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J Bacteriol. 1970 December; 104(3): 1045-1051
Copyright © 1970 American Society for Microbiology. All Rights Reserved.

Localization in the Cell and Extraction of Alkaline Phosphatase from Bacillus subtilis

^a Department of Botany and Microbiology, University College, London, W.C.1, England

ABSTRACT

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.

¹ Present address: Microbiology Unit, Department of Biochemistry, University of Oxford, Oxford, England.