O-DEALKYLATION OF COUMARIN AND RESORUFIN ETHERS BY UNICELLULAR GREEN-ALGAE - KINETIC-PROPERTIES OF CHLORELLA-FUSCA AND CHLORELLA-SOROKINIANA

Authors
Citation
F. Thies et Lh. Grimme, O-DEALKYLATION OF COUMARIN AND RESORUFIN ETHERS BY UNICELLULAR GREEN-ALGAE - KINETIC-PROPERTIES OF CHLORELLA-FUSCA AND CHLORELLA-SOROKINIANA, Archives of microbiology, 164(3), 1995, pp. 203-211
Citations number
26
Categorie Soggetti
Microbiology
Journal title
ISSN journal
03028933
Volume
164
Issue
3
Year of publication
1995
Pages
203 - 211
Database
ISI
SICI code
0302-8933(1995)164:3<203:OOCARE>2.0.ZU;2-T
Abstract
O-Dealkylations of resorufin and coumarin ethers, mediated by microsom al cytochrome P450 monooxygenases from animals, plants and microorgani sms, are shown here to be performed also by intact cells of the unicel lular green algae Chlorella fusca and Chlorella sorokiniana. The activ ity of the O-dealkylation of these ethers was up to tenfold higher wit h Chlorella sorokiniana. Both algae dealkylated methyl-, ethyl-, and p entylethers of resorufin and coumarin. Dealkylation in vivo indicated efficient absorption of methoxy- and ethoxyresorufin, confirmed by the respective absorption kinetics. Piperonylbutoxide and 1-aminobenzotri azole, known inhibitors of plant and mammalian cytochrome P450s, signi ficantly inhibited the O-dealkylase activity of both algal strains. Th e use of synchronized cultures of both algae revealed that efficiency of O-dealkylation depends on the stage of the cell cycle: during the g rowth phase, the O-dealkylase activities increased more than proportio nal, and the distinct drop in activity during the last hours of the li ght period indicated the appearance of an endogenous substrate.