Carbonetti N H, Sparling P F
Department of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill 27514.
Proc Natl Acad Sci U S A. 1987 Dec;84(24):9084-8. doi: 10.1073/pnas.84.24.9084.
Protein I (P.I) is the major outer membrane protein of Neisseria gonorrhoeae and serves as a porin. By using oligonucleotide probes derived from the known amino-terminal sequence of the mature protein, we have cloned the gene encoding the P.I of gonococcal strain FA19 in three overlapping fragments and determined the DNA sequence. The gene sequence predicts a protein with characteristics typical of the porins of other Gram-negative bacteria. A clone expressing P.I in Escherichia coli was obtained by removing a portion of the P.I gene promoter and reconstructing the entire P.I gene in a position just downstream from a phage T7 promoter. Expression of P.I was then achieved by introducing this recombinant plasmid into an E. coli strain containing an inducible T7 polymerase gene. The clone produced a protein that was identical in size to native P.I and reacted with anti-P.I monoclonal antibodies. Prolonged expression of the protein apparently was lethal for E. coli, possibly explaining failures to clone an intact P.I gene with its own promoter.
蛋白I(P.I)是淋病奈瑟菌的主要外膜蛋白,作为一种孔蛋白发挥作用。通过使用从成熟蛋白已知的氨基末端序列推导而来的寡核苷酸探针,我们已将淋病奈瑟菌菌株FA19编码P.I的基因克隆为三个重叠片段,并确定了DNA序列。该基因序列预测的蛋白质具有其他革兰氏阴性菌孔蛋白的典型特征。通过去除P.I基因启动子的一部分并将整个P.I基因重建到噬菌体T7启动子下游的位置,获得了在大肠杆菌中表达P.I的克隆。然后通过将这种重组质粒导入含有可诱导T7聚合酶基因的大肠杆菌菌株中来实现P.I的表达。该克隆产生的一种蛋白质在大小上与天然P.I相同,并能与抗P.I单克隆抗体发生反应。该蛋白质的长时间表达显然对大肠杆菌是致死性的,这可能解释了未能克隆带有自身启动子的完整P.I基因的原因。