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自然发生的启动子下调突变:痢疾志贺氏菌16型色氨酸启动子/操纵子/前导区的核苷酸序列

Naturally occurring promoter down mutation: nucleotide sequence of the trp promoter/operator/leader region of Shigella dysenteriae 16.

作者信息

Miozzari G, Yanofsky C

出版信息

Proc Natl Acad Sci U S A. 1978 Nov;75(11):5580-4. doi: 10.1073/pnas.75.11.5580.

DOI:10.1073/pnas.75.11.5580
PMID:364484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC393010/
Abstract

The promoter/operator/leader region of the trp operon of Shigella dysenteriae 16 has single base pair differences from the corresponding region of Escherichia coli at positions -24 and -13. The difference at -13 was shown to be responsible for the 90% reduction in promoter function characteristic of the trp operon of S. dysenteriae. The base pair difference at position -13 also renders the operator partially constitutive. This allows the organism to maintain relatively high repressed levels of the trp enzymes and increases the relative importance of attenuation as a transcription control mechanism. These findings and the earlier observation that the trpE protein of S. dysenteriae is only slightly active explain the low in vivo expression of the trp operon of this organism. Nutritional studies suggest that operons involved in other amino acid biosynthetic pathways in S. dysenteriae 16 may be similarly partially inactivated.

摘要

痢疾志贺氏菌16型色氨酸操纵子的启动子/操纵基因/前导区在-24和-13位与大肠杆菌的相应区域存在单碱基对差异。已证明-13位的差异导致痢疾志贺氏菌色氨酸操纵子启动子功能降低90%。-13位的碱基对差异还使操纵基因部分组成型表达。这使该生物体能够维持色氨酸酶相对较高的阻遏水平,并增加了衰减作为转录控制机制的相对重要性。这些发现以及早期观察到的痢疾志贺氏菌色氨酸E蛋白活性较低,解释了该生物体色氨酸操纵子在体内表达水平较低的原因。营养研究表明,痢疾志贺氏菌16型中参与其他氨基酸生物合成途径的操纵子可能同样部分失活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6561/393010/18ead09a2e77/pnas00021-0343-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6561/393010/18ead09a2e77/pnas00021-0343-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6561/393010/18ead09a2e77/pnas00021-0343-a.jpg

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本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Transduction by bacteriophage P-1 and the properties of the lac genetic region in E. coli and S. dysenteriae.噬菌体P-1的转导以及大肠杆菌和痢疾志贺氏菌中乳糖基因区域的特性
Virology. 1961 Nov;15:299-311. doi: 10.1016/0042-6822(61)90362-2.
3
Tryptophan synthetase levels in Escherichia coli, Shigella dysenteriae, and transduction hybrids.大肠杆菌、痢疾志贺氏菌及转导杂种中色氨酸合成酶的水平
麦双尾蚜的内共生菌(布赫纳氏菌属)含有由trpEG和trpEG假基因串联重复序列组成的质粒。
Appl Environ Microbiol. 1996 Feb;62(2):332-9. doi: 10.1128/aem.62.2.332-339.1996.
4
Gene inactivation in Lactococcus lactis: branched-chain amino acid biosynthesis.乳酸乳球菌中的基因失活:支链氨基酸生物合成
J Bacteriol. 1993 Jul;175(14):4383-90. doi: 10.1128/jb.175.14.4383-4390.1993.
5
The tryptophan repressor sequence is highly conserved among the Enterobacteriaceae.色氨酸阻遏物序列在肠杆菌科细菌中高度保守。
Nucleic Acids Res. 1994 May 25;22(10):1821-9. doi: 10.1093/nar/22.10.1821.
6
Regulatory regions of two transport operons under nitrogen control: nucleotide sequences.氮控制下两个转运操纵子的调控区域:核苷酸序列
Proc Natl Acad Sci U S A. 1982 Feb;79(4):1083-7. doi: 10.1073/pnas.79.4.1083.
7
The complete nucleotide sequence of the tryptophan operon of Escherichia coli.大肠杆菌色氨酸操纵子的完整核苷酸序列。
Nucleic Acids Res. 1981 Dec 21;9(24):6647-68. doi: 10.1093/nar/9.24.6647.
8
Interspecies homology of nitrogenase genes.固氮酶基因的种间同源性。
Proc Natl Acad Sci U S A. 1980 Jan;77(1):191-5. doi: 10.1073/pnas.77.1.191.
9
Direct selection and analysis of mutational events which diminish the level of expression of the trp operon.直接选择和分析降低色氨酸操纵子表达水平的突变事件。
J Bacteriol. 1980 Jan;141(1):422-6. doi: 10.1128/jb.141.1.422-426.1980.
10
Nucleotide sequence of a promoter recognized by Bacillus subtilis RNA polymerase.枯草芽孢杆菌RNA聚合酶识别的启动子的核苷酸序列。
Mol Gen Genet. 1980;180(1):57-65. doi: 10.1007/BF00267352.
J Bacteriol. 1962 Jan;83(1):193-204. doi: 10.1128/jb.83.1.193-204.1962.
4
Hybridization between Escherichia coli and Shigella.大肠杆菌与志贺氏菌之间的杂交。
J Bacteriol. 1957 Oct;74(4):461-76. doi: 10.1128/jb.74.4.461-476.1957.
5
Acetylornithinase of Escherichia coli: partial purification and some properties.大肠杆菌的乙酰鸟氨酸酶:部分纯化及某些性质
J Biol Chem. 1956 Jan;218(1):97-106.
6
A strain of Shigella dysenteriae. I. Requiring proline.一株痢疾志贺氏菌。I. 需要脯氨酸。
J Bacteriol. 1954 May;67(5):542-4. doi: 10.1128/jb.67.5.542-544.1954.
7
Comparison of the tryptophan synthetase alpha-subunits of several species of Enterobacteriaceae.几种肠杆菌科细菌色氨酸合成酶α亚基的比较。
J Bacteriol. 1966 May;91(5):1819-26. doi: 10.1128/jb.91.5.1819-1826.1966.
8
Properties and regulation of the beta-D-galactosidase in Shigella dysenteriae and in Escherichia coli-Shigella dysenteriae hybrids.痢疾志贺氏菌及大肠杆菌-痢疾志贺氏菌杂交体中β-D-半乳糖苷酶的性质与调控
J Bacteriol. 1966 Apr;91(4):1477-88. doi: 10.1128/jb.91.4.1477-1488.1966.
9
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J Mol Biol. 1973 May 5;76(1):89-101. doi: 10.1016/0022-2836(73)90082-x.
10
Detection of tryptophan messenger RNA in several bacterial species and examination of the properties of heterologous DNA-RNA hybrids.几种细菌物种中色氨酸信使核糖核酸的检测以及异源脱氧核糖核酸-核糖核酸杂交体性质的研究。
J Mol Biol. 1972 Mar 14;64(2):319-39. doi: 10.1016/0022-2836(72)90501-3.