Srijaruskul Kriangsuk, Charoenlap Nisanart, Namchaiw Poommaree, Chattrakarn Sorayut, Giengkam Suparat, Mongkolsuk Skorn, Vattanaviboon Paiboon
Laboratory of Biotechnology, Chulabhorn Research Institute, Bangkok, 10210, Thailand; Program in Applied Biological Sciences: Environmental Health, Chulabhorn Graduate Institute, Bangkok, 10210, Thailand.
Laboratory of Biotechnology, Chulabhorn Research Institute, Bangkok, 10210, Thailand.
PLoS One. 2015 Apr 27;10(4):e0123699. doi: 10.1371/journal.pone.0123699. eCollection 2015.
Stenotrophomonas maltophilia MfsA (Smlt1083) is an efflux pump in the major facilitator superfamily (MFS). Deletion of mfsA renders the strain more susceptible to paraquat, but no alteration in the susceptibility levels of other oxidants is observed. The expression of mfsA is inducible upon challenge with redox cycling/superoxide-generating drug (paraquat, menadione and plumbagin) treatments and is directly regulated by SoxR, which is a transcription regulator and sensor of superoxide-generating agents. Analysis of mfsA expression patterns in wild-type and a soxR mutant suggests that oxidized SoxR functions as a transcription activator of the gene. soxR (smlt1084) is located in a head-to-head fashion with mfsA, and these genes share the -10 motif of their promoter sequences. Purified SoxR specifically binds to the putative mfsA promoter motifs that contain a region that is highly homologous to the consensus SoxR binding site, and mutation of the SoxR binding site abolishes binding of purified SoxR protein. The SoxR box is located between the putative -35 and -10 promoter motifs of mfsA; and this position is typical for a promoter in which SoxR acts as a transcriptional activator. At the soxR promoter, the SoxR binding site covers the transcription start site of the soxR transcript; thus, binding of SoxR auto-represses its own transcription. Taken together, our results reveal for the first time that mfsA is a novel member of the SoxR regulon and that SoxR binds and directly regulates its expression.
嗜麦芽窄食单胞菌MfsA(Smlt1083)是主要易化子超家族(MFS)中的一种外排泵。mfsA基因的缺失使该菌株对百草枯更敏感,但未观察到对其他氧化剂敏感性水平的改变。在用氧化还原循环/超氧化物生成药物(百草枯、甲萘醌和白花丹素)处理后,mfsA的表达可被诱导,并且直接受SoxR调控,SoxR是一种转录调节因子和超氧化物生成剂的传感器。对野生型和soxR突变体中mfsA表达模式的分析表明,氧化型SoxR作为该基因的转录激活因子发挥作用。soxR(smlt1084)与mfsA呈头对头排列,并且这些基因共享其启动子序列的-10基序。纯化的SoxR特异性结合推定的mfsA启动子基序,该基序包含一个与共有SoxR结合位点高度同源的区域,并且SoxR结合位点的突变消除了纯化的SoxR蛋白的结合。SoxR框位于mfsA推定的-35和-10启动子基序之间;并且这个位置对于SoxR作为转录激活因子发挥作用的启动子来说是典型的。在soxR启动子处,SoxR结合位点覆盖soxR转录本的转录起始位点;因此,SoxR的结合会自动抑制其自身的转录。综上所述,我们的结果首次揭示mfsA是SoxR调控子的一个新成员,并且SoxR结合并直接调控其表达。