2-pyrone-4,6-dicarboxylate lactonase
| 2-pyrone-4,6-dicarboxylate lactonase (LigI) | |||||||||
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| Identifiers | |||||||||
| EC number | 3.1.1.57 | ||||||||
| CAS number | 84177-55-9 | ||||||||
| Databases | |||||||||
| IntEnz | IntEnz view | ||||||||
| BRENDA | BRENDA entry | ||||||||
| ExPASy | NiceZyme view | ||||||||
| KEGG | KEGG entry | ||||||||
| MetaCyc | metabolic pathway | ||||||||
| PRIAM | profile | ||||||||
| PDB structures | RCSB PDB PDBe PDBsum | ||||||||
| Gene Ontology | AmiGO / EGO | ||||||||
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In enzymology, 2-pyrone-4,6-dicarboxylate lactonase (EC 3.1.1.57) is an enzyme that catalyzes the reversible hydrolytic chemical reaction
- 2-pyrone-4,6-dicarboxylate + H2O
4-carboxy-2-hydroxyhexa-2,4-dienedioate and 4-oxalomesaconate
Thus, the two substrates of this enzyme are 2-pyrone-4,6-dicarboxylate[1] and H2O, whereas its product is a tautomeric mixture of 4-oxalomesaconate[2] and 4-carboxy-2-hydroxymuconate.[3]
This enzyme belongs to the Amidohydrolase superfamily of enzymes and is a member of Cluster of Orthologous Groups (COG) 3618. The systematic name of this enzyme is 2-pyrone-4,6-dicarboxylate lactonase but is also known as LigI. This enzyme is found to play an important role in the metabolism of lignin-derived aromatic compounds in both the syringate degradation pathway[4] and the protocatechuate 4,5-cleavage pathway.[5]
LigI from Sphingomonas is of particular interest as it has been shown to be the first member of the amidohydrolase superfamily to not require a divalent metal cation for catalytic activity.[6]
Mechanism
The mechanism of catalysis of LigI has been determined by crystallography and NMR analysis. More specifically, the hydrolytic water molecule is activated by the transfer of a proton to Asp-248 whereas the carbonyl group of the 2-pyrone-4,6-dicarboxylate (PDC) lactone substrate is activated by hydrogen bonding interactions with His-180, His-31, and His-33.[6]
References
- ↑ "2-pyrone-4,6-dicarboxylate". MetaCyc. SRI International.
- ↑ "(1E)-4-oxobut-1-ene-1,2,4-tricarboxylate". MetaCyc. SRI International.
- ↑ "(1Z,3Z)-4-hydroxybuta-1,3-diene-1,2,4-tricarboxylate". MetaCyc. SRI International.
- ↑ "syringate degradation". MetaCyc. SRI International.
- ↑ "protocatechuate degradation I (meta-cleavage pathway)". MetaCyc. SRI International.
- 1 2 Hobbs ME, Malashkevich V, Williams HJ, Xu C, Sauder JM, Burley SK, Almo SC, Raushel FM (April 2012). "Structure and Catalytic Mechanism of LigI: Insight into the Amidohydrolase Enzymes of cog3618 and Lignin Degradation". Biochemistry 51 (16): 3497–507. doi:10.1021/bi300307b. PMID 22475079.
Further reading
- Kersten PJ, Dagley S, Whittaker JW, Arciero DM, Lipscomb JD (1982). "2-pyrone-4,6-dicarboxylic acid, a catabolite of gallic acids in Pseudomonas species". J. Bacteriol. 152 (3): 1154–62. PMC 221622. PMID 7142106.
- Maruyama K (February 1983). "Purification and properties of 2-pyrone-4,6-dicarboxylate hydrolase". J. Biochem. 93 (2): 557–65. PMID 6841353.
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