High N J, Deadman M E, Hood D W, Moxon E R
Dept. of Paediatrics, University of Oxford, John Radcliffe Hospital, Headington, UK.
FEMS Microbiol Lett. 1996 Dec 15;145(3):325-31. doi: 10.1111/j.1574-6968.1996.tb08596.x.
Mutagenesis with the transposon Tn916 was used as a strategy to identify genes required for synthesis of the Gal alpha (1-4) beta Gal component of Haemophilus influenzae strain RM7004 lipopolysaccharide. Insertion of Tn916 into an open reading frame (ORF) encoding a protein with 75% homology to the Escherichia coli methionine related protein (Mrp) is described. Mutations in mrp resulted in loss of reactivity with monoclonal antibody (mAb) 4C4, which recognises Gal alpha (1-4) beta Gal, and expression of LPS with a different electrophoretic profile to that of wild-type RM7004. An unexpected feature of this mutation was that it appeared to influence the number of copies of 5'-CAAT-3' present in lic2A, a gene which is also required for biosynthesis and phase variable expression of the Gal alpha (1-4) beta Gal LPS epitope.
利用转座子Tn916进行诱变,作为一种策略来鉴定流感嗜血杆菌RM7004菌株脂多糖中Galα(1-4)βGal成分合成所需的基因。本文描述了将Tn916插入一个开放阅读框(ORF),该开放阅读框编码一种与大肠杆菌甲硫氨酸相关蛋白(Mrp)具有75%同源性的蛋白质。Mrp基因突变导致与识别Galα(1-4)βGal的单克隆抗体(mAb) 4C4失去反应性,并且脂多糖的表达具有与野生型RM7004不同的电泳图谱。该突变的一个意外特征是,它似乎影响了lic2A中5'-CAAT-3'的拷贝数,lic2A是Galα(1-4)βGal脂多糖表位生物合成和相变表达所必需的一个基因。