Hansen J B, Olsen R H
J Bacteriol. 1978 Jul;135(1):227-38. doi: 10.1128/jb.135.1.227-238.1978.
Large plasmids from Agrobacterium tumefaciens, Salmonella typhimurium, Escherichia coli, Pseudomonas putida, and Pseudomonas aeruginosa were routinely and consistently isolated using a procedure which does not require ultracentrifugation but includes steps designed to separate large-plasmid DNA from the bacterial folded chromosome. It also selectively removes fragments of broken chromosome. A variety of large plasmids was readily visualized with agarose gel electorphoresis, including five between 70 and 85 megadaltons (Mdal) in size, six between 90 and 143 Mdal, one that was larger than 200 Mdal, and one that was larger than 300 Mdal. This isolation procedure allowed initial estimation of the molecular sizes of the two IncP2 plasmids, pMG1 and pMG5, which were 312 and 280 Mdal, respectively. A standard curve for size determination by gel electrophoresis including plasmids between 23 and 143 Mdal in size did not extrapolate linearly for plasmids of the 300-Mdal size range. Unique response of different plasmids to the isolation procedure included sensitivity of IncP1 plasmids to high pH and the co-isolation of a 20-Mdal "cryptic" plasmid in conjunction.
利用一种无需超速离心的方法,可常规且稳定地从根癌土壤杆菌、鼠伤寒沙门氏菌、大肠杆菌、恶臭假单胞菌和铜绿假单胞菌中分离出大型质粒。该方法包含旨在将大型质粒DNA与细菌折叠染色体分离的步骤,还能选择性地去除破碎染色体的片段。通过琼脂糖凝胶电泳可轻松观察到多种大型质粒,包括5种大小在70至85兆道尔顿(Mdal)之间的、6种大小在90至143 Mdal之间的、1种大于200 Mdal的以及1种大于300 Mdal的。这种分离方法使得能够初步估计两种IncP2质粒pMG1和pMG5的分子大小,它们分别为312 Mdal和280 Mdal。用于通过凝胶电泳测定大小的标准曲线(包括大小在23至143 Mdal之间的质粒)对于300 Mdal大小范围的质粒并非呈线性外推。不同质粒对该分离方法的独特反应包括IncP1质粒对高pH的敏感性以及同时共分离出一个20 Mdal的“隐蔽”质粒。