Reusch V M, Foster J L, Haberkorn D S
J Bacteriol. 1983 Aug;155(2):896-9. doi: 10.1128/jb.155.2.896-899.1983.
Sacculi prepared from Streptococcus sanguis 34 by extensive extraction of cells with hot sodium dodecyl sulfate-2-mercaptoethanol retained the ability to coaggregate with Actinomyces viscosus T14V. When S. sanguis 34 was disrupted by homogenization with glass beads and fractionated by differential centrifugation, only the cell wall fraction agglutinated A. viscosus T14V. When strain 34 was treated with lysozyme, the coaggregating capability of the cells was essentially unaltered. Sacculi prepared from lysozyme-treated strain 34 and additionally purified by electrophoresis were agglutinated by strain T14V.
用热十二烷基硫酸钠 - 2 - 巯基乙醇对血链球菌34进行细胞大量抽提所制备的球囊,保留了与粘性放线菌T14V共聚集的能力。当血链球菌34用玻璃珠匀浆破碎并通过差速离心分级分离时,只有细胞壁部分能凝集粘性放线菌T14V。当34株用溶菌酶处理时,细胞的共聚集能力基本未改变。用溶菌酶处理过的34株制备并经电泳进一步纯化的球囊,能被T14V菌株凝集。