Porro D, Martegani E, Ranzi B M, Alberghina L
Dipartimento di Fisiologia e Biochimica Generali, sez di Biochimica Comparata, Università di Milano, 20133 Milan, Italy.
Biotechnol Bioeng. 1992 Apr 5;39(8):799-805. doi: 10.1002/bit.260390802.
Strains of Saccharomyces cerevisiae transformed with a multicopy expression vector bearing both the Escherichia coli beta-galactosidase gene under the control of the upstream activating sequence of the GAL1-10 genes and the GAL4 activator gene release part of beta-galactosidase in the growth medium. This release is due to cell lysis of the older mother cells; the enzyme maintains its activity in buffered growth media. Fermentation studies with transformed yeast strains showed that the release of beta-galactosidase allowed an efficient growth on buffered media containing lactose as carbon source as well as on whey-based media. The transformed strains utilized up to 95% of the lactose and a high growth yield was obtained in rich media. High productions of ethanol were also observed in stationary phase after growth in lactose minimal media.
用多拷贝表达载体转化的酿酒酵母菌株,该载体带有在GAL1 - 10基因上游激活序列控制下的大肠杆菌β - 半乳糖苷酶基因和GAL4激活基因,在生长培养基中释放部分β - 半乳糖苷酶。这种释放是由于老龄母细胞的细胞裂解;该酶在缓冲生长培养基中保持其活性。对转化酵母菌株的发酵研究表明,β - 半乳糖苷酶的释放使得在以乳糖为碳源的缓冲培养基以及乳清基培养基上能够高效生长。转化菌株利用了高达95%的乳糖,并且在丰富培养基中获得了高生长产量。在乳糖基本培养基中生长后,在稳定期也观察到了乙醇的高产量。