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ilv-lac融合操纵子高水平组成型表达的两株大肠杆菌K-12 ilv弱化子缺失突变体的分离与分析

Isolation and analysis of two Escherichia coli K-12 ilv attenuator deletion mutants with high-level constitutive expression of an ilv-lac fusion operon.

作者信息

Bennett D C, Umbarger H E

出版信息

J Bacteriol. 1984 Mar;157(3):839-45. doi: 10.1128/jb.157.3.839-845.1984.

DOI:10.1128/jb.157.3.839-845.1984
PMID:6230347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC215336/
Abstract

A lysogenizing lambda phage, lambda dilv-lac11, was constructed to carry an ilvD-lac operon fusion. Expression from the phage of the ilvE and lacZ genes is controlled by an intact ilv control region also carried by this phage. Two spontaneous mutants of lambda dilv-lac11 that have high-level constitutive expression of the ilv-lac fusion operon were isolated by growth on a beta-chloroalanine selective medium. The mutants were shown by nucleotide sequence determination to contain large deletions (delta 2216, approximately 1.6 kilobases; delta 2219, approximately 1.9 kilobases), which in both cases remove the proposed ilv attenuator terminator. The rest of the ilv leader and promoter region DNA remains intact in these mutants. Deletion 2216 also removed part of the downstream ilvG gene, whereas delta 2219 extended through the entire ilvG gene into the ilvGE intercistronic region. A possible mechanism of deletion formation is discussed.

摘要

构建了一种溶原化λ噬菌体λdilv-lac11,用于携带ilvD-lac操纵子融合体。ilvE和lacZ基因从该噬菌体的表达受该噬菌体所携带的完整ilv控制区调控。通过在β-氯丙氨酸选择培养基上生长,分离出了两个ilv-lac融合操纵子具有高水平组成型表达的λdilv-lac11自发突变体。通过核苷酸序列测定表明,这些突变体含有大的缺失(δ2216,约1.6千碱基;δ2219,约1.9千碱基),在这两种情况下都去除了推测的ilv衰减子终止子。在这些突变体中,ilv前导区和启动子区域的其余DNA保持完整。缺失2216还去除了下游ilvG基因的一部分,而δ2219则延伸穿过整个ilvG基因进入ilvGE基因间区域。讨论了缺失形成的一种可能机制。

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Isolation and analysis of two Escherichia coli K-12 ilv attenuator deletion mutants with high-level constitutive expression of an ilv-lac fusion operon.ilv-lac融合操纵子高水平组成型表达的两株大肠杆菌K-12 ilv弱化子缺失突变体的分离与分析
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引用本文的文献

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Mol Gen Genet. 1984;195(1-2):70-6. doi: 10.1007/BF00332726.
2
Internal promoter in the ilvGEDA transcription unit of Escherichia coli K-12.大肠杆菌K-12的ilvGEDA转录单元中的内部启动子。
J Bacteriol. 1985 Jan;161(1):128-32. doi: 10.1128/jb.161.1.128-132.1985.
3
Leucine regulation of the ilvGEDA operon of Serratia marcescens by attenuation is modulated by a single leucine codon.粘质沙雷氏菌ilvGEDA操纵子通过衰减作用进行的亮氨酸调控由一个单一的亮氨酸密码子调节。
J Bacteriol. 1985 Oct;164(1):217-22. doi: 10.1128/jb.164.1.217-222.1985.
4
Translational coupling between the ilvD and ilvA genes of Escherichia coli.大肠杆菌ilvD基因与ilvA基因之间的翻译偶联
J Bacteriol. 1988 Oct;170(10):4798-807. doi: 10.1128/jb.170.10.4798-4807.1988.
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Effects of deletion and insertion mutations in the ilvM gene of Escherichia coli.大肠杆菌ilvM基因中缺失和插入突变的影响。
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Physical and genetic localization of ilv regulatory sites in lambda ilv bacteriophages.λilv噬菌体中ilv调控位点的物理定位和遗传定位
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Regulation of ilvEDA expression occurs upstream of ilvG in Escherichia coli: additional evidence for an ilvGEDA operon.大肠杆菌中ilvEDA表达的调控发生在ilvG上游:ilvGEDA操纵子的更多证据。
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