Shuttleworth H L, Duggleby C J, Jones S A, Atkinson T, Minton N P
Microbial Technology Laboratory, PHLS, Centre for Applied Microbiology and Research, Porton Down, Salisbury, Wilts, U.K.
Gene. 1987;58(2-3):283-95. doi: 10.1016/0378-1119(87)90383-0.
Nucleotide sequence analysis of the gene (spa) for staphylococcal protein A (SPA) from Staphylococcus aureus strain Cowan 1 (NCTC8530) shows that the sequence differs from previously reported SPA nucleotide sequences, especially in the number of repeat units in the cell-wall-binding region of the gene. Dot matrix comparison with streptococcal protein G and the macrophage receptor for the constant fragment (Fc) of immunoglobulins shows a limited but significant homology. The homology to the latter probably identifies the Fc-binding region in the immunoglobulin-binding domains of SPA. Enhanced production of SPA in Escherichia coli was achieved using the lac promoter immediately upstream from the spa gene.
对金黄色葡萄球菌考恩1株(NCTC8530)的葡萄球菌蛋白A(SPA)基因(spa)进行核苷酸序列分析表明,该序列与先前报道的SPA核苷酸序列不同,尤其是在该基因细胞壁结合区域的重复单元数量上。与链球菌蛋白G以及免疫球蛋白恒定片段(Fc)的巨噬细胞受体进行点阵比较,结果显示存在有限但显著的同源性。与后者的同源性可能确定了SPA免疫球蛋白结合结构域中的Fc结合区域。利用spa基因上游紧邻的lac启动子,实现了大肠杆菌中SPA产量的提高。