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2-hydroxy-6-oxonona-2,4-dienedioate hydrolase

2-hydroxy-6-oxonona-2,4-dienedioate hydrolase (EC 3.7.1.14, mhpC (gene)) is an enzyme with systematic name (2Z,4E)-2-hydroxy-6-oxona-2,4-dienedioate succinylhydrolase.[1][2][3][4][5][6] This enzyme catalyses the following chemical reaction:

  1. (2Z,4E)-2-hydroxy-6-oxonona-2,4-diene-1,9-dioate + H2O (2Z)-2-hydroxypenta-2,4-dienoate + succinate
  2. (2Z,4E,7E)-2-hydroxy-6-oxonona-2,4,7-triene-1,9-dioate + H2O (2Z)-2-hydroxypenta-2,4-dienoate + fumarate
2-hydroxy-6-oxonona-2,4-dienedioate hydrolase
Identifiers
EC no.3.7.1.14
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Search
PMCarticles
PubMedarticles
NCBIproteins

This enzyme catalyses a step in a pathway of phenylpropanoid compounds degradation.

References edit

  1. ^ Burlingame R, Chapman PJ (July 1983). "Catabolism of phenylpropionic acid and its 3-hydroxy derivative by Escherichia coli". Journal of Bacteriology. 155 (1): 113–21. PMC 217659. PMID 6345502.
  2. ^ Burlingame RP, Wyman L, Chapman PJ (October 1986). "Isolation and characterization of Escherichia coli mutants defective for phenylpropionate degradation". Journal of Bacteriology. 168 (1): 55–64. PMC 213419. PMID 3531186.
  3. ^ Lam WW, Bugg TD (1994). "Chemistry of extradiol aromatic ring cleavage: isolation of a stable dienol ring fission intermediate and stereochemistry of its enzymatic hydrolytic cleavage". J. Chem. Soc., Chem. Commun. 10 (10): 1163–1164. doi:10.1039/c39940001163.
  4. ^ Lam WW, Bugg TD (October 1997). "Purification, characterization, and stereochemical analysis of a C-C hydrolase: 2-hydroxy-6-keto-nona-2,4-diene-1,9-dioic acid 5,6-hydrolase". Biochemistry. 36 (40): 12242–51. doi:10.1021/bi971115r. PMID 9315862.
  5. ^ Ferrández A, Garciá JL, Díaz E (April 1997). "Genetic characterization and expression in heterologous hosts of the 3-(3-hydroxyphenyl)propionate catabolic pathway of Escherichia coli K-12". Journal of Bacteriology. 179 (8): 2573–81. PMC 179006. PMID 9098055.
  6. ^ Díaz E, Ferrández A, García JL (June 1998). "Characterization of the hca cluster encoding the dioxygenolytic pathway for initial catabolism of 3-phenylpropionic acid in Escherichia coli K-12". Journal of Bacteriology. 180 (11): 2915–23. PMC 107259. PMID 9603882.

External links edit

hydroxy, oxonona, dienedioate, hydrolase, mhpc, gene, enzyme, with, systematic, name, hydroxy, oxona, dienedioate, succinylhydrolase, this, enzyme, catalyses, following, chemical, reaction, hydroxy, oxonona, diene, dioate, displaystyle, rightleftharpoons, hydr. 2 hydroxy 6 oxonona 2 4 dienedioate hydrolase EC 3 7 1 14 mhpC gene is an enzyme with systematic name 2Z 4E 2 hydroxy 6 oxona 2 4 dienedioate succinylhydrolase 1 2 3 4 5 6 This enzyme catalyses the following chemical reaction 2Z 4E 2 hydroxy 6 oxonona 2 4 diene 1 9 dioate H2O displaystyle rightleftharpoons 2Z 2 hydroxypenta 2 4 dienoate succinate 2Z 4E 7E 2 hydroxy 6 oxonona 2 4 7 triene 1 9 dioate H2O displaystyle rightleftharpoons 2Z 2 hydroxypenta 2 4 dienoate fumarate2 hydroxy 6 oxonona 2 4 dienedioate hydrolaseIdentifiersEC no 3 7 1 14DatabasesIntEnzIntEnz viewBRENDABRENDA entryExPASyNiceZyme viewKEGGKEGG entryMetaCycmetabolic pathwayPRIAMprofilePDB structuresRCSB PDB PDBe PDBsumSearchPMCarticlesPubMedarticlesNCBIproteins This enzyme catalyses a step in a pathway of phenylpropanoid compounds degradation References edit Burlingame R Chapman PJ July 1983 Catabolism of phenylpropionic acid and its 3 hydroxy derivative by Escherichia coli Journal of Bacteriology 155 1 113 21 PMC 217659 PMID 6345502 Burlingame RP Wyman L Chapman PJ October 1986 Isolation and characterization of Escherichia coli mutants defective for phenylpropionate degradation Journal of Bacteriology 168 1 55 64 PMC 213419 PMID 3531186 Lam WW Bugg TD 1994 Chemistry of extradiol aromatic ring cleavage isolation of a stable dienol ring fission intermediate and stereochemistry of its enzymatic hydrolytic cleavage J Chem Soc Chem Commun 10 10 1163 1164 doi 10 1039 c39940001163 Lam WW Bugg TD October 1997 Purification characterization and stereochemical analysis of a C C hydrolase 2 hydroxy 6 keto nona 2 4 diene 1 9 dioic acid 5 6 hydrolase Biochemistry 36 40 12242 51 doi 10 1021 bi971115r PMID 9315862 Ferrandez A Garcia JL Diaz E April 1997 Genetic characterization and expression in heterologous hosts of the 3 3 hydroxyphenyl propionate catabolic pathway of Escherichia coli K 12 Journal of Bacteriology 179 8 2573 81 PMC 179006 PMID 9098055 Diaz E Ferrandez A Garcia JL June 1998 Characterization of the hca cluster encoding the dioxygenolytic pathway for initial catabolism of 3 phenylpropionic acid in Escherichia coli K 12 Journal of Bacteriology 180 11 2915 23 PMC 107259 PMID 9603882 External links edit2 hydroxy 6 oxonona 2 4 dienedioate hydrolase at the U S National Library of Medicine Medical Subject Headings MeSH Portal nbsp Biology Retrieved from https en wikipedia org w index php title 2 hydroxy 6 oxonona 2 4 dienedioate hydrolase amp oldid 1172334855, wikipedia, wiki, book, books, library,

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