Jia J, Wheals A
Department of Biology and Biochemistry, University of Bath, UK.
Curr Genet. 2000 Dec;38(5):264-70. doi: 10.1007/s002940000160.
The gene encoding endopolygalacturonase (EC 3.2.1.15) has been cloned, sequenced and expressed from three strains of Saccharomyces cerevisiae (including nonsecretors) and three strains of Kluyveromyces marxianus. Both control and coding regions showed small differences within each species, one including loss of a potential glycosylation site. Two non-secreting S. cerevisiae strains (FY1679 and var. uvarum) had non-transcribed copies of functional genes. Maximum enzyme activity was achieved with the S. cerevisiae FY1679 gene in an expressing vector, with an enzyme activity of 51 micromol of reducing sugar released from polygalacturonic acid microg protein(-1) min(-1), the highest so far reported for a yeast.
编码内切多聚半乳糖醛酸酶(EC 3.2.1.15)的基因已从三株酿酒酵母(包括非分泌型)和三株马克斯克鲁维酵母中克隆、测序并表达。对照区和编码区在每个物种内都显示出微小差异,其中一个差异包括一个潜在糖基化位点的缺失。两株非分泌型酿酒酵母菌株(FY1679和葡萄变种)具有功能基因的非转录拷贝。在表达载体中,酿酒酵母FY1679基因实现了最大酶活性,从聚半乳糖醛酸释放还原糖的酶活性为51微摩尔微克蛋白⁻¹分钟⁻¹,这是迄今为止酵母中报道的最高值。