Beard J P, Howe T G, Richmond M H
J Bacteriol. 1972 Sep;111(3):814-20. doi: 10.1128/jb.111.3.814-820.1972.
A procedure for the purification of sex pili is described. Escherichia coli K-12 carrying Rldrd19 was grown in nutrient broth and blended at the time of peak sex pilus production. The cells were removed by centrifugation, and the supernatant fraction was concentrated, dialyzed, and clarified in an ultrafiltration system. After an additional blend and a clearing spin, the material was centrifuged in a CsCl gradient, and the fractions containing the sex pili were subjected to isoelectric focusing. About 5 mg of intact pili of approximately 98% purity were obtained by this method from about 100 g (wet weight) of cells.
本文描述了一种纯化性菌毛的方法。携带Rldrd19的大肠杆菌K-12在营养肉汤中培养,在性菌毛产生高峰期进行匀浆。通过离心去除细胞,将上清液浓缩、透析,并在超滤系统中澄清。经过再次匀浆和澄清离心后,将材料在CsCl梯度中离心,含有性菌毛的组分进行等电聚焦。通过这种方法,从约100 g(湿重)细胞中获得了约5 mg纯度约为98%的完整菌毛。