کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
18351 | 42719 | 2006 | 6 صفحه PDF | دانلود رایگان |
Chitin deacetylase is an enzyme, which catalyses the hydrolysis of N-acetamido bonds of chitin, converting it to chitosan. In the present report we purified the chitin deacetylase from mycelial extracts of a zygomycete Rhizopus nigricans by sequential ammonium sulfate precipitation, CM Sepharose chromatography and DEAE-cellulose chromatography. The progress of enzyme purification was followed by measurement of enzyme activity using partially O-hydroxyethylated chitin (glycol chitin) radiolabelled in N-acetyl groups as a substrate. The apparent molecular mass of chitin deacetylase obtained by SDS-PAGE was approximately 100 kDa. A cDNA library containing a chitin deacetylase gene from R. nigricans was constructed and the complete gene was sequenced. The complete gene contains an open reading frame of 1341 nucleotides, which encodes a sequence of 447 amino acid residues. The estimated molecular mass is 47 kDa, suggesting that carbohydrate content is 53% by weight of the protein. The gene sequence consists of nucleotides encoding a conserved polysaccharide deacetylase domain located in the middle, covering 34% of the entire sequence. Overall, there were eight possible N-linked glycosylation sites. The deduced amino acid sequence shows the highest identity with chitin deacetylases from other zygomycetes Phycomyces blakesleeanus, Gongronella butleri, Rhizopus oryzae and Mucor rouxii (55%, 48%, 43% and 41% identity, respectively).
Journal: Enzyme and Microbial Technology - Volume 39, Issue 6, 3 October 2006, Pages 1294–1299