Kulich S M, Frank D W, Barbieri J T
Department of Microbiology, Medical College of Wisconsin, Milwaukee 53226.
Infect Immun. 1995 Jan;63(1):1-8. doi: 10.1128/iai.63.1.1-8.1995.
The structural gene for the 49-kDa form of exoenzyme S (exoS) isolated from Pseudomonas aeruginosa 388 was expressed in both Escherichia coli and P. aeruginosa PA103. Expression of exoS in E. coli under the transcriptional regulation of the T7 promoter yielded a soluble cytosolic protein with an apparent molecular mass of 49 kDa, as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Expression of exoS in P. aeruginosa PA103 under the transcriptional regulation of the 0.9 kbp of Pseudomonas chromosomal DNA flanking the 5' end of exoS yielded a nitrilotriacetic acid-inducible extracellular protein with an apparent molecular mass of 49 kDa. Recombinant ExoS (rExoS) reacted with the anti-49-kDa form of exoenzyme S immunoglobulin G, existed as an aggregate as determined by gel filtration chromatography, and ADP-ribosylated soybean trypsin inhibitor at a specific activity that was similar (within twofold) to that of native exoenzyme S. Allelic exchange of exoS with a tetracycline gene cartridge yielded a strain of P. aeruginosa 388 that did not express detectable amounts of either ExoS in an immunoblot analysis using the anti-49-kDa form of exoenzyme S immunoglobulin G or ADP-ribosyltransferase activity under standard enzyme assay conditions. Expression of catalytically active rExoS in E. coli demonstrated that exoS was necessary and sufficient for the factor-activating exoenzyme S-dependent ADP-ribosyltransferase activity of exoenzyme S. Expression of nitrilotriacetic acid-inducible rExoS in P. aeruginosa PA103 demonstrated that the 0.9 kbp of Pseudomonas chromosomal DNA flanking the 5' end of exoS encoded a functional exoenzyme S promoter. Expression analysis and allelic exchange experiments suggest that the 49- and 53-kDa forms of exoenzyme S are encoded by separate genes.
从铜绿假单胞菌388中分离出的49 kDa形式的外毒素S(exoS)的结构基因在大肠杆菌和铜绿假单胞菌PA103中均有表达。在T7启动子的转录调控下,exoS在大肠杆菌中的表达产生了一种可溶性胞质蛋白,通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测定,其表观分子量为49 kDa。在exoS 5'端侧翼的0.9 kbp铜绿假单胞菌染色体DNA的转录调控下,exoS在铜绿假单胞菌PA103中的表达产生了一种次氮基三乙酸诱导的细胞外蛋白,其表观分子量为49 kDa。重组ExoS(rExoS)与抗49 kDa形式的外毒素S免疫球蛋白G发生反应,通过凝胶过滤色谱法测定其以聚集体形式存在,并且以与天然外毒素S相似(两倍以内)的比活性对大豆胰蛋白酶抑制剂进行ADP核糖基化。用四环素基因盒对exoS进行等位基因交换产生了一株铜绿假单胞菌388,在使用抗49 kDa形式的外毒素S免疫球蛋白G进行免疫印迹分析或在标准酶分析条件下,该菌株未表达可检测量的ExoS或ADP核糖基转移酶活性。在大肠杆菌中催化活性rExoS的表达表明,exoS对于外毒素S的因子激活外毒素S依赖性ADP核糖基转移酶活性是必需且足够的。在铜绿假单胞菌PA103中次氮基三乙酸诱导的rExoS的表达表明,exoS 5'端侧翼的0.9 kbp铜绿假单胞菌染色体DNA编码一个功能性外毒素S启动子。表达分析和等位基因交换实验表明,49 kDa和53 kDa形式的外毒素S由不同的基因编码。