Hart B A, Zahler S A
J Bacteriol. 1966 Dec;92(6):1632-7. doi: 10.1128/jb.92.6.1632-1637.1966.
Hart, Beth A. (Cornell University, Ithaca, N.Y.), and Stanley A. Zahler. Lytic enzyme produced by Myxococcus xanthus. J. Bacteriol. 92:1632-1637. 1966.-Strain FBa of Myxococcus xanthus releases into its culture medium an enzyme capable of lysing Micrococcus lysodeikticus cells and of releasing N-acetyl amino sugars from their cell walls. The lysin is stable at pH values near neutrality and at temperatures below 50 C. It lyses a number of bacterial species sensitive to egg-white lysozyme, and fails to lyse lysozyme-resistant species. Sensitivity of M. lysodeikticus cell walls to FBa lysin and to lysozyme is changed in a similar manner by addition and removal of O-acetyl groups. We describe methods for obtaining 190-fold purification of the lysin from culture filtrates, using acetone and ammonium sulfate precipitations and filtration through diethylaminoethyl cellulose. We also describe a gel filtration method for separating the lysin from a protease which is also produced by strain FBa.
哈特,贝丝·A.(纽约州伊萨卡市康奈尔大学),以及斯坦利·A.扎勒。黄色粘球菌产生的溶菌酶。《细菌学杂志》92:1632 - 1637。1966年。——黄色粘球菌菌株FBa向其培养基中释放一种能够裂解溶壁微球菌细胞并从其细胞壁释放N - 乙酰氨基糖的酶。该溶素在接近中性的pH值以及低于50摄氏度的温度下稳定。它能裂解一些对蛋清溶菌酶敏感的细菌种类,而不能裂解对溶菌酶有抗性的种类。通过添加和去除O - 乙酰基,溶壁微球菌细胞壁对FBa溶素和溶菌酶的敏感性以相似的方式发生变化。我们描述了使用丙酮和硫酸铵沉淀以及通过二乙氨基乙基纤维素过滤从培养滤液中获得190倍纯化溶素的方法。我们还描述了一种凝胶过滤方法,用于从FBa菌株也产生的一种蛋白酶中分离溶素。