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大肠杆菌中一个影响核糖体的基因座发生突变导致对新霉素和卡那霉素产生共抗性。

Coresistance to neomycin and kanamycin by mutations in an Escherichia coli locus that affects ribosomes.

作者信息

Apirion D, Schlessinger D

出版信息

J Bacteriol. 1968 Sep;96(3):768-76. doi: 10.1128/jb.96.3.768-776.1968.

Abstract

Mutant strains resistant to neomycin or to kanamycin sulfate were isolated from Escherichia coli K-12. Nine mutants were analyzed; all were resistant to both antibiotics (about 150 and 100 mug/ml, respectively), and were designated nek. In the mutant strains, the ribosomes are changed from those of the parental strain; for when they were used in assays for polypeptide formation directed by polyadenylic acid or polycytidylic acid, coding fidelity in presence of the drugs was increased and inhibition of synthesis by the drugs was lessened. Mating experiments and transduction tests showed that all of the nine nek mutants are either closely linked or allelic, and the nek locus is closely linked to two genes-str (streptomycin) and spc (spectinomycin)-known to affect the 30S ribosome. The two nek mutants tested were recessive to the sensitive, wild-type allele. When the nek mutants were compared to the parental strain, pleiotropic effects of the nek mutations were observed. Resistance to low levels of streptomycin and spectinomycin was increased, whereas resistance to chloramphenicol was decreased. Also, the mutants were less able to adapt to high concentrations of lincomycin, and could no longer show phenotypic suppression of an arginine requirement by neomycin or kanamycin. Such pleiotropic effects are suggested to be the rule for mutations in genes that participate in the biosynthesis of a cellular organelle.

摘要

从大肠杆菌K-12中分离出对新霉素或硫酸卡那霉素具有抗性的突变菌株。对9个突变体进行了分析;所有突变体对两种抗生素均具有抗性(分别约为150和100μg/ml),并被命名为nek。在突变菌株中,核糖体与亲本菌株的核糖体不同;因为当它们用于聚腺苷酸或聚胞苷酸指导的多肽形成测定时,在药物存在下编码保真度增加,并且药物对合成的抑制作用减弱。交配实验和转导测试表明,9个nek突变体中的所有突变体要么紧密连锁要么等位,并且nek基因座与已知影响30S核糖体的两个基因——str(链霉素)和spc(壮观霉素)紧密连锁。所测试的两个nek突变体对敏感的野生型等位基因呈隐性。当将nek突变体与亲本菌株进行比较时,观察到nek突变的多效性效应。对低水平链霉素和壮观霉素的抗性增加,而对氯霉素的抗性降低。此外,突变体适应高浓度林可霉素的能力较差,并且不再能通过新霉素或卡那霉素表现出对精氨酸需求的表型抑制。这种多效性效应被认为是参与细胞器生物合成的基因突变的规律。

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