Preparation and use of a cyclodextrinase for preparing maltooligosaccharides
AssigneeKikkoman Corporation
InventorsTetsuya Oguma, Mamoru Kikuchi, Kiyoshi Mizusawa, Shoichi Tokutake, Nobuyuki Yamaji
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Abstract
The present invention relates to the preparation of a cylodextrinase having specific physicochemical characteristics relating to action, substrate specificities, optimum pH, stable pH, inhibition, activation and molecular weight by culturing a specified microorganism belonging to the genus Bacillus, and also provides a process for preparing maltooligosaccharides by using the present enzyme on cylodextrins.
Claims1
A process for producing maltooligosaccharides which comprises catalytically acting a cyclodextrinase enzyme (EC 3.2.1.54) having the following physicochemical characteristics on cyclodextrins
- wherein the enzyme cleaves cyclodextrins to produce maltooligosaccharides corresponding to the polymerization degree of glucose of the cyclodextrins;
- the hydrolysis rate or affinity of said enzyme for cyclodextrins being higher than that of polysaccharides or linear maltooligosaccharides with the same polymerization degree of glucose as cylodextrins;
- when .alpha.-cyclodextrin is the substrate, Km=0.71;
- when .gamma.cyclodextrin is the substrate, Kn=1.43;
- and
- when .beta.-cyclodextrin is used as a substrate, Km=0.38, the optimum pH of said enzyme is around 8.0 and the stable pH range is 5.5-9.5;
- the working temperature of the enzyme is around 40.degree. C.;
- the enzyme is substantially inactivated by a treatment at a temperature of 50.degree. C. or more for a period of 15 minutes;
- the enzyme is inhibited by at least 90% by Hg.sup.2+, Cu.sup.2+, Zn.sup.2+, Ni.sup.2+, and Fe.sup.2+ and activated 10-30% by Ca.sup.2+ and Mg.sup.2+ ;
- and
- the molecular weight of the enzyme is 144,000 when measured according to gel filtration method and 72,000 when measured according to SDS PAGE method.
Dependencies are inferred from the claim text.