Süleymanoğlu E
Biophysics and Microscopy Group, Section of Molecular Cytology, Institute for Molecular Cell Biology, BioCentrum Amsterdam, University of Amsterdam, 1098 SM Amsterdam, The Netherlands.
Folia Microbiol (Praha). 2002;47(4):365-70. doi: 10.1007/BF02818691.
Bacterial chromosome is assembled and folded into one or several nucleoids, depending on the metabolic status of the cell. Development of reliable nucleoid isolation protocols has always been an objective for researchers. A rapid and reproducible procedure for isolation of E. coli nucleoids is described here, while the cell envelope is maintained. Membrane dispersions and vesicles were prepared by lysozyme-EDTA treatment with subsequent rupture of the spheroplasts by electric field. Under these conditions the yield of electroreleased nucleoids was around 90%. The extent of DNA-envelope contacts was determined by light microscopy employing phase contrast and fluorescence modes.
细菌染色体根据细胞的代谢状态组装并折叠成一个或几个类核。开发可靠的类核分离方案一直是研究人员的目标。本文描述了一种在保持细胞膜的同时快速且可重复的大肠杆菌类核分离程序。通过溶菌酶 - 乙二胺四乙酸(EDTA)处理制备膜分散体和囊泡,随后通过电场使原生质球破裂。在这些条件下,电释放类核的产量约为90%。采用相差和荧光模式的光学显微镜确定DNA与膜的接触程度。