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由独立转移和抗药性质粒组成的R因子系统的分子与遗传学研究。

Molecular and genetic studies of an R factor system consisting of independent transfer and drug resistance plasmids.

作者信息

van Embden J, Cohen S N

出版信息

J Bacteriol. 1973 Nov;116(2):699-709. doi: 10.1128/jb.116.2.699-709.1973.

Abstract

Certain genetic, structural, and biochemical properties of a class 2 R-factor system consisting of the conjugally proficient transfer plasmid I and the naturally occurring non-conjugative tetracycline (Tc) resistance plasmid 219 are reported. I and 219 exist as separate plasmid deoxyribonucleic acid (DNA) species in both Escherichia coli and Salmonella panama, having molecular weights of 42 x 10(6) and 5.8 x 10(6), respectively. The buoyant densities of I and 219 are 1.702 and 1.710 g/cm(3), respectively, in neutral cesium chloride. Although the Tc resistance plasmid is not transmissible in a normal conjugal mating, it is mobilized in a three-component mating by plasmid I and by certain other conjugative plasmids of the fi(+) or fi(-) phenotype. Mobilization does not appear to involve intermolecular recombination between plasmids, and no covalent linkage of resistance markers and fertility functions is observed. Transformation of CaCl(2)-treated E. coli by plasmid DNA is shown to be a useful procedure for studying the biological properties of different plasmid molecular species that have been fractionated in vitro, and for selectively inserting non-self-transmissible plasmids into specific bacterial strains. The effects of tetracycline on the rate of protein synthesis carried out by plasmid 219 were studied by using isolated E. coli minicells into which this plasmid had segregated. Consistent with the results of earlier investigations showing the inducibility of plasmid-mediated Tc resistance in E. coli, the antibiotic was observed to stimulate protein synthesis in minicells carrying the plasmid 219 and totally inhibit (3)H-leucine incorporation by minicells lacking the Tc resistance marker. Five discrete polypeptide species were synthesized by minicells carrying plasmid 219; exposure of minicells or parent bacteria to Tc resulted in specific and reproducible changes in polypeptide synthesis patterns.

摘要

报道了由具有高效接合转移能力的质粒I和天然存在的非接合型四环素(Tc)抗性质粒219组成的2类R因子系统的某些遗传、结构和生化特性。质粒I和219在大肠杆菌和巴拿马沙门氏菌中均以独立的质粒脱氧核糖核酸(DNA)形式存在,分子量分别为42×10⁶和5.8×10⁶。在中性氯化铯中,质粒I和219的浮力密度分别为1.702和1.710 g/cm³。虽然Tc抗性质粒在正常接合交配中不可转移,但在三元交配中可被质粒I和某些其他fi(+)或fi(-)表型的接合性质粒所动员。这种动员似乎不涉及质粒间的分子间重组,也未观察到抗性标记与育性功能的共价连接。经氯化钙处理的大肠杆菌被质粒DNA转化,这一方法被证明对于研究体外分离的不同质粒分子种类的生物学特性,以及将非自我传递性质粒选择性地插入特定细菌菌株很有用。利用分离出已携带该质粒的大肠杆菌微小细胞,研究了四环素对质粒219所进行的蛋白质合成速率的影响。与早期研究结果一致,早期研究表明大肠杆菌中质粒介导的Tc抗性具有诱导性,观察到抗生素刺激携带质粒219的微小细胞中的蛋白质合成,并完全抑制缺乏Tc抗性标记的微小细胞中³H-亮氨酸的掺入。携带质粒219的微小细胞合成了5种离散的多肽种类;微小细胞或亲代细菌暴露于Tc会导致多肽合成模式发生特定且可重复的变化。

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