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Escherichia coli mutants lacking NADH dehydrogenase I have a competitive disadvantage in stationary phase.缺乏NADH脱氢酶I的大肠杆菌突变体在稳定期具有竞争劣势。
J Bacteriol. 1993 Sep;175(17):5642-7. doi: 10.1128/jb.175.17.5642-5647.1993.
2
Genetic inactivation of the H(+)-translocating NADH:ubiquinone oxidoreductase of Paracoccus denitrificans is facilitated by insertion of the ndh gene from Escherichia coli.通过插入来自大肠杆菌的ndh基因,促进了反硝化副球菌H(+)-转运型NADH:泛醌氧化还原酶的基因失活。
FEBS Lett. 1996 Sep 9;393(1):81-5. doi: 10.1016/0014-5793(96)00831-9.
3
Modification of substrate specificity in single point mutants of Agrobacterium tumefaciens type II NADH dehydrogenase.根癌土壤杆菌II型NADH脱氢酶单点突变体中底物特异性的修饰
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4
Mutations in NADH:ubiquinone oxidoreductase of Escherichia coli affect growth on mixed amino acids.大肠杆菌NADH:泛醌氧化还原酶的突变影响其在混合氨基酸上的生长。
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5
Escherichia coli NADH dehydrogenase I, a minimal form of the mitochondrial complex I.大肠杆菌NADH脱氢酶I,线粒体复合物I的一种最小形式。
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Probing the mechanistic role of the long α-helix in subunit L of respiratory Complex I from Escherichia coli by site-directed mutagenesis.通过定点突变探究大肠杆菌呼吸复合物 I 亚基 L 中长α螺旋的作用机制。
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本文引用的文献

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Survival of hunger and stress: the role of rpoS in early stationary phase gene regulation in E. coli.饥饿与应激下的存活:rpoS在大肠杆菌稳定早期基因调控中的作用
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J Bacteriol. 1993 May;175(10):3013-9. doi: 10.1128/jb.175.10.3013-3019.1993.
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Characterization of the respiratory NADH dehydrogenase of Escherichia coli and reconstitution of NADH oxidase in ndh mutant membrane vesicles.大肠杆菌呼吸型NADH脱氢酶的特性及ndh突变体膜囊泡中NADH氧化酶的重组。
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Nucleotide sequence coding for the respiratory NADH dehydrogenase of Escherichia coli. UUG initiation codon.编码大肠杆菌呼吸型NADH脱氢酶的核苷酸序列。UUG起始密码子。
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The physical map of the whole E. coli chromosome: application of a new strategy for rapid analysis and sorting of a large genomic library.完整大肠杆菌染色体的物理图谱:一种用于大型基因组文库快速分析和分类的新策略的应用
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缺乏NADH脱氢酶I的大肠杆菌突变体在稳定期具有竞争劣势。

Escherichia coli mutants lacking NADH dehydrogenase I have a competitive disadvantage in stationary phase.

作者信息

Zambrano M M, Kolter R

机构信息

Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

J Bacteriol. 1993 Sep;175(17):5642-7. doi: 10.1128/jb.175.17.5642-5647.1993.

DOI:10.1128/jb.175.17.5642-5647.1993
PMID:8366049
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC206622/
Abstract

We have previously characterized mutant strains of Escherichia coli that are able to take over stationary-phase cultures. Here we describe two insertion mutations that prevent such strains from expressing this phenotype. Both insertions were mapped to min 51, and sequence analysis revealed that both mutated genes encode proteins homologous to subunits of mitochondrial NADH dehydrogenase I. Crude extracts prepared from both mutant strains were able to oxidize NADH but lacked the enzymatic activity needed to oxidize deamino-NADH, a substrate specific for NADH dehydrogenase I. This is the first identification of genes encoding subunits of NADH dehydrogenase I in E. coli. The significance of the inability of these mutant strains to compete in stationary-phase cultures is discussed.

摘要

我们之前已对能够接管稳定期培养物的大肠杆菌突变株进行了特征描述。在此,我们描述了两个插入突变,它们阻止了此类菌株表达该表型。两个插入位点均被定位到51分钟处,序列分析表明,这两个突变基因编码的蛋白质与线粒体NADH脱氢酶I的亚基同源。从这两个突变株制备的粗提取物能够氧化NADH,但缺乏氧化脱氨基NADH(NADH脱氢酶I的特异性底物)所需的酶活性。这是首次在大肠杆菌中鉴定出编码NADH脱氢酶I亚基的基因。我们还讨论了这些突变株在稳定期培养物中无法竞争的意义。