Abstract | AIMS: METHODS AND RESULTS: Site-directed mutagenesis of the conserved aromatic residues of PKD domain was performed by PCR. The aromatic residues, W30, Y48, W64 and W67, were replaced by alanine, and single- and double-mutant chitinases were produced in Escherichia coli XL10 and purified with HisTrap column. Single mutations were not quite effective on the hydrolysing activities against chitinous substrates when compared with wild-type ChiA. However, mutations of W30 and W67 decreased the activities against powdered chitin by 87.6%. Wild-type and mutant PKD domains were produced in E. coli TOP10 and purified with glutathione- Sepharose 4B column. Wild-type PKD domain showed significant binding activity to powdered chitin, whereas mutations of W30 and W67 reduced the binding activity to powdered chitin drastically. These results suggest that PKD domain of ChiA is essential for effective hydrolysis of powdered chitin through the interaction between two aromatic residues and chitin molecule. CONCLUSIONS: PKD domain of ChiA participates in the effective hydrolysis of powdered chitin through the interaction between two aromatic residues (W30 and W67) and chitin molecule. SIGNIFICANCE AND IMPACT OF THE STUDY: The findings of this study provide important information on chitin degradation by microbial chitinases.
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Authors | H Orikoshi, S Nakayama, C Hanato, K Miyamoto, H Tsujibo |
Journal | Journal of applied microbiology
(J Appl Microbiol)
Vol. 99
Issue 3
Pg. 551-7
( 2005)
ISSN: 1364-5072 [Print] England |
PMID | 16108796
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Bacterial Proteins
- Culture Media
- Recombinant Proteins
- Chitin
- Chitinases
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Topics |
- Adsorption
- Alteromonas
(enzymology)
- Amino Acid Sequence
- Bacterial Proteins
- Chitin
(genetics, metabolism)
- Chitinases
(genetics, metabolism)
- Culture Media
- Hydrolysis
- Mutagenesis
(genetics)
- Mutation
- Polycystic Kidney Diseases
(genetics)
- Recombinant Proteins
- Sequence Alignment
(methods)
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