Marugg J D, de Weger L A, Nielander H B, Oorthuizen M, Recourt K, Lugtenberg B, van der Hofstad G A, Weisbeek P J
Department of Molecular Cell Biology, University of Utrecht, The Netherlands.
J Bacteriol. 1989 May;171(5):2819-26. doi: 10.1128/jb.171.5.2819-2826.1989.
In iron-limited environments plant-growth-stimulating Pseudomonas putida WCS358 produces a yellow-green fluorescent siderophore called pseudobactin 358. Ferric pseudobactin 358 is efficiently taken up by cells of WCS358 but not by cells of another rhizophere-colonizing strain, Pseudomonas fluorescens WCS374. A gene bank containing partial Sau3A DNA fragments from WCS358 was constructed in a derivative of the broad-host-range cosmid pLAFR1. By mobilization of this gene bank to strain WCS374 a cosmid clone, pMR, which made WCS374 competent for the utilization of pseudobactin 358 was identified. By subcloning of the 29.4-kilobase (kb) insert of pMR the essential genetic information was localized on a BglII fragment of 5.3 kb. Tn5 mutagenesis limited the responsible gene to a region of approximately 2.5 kb within this fragment. Since the gene encodes an outer membrane protein with a predicted molecular mass of 90,000 daltons, it probably functions as the receptor for ferric pseudobactin 358. The gene is flanked by pseudobactin 358 biosynthesis genes on both sides and is on a separate transcriptional unit. WCS374 cells carrying pMR derivatives with Tn5 insertions in the putative receptor gene did not produce the 90,000-dalton protein anymore and were unable to take up Fe3+ via pseudobactin 358. In WCS358 cells as well as in WCS374 cells the gene is expressed only under iron-limited conditions.
在铁限制环境中,促进植物生长的恶臭假单胞菌WCS358产生一种黄绿色荧光铁载体,称为假铁载体358。假铁载体358铁被WCS358细胞有效摄取,但不能被另一种根际定殖菌株荧光假单胞菌WCS374的细胞摄取。在广宿主范围黏粒pLAFR1的衍生物中构建了一个包含来自WCS358的部分Sau3A DNA片段的基因文库。通过将该基因文库转移到WCS374菌株中,鉴定出一个黏粒克隆pMR,它使WCS374能够利用假铁载体358。通过对pMR的29.4千碱基(kb)插入片段进行亚克隆,将必需的遗传信息定位在一个5.3 kb的BglII片段上。Tn5诱变将负责的基因限制在该片段内大约2.5 kb的区域。由于该基因编码一种预测分子量为90,000道尔顿的外膜蛋白,它可能作为假铁载体358铁的受体发挥作用。该基因两侧都有假铁载体358生物合成基因,并且位于一个单独的转录单元上。携带在假定受体基因中插入Tn5的pMR衍生物的WCS374细胞不再产生90,000道尔顿的蛋白质,并且无法通过假铁载体358摄取Fe3+。在WCS358细胞以及WCS374细胞中,该基因仅在铁限制条件下表达。