Kharat Arun S, Coursange Evelyne, Noirclerc-Savoye Marjolaine, Lacoste Jérôme, Blot Michel
Plasticité et Expression des Génomes Microbiens, CNRS-FRE2383/CEA LRC12/Université Joseph Fourier, Grenoble, France.
Acta Biochim Pol. 2006;53(4):729-38. Epub 2006 Nov 14.
Transposition of insertion sequences (IS) is an enzyme-mediated process that only occurs in a minority of cells within a bacterial culture. Transposition is thus a rare event, but transposition frequency may vary depending on experimental conditions. For instance in a rich broth, IS elements are known to transpose during stationary phase but not during exponential growth. Using a reporter system which involves the activation of the cryptic bgl operon in Escherichia coli, we show that the frequency of IS1 transposition is a function of glucose concentration in the growth medium, it is increased by streptomycin amounts that are below minimum inhibitory concentration (sub-MIC) and is inhibited in an rpsL150 strain with high translation accuracy. Since starved cells are known to enhance ribosome frameshifting, our data suggests that growth conditions applied in this study could affect IS1 transposition by increasing translation infidelity.
插入序列(IS)的转座是一个酶介导的过程,仅发生在细菌培养物中的少数细胞内。因此,转座是一个罕见事件,但转座频率可能因实验条件而异。例如,在丰富肉汤中,已知IS元件在稳定期转座,但在指数生长期不转座。使用一个涉及激活大肠杆菌中隐秘bgl操纵子的报告系统,我们表明IS1转座频率是生长培养基中葡萄糖浓度的函数,低于最低抑菌浓度(亚MIC)的链霉素量可增加该频率,而在具有高翻译准确性的rpsL150菌株中则受到抑制。由于已知饥饿细胞会增强核糖体移码,我们的数据表明本研究中应用的生长条件可能通过增加翻译错误率来影响IS1转座。