Takuma S, Nakashima N, Tantirungkij M, Kinoshita S, Okada H, Seki T, Yoshida T
International Center of Cooperative Research in Biotechnology, Faculty of Engineering, Osaka University, Japan.
Appl Biochem Biotechnol. 1991 Spring;28-29:327-40. doi: 10.1007/BF02922612.
A NADPH/NADH-dependent xylose reductase gene was isolated from the xylose-assimilating yeast, Pichia stipitis. DNA sequence analysis showed that the gene consists of 951 bp. The gene introduced in Saccharomyces cerevisiae was transcribed to mRNA, and a considerable amount of enzyme activity was observed constitutively, whereas transcription and translation in P stipitis were inducible. S. cerevisiae carrying the xylose reductase gene could not, however, grow on xylose medium, and could not produce ethanol from xylose. Since xylose uptake and accumulation of xylitol by S. cerevisiae were observed, the conversion of xylitol to xylulose seemed to be limited.
从木糖同化酵母树干毕赤酵母中分离出一个依赖NADPH/NADH的木糖还原酶基因。DNA序列分析表明该基因由951个碱基对组成。导入酿酒酵母中的该基因转录成了mRNA,并且组成型地观察到了相当量的酶活性,而在树干毕赤酵母中,转录和翻译是可诱导的。然而,携带木糖还原酶基因的酿酒酵母不能在木糖培养基上生长,也不能从木糖生产乙醇。由于观察到酿酒酵母对木糖的摄取和木糖醇的积累,木糖醇向木酮糖的转化似乎受到限制。