Haake D A, Champion C I, Martinich C, Shang E S, Blanco D R, Miller J N, Lovett M A
Division of Infectious Diseases, West Los Angeles Veterans Affairs Medical Center, California 90073.
J Bacteriol. 1993 Jul;175(13):4225-34. doi: 10.1128/jb.175.13.4225-4234.1993.
Pathogenic Leptospira spp. are spirochetes that have a low transmembrane outer membrane protein content relative to that of enteric gram-negative bacteria. In a previous study we identified a 31-kDa surface protein that was present in strains of Leptospira alstoni in amounts which correlated with the outer membrane particle density observed by freeze fracture electron microscopy (D. A. Haake, E. M. Walker, D. R. Blanco, C. A. Bolin, J. N. Miller, and M. A. Lovett, Infect. Immun. 59:1131-1140, 1991). The N-terminal amino acid sequence was used to design a pair of oligonucleotides which were utilized to screen a lambda ZAP II library containing EcoRI fragments of L. alstoni DNA. A 2.5-kb DNA fragment which contained the entire structural ompL1 gene was identified. The structural gene deduced from the sequence of this DNA fragment would encode a 320-amino-acid polypeptide with a 24-amino-acid leader peptide and a leader peptidase I cleavage site. Processing of OmpL1 results in a mature protein with a predicted molecular mass of 31,113 Da. Secondary-structure prediction identified repeated stretches of amphipathic beta-sheets typical of outer membrane protein membrane-spanning sequences. A topological model of OmpL1 containing 10 transmembrane segments is suggested. A recombinant OmpL1 fusion protein was expressed in Escherichia coli in order to immunize rabbits with the purified protein. Upon Triton X-114 extraction of L. alstoni and phase separation, anti-OmpL1 antiserum recognized a single band on immunoblots of the hydrophobic detergent fraction which was not present in the hydrophilic aqueous fraction. Immunoelectron microscopy with anti-OmpL1 antiserum demonstrates binding to the surface of intact L. alstoni. DNA hybridization studies indicate that the ompL1 gene is present in a single copy in all pathogenic Leptospira species that have been tested and is absent in nonpathogenic Leptospira species. OmpL1 may be the first spirochetal transmembrane outer membrane protein for which the structural gene has been cloned and sequenced.
致病性钩端螺旋体属细菌是螺旋体,相对于肠道革兰氏阴性菌,其跨膜外膜蛋白含量较低。在之前的一项研究中,我们鉴定出一种31 kDa的表面蛋白,该蛋白存在于阿氏钩端螺旋体菌株中,其含量与通过冷冻断裂电子显微镜观察到的外膜颗粒密度相关(D. A. 哈克、E. M. 沃克、D. R. 布兰科、C. A. 博林、J. N. 米勒和M. A. 洛维特,《感染与免疫》59:1131 - 1140,1991)。利用N端氨基酸序列设计了一对寡核苷酸,用于筛选包含阿氏钩端螺旋体DNA的EcoRI片段的λZAP II文库。鉴定出一个包含完整ompL1结构基因的2.5 kb DNA片段。从该DNA片段序列推导的结构基因将编码一个含24个氨基酸前导肽和一个前导肽酶I切割位点的320个氨基酸的多肽。OmpL1的加工产生一个预测分子量为31,113 Da的成熟蛋白。二级结构预测确定了外膜蛋白跨膜序列典型的两亲性β折叠重复序列。提出了一个包含10个跨膜区段的OmpL1拓扑模型。为了用纯化蛋白免疫兔子,在大肠杆菌中表达了重组OmpL1融合蛋白。用Triton X - 114提取阿氏钩端螺旋体并进行相分离后,抗OmpL1抗血清在疏水去污剂部分的免疫印迹上识别出一条单一的条带,而在亲水水性部分不存在。用抗OmpL1抗血清进行免疫电子显微镜观察表明其与完整的阿氏钩端螺旋体表面结合。DNA杂交研究表明,ompL1基因在所有已测试的致病性钩端螺旋体物种中以单拷贝存在,而在非致病性钩端螺旋体物种中不存在。OmpL1可能是第一个其结构基因已被克隆和测序的螺旋体跨膜外膜蛋白。