Cytochrome P450 Alkane Hydroxylases of the CYP153 Family Are Common in Alkane-Degrading Eubacteria Lacking Integral Membrane Alkane Hydroxylases
Author(s) -
Jan B. van Beilen,
Enrico G. Funhoff,
Alexander van Loon,
Andrea Just,
Leo Kaysser,
Manuel Bouza,
René Holtackers,
Martina Röthlisberger,
Zhi Li,
Bernard Witholt
Publication year - 2006
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.72.1.59-65.2006
Subject(s) - alkane , hydroxylation , ferredoxin , cytochrome p450 , cytochrome , biology , biochemistry , gene , enzyme , pseudomonas putida , monooxygenase , chemistry , catalysis
Several strains that grow on medium-chain-length alkanes and catalyze interesting hydroxylation and epoxidation reactions do not possess integral membrane nonheme iron alkane hydroxylases. Using PCR, we show that most of these strains possess enzymes related to CYP153A1 and CYP153A6, cytochrome P450 enzymes that were characterized as alkane hydroxylases. A vector for the polycistronic coexpression of individual CYP153 genes with a ferredoxin gene and a ferredoxin reductase gene was constructed. Seven of the 11 CYP153 genes tested allowed Pseudomonas putida GPo12 recombinants to grow well on alkanes, providing evidence that the newly cloned P450s are indeed alkane hydroxylases.
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