Literature DB >> 20000468

Studies on the mechanism of p-hydroxyphenylacetate 3-hydroxylase from Pseudomonas aeruginosa: a system composed of a small flavin reductase and a large flavin-dependent oxygenase.

Sumita Chakraborty1, Mariliz Ortiz-Maldonado, Barrie Entsch, David P Ballou.   

Abstract

There are two known types of microbial two-component flavin-dependent monooxygenases that catalyze oxygenation of p-hydroxyphenylacetate (HPA), and they are distinguished by having structurally distinct reductases and oxygenases. This paper presents a detailed analysis of the properties of the enzyme from Pseudomonas aeruginosa, an example of one group, and compares its properties to those published for the Acinetobacter baumannii enzyme, an example of the alternative group. The reductase and oxygenase from P. aeruginosa were expressed in Escherichia coli. The reductase was purified as a stable C-terminally His-tagged yellow protein containing weakly bound FAD, and the oxygenase was purified as a stable colorless N-terminally His-tagged protein. The reductase catalyzes the reduction of FAD by NADH and releases the FADH(-) product into solution, but unlike the reductase from A. baumannii, this catalysis is not influenced by HPA. The oxygenase binds the released FADH(-) and catalyzes the oxygenation of HPA to form 3,4-dihydroxyphenylacetate, after which the FAD dissociates to be re-reduced by the reductase, a common overall pattern for two-component flavin-dependent oxygenases. With this system, it appears that interactions between the reductase and the oxygenase can facillitate the transfer of FADH(-) to the oxygenase, although they are not required. We show that the P. aeruginosa oxygenase system in complex with FADH(-) reacts with O(2) to form a quasi-stable, unusually high-extinction flavin hydroperoxide species that binds HPA and reacts to form the product. The resultant flavin hydroxide decomposes to FAD and water while still bound to the oxygenase and then releases product and FAD from the protein. Unlike the enzyme from A. baumannii, during normal catalysis involving both the reductase and oxygenase, the rate-determining step in catalysis is the dissociation of FAD from the oxygenase in a process that is independent of the concentration of HPA. Structures for the reductases and oxygenases from A. baumannii and from Thermus thermophilus (similar to the P. aeruginosa system) form a basis for interpreting the molecular origins of the differences between the two groups of flavin-dependent two-component oxygenases.

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Year:  2010        PMID: 20000468      PMCID: PMC2806516          DOI: 10.1021/bi901454u

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  25 in total

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Authors:  U Arunachalam; V Massey; C S Vaidyanathan
Journal:  J Biol Chem       Date:  1992-12-25       Impact factor: 5.157

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Authors:  Q H GIBSON; B E SWOBODA; V MASSEY
Journal:  J Biol Chem       Date:  1964-11       Impact factor: 5.157

Review 3.  Protein dynamics and electrostatics in the function of p-hydroxybenzoate hydroxylase.

Authors:  Barrie Entsch; Lindsay J Cole; David P Ballou
Journal:  Arch Biochem Biophys       Date:  2005-01-01       Impact factor: 4.013

Review 4.  Biosynthesis of flavocoenzymes.

Authors:  Markus Fischer; Adelbert Bacher
Journal:  Nat Prod Rep       Date:  2005-04-21       Impact factor: 13.423

5.  Evidence for flavin movement in the function of p-hydroxybenzoate hydroxylase from studies of the mutant Arg220Lys.

Authors:  G R Moran; B Entsch; B A Palfey; D P Ballou
Journal:  Biochemistry       Date:  1996-07-16       Impact factor: 3.162

6.  Crystal structure of the p-hydroxybenzoate hydroxylase-substrate complex refined at 1.9 A resolution. Analysis of the enzyme-substrate and enzyme-product complexes.

Authors:  H A Schreuder; P A Prick; R K Wierenga; G Vriend; K S Wilson; W G Hol; J Drenth
Journal:  J Mol Biol       Date:  1989-08-20       Impact factor: 5.469

7.  Oxidation of reduced flavins by quinones.

Authors:  M J Gibian; J A Rynd
Journal:  Biochem Biophys Res Commun       Date:  1969-03-10       Impact factor: 3.575

8.  A sensitive method for the determination of RNA in DNA and vice versa.

Authors:  D S Duch; M Laskowski
Journal:  Anal Biochem       Date:  1971-11       Impact factor: 3.365

