Wang T, Penttilä M, Gao P, Wang C, Zhong L
State Key Laboratory of Microbial Technology, Shandong University, Jinan, China.
Chin J Biotechnol. 1998;14(3):179-85.
A cDNA sub-library from the fungus Trichoderma reesei grown on xylan was constructed in S.cerevisiae recombinant strain H475 harboring a xylose reductase (XR) gene from Pichia stipitis. The xylitol dehydrogenase (XDH) gene was screened from sub-library on a SC selective medium in which xylose was used as a sole carbon source. The length of XDH gene, xdh1, was about 1.3 kb. Southern, Northern and Western blots were carried out, indicating that xdh1 has high affinity with T.reesei and the molecular weight of the xylitol dehydrogenase from T.reesei was about 40 kDa. The strain HX1 harboring both the XR gene from P.stipitis and the XDH gene from T.reesei was able to grow on the xylose medium and converted more than 90% of the xylose into xylitol, ethanol, and other by-products.
在含有树干毕赤酵母木糖还原酶(XR)基因的酿酒酵母重组菌株H475中构建了来自在木聚糖上生长的里氏木霉的cDNA亚文库。在以木糖作为唯一碳源的SC选择培养基上从亚文库中筛选木糖醇脱氢酶(XDH)基因。XDH基因xdh1的长度约为1.3 kb。进行了Southern、Northern和Western印迹分析,表明xdh1与里氏木霉具有高亲和力,且里氏木霉木糖醇脱氢酶的分子量约为40 kDa。同时含有树干毕赤酵母XR基因和里氏木霉XDH基因的菌株HX1能够在木糖培养基上生长,并将90%以上的木糖转化为木糖醇、乙醇和其他副产物。