides can bind simultaneously to core.枯草芽孢杆菌RNA聚合酶与决定起始特异性的亚基之间的相互作用。σ肽和δ肽可同时与核心结合。
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Altered promoter selection by a novel form of Bacillus subtilis RNA polymerase.枯草芽孢杆菌新型RNA聚合酶对启动子选择的改变
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Interaction of Bacillus subtilis RNA polymerase core with two specificity-determining subunits. Competition between sigma and the SPO1 gene 28 protein.枯草芽孢杆菌RNA聚合酶核心与两个特异性决定亚基的相互作用。σ因子与SPO1基因28蛋白之间的竞争
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Specificity of promoter site utilization in vitro by bacterial RNA polymerases on Bacillus phage phi 29 DNA. Transcription mapping with exonuclease III.细菌RNA聚合酶在体外对芽孢杆菌噬菌体φ29 DNA上启动子位点利用的特异性。用核酸外切酶III进行转录图谱分析。
J Biol Chem. 1980 Sep 25;255(18):8819-30.

引用本文的文献

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Cloning and characterization of the Bacillus licheniformis gene coding for alkaline phosphatase.地衣芽孢杆菌碱性磷酸酶编码基因的克隆与特性分析
J Bacteriol. 1984 Jun;158(3):978-82. doi: 10.1128/jb.158.3.978-982.1984.
2
A temporally regulated promoter from Bacillus subtilis is transcribed only by an RNA polymerase with a 37,000 dalton sigma factor.来自枯草芽孢杆菌的一个时间调控启动子仅由带有37,000道尔顿σ因子的RNA聚合酶转录。
Mol Gen Genet. 1983;191(2):319-25. doi: 10.1007/BF00334833.
3
Isolation and physical mapping of the gene encoding the major sigma factor of Bacillus subtilis RNA polymerase.
枯草芽孢杆菌RNA聚合酶主要σ因子编码基因的分离与物理图谱绘制。
Proc Natl Acad Sci U S A. 1983 Jul;80(13):4074-8. doi: 10.1073/pnas.80.13.4074.
4
Isolation of Bacillus subtilis mutants altered in expression of a gene transcribed in vitro by a minor form of RNA polymerase (E-sigma 37).枯草芽孢杆菌突变体的分离,这些突变体在一种由次要形式的RNA聚合酶(E-σ37)体外转录的基因的表达上发生了改变。
J Bacteriol. 1985 Feb;161(2):515-22. doi: 10.1128/jb.161.2.515-522.1985.
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Two alkaline phosphatase genes positioned in tandem in Bacillus licheniformis MC14 require different RNA polymerase holoenzymes for transcription.地衣芽孢杆菌MC14中串联排列的两个碱性磷酸酶基因转录时需要不同的RNA聚合酶全酶。
Proc Natl Acad Sci U S A. 1985 Feb;82(4):1035-9. doi: 10.1073/pnas.82.4.1035.
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Multiple procaryotic ribonucleic acid polymerase sigma factors.多种原核生物核糖核酸聚合酶σ因子
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In vivo selected promoter and ribosome binding site up-mutations: demonstration that the Escherichia coli bla promoter and a Shine-Dalgarno region with low complementarity to the 16 S ribosomal RNA function in Bacillus subtilis.体内筛选的启动子和核糖体结合位点向上突变:证明大肠杆菌bla启动子和与16S核糖体RNA互补性低的Shine-Dalgarno区域在枯草芽孢杆菌中起作用。
Mol Gen Genet. 1989 Oct;219(1-2):129-36. doi: 10.1007/BF00261168.