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{{enzyme
| Name = Ethylbenzene hydroxylase (Ethylbenzene dehydrogenase)
| EC_number = 1.17.99.2
| CAS_number =
| IUBMB_EC_number = 1/17/99/2
| GO_code =
| image =
| width =
| caption =
}}
In [[enzymology]], an '''ethylbenzene hydroxylase''' ({{EC number|1.17.99.2}}) is an [[enzyme]] that [[catalysis|catalyzes]] the [[chemical reaction]]
 
:ethylbenzene + H<sub>2</sub>O + acceptor <math>\rightleftharpoons</math> (S)-1-phenylethanol + reduced acceptor
 
The 3 [[substrate (biochemistry)|substrates]] of this enzyme are [[ethylbenzene]], [[water|H<sub>2</sub>O]], and [[Electron acceptor|acceptor]], whereas its two [[product (chemistry)|products]] are [[(S)-1-phenylethanol]] and [[reduced acceptor]].
 
This enzyme belongs to the family of [[oxidoreductase]]s, specifically those acting on CH or CH<sub>2</sub> groups with other acceptors. The systematic name of this enzyme class is '''ethylbenzene:acceptor oxidoreductase'''. Other names in common use include '''ethylbenzene dehydrogenase''', and '''ethylbenzene:(acceptor) oxidoreductase'''. This enzyme participates in [[ethylbenzene degradation]] by ''Aromatoleum aromaticum'', a denitrifying bacterium related to the genera ''Azoarcus'' and ''Thauera''. It is a molybdenum enzyme belonging to the [[DMSO reductase]] family. Molybdenum enzymes are distinguished by the presence of a unique active site containing molybdenum atom, one or two [[molybdopterin]]s and additional ligands (i.e. aminoacid residue of Ser, Cys, SeCys or Asp and very often oxygen Mo=O ligand). EBDH is synthesized exclusively in cells grown anaerobically on ethylbenzene and has been identified as a soluble periplasmic protein.
 
==Structural studies==
 
As of late 2007, only one [[tertiary structure|structure]] has been solved for this class of enzymes, with the [[Protein Data Bank|PDB]] accession code {{PDB link|2IVF}}. EBDH consists of three subunits of 96, 43, and 23 kDa, and contains a molybdenum cofactor and a heme b559 cofactor linked by a linear row of five iron-sulfur clusters.
 
==Mechanism==
The reaction is catalyzed by the enzyme using a molybdenum cofactor (MoCo), which in the native state consists of a molybdenum (VI) nucleus ligated by two molybdopterin guanine dinucleotide (MGD) ligands and an aspartic acid residue. Two electrons acquired by the cofactor during the reaction, i.e., the hydroxylation of the hydrocarbon, are then transferred via a chain of iron-sulfur clusters connecting the molybdenum with a heme b cofactor in the alpha subunit, from which the electrons are donated to a yet-unknown acceptor. Notably, EBDH exhibits in vitro activity only with artificial electron acceptors of high redox potential, like the ferricenium ion (E0’= +380 mV). This suggests that its natural electron acceptor may be a periplasmic cytochrome c of similarly high potential, which would couple the ethylbenzene oxidation to the nitrate respiration of ''A. aromaticum''.
 
The EBDH catalytic cycle has two parts: i) oxidation part, where substrate is oxidized to alcohols and the enzyme is reduced to its catalytically inactive form, and ii) enzyme re-oxidation part, where EBDH active site (MoCo) is oxidized and restored to its catalytically active form.
 
Recent theoretical and experimental studies point toward radical C-H activation as the initial reaction and rate limiting step. A possible alternative hydride transfer seems to be less likely. The mechanism concludes with conversion of the hydrocarbon to a carbocation intermediate and rebound of a hydroxide to form the hydroxylated product. Moreover, a histidine residue (His192) of the active site seems to be involved in the reaction mechanism.
 
