New Centrifugation Technique for Isolating Enzymes from Large Cell Structures: Isolation and Characterization of Two Bacillus subtilis Autolysins

Author:

Fan David P.1,Beckman Mary M.1

Affiliation:

1. Department of Genetics and Cell Biology, University of Minnesota, St. Paul, Minnesota 55101

Abstract

Bacillus subtilis cell walls can be centrifuged through a linear gradient of 0 to 2 m LiCl and 10 to 25% sucrose so that different autolysins are removed by different salt concentrations and banded in separate positions as the walls pass through the gradient. Using this technique we have found that B. subtilis cell walls are isolated with two autolytic enzymes attached. One autolysin, a glycosidase, can be eluted from walls with 0.5 m LiCl, has a p H optimum between 5 and 8, is relatively heat-sensitive, and has a molecular weight of 60,000. The other autolysin, an alanine amidase, can be eluted from walls with 1.5 m LiCl, has a p H optimum around 8, is relatively heat-stable, has a molecular weight of 35,000, and is present in quantities ten times greater than the glycosidase.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference14 articles.

1. Studies on the competence inducing factor of Bacillus subtilis;Akrigg A.;Biochem. J.,1970

2. Problems in purification of a Bacillus subtilis autolytic enzyme caused by association with teichoic acid;Brown W. C.;Biochem. Biophys. Acta,1970

3. Dynamic interactions between cell wall polymers, extracellular proteases and autolytic enzymes;Brown W. C.;Biochem. Biophys. Res. Commun.,1970

4. Microdetermination of phosphorous;Chen P. S.;Anal. Chem.,1956

5. Cell wall binding properties of the Bacillus subtilis autolysin(s);Fan D. P.;J. Bacteriol.,1970

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