Azakami H, Yumoto H, Nakae H, Matsuo T, Ebisu S
Department of Conservative Dentistry, Tokushima University School of Dentistry, Japan.
Gene. 1996 Nov 21;180(1-2):207-12. doi: 10.1016/s0378-1119(96)00639-7.
A monoclonal antibody against a lectin-like substance (LS) of Eikenella corrodens (Ec) was used for screening the Ec DNA library. Three positive clones that carried an identical 12-kb segment were obtained. A 25-kDa protein, which specifically binds to the antibody, was overproduced in all of the Escherichia coli clones. Deletion analysis showed that the gene encoding the 25-kDa protein was located within a 1.2-kb segment. The nucleotide (nt) sequence of this segment contained an open reading frame encoding a protein of 24600 Da. We purified the 25-kDa protein from the cloned E. coli strain. The sequence of the first 10 amino acids(aa) from the N-terminus of the purified 25-kDa protein agreed with that deduced from the nt sequence. Since the monoclonal antibody used in this study inhibits the physiological activity of EcLS, we concluded that the 25-kDa protein is a component of the adhesin complex, which is located near the carbohydrate recognition domain of lectin in EcLS.
一种针对腐蚀艾肯菌(Ec)凝集素样物质(LS)的单克隆抗体被用于筛选Ec DNA文库。获得了三个携带相同12 kb片段的阳性克隆。在所有大肠杆菌克隆中均过量产生了一种与该抗体特异性结合的25 kDa蛋白。缺失分析表明,编码25 kDa蛋白的基因位于一个1.2 kb的片段内。该片段的核苷酸(nt)序列包含一个编码24600 Da蛋白的开放阅读框。我们从克隆的大肠杆菌菌株中纯化了25 kDa蛋白。纯化的25 kDa蛋白N端前10个氨基酸(aa)的序列与从nt序列推导的序列一致。由于本研究中使用的单克隆抗体抑制EcLS的生理活性,我们得出结论,25 kDa蛋白是粘附素复合物的一个组成部分,位于EcLS中凝集素的碳水化合物识别结构域附近。