Isolation and Characterization of a Pseudomonas Strain Producing Glutaryl-7-Aminocephalosporanic Acid Acylase

Author:

Binder R. G.1,Numata K.1,Lowe D. A.1,Murakami T.1,Brown J. L.1

Affiliation:

1. Bio/Chem Division, Bristol-Myers Squibb Company, P.O. Box 4755, Syracuse, New York 13221-4755, and Bristol-Myers Squibb Research Institute, 2-9-3 Shimo-meguro, Meguro-ku, Tokyo 153, Japan2

Abstract

Several screening methods were developed for the selection of Pseudomonas strains capable of hydrolyzing glutaryl-7-aminocephalosporanic acid to 7-aminocephalosporanic acid. An isolate exhibiting high acylase activity, designated BL072, was identified as a strain of Pseudomonas diminuta . It grew optimally at pH 7 to 8 and at a temperature of 32 to 40°C, but acylase activity was highest when the strain was grown at 28°C. Mutants of BL072 were generated by nitrosoguanidine treatment and screened for increased production of glutaryl-7-aminocephalosporanic acid acylase. A superior mutant gave a fourfold increase in acylase titer. The cell-associated acylase had similar activities against various glutaryl-cephems but had undetectable activity against cephalosporin C. This acylase may prove useful for the conversion of cephalosporin C to 7-aminocephalosporanic acid.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference30 articles.

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3. Isolation of soil strains producing new cephalosporin acylases;Aramori I.;J. Ferment. Bioeng.,1991

4. Aretz W. and K. Sauber (Hoechst AG). May 1988. European patent 0275901.

5. Arnold B. R. Fildes and D. Gilbert (Glaxo). April 1972. U.S. patent 3658649.

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