Graduate School of Biosphere Science, Hiroshima University, 1-4-4, Kagamiyama, Higashihiroshima, Hiroshima 739-8527, Japan.
AMB Express. 2011 May 25;1(1):7. doi: 10.1186/2191-0855-1-7.
We previously developed a host vector system for the wastewater treatment yeast Hansenula fabianii J640. The promoter and terminator regions of the gene encoding glucoamylase from H. fabianii J640 were used for a new expression vector, pHFGE-1. The performance of pHFGE-1 was compared with that of the widely used pG-1 transformant vector. H. fabianii J640 (HF-TAMY) cells were transformed with pHFGE-1, and Saccharomyces cerevisiae YPH-499 (SC-TAMY) cells were transformed with pG-1, both of which carried the Taka-amylase. Expression of Taka-amylase by HF-TAMY showed higher than that by SC-TAMY. By using this new system, we bred the new wastewater treatment yeast that shows α-amylase activity. This yeast appears to grow well under experimental wastewater conditions, and is effective in treating model wastewater containing soluble and insoluble starch.
我们先前开发了一种用于废水处理酵母汉逊德巴利酵母 J640 的宿主载体系统。汉逊德巴利酵母 J640 编码葡萄糖淀粉酶的启动子和终止子区域被用于一个新的表达载体 pHFGE-1。pHFGE-1 的性能与广泛使用的 pG-1 转化载体进行了比较。pHFGE-1 转化了汉逊德巴利酵母 J640(HF-TAMY)细胞,pG-1 转化了酿酒酵母 YPH-499(SC-TAMY)细胞,两者都携带了 Takara 淀粉酶。HF-TAMY 中的 Takara 淀粉酶表达高于 SC-TAMY。通过使用这个新系统,我们培育了一种具有 α-淀粉酶活性的新型废水处理酵母。这种酵母在实验性废水条件下似乎生长良好,并且在处理含有可溶性和不溶性淀粉的模型废水中有效。