Bolen P L, Hayman G T, Shepherd H S
National Center for Agricultural Utilization Research, U.S. Department of Agriculture, Peoria, IL 61604, USA.
Yeast. 1996 Oct;12(13):1367-75. doi: 10.1002/(SICI)1097-0061(199610)12:13%3C1367::AID-YEA33%3E3.0.CO;2-#.
A xylose reductase gene was isolated from the xylose-fermenting yeast Pachysolen tannophilus as a cDNA clone by selecting clones that hybridized specifically to xylose-inducible messenger RNA. Use of the cDNA clone as a probe in Northern hybridizations identified a xylose-inducible mRNA species large enough to encode a 36 kDa xylose reductase protein known to be produced by this yeast. A corresponding genomic clone was isolated as a 3 kb EcoRI fragment that specifically hybridized to the cDNA clone. The sequence of the cDNA and the largest open reading frame of the genomic clone are identical. The predicted translation product exhibits: (1) significant sequence identity with a previously published N-terminal amino acid sequence from purified P. tannophilus xylose (aldose) reductase protein exhibiting NADH/NADPH-dependent activities (aldose reductase, EC 1.1.1.21); (2) identity with a protein composed of 317 amino acid residues with a calculated molecular mass of 36.2 kDa, equivalent to that reported for purified P. tannophilus xylose reductase; and (3) considerable sequence similarity to, and features of, a superfamily of oxidoreductases.
通过筛选与木糖诱导型信使核糖核酸特异性杂交的克隆,从木糖发酵酵母嗜鞣管囊酵母中分离出一个木糖还原酶基因作为cDNA克隆。在Northern杂交中使用该cDNA克隆作为探针,鉴定出一种木糖诱导型mRNA,其大小足以编码一种已知由该酵母产生的36 kDa木糖还原酶蛋白。一个相应的基因组克隆作为一个3 kb的EcoRI片段被分离出来,该片段与cDNA克隆特异性杂交。cDNA和基因组克隆的最大开放阅读框的序列是相同的。预测的翻译产物表现出:(1)与先前发表的来自纯化的嗜鞣管囊酵母木糖(醛糖)还原酶蛋白的N端氨基酸序列具有显著的序列同一性,该蛋白具有NADH/NADPH依赖性活性(醛糖还原酶,EC 1.1.1.21);(2)与一种由317个氨基酸残基组成、计算分子量为36.2 kDa的蛋白质相同,这与报道的纯化的嗜鞣管囊酵母木糖还原酶的分子量相当;(3)与氧化还原酶超家族有相当的序列相似性和特征。