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J Bacteriol. 1969 October; 100(1): 187-194
Copyright © 1969 American Society for Microbiology. All Rights Reserved.

Immunological Analysis of Mycoplasma Membranes

Itzhak Kahane and Shmuel Razin

Department of Clinical Microbiology, the Hebrew University-Hadassah Medical School, Jerusalem, Israel

ABSTRACT

The antigens responsible for the production of antibodies to Mycoplasma laidlawii and M. gallisepticum causing growth and metabolic inhibition of these organisms were localized in the cell membrane. Various membrane fractions were tested for serological activity. Membrane lipids were completely or almost completely inactive, whereas several preparations of defatted membrane proteins retained some serological activity, shown by their ability to stimulate metabolic inhibition antibody in rabbits and to adsorb metabolic inhibition antibody and form precipitation lines with an antiserum to the membrane. When the membranes were heated to 65 C for 1 hr, they virtually lost their ability to adsorb metabolic inhibition antibody, which suggests that the antigenic determinants are proteins. Serological activity was retained in reaggregated membranes obtained by dialysis against Mg2+ of membranes solubilized in sodium dodecyl sulfate. The amount of solubilized membrane protein and lipid incorporated into the reaggregated membranes could be regulated by varying the Mg2+ concentration. As the serological tests indicated that the various membrane antigens were selectively incorporated into the different reaggregated membranes, the use of controlled reaggregation of solubilized membranes is suggested as a new tool for the fractionation and antigenic analysis of membrane proteins.


J Bacteriol. 1969 October; 100(1): 187-194
Copyright © 1969 American Society for Microbiology. All Rights Reserved.







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