Davis M A, Cobbett C S, Hynes M J
Department of Genetics, University of Melbourne, Parkville, Victoria, Australia.
Gene. 1988 Mar 31;63(2):199-212. doi: 10.1016/0378-1119(88)90525-2.
A translational fusion has been constructed between the amdS gene of Aspergillus nidulans and the lacZ gene of Escherichia coli. Sequencing across the fusion junction confirmed the generation of an in-frame fusion at amino acid 34 of amdS and a novel protein has been detected in transformants carrying the fusion plasmid. Transformants of A. nidulans and Aspergillus niger carrying the fusion plasmid were obtained by co-transformation with a second selectable plasmid. These transformants were readily identified on media containing XGal. The intensity of the reaction on XGal media was indicative of the number of copies of the fusion plasmid carried by the transformants. The growth of highly expressing strains of A. nidulans was inhibited on XGal media. The fusion plasmid was used to develop a two-step gene replacement strategy in which the resident amdS gene was replaced with the fusion gene free of vector sequences. Plate tests and in vitro assays of the beta-galactosidase enzyme confirmed that expression of the fusion gene was regulated by amdS flanking sequences and trans-acting regulatory genes.
已构建了构巢曲霉的amdS基因与大肠杆菌的lacZ基因之间的翻译融合体。对融合位点进行测序证实,在amdS的第34位氨基酸处产生了读码框内融合,并且在携带融合质粒的转化子中检测到了一种新蛋白质。通过与第二个选择性质粒共转化,获得了携带融合质粒的构巢曲霉和黑曲霉的转化子。这些转化子在含有XGal的培养基上很容易被鉴定出来。在XGal培养基上反应的强度表明转化子携带的融合质粒的拷贝数。在XGal培养基上,构巢曲霉高表达菌株的生长受到抑制。该融合质粒被用于开发一种两步基因置换策略,其中常驻的amdS基因被不含载体序列的融合基因所取代。β-半乳糖苷酶的平板试验和体外测定证实,融合基因的表达受amdS侧翼序列和顺式作用调控基因的调节。