Advanced Synthesis & Catalysis · 2002 · 57 citations · 98 references
Life SciencesBiochemistryBiotechnologyBiocatalysisEnzyme MechanismEnzymologyBiocatalytic OxidationCatalytic MechanismsEnzyme DiscoveryFlavin-containing MonooxygenasesRedox EnzymesBiocatalytic SynthesisDirected Random MutagenesisMonooxygenase CatalysisPhenolic CompoundsPhenolic SubstratesPolyphenol OxidasesRandom MutagenesisRegioselectivity
Flavin-dependent monooxygenases and oxidases play an important role in the mineralization of phenolic compounds. Because of their exquisite regioselectivity and stereoselectivity, these enzymes are of interest for the biocatalytic production of fine chemicals and food ingredients. In our group, we have characterized several flavoenzymes that act on phenolic compounds, including 4-hydroxybenzoate 3-hydroxylase, 3-hydroxyphenylacetate 6-hydroxylase, 4-hydroxybenzoate 1-hydroxylase (decarboxylating), hydroquinone hydroxylase, 2-hydroxybiphenyl 3-monooxygenase, phenol hydroxylase, 4-hydroxyacetophenone monooxygenase and vanillyl-alcohol oxidase. The catalytic properties of these enzymes are reviewed here, together with insights obtained from site-directed and random mutagenesis.
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Philip J. Geary · Biochemical Society Transactions · 1977 · 805 citations
Structural proteomics of an archaeon.
A.M. Edwards, C.H. Arrowsmith, Dinesh Christendat et al. · Nature Structural Biology · 2000 · 291 citations