Park Myeong Soo, Kwon Bin, Shim Jae Jung, Huh Chul Sung, Ji Geun Eog
Research center, BIFIDO Co., Ltd., Seoul 151-818, Korea.
Biotechnol Lett. 2008 Jan;30(1):165-72. doi: 10.1007/s10529-007-9514-3. Epub 2007 Sep 12.
We have constructed a constitutive high-level-expression vector for the genus Bifidobacterium and used it to express cholesterol oxidase from Streptomyces coelicola. The promoter region of the 16S rRNA gene was amplified by inverse PCR and used for the construction of pBES16PR. The optimal ribosome-binding site (RBS) for Bifidobacterium was incorporated in pBES16PR. In order to test the efficacy of this expression vector, we constructed pBES16PR-CHOL with the structural gene for cholesterol oxidase under the control of the 16S rRNA promoter, and used it to transform Bifidobacterium longum. The gene was successfully expressed and high level of cholesterol oxidase activity was obtained in B. longum. This is the first report of an expression vector for the genus Bifidobacterium using a 16S rRNA gene promoter and successful expression of cholesterol oxidase.
我们构建了一种用于双歧杆菌属的组成型高表达载体,并利用它来表达来自天蓝色链霉菌的胆固醇氧化酶。通过反向PCR扩增16S rRNA基因的启动子区域,并将其用于构建pBES16PR。将双歧杆菌的最佳核糖体结合位点(RBS)整合到pBES16PR中。为了测试该表达载体的功效,我们构建了pBES16PR-CHOL,其胆固醇氧化酶结构基因受16S rRNA启动子控制,并用于转化长双歧杆菌。该基因成功表达,并且在长双歧杆菌中获得了高水平的胆固醇氧化酶活性。这是首次报道使用16S rRNA基因启动子的双歧杆菌属表达载体以及胆固醇氧化酶的成功表达。