Accetto Tomaz, Peterka Matjaz, Avgustin Gorazd
University of Ljubljana, Biotechnical Faculty, Zootechnical Department, Groblje 3, 1230 Domzale, Slovenia.
FEMS Microbiol Lett. 2005 Jun 15;247(2):177-83. doi: 10.1016/j.femsle.2005.05.016.
The restriction endonucleases PbrTI and Pru2I, isoschizomers of Sau3AI and HaeIII, were partially purified and characterized from anaerobic rumen bacteria Prevotella bryantii TC1-1 and Prevotella ruminicola 23, respectively. These are the first type II restriction endonucleases discovered in strains of the genus Prevotella, and they represent one of the barriers hindering gene transfer in these microorganisms. Heterologous DNA was protected against the action of the PbrTI or Pru2I by incubation in a cell-free extract of the respective strain which contained 20 mM EDTA. This led to the development of a protocol enabling successful electrotransformation of the P. bryantii TC1-1 strain with a pRH3 Bacteroides--Escherichia coli shuttle vector containing up to 7-kb long DNA inserts. Plasmid DNA isolated from the transformed strain facilitated the transfer with further increased efficiency and made possible the introduction of ligation reaction products directly to P. bryantii TC1-1 without passing them first through E. coli.
限制性内切酶PbrTI和Pru2I分别是Sau3AI和HaeIII的同裂酶,它们分别从厌氧瘤胃细菌布氏普雷沃氏菌TC1-1和反刍普雷沃氏菌23中部分纯化并进行了表征。这些是在普雷沃氏菌属菌株中首次发现的II型限制性内切酶,它们是阻碍这些微生物中基因转移的障碍之一。通过在含有20 mM EDTA的相应菌株的无细胞提取物中孵育,可保护异源DNA免受PbrTI或Pru2I的作用。这导致了一种方案的开发,该方案能够用含有长达7 kb长DNA插入片段的pRH3拟杆菌-大肠杆菌穿梭载体成功地对布氏普雷沃氏菌TC1-1菌株进行电转化。从转化菌株中分离出的质粒DNA促进了转移,效率进一步提高,并使得无需先将连接反应产物通过大肠杆菌,就可直接将其导入布氏普雷沃氏菌TC1-1。