Blanco P, Sieiro C, Reboredo N M, Villa T G
Department of Microbiology, Faculty of Pharmacy, University of Santiago, Santiago de Compostela, Spain.
FEMS Microbiol Lett. 1998 Jul 15;164(2):249-55. doi: 10.1111/j.1574-6968.1998.tb13094.x.
A structural polygalacturonase-encoding gene (PGU1) from Saccharomyces cerevisiae IM1-8b was cloned and sequenced. The predicted protein comprises 361 amino acids, with a signal peptide between residues 1 and 18 and two potential glycosylation points in residues 318 and 330. The putative active site is a conserved histidine in position 222. This polygalacturonase showed 54% homology with the fungal ones and only 24% homology with their plant and bacterial counterparts. The gene is present in a single gene copy per haploid genome and it is detected in all strains, regardless of their phenotype. The expression of PGU1 gene in several strains of S. cerevisiae revealed that the polygalacturonase activity depended on the plasmid used and also on the genetic background of each strain but in all cases the enzymatic activity increased.
克隆并测序了来自酿酒酵母IM1-8b的一个编码结构多聚半乳糖醛酸酶的基因(PGU1)。预测的蛋白质由361个氨基酸组成,在第1至18位残基之间有一个信号肽,在第318和330位残基处有两个潜在的糖基化位点。推定的活性位点是位于第222位的保守组氨酸。这种多聚半乳糖醛酸酶与真菌的多聚半乳糖醛酸酶有54%的同源性,与植物和细菌的多聚半乳糖醛酸酶只有24%的同源性。该基因在每个单倍体基因组中以单基因拷贝形式存在,并且在所有菌株中都能检测到,无论其表型如何。PGU1基因在几种酿酒酵母菌株中的表达表明,多聚半乳糖醛酸酶活性取决于所用的质粒以及每个菌株的遗传背景,但在所有情况下酶活性都有所增加。