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Appl Environ Microbiol. 1968 October; 16(10): 1557-1563
Copyright © 1968 American Society for Microbiology. All Rights Reserved.

Specificity of Penicillin Acylase of Fusarium and of Penicillium chrysogenum

H. Vanderhaeghe, M. Claesen, A. Vlietinck and G. Parmentier

Rega Institute, University of Louvain, Louvain, Belgium

ABSTRACT

Extracts containing penicillin acylase were obtained by shaking the mycelium of Fusarium avenaceum and of Penicillium chrysogenum in 0.2 M sodium acetate or sodium chloride solution. The optimum pH for conversion of penicillin V into 6-aminopenicillanic acid (6-APA) by the enzyme of Fusarium was about 7.5, and the reaction velocity was increased by a rise in temperature from 27 to 37 C. Penicillin G and penicillins with an aliphatic side chain were cleaved much less readily than was penicillin V. With the enzyme preparation obtained from a nonpenicillin-producing strain of P. chrysogenum, the reaction rate was higher at pH 8.5 than at pH 7.5 and pH 6.5. The acylase of P. chrysogenum hydrolyzes penicillin V more readily than penicillin G. In a series of aliphatic penicillins, the amount of 6-APA formed through the action of this enzyme increased with the number of carbon atoms of the side chain. Penicillins with a glutaryl or an adipyl group as side chain were unaffected by the enzyme of Fusarium and of Penicillium. No reaction was observed upon incubation of penicillin N (with a D-aminoadipyl side chain) or isopenicillin N (with an L-aminoadipyl side chain) with Fusarium and Penicillium extract. When the carboxy group of the side chain of these penicillins was esterified, formation of 6-APA was observed upon incubation with Penicillium extract, whereas no 6-APA or only very small amounts were obtained by acylase of Fusarium.


Appl Environ Microbiol. 1968 October; 16(10): 1557-1563
Copyright © 1968 American Society for Microbiology. All Rights Reserved.







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Copyright © 1968 by the American Society for Microbiology. All rights reserved.