Lee K Y, Birkbeck T H
Infect Immun. 1984 May;44(2):434-8. doi: 10.1128/iai.44.2.434-438.1984.
The stability of mRNA for the delta-lysin of Staphylococcus aureus was determined by measuring the residual lysin synthesis after inhibition of DNA-dependent RNA polymerase activity with rifampin. At the late logarithmic-early stationary phase of growth the delta-lysin mRNA was very stable, with a half-life of ca. 20 min. Total cellular RNA was extracted from S. aureus and translated with a modified Escherichia coli S-30 system; delta-lysin was identified amongst the translation products by immunoprecipitation and immunoabsorption. The delta-lysin synthesized in vitro was of a size similar to mature delta-lysin and did not require a signal sequence for secretion from the cell.
通过用利福平抑制依赖DNA的RNA聚合酶活性后测量残余溶菌素合成,来测定金黄色葡萄球菌δ-溶菌素mRNA的稳定性。在生长的对数后期-早期稳定期,δ-溶菌素mRNA非常稳定,半衰期约为20分钟。从金黄色葡萄球菌中提取总细胞RNA,并使用改良的大肠杆菌S-30系统进行翻译;通过免疫沉淀和免疫吸附在翻译产物中鉴定出δ-溶菌素。体外合成的δ-溶菌素大小与成熟的δ-溶菌素相似,并且从细胞分泌不需要信号序列。