Wood D A, Tristram H
Department of Botany and Microbiology, University College, London, W.C.1, England.
J Bacteriol. 1970 Dec;104(3):1045-51. doi: 10.1128/jb.104.3.1045-1051.1970.
Study of protoplasts, lysed protoplasts, and cells treated with lysozyme in the absence of osmotic stabilizer suggested that the alkaline phosphatase (EC 3.1.3.1.) of Bacillus subtilis is located in the protoplasmic membrane. Cytochemical evidence in support of this view is presented. The enzyme protein was strongly bound to the membrane structure and could not be solubilized by a number of treatments known to release enzymes from membranes and other lipoprotein structures. Alkaline phosphatase was, however, solubilized by treatment of intact B. subtilis cells or isolated protoplasmic membranes with strong salt solutions at pH 7.2, suggesting that electrostatic forces are responsible for the association between membrane and enzyme protein. Dialysis of alkaline phosphatase solutions against buffer of low ionic strength resulted in precipitation of the enzyme.
对原生质体、裂解的原生质体以及在没有渗透稳定剂的情况下用溶菌酶处理的细胞的研究表明,枯草芽孢杆菌的碱性磷酸酶(EC 3.1.3.1.)位于原生质膜中。本文提供了支持这一观点的细胞化学证据。酶蛋白与膜结构紧密结合,并且不能通过已知的从膜和其他脂蛋白结构释放酶的多种处理方法来溶解。然而,通过在pH 7.2下用强盐溶液处理完整的枯草芽孢杆菌细胞或分离的原生质膜,碱性磷酸酶可被溶解,这表明静电力是膜与酶蛋白之间结合的原因。将碱性磷酸酶溶液对低离子强度的缓冲液进行透析会导致酶沉淀。