1.14.13.84: 4-hydroxyacetophenone monooxygenase
This is an abbreviated version!
For detailed information about 4-hydroxyacetophenone monooxygenase, go to the full flat file.
Word Map on EC 1.14.13.84
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1.14.13.84
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baeyer-villiger
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fluorescens
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ketones
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bvmos
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acetophenones
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cyclohexanone
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nadph-dependent
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biocatalytic
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putida
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enantioselectivity
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resin
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base-catalysed
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stabilised
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ring-substituted
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characterise
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fad
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flavoproteins
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synthesis
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4-fluorophenol
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fluorophenyl
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fluoride
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flavin-containing
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synthons
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4-fluorocatechol
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sulfides
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lactones
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fluorinated
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noncovalent
- 1.14.13.84
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baeyer-villiger
- fluorescens
- ketones
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bvmos
- acetophenones
- cyclohexanone
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nadph-dependent
-
biocatalytic
- putida
-
enantioselectivity
- resin
-
base-catalysed
-
stabilised
-
ring-substituted
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characterise
- fad
- flavoproteins
- synthesis
- 4-fluorophenol
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fluorophenyl
- fluoride
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flavin-containing
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synthons
- 4-fluorocatechol
- sulfides
- lactones
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fluorinated
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noncovalent
Reaction
Synonyms
4-hydroxyacetophenone monooxygenase, arylketone monooxygenase, Baeyer-Villiger monooxygenase, hAPA, HAPMO, More, oxygenase, 4-hydroxyacetophenone mono-
ECTree
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General Information on EC 1.14.13.84 - 4-hydroxyacetophenone monooxygenase
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GENERAL INFORMATION 
ORGANISM
UNIPROT
COMMENTARY 
LITERATURE
metabolism
metabolism
recombinant Baeyer-Villiger monooxygenases converts arylaliphatic ketones into the corresponding esters with preference for para-substitution at the aromatic ring, oxidation of aldehydes and some heteroaromatic compounds are also converted while cycloketones and open-chain ketones are not or poorly accepted as substrates, aromatic ketones such as 3-phenyl-2-butanone are oxidized with excellent enantioselectivity
metabolism
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recombinant Baeyer-Villiger monooxygenases converts arylaliphatic ketones into the corresponding esters with preference for para-substitution at the aromatic ring, oxidation of aldehydes and some heteroaromatic compounds are also converted while cycloketones and open-chain ketones are not or poorly accepted as substrates, aromatic ketones such as 3-phenyl-2-butanone are oxidized with excellent enantioselectivity
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