检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:秦楠[1] 洪雪莹[1] 陈其新[1] 李明[1] 路鹏[1]
出 处:《中国草食动物》2011年第2期5-9,共5页China Herbivores
基 金:河南省科技攻关项目(0422011200)
摘 要:为实现家兔BMP7基因原核表达及探索适宜的表达条件,采用PCR技术从pMD18-T-BMP7重组质粒中扩增获得BMP7基因成熟肽片段(mBMP7),构建原核表达工程菌pET32a-mBMP7/BL21(DE3)和pET32a-mBMP7/BL21(DE3)pLysS,并比较温度、IPTG浓度、诱导时间等因素对目的蛋白表达的影响。结果表明,mBMP7原核表达载体构建正确;工程菌pET32a-mBMP7/BL21(DE3)和pET32a-mBMP7/BL21(DE3)pLysS经IPTG诱导均可表达含有家兔BMP7成熟肽的34KDa的融合蛋白,表达产物约占菌体总蛋白的30%。在37℃、0.75 mM IPTG以及诱导150 min时,能取得较高的目的蛋白表达量;在20℃低温条件下,IPTG浓度和诱导表达时间应分别以0.20 mM和7 h为宜;另外,目的蛋白表达对工程菌生长无明显的不利影响。因此,成功地构建了家兔BMP7基因工程菌,并确定了适宜的表达条件,为进一步研究该蛋白的结构和功能奠定基础。To realize the prokaryotic expression and explore its reasonable expression conditions,the study subcloned the coding DNA for the mature protein of rabbit BMP7,and constructed the Engineered Escherichia Coli pET32a-mBMP7/BL21(DE3) and pET32a-mBMP7/BL21(DE3) pLysS,respectively.The effects of culture temperature,IPTG levels and induction time on the expression of desired fusion protein were also analyzed.The results showed that the interest fragment of DNA coding the mature protein of rabbit BMP7 was correctly inserted into the prokaryotic expression vector pET32a.under the induction of IPTG,the both engineered Escherichia Coli produced the desired 34 KD fusion protein consisting of the target mature protein as well as a vector tag protein,and the output of fusion protein reached to nearly 30% of the total protein of Escherichia Coli.The comparative expressions implied that a higher amount of fusion protein could be harvested when the hosts were cultured at the temperature of 37 ℃,and with the use of a IPTG level of 0.75 mM as well as with a induction time of 150min,while at a lower temperature(20 ℃) culture,the 0.2 mM IPTG and a induction time of 7 h seemed to be suitable.In addition,the foreign protein was found not to be deleterious to the growth of host.It then been concluded that the engineering Escherichia Coli are successively constructed,and suitable conditions for the expression of target protein are proposed.These will lie a good foundation to the further studies on the either structure or the functions of this proteins.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.113