Laboratory of Animal Microbiology, Department of Microbial Biotechnology, Graduate School of Agricultural Science, Tohoku University, 1-1 Tsutsumidori Amamiya-machi Aoba-ku, Sendai 981-8555, Japan.
Antimicrob Agents Chemother. 2010 Apr;54(4):1492-7. doi: 10.1128/AAC.01495-09. Epub 2010 Jan 25.
Pseudomonas aeruginosa is equipped with the Sec and Tat protein secretion systems, which translocate the xenobiotic transporter MexAB-OprM and the pathogenic factor phospholipase C (PlcH), respectively. When the signal sequence of MexA was replaced with that of PlcH, the hybrid protein was successfully expressed and recovered from the periplasmic fraction, suggesting that the hybrid protein had been translocated across the inner membrane. MexA-deficient cells harboring the plasmid carrying the plcH-mexA fusion gene showed antibiotic resistance comparable to that of the wild-type cells. This result suggested that MexA secreted via the Tat machinery was properly assembled and functioned as a subunit of the MexAB-OprM efflux pump. A mutation was introduced into the chromosomal tatC gene encoding an inner membrane component of the Tat protein secretion machinery in mexA-deficient cells, and they were transformed with the plasmid carrying the plcH-mexA fusion gene. The transformants showed antibiotic susceptibility comparable to that of mexA-deficient cells, indicating that the hybrid protein was not transported to the periplasm. Whole-cell lysate of the mexA-tatC double mutant harboring the plcH-mexA plasmid produced mainly unprocessed PlcH-MexA. The periplasmic fraction showed no detectable anti-MexA antibody-reactive material. On the basis of these results, we concluded that MexA could be translocated across the inner membrane through the Tat pathway and assembled with its cognate partners, MexB and OprM, and that this complex machinery was fully functional. This hybrid protein translocation system has the potential to be a powerful screening tool for antimicrobial agents targeting the Tat system, which is not present in mammalian cells.
铜绿假单胞菌配备了 Sec 和 Tat 蛋白分泌系统,分别将外源性转运体 MexAB-OprM 和致病因子磷脂酶 C(PlcH)转运至细胞外。当 MexA 的信号序列被 PlcH 的信号序列取代时,杂交蛋白成功地从周质部分表达和回收,表明杂交蛋白已穿过内膜转运。携带 plcH-mexA 融合基因质粒的 MexA 缺陷细胞表现出与野生型细胞相当的抗生素抗性。这一结果表明,通过 Tat 机制分泌的 MexA 正确组装并作为 MexAB-OprM 外排泵的亚基发挥作用。在 MexA 缺陷细胞中,引入编码 Tat 蛋白分泌机制内膜成分的 tatC 基因的突变,并用携带 plcH-mexA 融合基因的质粒转化它们。转化体表现出与 MexA 缺陷细胞相当的抗生素敏感性,表明杂交蛋白未被转运至周质。携带 plcH-mexA 质粒的 MexA-tatC 双突变体细胞的全细胞裂解物主要产生未加工的 PlcH-MexA。周质部分没有检测到抗 MexA 抗体反应性物质。基于这些结果,我们得出结论,MexA 可以通过 Tat 途径穿过内膜转运,并与它的同源伴侣 MexB 和 OprM 组装,并且这个复杂的机器是完全功能性的。这种杂交蛋白转运系统有可能成为针对 Tat 系统的抗菌剂的有效筛选工具,因为哺乳动物细胞中不存在 Tat 系统。