Essich E, Stevens S E, Porter R D
Department of Molecular and Cell Biology, Pennsylvania State University, University Park 16802.
J Bacteriol. 1990 Apr;172(4):1916-22. doi: 10.1128/jb.172.4.1916-1922.1990.
Chromosomal transformation of Agmenellum quadruplicatum PR-6 (= Synechococcus sp. strain 7002) was characterized for phenotypic expression, for exposure time to DNA, and for dependence on DNA concentration with regard to Rifr donor DNA. Exponentially growing cells of PR-6 were competent for chromosomal transformation. Competence decreased in cells in the stationary phase of growth or in cells deprived of a nitrogen source. Dark incubation of cells before exposure to donor DNA also decreased competence. Homologous Rifr and Strr DNA and heterologous Escherichia coli W3110 DNA were used in DNA-DNA competition studies, which clearly showed that DNA binding by PR-6 was nonspecific. DNA binding and uptake by PR-6 exhibited single-hit kinetics. Single-stranded DNA failed to transform competent cells of PR-6, and DNA eclipse was not observed, suggesting that double-stranded DNA was the substrate for the binding and uptake reactions during the transformation of PR-6. A significant improvement in transformation frequency was achieved by increasing the nitrate content of the culture medium and by lowering the temperature at which cells were exposed to donor DNA from 39 degrees C (the optimal temperature for growth) to 30 degrees C.
对四倍体阿格门氏蓝细菌PR-6(=聚球藻属菌株7002)的染色体转化进行了表征,包括表型表达、DNA暴露时间以及对利福平抗性(Rifr)供体DNA浓度的依赖性。处于指数生长期的PR-6细胞具有染色体转化能力。在生长稳定期的细胞或缺乏氮源的细胞中,转化能力下降。在暴露于供体DNA之前对细胞进行暗培养也会降低转化能力。在DNA-DNA竞争研究中使用了同源的利福平抗性和链霉素抗性(Strr)DNA以及异源的大肠杆菌W3110 DNA,结果清楚地表明PR-6的DNA结合是非特异性的。PR-6的DNA结合和摄取表现出单次打击动力学。单链DNA无法转化PR-6的感受态细胞,并且未观察到DNA隐蔽现象,这表明双链DNA是PR-6转化过程中结合和摄取反应的底物。通过增加培养基中的硝酸盐含量以及将细胞暴露于供体DNA的温度从39℃(生长的最佳温度)降低到30℃,转化频率得到了显著提高。