Bui D M, Kunze I, Horstmann C, Schmidt T, Breunig K D, Kunze G
Institut für Pflanzengenetik und Kulturpflanzenforschung, Gatersleben, Germany.
Appl Microbiol Biotechnol. 1996 Mar;45(1-2):102-6. doi: 10.1007/s002530050655.
The glucoamylase gene of the yeast Arxula adeninivorans was expressed in Kluyveromyces lactis by using the GAP promoter from Saccharomyces cerevisiae and a multicopy plasmid vector. The transformants secreted 90.1% of the synthesized glucoamylase into the culture medium. The secreted glucoamylase activities are about 20 times higher in comparison to those of Saccharomyces cerevisiae transformants using the same promoter. Secreted glucoamylase possesses identical N-terminal amino acid sequences to those secreted by A. adeninivorans showing that cleavage of the N-terminal signal peptide takes place at the same site. Biochemical characteristics of glucoamylase expressed by K. lactis and A. adeninivorans are very similar.
通过使用来自酿酒酵母的GAP启动子和多拷贝质粒载体,将酵母嗜腺嘌呤丛赤壳菌的葡糖淀粉酶基因在乳酸克鲁维酵母中进行表达。转化子将合成的葡糖淀粉酶的90.1%分泌到培养基中。与使用相同启动子的酿酒酵母转化子相比,分泌的葡糖淀粉酶活性高约20倍。分泌的葡糖淀粉酶具有与嗜腺嘌呤丛赤壳菌分泌的相同的N端氨基酸序列,表明N端信号肽在相同位点发生切割。乳酸克鲁维酵母和嗜腺嘌呤丛赤壳菌表达的葡糖淀粉酶的生化特性非常相似。