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Enzymatic properties of wild‐type and active site mutants of chitinase A from Vibrio carchariae , as revealed by HPLC‐MS
Author(s) -
Suginta Wipa,
Vongsuwan Archara,
Songsiriritthigul Chomphunuch,
Svasti Jisnuson,
Prinz Heino
Publication year - 2005
Publication title -
the febs journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 204
eISSN - 1742-4658
pISSN - 1742-464X
DOI - 10.1111/j.1742-4658.2005.04753.x
Subject(s) - chitinase , enzyme , mutant , chemistry , high performance liquid chromatography , wild type , biochemistry , vibrio , biology , chromatography , microbiology and biotechnology , bacteria , gene , genetics
The enzymatic properties of chitinase A from Vibrio carchariae have been studied in detail by using combined HPLC and electrospray MS. This approach allowed the separation of α and β anomers and the simultaneous monitoring of chitooligosaccharide products down to picomole levels. Chitinase A primarily generated β‐anomeric products, indicating that it catalyzed hydrolysis through a retaining mechanism. The enzyme exhibited endo characteristics, requiring a minimum of two glycosidic bonds for hydrolysis. The kinetics of hydrolysis revealed that chitinase A had greater affinity towards higher M r chitooligomers, in the order of (GlcNAc) 6 > (GlcNAc) 4 > (GlcNAc) 3 , and showed no activity towards (GlcNAc) 2 and pNP‐GlcNAc. This suggested that the binding site of chitinase A was probably composed of an array of six binding subsites. Point mutations were introduced into two active site residues – Glu315 and Asp392 – by site‐directed mutagenesis. The D392N mutant retained significant chitinase activity in the gel activity assay and showed ≈ 20% residual activity towards chitooligosaccharides and colloidal chitin in HPLC‐MS measurements. The complete loss of substrate utilization with the E315M and E315Q mutants suggested that Glu315 is an essential residue in enzyme catalysis. The recombinant wild‐type enzyme acted on chitooligosaccharides, releasing higher quantities of small oligomers, while the D392N mutant favored the formation of transient intermediates. Under standard hydrolytic conditions, all chitinases also exhibited transglycosylation activity towards chitooligosaccharides and pNP‐glycosides, yielding picomole quantities of synthesized chitooligomers. The D392N mutant displayed strikingly greater efficiency in oligosaccharide synthesis than the wild‐type enzyme.