Literature DB >> 3690421

alpha-Santonin 1,2-reductase and its role in the formation of dihydrosantonin and lumisantonin by Pseudomonas cichorii S.

U Naik1, S Mavuinkurve.   

Abstract

1,2-Dihydrosantonin is the first stable product in the degradative pathway of alpha-santonin by Pseudomonas cichorii S. Its formation is catalyzed by an oxidoreductase, which is NADH or NADPH dependent and has an apparent Km value of 66.66 microM for santonin and 44.33 microM for NADH. The enzyme activity is stable at pH 6.0, 7.0, and 8.0, and is not affected by EDTA and divalent metal ions. It is postulated that the enzymic reduction of santonin occurs via formation of a transient zwitterionic intermediate, which undergoes nonenzymatic 1,4-sigmatropic rearrangement to yield lumisantonin during the solvent extraction process. Lumisantonin is, thus, not a true metabolic intermediate but an artifact.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3690421     DOI: 10.1139/m87-115

Source DB:  PubMed          Journal:  Can J Microbiol        ISSN: 0008-4166            Impact factor:   2.419


  1 in total

1.  Periplasmically located α-santonin binding factor in Sphingomonas paucimobilis strain S ATCC 43388.

Authors:  M Shailaja Raj; I Furtado; S Mavinkurve
Journal:  Indian J Microbiol       Date:  2008-01-11       Impact factor: 2.461

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.