Whiteside T L, Corpe W A
J Bacteriol. 1969 Mar;97(3):1449-59. doi: 10.1128/jb.97.3.1449-1459.1969.
Cell envelopes of Chromobacterium violaceum were isolated and treated under controlled conditions with trypsin, Pronase, lipase, phospholipase C, lysozyme, and a mixture of enzymes produced by a bacteriolytic Pseudomonas sp. After each enzyme treatment, losses in dry weight, protein, lipid, carbohydrate, 2,6-diaminopimelic acid, and total phosphorus were determined. Electron-microscopic examination of the enzyme-treated envelopes indicated complete or partial loss of envelope rigidity or some envelope fragmentation, or both. Each enzyme hydrolyzed at least one envelope component and liberated several others into the supernatant fluid, where they appeared as nondialyzable particulate components, identified by means of electron microscopy. Unlike the other enzymes, the Pseudomonas sp. enzyme mixture partially liberated all major envelope components except phosphorus, heptose, and 2-keto-3-deoxy octonic acid. In spite of these large losses, the envelopes preserved some features of their integrity and elongated shape.
对紫色色杆菌的细胞包膜进行分离,并在可控条件下用胰蛋白酶、链霉蛋白酶、脂肪酶、磷脂酶C、溶菌酶以及一种溶菌假单胞菌产生的混合酶进行处理。每次酶处理后,测定干重、蛋白质、脂质、碳水化合物、2,6 - 二氨基庚二酸和总磷的损失。对经酶处理的包膜进行电子显微镜检查发现,包膜的刚性完全或部分丧失,或出现一些包膜破碎,或两者皆有。每种酶至少水解一种包膜成分,并将其他几种成分释放到上清液中,通过电子显微镜鉴定,这些成分以上清液中不可透析的颗粒成分形式出现。与其他酶不同,假单胞菌的混合酶部分释放了除磷、庚糖和2 - 酮 - 3 - 脱氧辛酸之外的所有主要包膜成分。尽管有这些大量损失,包膜仍保留了一些完整性特征和细长形状。