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- W2120092337 abstract "ABSTRACT 4-Ethylphenol methylenehydroxylase from Pseudomonas putida JD1 acts by dehydrogenation of its substrate to give a quinone methide, which is then hydrated to an alcohol. It was shown to be active with a range of 4-alkylphenols as substrates. 4- n -Propylphenol, 4- n -butylphenol, chavicol, and 4-hydroxydiphenylmethane were hydroxylated on the methylene group next to the benzene ring and produced the corresponding chiral alcohol as the major product. The alcohols 1-(4′-hydroxyphenyl)propanol and 1-(4′-hydroxyphenyl)-2-propen-1-ol, produced by the biotransformation of 4- n -propylphenol and chavicol, respectively, were shown to be R (+) enantiomers. 5-Indanol, 6-hydroxytetralin, 4-isopropylphenol, and cyclohexylphenol, with cyclic or branched alkyl groups, gave the corresponding vinyl compounds as their major products." @default.
- W2120092337 created "2016-06-24" @default.
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- W2120092337 date "2003-06-01" @default.
- W2120092337 modified "2023-10-17" @default.
- W2120092337 title "Alkylphenol Biotransformations Catalyzed by 4-Ethylphenol Methylenehydroxylase" @default.
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- W2120092337 doi "https://doi.org/10.1128/aem.69.6.3650-3652.2003" @default.
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