Department of Biological and Physical Sciences, Montana State University Billings, Billings, Montana, USA.
J Bacteriol. 2013 Sep;195(17):3876-87. doi: 10.1128/JB.00528-13. Epub 2013 Jun 21.
Pyridine-2,6-bis(thiocarboxylate) (PDTC), produced by certain pseudomonads, is a sulfur-containing siderophore that binds iron, as well as a wide range of transition metals, and it affects the net hydrolysis of the environmental contaminant carbon tetrachloride. The pathway of PDTC biosynthesis has not been defined. Here, we performed a transposon screen of Pseudomonas putida DSM 3601 to identify genes necessary for PDTC production (Pdt phenotype). Transposon insertions within genes for sulfate assimilation (cysD, cysNC, and cysG [cobA2]) dominated the collection of Pdt mutations. In addition, two insertions were within the gene for the LysR-type transcriptional activator FinR (PP1637). Phenotypic characterization indicated that finR mutants were cysteine bradytrophs. The Pdt phenotype of finR mutants could be complemented by the known target of FinR regulation, fprA (encoding ferredoxin:NADP(+) oxidoreductase), or by Escherichia coli cysJI (encoding sulfite reductase). These data indicate that fprA is necessary for effective sulfate assimilation by P. putida and that the effect of finR mutation on PDTC production was due to deficient expression of fprA and sulfite reduction. fprA expression in both P. putida and P. aeruginosa was found to be regulated by FinR, but in a manner dependent upon reduced sulfur sources, implicating FinR in sulfur regulatory physiology. The genes and phenotypes identified in this study indicated a strong dependence upon intracellular reduced sulfur/cysteine for PDTC biosynthesis and that pseudomonads utilize sulfite reduction enzymology distinct from that of E. coli and possibly similar to that of chloroplasts and other proteobacteria.
吡啶-2,6-双(硫代羧酸酯)(PDTC)是某些假单胞菌产生的一种含硫铁载体,可与铁以及广泛的过渡金属结合,并影响环境污染物四氯化碳的净水解。PDTC 的生物合成途径尚未确定。在这里,我们对 Pseudomonas putida DSM 3601 进行了转座子筛选,以鉴定 PDTC 产生所必需的基因(Pdt 表型)。转座子插入到硫酸盐同化基因(cysD、cysNC 和 cysG [cobA2])内,占据了 Pdt 突变体的大部分。此外,两个插入位于 LysR 型转录激活因子 FinR(PP1637)的基因内。表型特征表明,finR 突变体是半胱氨酸迟缓生长体。finR 突变体的 Pdt 表型可以通过已知的 FinR 调节靶标 fprA(编码铁氧还蛋白:NADP(+)氧化还原酶)或大肠杆菌 cysJI(编码亚硫酸盐还原酶)来互补。这些数据表明,fprA 是 P. putida 有效同化硫酸盐所必需的,finR 突变对 PDTC 产生的影响是由于 fprA 和亚硫酸盐还原的表达不足。发现 fprA 在 P. putida 和 P. aeruginosa 中的表达均受 FinR 调节,但方式依赖于还原硫源,表明 FinR 参与了硫调节生理学。本研究中鉴定的基因和表型表明,PDTC 生物合成强烈依赖于细胞内还原态硫/半胱氨酸,假单胞菌利用的亚硫酸盐还原酶学与大肠杆菌不同,可能与叶绿体和其他变形菌相似。