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萘啶酸对大肠杆菌的作用机制。六、无细胞研究。

Mechanism of action of nalidixic acid on Escherichia coli. Vi. Cell-free studies.

作者信息

Boyle J V, Cook T M, Goss W A

出版信息

J Bacteriol. 1969 Jan;97(1):230-6. doi: 10.1128/jb.97.1.230-236.1969.

Abstract

The effects of nalidixic acid in vitro on deoxyribonucleic acid (DNA)- polymerase (deoxyribonucleosidetriphosphate: DNA deoxynucleotidyltransferase, EC 2.7.7.7), deoxyribonucleotide kinases (ATP: deoxymono- and diphosphate phosphotransferases), and deoxyribosyl transferase (nucleoside: purine deoxyribosyltransferase, EC 2.4.2.6) were examined employing partially purified and crude extracts of Escherichia coli ATCC 11229 and E. coli 15TAU. Nalidixic acid had no inhibitory effect on the DNA-polymerase of the wild-type strain E. coli ATCC 11229 at concentrations of 1.4 x 10(-3) to 2.8 x 10(-3)m. No inhibition of deoxyribonucleotide kinase activity was observed at concentrations of nalidixic acid ranging from 2 x 10(-3) to 8.6 x 10(-3)m. Nalidixic acid (0.43 x 10(-4) to 0.43 x 10(-3)m) had no inhibitory effect on the deoxyribosyl transferase activity of crude extracts obtained from E. coli ATCC 11229 or E. coli 15TAU. Analytical CsCl density gradient centrifugation demonstrated that the DNA obtained after treatment of E. coli 15TAU with nalidixic acid was not cross-linked. These results suggest that the prevention of DNA synthesis in vivo by nalidixic acid is not attributable to inhibition of DNA polymerase, deoxyribonucleotide kinase, deoxyribosyl transferase, or to cross-linking of the DNA of treated cells.

摘要

采用大肠杆菌ATCC 11229和大肠杆菌15TAU的部分纯化提取物和粗提物,研究了萘啶酸在体外对脱氧核糖核酸(DNA)聚合酶(脱氧核苷三磷酸:DNA脱氧核苷酸转移酶,EC 2.7.7.7)、脱氧核苷酸激酶(ATP:脱氧单磷酸和二磷酸磷酸转移酶)以及脱氧核糖基转移酶(核苷:嘌呤脱氧核糖基转移酶,EC 2.4.2.6)的影响。在浓度为1.4×10⁻³至2.8×10⁻³m时,萘啶酸对野生型菌株大肠杆菌ATCC 11229的DNA聚合酶没有抑制作用。在萘啶酸浓度范围为2×10⁻³至8.6×10⁻³m时,未观察到对脱氧核苷酸激酶活性的抑制作用。萘啶酸(0.43×10⁻⁴至0.43×10⁻³m)对从大肠杆菌ATCC 11229或大肠杆菌15TAU获得的粗提物的脱氧核糖基转移酶活性没有抑制作用。分析性氯化铯密度梯度离心表明,用萘啶酸处理大肠杆菌15TAU后获得的DNA没有交联。这些结果表明,萘啶酸在体内对DNA合成的抑制作用并非归因于对DNA聚合酶、脱氧核苷酸激酶、脱氧核糖基转移酶的抑制,也不是由于处理细胞的DNA交联。

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