{"title":"奶牛场污泥中铜绿假单胞菌RGSS-09耐热有机耐溶剂酸性蛋白酶的制备及特性研究。","authors":"R. Gaur, S. Tiwari, Sheffalika Singh","doi":"10.3923/AJB.2015.52.66","DOIUrl":null,"url":null,"abstract":"Fifteen bacterial strains isolated from the dairy soil samples for acidic protease production. Among them, culture RGSS-09 was adjudged as the best protease producer and was identified as Pseudomonas aeruginosa RGSS-09 from MTCC Chandigarh. The isolate showed maximum protease production (1256 U mLG) with 2.5 g LG biomass production in the presence of wheat bran and yeast extract at 37°C pH 6.5 within 48 h of incubation. Pseudomonas aeruginosa RGSS-09 also showed enhanced activity and stability in presence of Ca, Mg, Tween-20, Tween-40, triton-X-100 and SDS at 5 and 10 mM concentration. The enzyme was also stable in the presence of n-dodecane, isooctane, n-decane, xylene, toluene, n-haxane, n-butanol and cyclohexane, respectively. The presence of benzene, methanol and ethanol marginally reduced the protease stability, respectively. The enzyme was showed it 100% activity at 75°C and pH 7.5 with 110 and 100% stability at 70°C and pH 7.0, respectively. The purity of the enzyme was confirmed by the presence of a single band on SDS-PAGE and its molecular weight was approximately 42 kDa. Pseudomonas aeruginosa can be used profitably for the large scale production of protease to meet the present day demand of the industrial sector.","PeriodicalId":8510,"journal":{"name":"Asian Journal of Biochemistry","volume":"13 1","pages":"52-66"},"PeriodicalIF":0.0000,"publicationDate":"2015-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Production and characterization of thermotolerant-organic solvent resistant acidic protease by Pseudomonas aeruginosa RGSS-09 isolated from dairy sludge.\",\"authors\":\"R. Gaur, S. Tiwari, Sheffalika Singh\",\"doi\":\"10.3923/AJB.2015.52.66\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Fifteen bacterial strains isolated from the dairy soil samples for acidic protease production. Among them, culture RGSS-09 was adjudged as the best protease producer and was identified as Pseudomonas aeruginosa RGSS-09 from MTCC Chandigarh. The isolate showed maximum protease production (1256 U mLG) with 2.5 g LG biomass production in the presence of wheat bran and yeast extract at 37°C pH 6.5 within 48 h of incubation. Pseudomonas aeruginosa RGSS-09 also showed enhanced activity and stability in presence of Ca, Mg, Tween-20, Tween-40, triton-X-100 and SDS at 5 and 10 mM concentration. The enzyme was also stable in the presence of n-dodecane, isooctane, n-decane, xylene, toluene, n-haxane, n-butanol and cyclohexane, respectively. The presence of benzene, methanol and ethanol marginally reduced the protease stability, respectively. The enzyme was showed it 100% activity at 75°C and pH 7.5 with 110 and 100% stability at 70°C and pH 7.0, respectively. The purity of the enzyme was confirmed by the presence of a single band on SDS-PAGE and its molecular weight was approximately 42 kDa. Pseudomonas aeruginosa can be used profitably for the large scale production of protease to meet the present day demand of the industrial sector.\",\"PeriodicalId\":8510,\"journal\":{\"name\":\"Asian Journal of Biochemistry\",\"volume\":\"13 1\",\"pages\":\"52-66\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Biochemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3923/AJB.2015.52.66\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Biochemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3923/AJB.2015.52.66","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
摘要
从奶牛场土壤样品中分离出15株产酸性蛋白酶的菌株。其中,培养物RGSS-09为最佳蛋白酶产生菌,经鉴定为铜绿假单胞菌RGSS-09来自昌迪加尔MTCC。在37°C pH 6.5的条件下,分离物在培养48 h内显示出最大的蛋白酶产量(1256 U mLG)和2.5 g LG生物质产量。铜绿假单胞菌RGSS-09在Ca、Mg、Tween-20、Tween-40、triton-X-100和SDS浓度为5和10 mM时也表现出较强的活性和稳定性。该酶在正十二烷、异辛烷、正癸烷、二甲苯、正己烷、正己烷、正丁醇和环己烷的存在下也保持稳定。苯、甲醇和乙醇的存在分别略微降低了蛋白酶的稳定性。该酶在75℃和pH 7.5条件下具有100%的活性,在70℃和pH 7.0条件下具有110和100%的稳定性。酶的纯度通过SDS-PAGE上的单条带证实,其分子量约为42 kDa。铜绿假单胞菌可有效地用于蛋白酶的大规模生产,以满足当今工业部门的需求。
Production and characterization of thermotolerant-organic solvent resistant acidic protease by Pseudomonas aeruginosa RGSS-09 isolated from dairy sludge.
Fifteen bacterial strains isolated from the dairy soil samples for acidic protease production. Among them, culture RGSS-09 was adjudged as the best protease producer and was identified as Pseudomonas aeruginosa RGSS-09 from MTCC Chandigarh. The isolate showed maximum protease production (1256 U mLG) with 2.5 g LG biomass production in the presence of wheat bran and yeast extract at 37°C pH 6.5 within 48 h of incubation. Pseudomonas aeruginosa RGSS-09 also showed enhanced activity and stability in presence of Ca, Mg, Tween-20, Tween-40, triton-X-100 and SDS at 5 and 10 mM concentration. The enzyme was also stable in the presence of n-dodecane, isooctane, n-decane, xylene, toluene, n-haxane, n-butanol and cyclohexane, respectively. The presence of benzene, methanol and ethanol marginally reduced the protease stability, respectively. The enzyme was showed it 100% activity at 75°C and pH 7.5 with 110 and 100% stability at 70°C and pH 7.0, respectively. The purity of the enzyme was confirmed by the presence of a single band on SDS-PAGE and its molecular weight was approximately 42 kDa. Pseudomonas aeruginosa can be used profitably for the large scale production of protease to meet the present day demand of the industrial sector.