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Identification of a Genetic Locus in Pseudomonas aureofaciens Involved in Fungal Inhibition

机译:金黄色假单胞菌中涉及真菌抑制的遗传基因座的鉴定。

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In iron-rich conditions, Pseudomonas aureofaciens PA147-2 produces an antibiotic-like compound that inhibits the growth of a plant fungal pathogen, Aphanomyces euteiches. To contribute to the potential use of PA147-2 as a biocontrol organism, we report the identification of a genetic locus important for antibiotic biosynthesis. Mutants defective for fungal inhibition (Af-) were generated by Tn5 mutagenesis. Southern hybridization of total DNAs from three Af- mutants indicated that loss of fungal inhibition was due to a single Tn5 insertion in each mutant. Restriction mapping of the mutation points showed that in two mutants the Tn5 insertions were in the same 16.0-kb EcoRI fragment and were separated by 2.1 kb. A genomic library of PA147-2 was constructed and screened by using a region of DNA flanking the Tn5 insertion in one mutant (PA109) as a probe to recover complementing cosmids. Three cosmids containing a 16.0-kb EcoRI fragment complementary to the two mutants were recovered. Allele replacement by homologous recombination with putative complementing cosmids restored one mutant to antifungal activity against A. euteiches. Southern analysis of the complemented mutants confirmed that allele replacement had occurred between cosmid DNA and Tn5. The wild-type 16.0-kb EcoRI fragment was cloned from the cosmid and complemented the two mutants to antifungal activity. An antifungal compound was isolated from PA147-2 grown on solid medium. Antifungal activity correlated to a peak on high-pressure liquid chromatography analysis. Under the same growth and extraction conditions, the antifungal activity seen in PA147-2 was absent in two Af- mutants. Furthermore, absence of an antifungal compound in each mutant correlated to the absence of the wild-type “antifungal” peak on high-pressure liquid chromatography analysis.
机译:在富铁条件下,金黄色假单胞菌PA147-2产生一种类抗生素化合物,该化合物抑制植物真菌病原体Aphanomyces euteiches的生长。为了有助于PA147-2作为生物防治生物的潜在用途,我们报告了对抗生素生物合成很重要的遗传位点的鉴定。 Tn5诱变产生了真菌抑制(Af-)缺陷的突变体。来自三个Af-突变体的总DNA的Southern杂交表明,真菌抑制作用的丧失是由于每个突变体中插入了一个Tn5。突变点的限制性图谱显示,在两个突变体中,Tn5插入片段位于相同的16.0-kb EcoRI片段中,相隔2.1 kb。通过使用一个突变体(PA109)中位于Tn5插入侧翼的DNA区域作为回收互补粘粒的探针,构建和筛选PA147-2的基因组文库。回收了含有与两个突变体互补的16.0-kb EcoRI片段的三个粘粒。通过与假定的互补粘粒的同源重组进行等位基因置换,使一种突变体恢复了针对真菌的抗真菌活性。对互补突变体的Southern分析证实,等位基因置换发生在粘粒DNA和Tn5之间。从粘粒中克隆了野生型16.0 kb EcoRI片段,并使这两个突变体具有抗真菌活性。从在固体培养基上生长的PA147-2中分离出抗真菌化合物。抗真菌活性与高压液相色谱分析中的峰相关。在相同的生长和提取条件下,两个Af突变体均不存在PA147-2中的抗真菌活性。此外,在高压液相色谱分析中,每个突变体中均不存在抗真菌化合物,这与野生型“抗真菌”峰不存在相关。

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