9.  Catalytic mechanism of p-hydroxybenzoate hydroxylase with p-mercaptobenzoate as substrate.

Authors:  B Entsch; D P Ballou; M Husain; V Massey
Journal:  J Biol Chem       Date:  1976-12-10       Impact factor: 5.157

10.  Flavin-oxygen derivatives involved in hydroxylation by p-hydroxybenzoate hydroxylase.

Authors:  B Entsch; D P Ballou; V Massey
Journal:  J Biol Chem       Date:  1976-05-10       Impact factor: 5.157

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  16 in total

1.  Interactions with the substrate phenolic group are essential for hydroxylation by the oxygenase component of p-hydroxyphenylacetate 3-hydroxylase.

Authors:  Chanakan Tongsook; Jeerus Sucharitakul; Kittisak Thotsaporn; Pimchai Chaiyen
Journal:  J Biol Chem       Date:  2011-11-03       Impact factor: 5.157

2.  The C-terminal domain of 4-hydroxyphenylacetate 3-hydroxylase from Acinetobacter baumannii is an autoinhibitory domain.

Authors:  Thanawat Phongsak; Jeerus Sucharitakul; Kittisak Thotsaporn; Worrapoj Oonanant; Jirundon Yuvaniyama; Jisnuson Svasti; David P Ballou; Pimchai Chaiyen
Journal:  J Biol Chem       Date:  2012-06-03       Impact factor: 5.157

3.  StyA1 and StyA2B from Rhodococcus opacus 1CP: a multifunctional styrene monooxygenase system.

Authors:  Dirk Tischler; René Kermer; Janosch A D Gröning; Stefan R Kaschabek; Willem J H van Berkel; Michael Schlömann
Journal:  J Bacteriol       Date:  2010-07-30       Impact factor: 3.490

4.  pH-dependent studies reveal an efficient hydroxylation mechanism of the oxygenase component of p-hydroxyphenylacetate 3-hydroxylase.

Authors:  Nantidaporn Ruangchan; Chanakan Tongsook; Jeerus Sucharitakul; Pimchai Chaiyen
Journal:  J Biol Chem       Date:  2010-10-28       Impact factor: 5.157

5.  Hydrolase CehA and Monooxygenase CfdC Are Responsible for Carbofuran Degradation in Sphingomonas sp. Strain CDS-1.

Authors:  Xin Yan; Wen Jin; Guang Wu; Wankui Jiang; Zhangong Yang; Junbin Ji; Jiguo Qiu; Jian He; Jiandong Jiang; Qing Hong
Journal:  Appl Environ Microbiol       Date:  2018-08-01       Impact factor: 4.792

6.  Kinetic Mechanism of the Dechlorinating Flavin-dependent Monooxygenase HadA.

Authors:  Panu Pimviriyakul; Kittisak Thotsaporn; Jeerus Sucharitakul; Pimchai Chaiyen
Journal:  J Biol Chem       Date:  2017-02-03       Impact factor: 5.157

Review 7.  Monooxygenation of aromatic compounds by flavin-dependent monooxygenases.

Authors:  Pirom Chenprakhon; Thanyaporn Wongnate; Pimchai Chaiyen
Journal:  Protein Sci       Date:  2019-01       Impact factor: 6.725

8.  Stabilization of C4a-hydroperoxyflavin in a two-component flavin-dependent monooxygenase is achieved through interactions at flavin N5 and C4a atoms.

Authors:  Kittisak Thotsaporn; Pirom Chenprakhon; Jeerus Sucharitakul; Andrea Mattevi; Pimchai Chaiyen
Journal:  J Biol Chem       Date:  2011-06-16       Impact factor: 5.157

9.  Crystallization and preliminary X-ray analysis of the reductase component of p-hydroxyphenylacetate 3-hydroxylase from Acinetobacter baumannii.

Authors:  Worrapoj Oonanant; Jeerus Sucharitakul; Pimchai Chaiyen; Jirundon Yuvaniyama
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2012-05-24

10.  PqsL uses reduced flavin to produce 2-hydroxylaminobenzoylacetate, a preferred PqsBC substrate in alkyl quinolone biosynthesis in Pseudomonas aeruginosa.

Authors:  Steffen Lorenz Drees; Simon Ernst; Benny Danilo Belviso; Nina Jagmann; Ulrich Hennecke; Susanne Fetzner
Journal:  J Biol Chem       Date:  2018-04-18       Impact factor: 5.157

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