Microbiology and Biotechnology Letters (한국미생물·생명공학회지)
- Volume 20 Issue 2
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- Pages.169-177
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- 1992
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- 1598-642X(pISSN)
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- 2234-7305(eISSN)
Production and Purification of Alkaline Protease from Streptomyces sp.
Streptomyces속 균주가 생성하는 Alkaline Protease의 생산 및 정제
- Choi, Cheong (Department of Food Science & Technology, Yeungnam Univ.) ;
- Chung, Yung-Gun (Department of Food Science & Technology, Yeungnam Univ.) ;
- Sung, Sam-Kyung (Department of Food Science & Technology, Yeungnam Univ.) ;
- Choi, Kwang-Soo (Department of Food Science & Technology, Yeungnam Univ.) ;
- Lee, Jae-Sung (Department of Food Science & Technology, Yeungnam Univ.) ;
- Cho, Young-Je (Department of Food Science & Technology, Yeungnam Univ.) ;
- Kwon, Oh-Jin (Department of Food Science & Technology, Yeungnam Univ.)
- 최청 (영남대학교 식품가공학과) ;
- 정영건 (영남대학교 식품가공학과) ;
- 성삼경 (영남대학교 식품가공학과) ;
- 최광수 (영남대학교 식품가공학과) ;
- 이재성 (영남대학교 식품가공학과) ;
- 조영제 (영남대학교 식품가공학과) ;
- 권오진 (영남대학교 식품가공학과)
- Published : 1992.04.01
Abstract
An alkaline protease producing microorganism was isolated from soil and identified as Streptomyces griseus HC-1141. The optimum culture condition of Streptomyces griseus HC- 1141 for the production of alkaline protease was as follows; 0.5% casein, 0.05% ammonium chloride, 0.1% ferrous sulfate. 2.0% lactose, pH 8.0 and 84 hrs. The enzyme was purified about 53 folds by ammonium sulfate treatment, DEAE-cellulose ion exchange chromatography and gel filtratioo on Sephadex G-150. The homogeneity of the purified enzyme was verified by polyacrylamide gel electrophoresis. The molecular weight was estimated to be 31,000 on sodium dodecyl sulfate polyacrylamide gel electrophoresis. This enzyme consists of glycine and glutamic acid as major amino acids. The N-terminal and C-terminal residues of the alkaline protease were leucine and histidine respectively.
토양으로부터 alkaline protease 생성능이 강한 Streptomyces griseus HC-1141을 분리하였으며, 효소생산의 최적 배양조건은 0.5 casein, 0.05 ammonium chloride, 0.1 ferrous sulfate, 2.0의 lactose, pH 8.0에서 84시간 배양했을 때이다. 효소의 정제는 ammonium sulfate 침전, DEAE-cellulose ion exchange chromatography, Sephadex G-150 gel filtration, crystallization으로 하여 53.23배 정제할 수 있었으며 polyacrylamide gel 전기영동상 단일밴드를 나타내었다.