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PMID: 1935954 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Purification and characterisation of 3-hydroxyphenylacetate 6-hydroxylase: a novel FAD-dependent monooxygenase from a Flavobacterium species.

European journal of biochemistry ·Vol. 201 ·No. 3 ·1991-11-01 ·Pages 585-92

Van Berkel WJ, Van Den Tweel WJ

Abstract

3-Hydroxyphenylacetate 6-hydroxylase was purified 70-fold from a Flavobacterium sp. grown upon phenylacetic acid as its sole carbon and energy source. The presence of FAD and dithiothreitol during purification is essential for high recovery of active enzyme. SDS/PAGE of purified enzyme reveals a single band with a minimum molecular mass of 63 kDa. Analytical gel-filtration, sedimentation-equilibrium and sedimentation-velocity experiments indicate that the purified enzyme exists in solution mainly as a dimer, containing 1 molecule non-covalently bound FAD/subunit. 3-Hydroxyphenylacetate 6-hydroxylase utilizes NADH and NADPH as external electron donors with similar efficiency. The enzyme shows a narrow substrate specificity. Only the primary substrate 3-hydroxyphenylacetate is hydroxylated efficiently, yielding 2,5-dihydroxyphenylacetate as a product. During turnover, the substrate analogues 3,4-dihydroxyphenylacetate and 4-hydroxyphenylacetate are partially hydroxylated, exclusively at the 6' (2') position. The physiological product 2,5-dihydroxyphenylacetate acts as an effector, strongly stimulating NAD(P)H oxidation. The activity of 3-hydroxyphenylacetate 6-hydroxylase is severely inhibited by chloride ions, competitive to the aromatic substrate. In the native state of enzyme, two sulfhydryl groups are accessible to 5,5'-dithiobis(2-nitrobenzoate). Titration with stoichiometric amounts of either 5,5'-dithiobis(2-nitrobenzoate) or mercurial reagents completely blocks enzyme activity. Inactivation by cysteine reagents is inhibited by the substrate 3-hydroxyphenylacetate. The original activity is fully restored by treatment of the modified enzyme with dithiothreitol. The N-terminal amino acid sequence of the enzyme lacks the consensus sequence GXGXXG, found at the N-termini of all flavin-dependent external monooxygenases sequenced so far. The amino acid composition of 3-hydroxyphenylacetate 6-hydroxylase is also presented.

MeSH Terms
Amino Acid Sequence Catalysis Enzyme Stability Flavobacterium/enzymology Kinetics Mixed Function Oxygenases/chemistry,isolation & purification,metabolism Molecular Sequence Data Oxidation-Reduction Spectrophotometry Substrate Specificity Sulfhydryl Compounds/analysis
Chemicals
3-hydroxyphenylacetate 6-hydroxylase Sulfhydryl Compounds Mixed Function Oxygenases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Van Berkel W J
Department of Biochemistry, Agricultural University, Wageningen, The Netherlands.
Van Den Tweel W J
Article Info
Journal
European journal of biochemistry
Abbr.
Eur J Biochem
ISSN
0014-2956
Published
1991-11-01
Pages
585-92
Language
English
Region
England
NLM ID
0107600
Subset
IM
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