Formation and Purification of Serratia marcescens Arylsulfatase

Author:

Murooka Yoshikatsu1,Yim Moo-Hyun1,Harada Tokuya1

Affiliation:

1. Institute of Scientific and Industrial Research, Osaka University, Suita-shi, Osaka 565, Japan

Abstract

The effects of culture conditions on arylsulfatase production by six strains of the genus Serratia were studied. Synthesis of arylsulfatases in all six strains was repressed in media with inorganic sulfate or methionine as the sole source of sulfur and derepressed by the addition of tyramine. Serratia marcescens IFO 3046 grew most rapidly and produced a high level of arylsulfatase when cultured on mannitol with inorganic sulfate and tyramine. The derepressed synthesis of arylsulfatase in S. marcescens was not subject to strong catabolite repression. The molecular weight of purified arylsulfatase was determined to be between 46,000 and 49,000. Arylsulfatase from S. marcescens differed in K m and V max values, substrate specificities, fluoride inhibition, and electrophoretic mobility from the enzyme from K. aerogenes , but had the same molecular weight as the latter.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference28 articles.

1. Derepression of arylsulfatase synthesis in Aerobacter aerogenes by tyramine;Adachi T.;J. Bacteriol.,1973

2. Regulation of arylsulfatase synthesis by sulfur compounds in Klebsiella aerogenes;Adachi T.;J. Bacteriol.,1975

3. Catabolite repression and derepression of arylsulfatase synthesis in KiebsieUa aerogenes;Adachi T.;J. Bacteriol.,1974

4. The isolation of arylsulfatase isoenzymes from Pseudomonas aeruginosa;Delisle G. J.;Biochim. Biophys. Acta,1970

5. Observations on the arylsulfatase of Proteus vulgaris;Dodgson K. S.;Enzymologia,1959

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