==References==
{{reflist|1}}
* {{cite journal | author = Kniemeyer O, Heider J | year = 2001 | title = Ethylbenzene Dehydrogenase, a Novel Hydrocarbon-oxidizing Molybdenum/Iron-Sulfur/Heme Enzyme | journal = J. Biol. Chem. | volume = 276 | pages = 21381&ndash;6 | pmid = 11294876 | doi = 10.1074/jbc.M101679200 | issue = 24 }}
* {{cite journal | author = Johnson HA, Pelletier DA, Spormann AM | year = 2001 | title = Isolation and Characterization of Anaerobic Ethylbenzene Dehydrogenase, a Novel Mo-Fe-S Enzyme | journal = J. Bacteriol. | volume = 183 | pages = 4536&ndash;42 | pmid = 11443088 | doi = 10.1128/JB.183.15.4536-4542.2001 | issue = 15 | pmc = 95348 }}
* {{cite journal | author = Szaleniec M, Hagel C, Menke M, Nowak P, Witko M, Heider J | year = 2007 | title = Kinetics and Mechanism of Oxygen-Independent Hydrocarbon Hydroxylation by Ethylbenzene Dehydrogenase | journal = Biochemistry | volume = 46, | pages = 7637&ndash;46 | pmid = 17542621 | doi = 10.1021/bi700633c | issue = 25 }}
* {{cite journal | author = Szaleniec M, Borowski T, Schühle K, Witko M, Heider J | year = 2010 | title = ''Ab Inito'' Modeling of Ethylbenzene Dehydrogenase Reaction Mechanism | journal = J. Am. Chem. Soc. | volume = 132 , | pages = 6014&ndash;24 | pmid = 20387836 | doi = 10.1021/ja907208k | issue = 17 }}
 
[[Category:EC 1.17.99]]
[[Category:Enzymes of known structure]]

Latest revision as of 02:56, 2 March 2013

Template:Enzyme In enzymology, an ethylbenzene hydroxylase (Air Transportation Experts Kull from Wingham, has many interests that include butterflies, property developers in singapore and digital photography. Is a travel freak and in recent past made buy a house in singapore journey to Paleochristian and Byzantine Monuments of Thessalonika.) is an enzyme that catalyzes the chemical reaction

ethylbenzene + H2O + acceptor (S)-1-phenylethanol + reduced acceptor

The 3 substrates of this enzyme are ethylbenzene, H2O, and acceptor, whereas its two products are (S)-1-phenylethanol and reduced acceptor.

This enzyme belongs to the family of oxidoreductases, specifically those acting on CH or CH2 groups with other acceptors. The systematic name of this enzyme class is ethylbenzene:acceptor oxidoreductase. Other names in common use include ethylbenzene dehydrogenase, and ethylbenzene:(acceptor) oxidoreductase. This enzyme participates in ethylbenzene degradation by Aromatoleum aromaticum, a denitrifying bacterium related to the genera Azoarcus and Thauera. It is a molybdenum enzyme belonging to the DMSO reductase family. Molybdenum enzymes are distinguished by the presence of a unique active site containing molybdenum atom, one or two molybdopterins and additional ligands (i.e. aminoacid residue of Ser, Cys, SeCys or Asp and very often oxygen Mo=O ligand). EBDH is synthesized exclusively in cells grown anaerobically on ethylbenzene and has been identified as a soluble periplasmic protein.

Structural studies

As of late 2007, only one structure has been solved for this class of enzymes, with the PDB accession code Template:PDB link. EBDH consists of three subunits of 96, 43, and 23 kDa, and contains a molybdenum cofactor and a heme b559 cofactor linked by a linear row of five iron-sulfur clusters.

Mechanism

The reaction is catalyzed by the enzyme using a molybdenum cofactor (MoCo), which in the native state consists of a molybdenum (VI) nucleus ligated by two molybdopterin guanine dinucleotide (MGD) ligands and an aspartic acid residue. Two electrons acquired by the cofactor during the reaction, i.e., the hydroxylation of the hydrocarbon, are then transferred via a chain of iron-sulfur clusters connecting the molybdenum with a heme b cofactor in the alpha subunit, from which the electrons are donated to a yet-unknown acceptor. Notably, EBDH exhibits in vitro activity only with artificial electron acceptors of high redox potential, like the ferricenium ion (E0’= +380 mV). This suggests that its natural electron acceptor may be a periplasmic cytochrome c of similarly high potential, which would couple the ethylbenzene oxidation to the nitrate respiration of A. aromaticum.

The EBDH catalytic cycle has two parts: i) oxidation part, where substrate is oxidized to alcohols and the enzyme is reduced to its catalytically inactive form, and ii) enzyme re-oxidation part, where EBDH active site (MoCo) is oxidized and restored to its catalytically active form.

Recent theoretical and experimental studies point toward radical C-H activation as the initial reaction and rate limiting step. A possible alternative hydride transfer seems to be less likely. The mechanism concludes with conversion of the hydrocarbon to a carbocation intermediate and rebound of a hydroxide to form the hydroxylated product. Moreover, a histidine residue (His192) of the active site seems to be involved in the reaction mechanism.

References

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