Mansur Manuel, Cabello Cecilia, Hernández Lester, País José, Varas Laura, Valdés Jorge, Terrero Yanet, Hidalgo Abdel, Plana Liuba, Besada Vladimir, García Liudys, Lamazares Emilio, Castellanos Lila, Martínez Eduardo
Center for Genetic Engineering and Biotechnology (CIGB), P.O. Box 6162, Havana 11600, Cuba.
Biotechnol Lett. 2005 Mar;27(5):339-45. doi: 10.1007/s10529-005-1007-7.
We have found a direct relationship between protein production in Pichia pastoris and the number of introduced synthetic genes of miniproinsulin (MPI), fused to the Saccharomyces cerevisiae pre-pro alpha factor used as secretion signal, and inserted between the alcohol oxidase 1 (AOX1) promoter and terminator sequences. Two consecutive approaches were followed to increase the number of integrated cassettes: the head-to-tail expression cassette multimerization procedure and re-transformation with a dominant selection marker. This increased expression from 19 to 250 mg l(-1) when about 11 copies have been integrated. Further, the correct position of one of the disulphide bridges of the purified molecule was verified by digestion with Glu-C endoprotease, followed by mass spectrometry of the isolated fragments.
我们发现,在巴斯德毕赤酵母中,蛋白质产量与引入的微小胰岛素(MPI)合成基因数量之间存在直接关系。这些基因与用作分泌信号的酿酒酵母前原α因子融合,并插入到醇氧化酶1(AOX1)启动子和终止子序列之间。为了增加整合盒的数量,我们采用了两种连续的方法:头尾相连的表达盒多聚化程序和用显性选择标记进行再转化。当整合了约11个拷贝时,表达量从19毫克/升提高到了250毫克/升。此外,通过用Glu-C内切蛋白酶消化,随后对分离的片段进行质谱分析,验证了纯化分子中二硫键之一的正确位置。