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.
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CITATION STYLE
Binder, R. G., Numata, K., Lowe, D. A., Murakami, T., & Brown, J. L. (1993). Isolation and characterization of a Pseudomonas strain producing glutaryl- 7-aminocephalosporanic acid acylase. Applied and Environmental Microbiology, 59(10), 3321–3326. https://doi.org/10.1128/aem.59.10.3321-3326.1993
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