Gill R E, Bornemann M C
Department of Microbiology and Immunology, University of Colorado Health Sciences Center, Denver 80262.
J Bacteriol. 1988 Nov;170(11):5289-97. doi: 10.1128/jb.170.11.5289-5297.1988.
The bsgA mutants of Myxococcus xanthus are blocked at a very early stage of the developmental program. They fail to produce fruiting bodies or to sporulate under normal conditions but can be rescued by extracellular complementation in mixtures with wild-type cells. A bsgA-lacZ gene fusion was constructed and expressed in Escherichia coli. The resulting fusion protein, which has beta-galactosidase enzyme activity, was partially purified by affinity chromatography and preparative polyacrylamide gel electrophoresis. The protein was used to immunize mice, which produced a hybridoma secreting monoclonal antibody that was specific for the bsgA gene product. The monoclonal antibody was used in Western blot (immunoblot) experiments to determine the apparent cellular location of the bsgA protein in M. xanthus and to compare the level of this protein at various times in the Myxococcus life cycle.
黄色黏球菌的bsgA突变体在发育程序的非常早期阶段就被阻断。它们在正常条件下无法产生子实体或形成孢子,但与野生型细胞混合时可通过细胞外互补得到拯救。构建了bsgA-lacZ基因融合体并在大肠杆菌中表达。产生的具有β-半乳糖苷酶活性的融合蛋白通过亲和层析和制备性聚丙烯酰胺凝胶电泳进行了部分纯化。该蛋白用于免疫小鼠,产生了分泌对bsgA基因产物具有特异性的单克隆抗体的杂交瘤。该单克隆抗体用于蛋白质印迹(免疫印迹)实验,以确定bsgA蛋白在黄色黏球菌中的表观细胞定位,并比较该蛋白在黏球菌生命周期不同时间的水平。