Frank D W, Iglewski B H
Department of Microbiology, Medical College of Wisconsin, Milwaukee 53226.
J Bacteriol. 1991 Oct;173(20):6460-8. doi: 10.1128/jb.173.20.6460-6468.1991.
Exoenzyme S is an ADP-ribosyltransferase enzyme distinct from exotoxin A that is synthesized and secreted by Pseudomonas aeruginosa. Yields of exoenzyme S are variable and depend on strain and growth conditions. Since certain medium additives are required for exoenzyme S production, its regulation may be influenced by environmental stimuli. In this study, we have cloned a region that complements the exoenzyme S-deficient phenotype of strain 388 exs1::Tn1, a chromosomal Tn1 insertional mutation. A large clone (28 kb) was shown to restore both synthesis and secretory functions to the mutant strain. Subcloning and Tn501 mutagenesis experiments localized the region required for exoenzyme S synthesis to a 3.2-kb fragment. Nucleotide sequence analysis demonstrated several open reading frames. Comparison of the N-terminal amino acid sequence of purified exoenzyme S with predicted amino acid sequences of all open reading frames indicated that the structural gene was not encoded within the sequenced region. Homology studies suggested that the region encoded three regulatory genes, exsC, exsB, and exsA. ExsA was homologous to the AraC family of transcriptional activator proteins, with extensive homology being found with one member of this family, VirF of Yersinia enterocolitica. VirF and ExsA both contain carboxy-terminal domains with the helix-turn-helix motif of DNA-binding proteins. The ExsA gene product appeared to be required for induction of exoenzyme S synthesis above a low basal level. Expression of ExsA was demonstrated by cloning the region under the control of the T7 promoter. Gene replacement experiments suggested that the expression of ExsC affects the final yield of exoenzyme S.
外毒素S是一种与外毒素A不同的ADP核糖基转移酶,由铜绿假单胞菌合成并分泌。外毒素S的产量各不相同,取决于菌株和生长条件。由于外毒素S的产生需要某些培养基添加剂,其调控可能受环境刺激的影响。在本研究中,我们克隆了一个区域,该区域可弥补菌株388 exs1::Tn1(一种染色体Tn1插入突变体)的外毒素S缺陷表型。一个大的克隆(28 kb)被证明可恢复突变菌株的合成和分泌功能。亚克隆和Tn501诱变实验将外毒素S合成所需区域定位到一个3.2 kb的片段。核苷酸序列分析显示了几个开放阅读框。将纯化的外毒素S的N端氨基酸序列与所有开放阅读框的预测氨基酸序列进行比较,表明结构基因不在测序区域内编码。同源性研究表明,该区域编码三个调控基因,即exsC、exsB和exsA。ExsA与转录激活蛋白的AraC家族同源,与该家族的一个成员——小肠结肠炎耶尔森菌的VirF有广泛的同源性。VirF和ExsA都含有羧基末端结构域,具有DNA结合蛋白的螺旋-转角-螺旋基序。ExsA基因产物似乎是将外毒素S合成诱导至低基础水平以上所必需的。通过将该区域克隆到T7启动子的控制下,证明了ExsA的表达。基因替换实验表明,ExsC的表达影响外毒素S的最终产量。