Biology:Chitin synthase
| chitin synthase | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||
| EC number | 2.4.1.16 | ||||||||
| CAS number | 9030-18-6 | ||||||||
| 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 / QuickGO | ||||||||
| |||||||||
In enzymology, a chitin synthase (EC 2.4.1.16) is an enzyme that catalyzes the chemical reaction
- UDP-N-acetyl-D-glucosamine + [1,4-(N-acetyl-beta-D-glucosaminyl)]n [math]\displaystyle{ \rightleftharpoons }[/math] UDP + [1,4-(N-acetyl-beta-D-glucosaminyl)]n+1
Thus, the two substrates of this enzyme are UDP-N-acetyl-D-glucosamine and [1,4-(N-acetyl-beta-D-glucosaminyl)]n, whereas its two products are UDP and [1,4-(N-acetyl-beta-D-glucosaminyl)]n+1.
This enzyme belongs to the family of glycosyltransferases, specifically the hexosyltransferases. The systematic name of this enzyme class is UDP-N-acetyl-D-glucosamine:chitin 4-beta-N-acetylglucosaminyl-transferase. Other names in common use include chitin-UDP N-acetylglucosaminyltransferase, chitin-uridine diphosphate acetylglucosaminyltransferase, chitin synthetase, and trans-N-acetylglucosaminosylase. This enzyme participates in aminosugars metabolism.
Production
Chitin Synthase is manufactured in the rough endoplasmic reticulum of fungi as the inactive form, zymogen. The zymogen is then packaged into chitosomes in the golgi apparatus. Chitosomes bring the zymogen to the hyphal tip of a mold or yeast cell membrane. Chitin synthase is placed into the interior side of the cell membrane and then activated.[citation needed]
References
- "The synthesis of chitin in cell-free extracts of Neurospora crassa". J. Biol. Chem. 228 (2): 729–42. 1957. PMID 13475355.
- "Chitin synthetase 2, a presumptive participant in septum formation in Saccharomyces cerevisiae". J. Biol. Chem. 261 (32): 15147–52. 1986. PMID 2945823.
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