Choi Young-Seok, Shin Dong-Ho, Chung In-Young, Kim Seol-Hee, Heo Yun-Jeong, Cho You-Hee
Department of Life Science, Sogang University, Seoul 121-742, Korea.
J Microbiol Biotechnol. 2007 Aug;17(8):1344-52.
An opportunistic human pathogen, Pseudomonas aeruginosa, contains the major catalase KatA, which is required to cope with oxidative and osmotic stresses. As an attempt to uncover the H2O2-dependent regulatory mechanism delineating katA gene expression, four prototrophic H2O2-sensitive mutants were isolated from about 1,500 TnphoA mutant clones of P. aeruginosa strain PA14. Arbitrary PCR and direct cloning of the transposon insertion sites revealed that one insertion is located within the katA coding region and two are within the coding region of oxyR, which is responsible for transcriptional activation of several antioxidant enzyme genes in response to oxidative challenges. The fourth insertion was within PA3815 (IscR), which encodes a homolog of the Escherichia coli iron-sulfur assembly regulator, IscR. The levels of catalase and SOD activities were significantly reduced in the iscR mutant, but not in the oxyR mutant, during the normal planktonic culture conditions. These results suggest that both IscR and OxyR are required for the optimal resistance to H2O2, which involves the expression of multiple antioxidant enzymes including KatA.
铜绿假单胞菌是一种机会性人类病原体,它含有主要的过氧化氢酶KatA,该酶是应对氧化应激和渗透压应激所必需的。为了揭示描述katA基因表达的H2O2依赖性调控机制,从约1500个铜绿假单胞菌PA14菌株的TnphoA突变体克隆中分离出四个原养型H2O2敏感突变体。转座子插入位点的任意PCR和直接克隆显示,一个插入位于katA编码区内,两个位于oxyR编码区内,oxyR负责响应氧化应激激活几个抗氧化酶基因的转录。第四个插入位于PA3815(IscR)内,该基因编码大肠杆菌铁硫组装调节因子IscR的同源物。在正常浮游培养条件下,iscR突变体中过氧化氢酶和超氧化物歧化酶活性水平显著降低,但oxyR突变体中未降低。这些结果表明,IscR和OxyR都是对H2O2产生最佳抗性所必需的,这涉及包括KatA在内的多种抗氧化酶的表达。