Bergkamp R J, Bootsman T C, Toschka H Y, Mooren A T, Kox L, Verbakel J M, Geerse R H, Planta R J
Laboratorium voor Biochemie en Moleculaire Biologie, Vrije Universiteit, Amsterdam, The Netherlands.
Appl Microbiol Biotechnol. 1993 Nov;40(2-3):309-17. doi: 10.1007/BF00170386.
For expression of the alpha-galactosidase gene from Cyamopsis tetragonoloba in Kluyveromyces marxianus CBS 6556 we have used the promoter of the homologous inulinase-encoding gene (INU1). The INU1 gene has been cloned and sequenced and the coding region shows an identity of 59% with the Saccharomyces cerevisiae invertase gene (SUC2). In the 5'-flanking region of INU1 we found a sequence (TAAATCCGGGG) that perfectly matches to the MIG1 binding consensus sequence (WWWWTSYGGGG) of the S. cerevisiae GAL1, GAL4 and SUC2 genes. Using the K. marxianus INU1 promoter and prepro-signal sequence, we obtained a high alpha-galactosidase production level (153 mg/l) and a secretion efficiency of 99%. Both the production level and the secretion efficiency were significantly reduced when the INU1 pro-peptide was deleted. With either the S. cerevisiae PGK or GAL7 promoter we could obtain only low alpha-galactosidase production levels (2 mg/l).
为了在马克斯克鲁维酵母CBS 6556中表达来自四角瓜尔豆的α-半乳糖苷酶基因,我们使用了同源菊粉酶编码基因(INU1)的启动子。INU1基因已被克隆和测序,其编码区与酿酒酵母转化酶基因(SUC2)的同一性为59%。在INU1的5'侧翼区域,我们发现了一个序列(TAAATCCGGGG),它与酿酒酵母GAL1、GAL4和SUC2基因的MIG1结合共有序列(WWWWTSYGGGG)完全匹配。使用马克斯克鲁维酵母INU1启动子和前原信号序列,我们获得了较高的α-半乳糖苷酶产量水平(153 mg/l)和99%的分泌效率。当删除INU1前肽时,产量水平和分泌效率均显著降低。使用酿酒酵母PGK或GAL7启动子,我们只能获得较低的α-半乳糖苷酶产量水平(2 mg/l)。