van Nieuwenhoven M H, Hellingwerf K J, Venema G, Konings W N
J Bacteriol. 1982 Aug;151(2):771-6. doi: 10.1128/jb.151.2.771-776.1982.
This study explored the role of the proton motive force in the processes of DNA binding and DNA transport of genetic transformation of Bacillus subtilis 168 strain 8G-5 (trpC2). Transformation was severely inhibited by the ionophores valinomycin, nigericin, and 3,5-di-tert-4-hydroxybenzylidenemalononitrite (SF-6847) and by tetraphenylphosphonium. The ionophores valinomycin and nigericin also severely inhibited binding of transforming DNA to the cell envelope, whereas SF-6847 and carbonylcyanide-p-trifluoromethoxyphenylhydrazone hardly affected binding. The proton motive force, therefore, does not contribute to the process of DNA binding, and valinomycin and nigericin interact directly with the DNA binding sites at the cell envelope. The effects of ionophores, weak acids, and tetraphenylphosphonium on the components of the proton motive force and on the entry of transforming DNA after binding to the cell envelope was investigated. DNA entry, as measured by the amount of DNase I-resistant cell-associated [3H]DNA and by the formation of DNA breakdown products, was severely inhibited under conditions of a small proton motive force and also under conditions of a small delta pH and a high electrical potential. These results suggest that the proton motive force and especially the delta pH component functions as a driving force for DNA uptake in transformation.
本研究探讨了质子动力在枯草芽孢杆菌168菌株8G-5(trpC2)遗传转化的DNA结合和DNA转运过程中的作用。缬氨霉素、尼日利亚菌素和3,5-二叔丁基-4-羟基亚苄基丙二腈(SF-6847)等离子载体以及四苯基鏻严重抑制了转化。缬氨霉素和尼日利亚菌素也严重抑制了转化DNA与细胞包膜的结合,而SF-6847和羰基氰对三氟甲氧基苯腙几乎不影响结合。因此,质子动力对DNA结合过程没有贡献,缬氨霉素和尼日利亚菌素直接与细胞包膜上的DNA结合位点相互作用。研究了离子载体、弱酸和四苯基鏻对质子动力成分以及转化DNA与细胞包膜结合后进入细胞的影响。通过抗DNase I的细胞相关[3H]DNA量和DNA降解产物的形成来衡量,在质子动力较小的条件下以及在ΔpH较小和电势较高的条件下,DNA进入均受到严重抑制。这些结果表明,质子动力尤其是ΔpH成分在转化过程中作为DNA摄取的驱动力发挥作用。