Applied Biological Chemistry
- 제33권1호
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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)
Cyclodextrin분해효소의 정제 및 그 특성
Purification and Some Properties of Cyclodextrin Hydrolase
- Kim, Yong-Hwi (Chonbuk National Univ.) ;
- Shim, Kyu-Kwnag (Chonju Woosuk Univ.) ;
- Moon, Young-Hee (Chonbuk National Univ.)
- 발행 : 1990.03.31
초록
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
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