Tanabe Tomotaka, Naka Ayaka, Aso Hiroaki, Nakao Hiroshi, Narimatsu Shizuo, Inoue Yuji, Ono Tomomichi, Yamamoto Shigeo
Department of Molecular Biopharmaceutical Sciences, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 1-1-1 Tsushima-naka, Okayama, Japan.
Microbiol Immunol. 2005;49(9):823-34. doi: 10.1111/j.1348-0421.2005.tb03671.x.
We demonstrated that Vibrio vulnificus M2799 utilizes aerobactin for growth as an exogenous siderophore under iron-limiting conditions, concomitant with enhanced production of the 76-kDa iron-repressible outer membrane protein. Subsequently, by applying the Fur titration assay method to the M2799 genomic libraries followed by further cloning of the regions surrounding the candidate genes, we identified the 8.4-kb aerobactin utilization gene cluster which consists of five genes arranged in three distinct transcriptional units. It was confirmed by disruption of the corresponding genes that the first unit forming a three-gene operon (vatCDB) and the third unit of a single gene (iutA) encode an ATP-binding cassette transport component and the 76-kDa ferric aerobactin receptor, respectively. The second unit of another single gene (iutR), encodes a homologue of the GntR family of transcriptional repressors. Although transcription of the first and third units was iron-regulated, the iutR gene was transcribed regardless of iron status in the growth medium. Construction of an iutR disruptant coupled with genetic complementation experiments suggested that the gene encodes a transcriptional repressor for iutA. This is the first example of a regulator gene involved in aerobactin-enhanced production of IutA.
我们证明,创伤弧菌M2799在铁限制条件下利用气杆菌素作为外源性铁载体进行生长,同时76 kDa的铁抑制外膜蛋白产量增加。随后,通过将Fur滴定分析法应用于M2799基因组文库,然后进一步克隆候选基因周围的区域,我们鉴定出了8.4 kb的气杆菌素利用基因簇,该基因簇由五个基因组成,排列在三个不同的转录单元中。通过破坏相应基因证实,形成三基因操纵子的第一个单元(vatCDB)和单个基因的第三个单元(iutA)分别编码一个ATP结合盒转运成分和76 kDa的铁气杆菌素受体。另一个单基因(iutR)的第二个单元编码转录抑制因子GntR家族的一个同源物。虽然第一个和第三个单元的转录受铁调节,但iutR基因的转录与生长培养基中的铁状态无关。构建iutR缺失突变体并结合基因互补实验表明,该基因编码iutA的转录抑制因子。这是参与气杆菌素增强IutA产生的调节基因的第一个例子。