Fan D P, Beckman M M
J Bacteriol. 1972 Mar;109(3):1258-65. doi: 10.1128/jb.109.3.1258-1265.1972.
Bacillus subtilis cell walls can be centrifuged through a linear gradient of 0 to 2 m LiCl and 10 to 25% sucrose so that different autolysins are removed by different salt concentrations and banded in separate positions as the walls pass through the gradient. Using this technique we have found that B. subtilis cell walls are isolated with two autolytic enzymes attached. One autolysin, a glycosidase, can be eluted from walls with 0.5 m LiCl, has a pH optimum between 5 and 8, is relatively heat-sensitive, and has a molecular weight of 60,000. The other autolysin, an alanine amidase, can be eluted from walls with 1.5 m LiCl, has a pH optimum around 8, is relatively heat-stable, has a molecular weight of 35,000, and is present in quantities ten times greater than the glycosidase.
枯草芽孢杆菌细胞壁可通过0至2m LiCl和10至25%蔗糖的线性梯度进行离心,这样不同的自溶素会被不同的盐浓度去除,并在细胞壁穿过梯度时在不同位置形成条带。利用这项技术,我们发现分离得到的枯草芽孢杆菌细胞壁附着有两种自溶酶。一种自溶素是糖苷酶,可用0.5m LiCl从细胞壁上洗脱下来,最适pH在5至8之间,相对热敏感,分子量为60,000。另一种自溶素是丙氨酸酰胺酶,可用1.5m LiCl从细胞壁上洗脱下来,最适pH约为8,相对热稳定,分子量为35,000,其含量比糖苷酶高十倍。