Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2006-1-10
pubmed:abstractText
Cytochromes P450cam and P450BM3 oxidize alpha- and beta-thujone into multiple products, including 7-hydroxy-alpha-(or beta-)thujone, 7,8-dehydro-alpha-(or beta-)thujone, 4-hydroxy-alpha-(or beta-)thujone, 2-hydroxy-alpha-(or beta-)thujone, 5-hydroxy-5-isopropyl-2-methyl-2-cyclohexen-1-one, 4,10-dehydrothujone, and carvacrol. Quantitative analysis of the 4-hydroxylated isomers and the ring-opened product indicates that the hydroxylation proceeds via a radical mechanism with a radical recombination rate ranging from 0.7 +/- 0.3 x 10(10) s(-1) to 12.5 +/- 3 x 10(10) s(-1) for the trapping of the carbon radical by the iron-bound hydroxyl radical equivalent. 7-[2H]-alpha-Thujone has been synthesized and used to amplify C-4 hydroxylation in situations where uninformative C-7 hydroxylation is the dominant reaction. The involvement of a carbon radical intermediate is confirmed by the observation of inversion of stereochemistry of the methyl-substituted C-4 carbon during the hydroxylation. With an L244A mutation that slightly increases the P450(cam) active-site volume, this inversion is observed in up to 40% of the C-4 hydroxylated products. The oxidation of alpha-thujone by human CYP1A2, CYP2C9, CYP2C19, CYP2D6, CYP2E1, and CYP3A4 occurs with up to 80% C-4 methyl inversion, in agreement with a dominant radical hydroxylation mechanism. Three minor desaturation products are produced, with at least one of them via a cationic pathway. The cation involved is proposed to form by electron abstraction from a radical intermediate. The absence of a solvent deuterium isotope effect on product distribution in the P450cam reaction precludes a significant role for the P450 ferric hydroperoxide intermediate in substrate hydroxylation. The results indicate that carbon hydroxylation is catalyzed exclusively by a P450 ferryl species via radical intermediates whose detailed properties are substrate- and enzyme-dependent.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-1027445, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-10725394, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-10913233, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-11308346, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-11368559, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-12022835, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-12643683, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-15237977, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-15258138, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-15307740, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-15787531, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-15994329, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-1742281, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-2510153, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-3138238, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-656092, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-8369287, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-8424677, http://linkedlifedata.com/resource/pubmed/commentcorrection/16401082-9649301
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Alanine, http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Proteins, http://linkedlifedata.com/resource/pubmed/chemical/CYP1A2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/CYP3A protein, human, http://linkedlifedata.com/resource/pubmed/chemical/CYP3A4 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Camphor 5-Monooxygenase, http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 CYP1A2, http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 CYP2D6, http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 CYP3A, http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 Enzyme System, http://linkedlifedata.com/resource/pubmed/chemical/Deuterium Oxide, http://linkedlifedata.com/resource/pubmed/chemical/Free Radicals, http://linkedlifedata.com/resource/pubmed/chemical/Leucine, http://linkedlifedata.com/resource/pubmed/chemical/Monoterpenes, http://linkedlifedata.com/resource/pubmed/chemical/beta-thujone
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0006-2960
pubmed:author
pubmed:issnType
Print
pubmed:day
17
pubmed:volume
45
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
533-42
pubmed:dateRevised
2011-4-14
pubmed:meshHeading
pubmed-meshheading:16401082-Alanine, pubmed-meshheading:16401082-Amino Acid Substitution, pubmed-meshheading:16401082-Bacterial Proteins, pubmed-meshheading:16401082-Camphor 5-Monooxygenase, pubmed-meshheading:16401082-Catalysis, pubmed-meshheading:16401082-Cytochrome P-450 CYP1A2, pubmed-meshheading:16401082-Cytochrome P-450 CYP2D6, pubmed-meshheading:16401082-Cytochrome P-450 CYP3A, pubmed-meshheading:16401082-Cytochrome P-450 Enzyme System, pubmed-meshheading:16401082-Deuterium Oxide, pubmed-meshheading:16401082-Free Radicals, pubmed-meshheading:16401082-Gas Chromatography-Mass Spectrometry, pubmed-meshheading:16401082-Humans, pubmed-meshheading:16401082-Hydrogen-Ion Concentration, pubmed-meshheading:16401082-Hydroxylation, pubmed-meshheading:16401082-Isomerism, pubmed-meshheading:16401082-Leucine, pubmed-meshheading:16401082-Monoterpenes, pubmed-meshheading:16401082-Oxidation-Reduction
pubmed:year
2006
pubmed:articleTitle
Radical intermediates in the catalytic oxidation of hydrocarbons by bacterial and human cytochrome P450 enzymes.
pubmed:affiliation
Department of Pharmaceutical Chemistry, University of California, 600 16th Street, San Francisco, California 94143-2280, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural