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对氧化磷酸化解偶联剂具有抗性的大肠杆菌突变体。

Escherichia coli mutants resistant to uncouplers of oxidative phosphorylation.

作者信息

Jones M R, Beechey R B

机构信息

Department of Biochemistry and Agricultural Biochemistry, University College of Wales, Aberystwyth, Dyfed, UK.

出版信息

J Gen Microbiol. 1987 Oct;133(10):2759-66. doi: 10.1099/00221287-133-10-2759.

Abstract

Two mutant strains of Escherichia coli K 12 Doc-S resistant to the uncoupling agents 4,5,6,7-tetrachloro-2-trifluoromethyl benzimidazole and carbonyl cyanide m-chlorophenylhydrazone were isolated. These strains, designated TUV and CUV, were capable of (a) growth, (b) the transport of succinate and L-proline and (c) electron-transport-linked oxidative synthesis of ATP in the presence of titres of uncoupler which inhibited these processes in strain Doc-S. The inhibition of transport of L-proline by a fixed titre of uncoupler was sharply pH dependent in strain Doc-S: uptake was unaffected at pH 7.6 but completely inhibited at pH 5.6. This pH dependence was not shown by the resistant strains. We believe that uncouplers were equally accessible to their site(s) of action in the energy-conserving membrane of the sensitive and resistant strains. We conclude that uncoupler resistance in these strains of E. coli has arisen as a consequence of mutations which directly affect a specific site of uncoupler action within the cytoplasmic membrane, rather than as a consequence of a decrease in the permeability of cells to uncoupler.

摘要

分离出了对解偶联剂4,5,6,7-四氯-2-三氟甲基苯并咪唑和羰基氰化物间氯苯腙具有抗性的两种大肠杆菌K 12 Doc-S突变菌株。这些菌株,命名为TUV和CUV,能够(a)生长,(b)转运琥珀酸和L-脯氨酸,以及(c)在一定剂量的解偶联剂存在下进行与电子传递相关的ATP氧化合成,而这些解偶联剂在Doc-S菌株中会抑制这些过程。在Doc-S菌株中,固定剂量的解偶联剂对L-脯氨酸转运的抑制作用强烈依赖于pH值:在pH 7.6时摄取不受影响,但在pH 5.6时完全被抑制。抗性菌株未表现出这种pH依赖性。我们认为解偶联剂在敏感菌株和抗性菌株的能量保存膜中的作用位点上同样容易接近。我们得出结论,这些大肠杆菌菌株中的解偶联剂抗性是由于直接影响细胞质膜内解偶联剂作用特定位点的突变而产生的,而不是由于细胞对解偶联剂的通透性降低所致。

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