通过培养基优化、核糖体工程对链霉菌(Streptomyces sp.)FJS31-2外分泌物产生条件进行了优化,利用高分辨质谱(HRMS)技术对其主要活性产物的成分进行了初步分析,采用磺酰罗丹明B(SRB)比色法测定了外分泌物对肝癌细胞MHCC97H的抑制活性。...通过培养基优化、核糖体工程对链霉菌(Streptomyces sp.)FJS31-2外分泌物产生条件进行了优化,利用高分辨质谱(HRMS)技术对其主要活性产物的成分进行了初步分析,采用磺酰罗丹明B(SRB)比色法测定了外分泌物对肝癌细胞MHCC97H的抑制活性。结果表明,经链霉素多代胁迫结合培养基优化诱导链霉菌FJS31-2产生了分子式为C 28 H 40 O 2的四环萜类化合物,该化合物可抑制肝癌细胞MHCC97H的生长,并呈浓度依赖性。为从链霉菌FJS31-2获取新型抗生素奠定了技术和物质基础。展开更多
A pair of primers containing BamHI and XhoI sites was designed to amplify n gene of 1149bp from the positive pMD18-TN plasmid of transmissible gastroenteritis virus n gene by PCR.PCR product was subcloned into multipl...A pair of primers containing BamHI and XhoI sites was designed to amplify n gene of 1149bp from the positive pMD18-TN plasmid of transmissible gastroenteritis virus n gene by PCR.PCR product was subcloned into multiple cloning sites of pET-30a containing 6 His·Tag.Recombinant plasmid pET-30a of n gene named pET30a-N was transfected into E.coli BL21 and the bacteria was induced with IPTG at 37℃.It was demonstrated by SDS-PAGE that recombinant N protein expressed in E.coli BL21 was soluble protein and its molecular weight was about 52kD.The result of Western blot test showed that immunoactivity of the recombinant N protein was the same to that of the natural N protein.展开更多
文摘通过培养基优化、核糖体工程对链霉菌(Streptomyces sp.)FJS31-2外分泌物产生条件进行了优化,利用高分辨质谱(HRMS)技术对其主要活性产物的成分进行了初步分析,采用磺酰罗丹明B(SRB)比色法测定了外分泌物对肝癌细胞MHCC97H的抑制活性。结果表明,经链霉素多代胁迫结合培养基优化诱导链霉菌FJS31-2产生了分子式为C 28 H 40 O 2的四环萜类化合物,该化合物可抑制肝癌细胞MHCC97H的生长,并呈浓度依赖性。为从链霉菌FJS31-2获取新型抗生素奠定了技术和物质基础。
文摘A pair of primers containing BamHI and XhoI sites was designed to amplify n gene of 1149bp from the positive pMD18-TN plasmid of transmissible gastroenteritis virus n gene by PCR.PCR product was subcloned into multiple cloning sites of pET-30a containing 6 His·Tag.Recombinant plasmid pET-30a of n gene named pET30a-N was transfected into E.coli BL21 and the bacteria was induced with IPTG at 37℃.It was demonstrated by SDS-PAGE that recombinant N protein expressed in E.coli BL21 was soluble protein and its molecular weight was about 52kD.The result of Western blot test showed that immunoactivity of the recombinant N protein was the same to that of the natural N protein.