Literature DB >> 411518

Effects of carrier morphology and buffer diffusion on the expression of enzymatic activity.

J Konecny, W Voser.   

Abstract

A very stable esterase (EC 3.1.1.-), which hydrolyses ethyl acetate, cephalosporin C and other acetyl esters with a maximum turnover number of 3-10(2) s-1, was isolated from Bacillus subtilis ATCC 6633 and immobilized on two supports: controlled-pore glass and powdered brick, a representative of carriers having a wide pore-size distribution. Carrier morphology determines diffusion rates and the expression of activity. Rate-limiting mass transfer of buffer leads to apparent losses of activity, gross distortions of molecular pH vs. activity profiles and to apparent deviations from Michaelis-Menten kinetics.

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Year:  1977        PMID: 411518     DOI: 10.1016/0005-2744(77)90172-3

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  2 in total

1.  Purification and characterization of a cephalosporin esterase from Rhodosporidium toruloides.

Authors:  M Politino; S M Tonzi; W V Burnett; G Romancik; J J Usher
Journal:  Appl Environ Microbiol       Date:  1997-12       Impact factor: 4.792

2.  Gene cloning, nucleotide sequence, and expression of a cephalosporin-C deacetylase from Bacillus subtilis.

Authors:  K Mitsushima; A Takimoto; T Sonoyama; S Yagi
Journal:  Appl Environ Microbiol       Date:  1995-06       Impact factor: 4.792

  2 in total

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