{"title":"枯草芽孢杆菌胶原酶的分离与鉴定(Ehrenberg, 1835)ATCC 6633用于降解印度尼西亚Cirata水库的鱼皮胶原蛋白废物","authors":"Emma Rochima , Nadia Sekar , Ibnu Dwi Buwono , Eddy Afrianto , Rusky Intan Pratama","doi":"10.1016/j.aqpro.2016.07.010","DOIUrl":null,"url":null,"abstract":"<div><p>The objective of this research was to isolate and characterize collagenase from <em>Bacillus subtilis</em> ATCC 6633 collection of Microbiology Laboratory, Department Pharmacy Biology, Faculty Pharmacy Padjadjaran University. The substrate collagen derived of Tilapia fish skin waste from Cirata Reservoar which has’nt exploited fully yet. The experimental design used and the data analysed descriptively. Collagen as substrate from Tilapia skin waste had extracted by Yuniarti (2010) method in Luria Broth media. The production time of collagenase used <span>Rahmayanti (2014)</span> methods which incubated the isolate for 24<!--> <!-->hours and the OD of absorbances from 0.2 to 0.8 evaluated. The effect of temperature on collagenase activity evaluated by temperature from 20 to 70<sup>o</sup>C. The effect of pH collagenase activity evaluated pH from 5 to 10. The conclusion of the research that <em>B. subtilis</em> ATCC 6633 has colagenolitik activity showed by the clear zone in the Luria media. The optimum production time of collagenase was 24<!--> <!-->h of incubation. Collagenase activity reached the optimum temperature was 50° C (1,298 Unit mL<sup>–1</sup>), while the pH optimum collagenase obtained in the range of 7-9 (from 1.298 Unit mL<sup>–1</sup> to 1,321 U mL<sup>–1</sup>.</p></div>","PeriodicalId":92478,"journal":{"name":"Aquatic procedia","volume":"7 ","pages":"Pages 76-84"},"PeriodicalIF":0.0000,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.aqpro.2016.07.010","citationCount":"12","resultStr":"{\"title\":\"Isolation and Characterization of Collagenase from Bacillus Subtilis (Ehrenberg, 1835); ATCC 6633 for Degrading Fish Skin Collagen Waste from Cirata Reservoir, Indonesia\",\"authors\":\"Emma Rochima , Nadia Sekar , Ibnu Dwi Buwono , Eddy Afrianto , Rusky Intan Pratama\",\"doi\":\"10.1016/j.aqpro.2016.07.010\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The objective of this research was to isolate and characterize collagenase from <em>Bacillus subtilis</em> ATCC 6633 collection of Microbiology Laboratory, Department Pharmacy Biology, Faculty Pharmacy Padjadjaran University. The substrate collagen derived of Tilapia fish skin waste from Cirata Reservoar which has’nt exploited fully yet. The experimental design used and the data analysed descriptively. Collagen as substrate from Tilapia skin waste had extracted by Yuniarti (2010) method in Luria Broth media. The production time of collagenase used <span>Rahmayanti (2014)</span> methods which incubated the isolate for 24<!--> <!-->hours and the OD of absorbances from 0.2 to 0.8 evaluated. The effect of temperature on collagenase activity evaluated by temperature from 20 to 70<sup>o</sup>C. The effect of pH collagenase activity evaluated pH from 5 to 10. The conclusion of the research that <em>B. subtilis</em> ATCC 6633 has colagenolitik activity showed by the clear zone in the Luria media. The optimum production time of collagenase was 24<!--> <!-->h of incubation. Collagenase activity reached the optimum temperature was 50° C (1,298 Unit mL<sup>–1</sup>), while the pH optimum collagenase obtained in the range of 7-9 (from 1.298 Unit mL<sup>–1</sup> to 1,321 U mL<sup>–1</sup>.</p></div>\",\"PeriodicalId\":92478,\"journal\":{\"name\":\"Aquatic procedia\",\"volume\":\"7 \",\"pages\":\"Pages 76-84\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.aqpro.2016.07.010\",\"citationCount\":\"12\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Aquatic procedia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2214241X16300311\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aquatic procedia","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214241X16300311","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 12
摘要
本研究的目的是分离和鉴定枯草芽孢杆菌ATCC 6633的胶原酶,这些胶原酶来自印度帕贾贾兰大学药学院生物学系微生物实验室。底物胶原蛋白来源于尚未充分开发利用的Cirata水库罗非鱼鱼皮废弃物。采用了实验设计,并对数据进行了描述性分析。采用Yuniarti(2010)的方法,在Luria肉汤培养基中提取罗非鱼废皮中的胶原蛋白作为底物。胶原酶生产时间采用Rahmayanti(2014)方法,培养24小时,吸光度OD值为0.2 ~ 0.8。温度对胶原酶活性的影响通过20 ~ 70℃的温度来评估。pH值对胶原酶活性的影响评价pH值为5 ~ 10。研究结果表明,枯草芽孢杆菌ATCC 6633在Luria培养基中具有胶原蛋白活性。胶原酶的最佳产酶时间为24 h。胶原酶的最佳活性温度为50℃(1,298 Unit mL-1), pH值为7 ~ 9 (1.298 ~ 1,321 U mL-1)。
Isolation and Characterization of Collagenase from Bacillus Subtilis (Ehrenberg, 1835); ATCC 6633 for Degrading Fish Skin Collagen Waste from Cirata Reservoir, Indonesia
The objective of this research was to isolate and characterize collagenase from Bacillus subtilis ATCC 6633 collection of Microbiology Laboratory, Department Pharmacy Biology, Faculty Pharmacy Padjadjaran University. The substrate collagen derived of Tilapia fish skin waste from Cirata Reservoar which has’nt exploited fully yet. The experimental design used and the data analysed descriptively. Collagen as substrate from Tilapia skin waste had extracted by Yuniarti (2010) method in Luria Broth media. The production time of collagenase used Rahmayanti (2014) methods which incubated the isolate for 24 hours and the OD of absorbances from 0.2 to 0.8 evaluated. The effect of temperature on collagenase activity evaluated by temperature from 20 to 70oC. The effect of pH collagenase activity evaluated pH from 5 to 10. The conclusion of the research that B. subtilis ATCC 6633 has colagenolitik activity showed by the clear zone in the Luria media. The optimum production time of collagenase was 24 h of incubation. Collagenase activity reached the optimum temperature was 50° C (1,298 Unit mL–1), while the pH optimum collagenase obtained in the range of 7-9 (from 1.298 Unit mL–1 to 1,321 U mL–1.