Isaacson R E
Infect Immun. 1978 Nov;22(2):555-9. doi: 10.1128/iai.22.2.555-559.1978.
K99 prepared by acid precipitation hemagglutinated guinea pig erythrocytes, whereas K99 prepared by chromatography on diethylaminoethyl-Sephadex did not. K99 purified by either procedure hemagglutinated horse erythrocytes. K99 prepared by acid precipitation contained a second antigen not presnet in the K99 prepared by chromatography on diethylaminoethyl-Sephadex. This antigen could be detected by immunoprecipitation with some, but not all, sera prepared against K99-positive Escherichia coli strains. It was assumed that this second antigen is not K99 and is responsible for the guinea pig erythrocyte hemagglutination reaction. Furthermore, the second antigen has an isoelectric point of 4.2, which has been reported by Morris and co-workers to be the isoelectric point of K99.
通过酸沉淀法制备的K99能使豚鼠红细胞发生血凝,而通过二乙氨基乙基-葡聚糖凝胶柱层析法制备的K99则不能。通过任何一种方法纯化的K99都能使马红细胞发生血凝。通过酸沉淀法制备的K99含有一种第二种抗原,而通过二乙氨基乙基-葡聚糖凝胶柱层析法制备的K99中不存在这种抗原。这种抗原可以用一些(但不是所有)针对K99阳性大肠杆菌菌株制备的血清通过免疫沉淀法检测到。据推测,这种第二种抗原不是K99,并且是豚鼠红细胞血凝反应的原因。此外,第二种抗原的等电点为4.2,莫里斯及其同事曾报道该等电点是K99的等电点。