Marugg J D, van Spanje M, Hoekstra W P, Schippers B, Weisbeek P J
J Bacteriol. 1985 Nov;164(2):563-70. doi: 10.1128/jb.164.2.563-570.1985.
The plant-growth-stimulating Pseudomonas putida WCS358 was mutagenized with transposon Tn5. The resulting mutant colony bank was screened for mutants defective in the biosynthesis of the fluorescent siderophore. A total of 28 mutants, divided into six different classes, were isolated that were nonfluorescent or defective in iron acquisition or both. These different types of mutants together with the probable overall structure of the siderophore, i.e., a small peptide chain attached to a fluorescing group, suggest a biosynthetic pathway in which the synthesis of the fluorescing group is preceded by the synthesis of the peptide part. A gene colony bank of P. putida WCS358 was constructed with the broad-host-range cosmid vector pLAFR1. This genomic library, established in Escherichia coli, was mobilized into the 28 individual mutants, screening for transconjugants restored in fluorescence or growth under iron-limiting conditions or both. A total of 13 cosmids were found to complement 13 distinct mutants. The complementation analysis revealed that at least five gene clusters, with a minimum of seven genes, are needed for siderophore biosynthesis. Some of these genes seem to be arranged in an operon-like structure.
能促进植物生长的恶臭假单胞菌WCS358用转座子Tn5进行诱变。对所得的突变菌落文库进行筛选,以找出荧光铁载体生物合成有缺陷的突变体。共分离出28个突变体,分为六个不同类别,这些突变体无荧光或在铁摄取方面有缺陷或两者皆有。这些不同类型的突变体连同铁载体可能的整体结构,即连接到荧光基团的小肽链,提示了一种生物合成途径,其中荧光基团的合成先于肽部分的合成。用广宿主范围的黏粒载体pLAFR1构建了恶臭假单胞菌WCS358的基因文库。这个在大肠杆菌中建立起来的基因组文库被转入28个单独的突变体中,筛选在铁限制条件下荧光或生长或两者都恢复的接合子。共发现13个黏粒可互补13个不同的突变体。互补分析表明,铁载体生物合成至少需要五个基因簇,最少七个基因。其中一些基因似乎以操纵子样结构排列。