Sears I B, O'Connor J, Rossanese O W, Glick B S
Department of Molecular Genetics and Cell Biology, University of Chicago, IL 60637, USA.
Yeast. 1998 Jun 15;14(8):783-90. doi: 10.1002/(SICI)1097-0061(19980615)14:8<783::AID-YEA272>3.0.CO;2-Y.
The budding yeast Pichia pastoris is an attractive system for exploring certain questions in cell biology, but experimental use of this organism has been limited by a lack of convenient expression vectors. Here we describe a set of compact vectors that should allow for the expression of a wide range of endogenous or foreign genes in P. pastoris. A gene of interest is inserted into a modified pUC19 polylinker; targeted integration into the genome then results in stable and uniform expression of this gene. The utility of these vectors was illustrated by expressing the bacterial beta-glucuronidase (GUS) gene. Constitutive GUS expression was obtained with the strong GAP promoter or the moderate YPT1 promoter. The regulatable AOX1 promoter yielded very strong GUS expression in methanol-grown cells, negligible expression in glucose-grown cells, and intermediate expression in mannitol-grown cells. GenBank Accession Numbers are: pIB1, AF027958; pIB2, AF0279959; pIB3, AF027960; pIB4, AF027961.
出芽酵母巴斯德毕赤酵母是探索细胞生物学中某些问题的一个有吸引力的系统,但该生物体的实验应用一直受到缺乏便捷表达载体的限制。在此,我们描述了一组紧凑型载体,它们应能使多种内源或外源基因在巴斯德毕赤酵母中得以表达。将感兴趣的基因插入到经修饰的pUC19多克隆位点;随后靶向整合到基因组中可导致该基因稳定且均匀的表达。通过表达细菌β-葡萄糖醛酸酶(GUS)基因证明了这些载体的实用性。用强GAP启动子或中度YPT1启动子可实现组成型GUS表达。可调控的AOX1启动子在甲醇培养的细胞中产生非常强的GUS表达,在葡萄糖培养的细胞中表达可忽略不计,而在甘露醇培养的细胞中表达处于中等水平。GenBank登录号为:pIB1,AF027958;pIB2,AF0279959;pIB3,AF027960;pIB4,AF027961。