Applied Biological Chemistry
- Volume 33 Issue 1
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- Pages.79-86
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- 1990
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- 2468-0834(pISSN)
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- 2468-0842(eISSN)
Purification and Some Properties of Cyclodextrin Hydrolase
Cyclodextrin분해효소의 정제 및 그 특성
- Kim, Yong-Hwi (Chonbuk National Univ.) ;
- Shim, Kyu-Kwnag (Chonju Woosuk Univ.) ;
- Moon, Young-Hee (Chonbuk National Univ.)
- Published : 1990.03.31
Abstract
Cyclodextrin hydrolase from Bacillus stearothermophilus KFCC 21203 was purified and the properties of the purified enzyme were investigated. The enzyme was purified 15 folds with 77 % recovery by ammonium sulfate fractionation, DEAE-cellulose chromatography, and Ultro AcA 34 gel filtration. The specific activity and the molecular weight of the enzyme were 1.30 units/mg protein and about 29,500, respectively, The maximum activity of the enzyme was shown at
Bacillus stearothermophilus KFCC 21203를 배양하여 cyclodextrin(CD)을 분해하는 효소를 분리, 정제하고 정제효소의 몇 가지 특성을 조사하였다. 배양액에서 얻은 조효소를 염석, DEAE-cellulose column chromatography, Ultro AcA 34 gel filtration등의 방법으로 15배 정제하였으며 회수율은 77.2%이었다. 정제효소의 specific activity는 12.30units/mg protein 이었고 분자량은 약 29,500정도였다. 이 효소의 작용최적 PH는 5.5, 작용최적온도는