{"title":"玉米蛋白磷酸酶2C基因(ZmPP2C2)的原核表达和蛋白纯化","authors":"Lixia Liu, Xiaoli Hu","doi":"10.1109/FBIE.2009.5405877","DOIUrl":null,"url":null,"abstract":"The coding region of the protein phosphatase 2C gene (ZmPP2C2) from Zea mays (maize) was sub-cloned into expression vector, pET30a-c(+), and introduced into E. coli BL21 (DE3) for expression. SDS-PAGE analysis indicated ZmPP2C2 was great expressed at 37°C for 4 h with 1mM IPTG. Ultrasonic extraction experiment showed this recombinant protein was little in lysis buffer solution, but most in inclusion body. Inclusion body was collected and dissolved by lysis buffer solution with carbamide. The hexahistidine-tagged ZmPP2C2 fusion protein was purified by Ni-NTA column by 300 mM imidazole elution.","PeriodicalId":333255,"journal":{"name":"2009 International Conference on Future BioMedical Information Engineering (FBIE)","volume":"140 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2009-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Prokaryotic expression, protein purification of a protein phosphatase 2C gene (ZmPP2C2) from maize\",\"authors\":\"Lixia Liu, Xiaoli Hu\",\"doi\":\"10.1109/FBIE.2009.5405877\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The coding region of the protein phosphatase 2C gene (ZmPP2C2) from Zea mays (maize) was sub-cloned into expression vector, pET30a-c(+), and introduced into E. coli BL21 (DE3) for expression. SDS-PAGE analysis indicated ZmPP2C2 was great expressed at 37°C for 4 h with 1mM IPTG. Ultrasonic extraction experiment showed this recombinant protein was little in lysis buffer solution, but most in inclusion body. Inclusion body was collected and dissolved by lysis buffer solution with carbamide. The hexahistidine-tagged ZmPP2C2 fusion protein was purified by Ni-NTA column by 300 mM imidazole elution.\",\"PeriodicalId\":333255,\"journal\":{\"name\":\"2009 International Conference on Future BioMedical Information Engineering (FBIE)\",\"volume\":\"140 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2009 International Conference on Future BioMedical Information Engineering (FBIE)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/FBIE.2009.5405877\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2009 International Conference on Future BioMedical Information Engineering (FBIE)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/FBIE.2009.5405877","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Prokaryotic expression, protein purification of a protein phosphatase 2C gene (ZmPP2C2) from maize
The coding region of the protein phosphatase 2C gene (ZmPP2C2) from Zea mays (maize) was sub-cloned into expression vector, pET30a-c(+), and introduced into E. coli BL21 (DE3) for expression. SDS-PAGE analysis indicated ZmPP2C2 was great expressed at 37°C for 4 h with 1mM IPTG. Ultrasonic extraction experiment showed this recombinant protein was little in lysis buffer solution, but most in inclusion body. Inclusion body was collected and dissolved by lysis buffer solution with carbamide. The hexahistidine-tagged ZmPP2C2 fusion protein was purified by Ni-NTA column by 300 mM imidazole elution.