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耐萘啶酸的大肠杆菌K-12突变体:基因定位与显性研究。

Escherichia coli K-12 mutants resistant to nalidixic acid: genetic mapping and dominance studies.

作者信息

Hane M W, Wood T H

出版信息

J Bacteriol. 1969 Jul;99(1):238-41. doi: 10.1128/jb.99.1.238-241.1969.

Abstract

Escherichia coli K-12 strains tested so far (approximately 20) can be separated into three groups on the basis of their abilities to form colonies on nutrient agar supplemented with nalidixic acid (NAL): (i) Nal(s) or wild type (no growth at 1 to 2 mug/ml); (ii) NalA(r) (growth at 40 mug/ml or higher); and (iii) NalB(r) (growth at 4 mug/ml, but no growth at 10 mug/ml). The NalA(r) group has a spectrum of sensitivity ranging from 60 to over 100 mug/ml. All Hfr strains of the NalA(r) and NalB(r) groups transfer NAL resistance to recipient cells at genetic loci which are at 42.5 +/- 0.5 and 51 +/- 1 min, respectively, on the Taylor-Trotter map. Some members of the NalA(r) group also have the genetic locus for NalB(r). The nalA(s) allele is completely dominant to nalA(r) in a partial diploid configuration. In haploids, nalA(r)-nalB(r) is phenotypically NalA(r); nalA(r)-nalB(s) is NalA(r); and nalA(s)-nalB(r) is NalB(r). The map location of nalA and the easy differentiation between NalA(r) and NalA(s) allow this marker to be used as a counterselector in bacterial conjugation experiments.

摘要

迄今为止所测试的大肠杆菌K-12菌株(约20株),根据其在添加萘啶酸(NAL)的营养琼脂上形成菌落的能力可分为三组:(i)Nal(s)或野生型(在1至2微克/毫升时不生长);(ii)NalA(r)(在40微克/毫升或更高浓度时生长);以及(iii)NalB(r)(在4微克/毫升时生长,但在10微克/毫升时不生长)。NalA(r)组的敏感范围为60至100微克/毫升以上。NalA(r)组和NalB(r)组的所有高频重组(Hfr)菌株分别在泰勒-特罗特图谱上42.5±0.5分钟和51±1分钟的基因位点将NAL抗性转移给受体细胞。NalA(r)组的一些成员也具有NalB(r)的基因位点。在部分二倍体构型中,nalA(s)等位基因对nalA(r)完全显性。在单倍体中,nalA(r)-nalB(r)表型为NalA(r);nalA(r)-nalB(s)为NalA(r);而nalA(s)-nalB(r)为NalB(r)。nalA的图谱位置以及NalA(r)和NalA(s)之间易于区分,使得该标记可在细菌接合实验中用作反选择标记。

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