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首页> 外文期刊>Molecular Plant-Microbe Interactions >Polymorphism of the Polyketide Synthase Gene phlD in Biocontrol Fluorescent Pseudomonads Producing 2,4-Diacetylphloroglucinol and Comparison of PhlD with Plant Polyketide Synthases
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Polymorphism of the Polyketide Synthase Gene phlD in Biocontrol Fluorescent Pseudomonads Producing 2,4-Diacetylphloroglucinol and Comparison of PhlD with Plant Polyketide Synthases

机译:聚酮化合物合酶基因phlD在生产2,4-二乙酰基间苯三酚的生物控制荧光假单胞菌中的多态性及与植物聚酮化合物合酶的PhlD比较

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Many biocontrol fluorescent pseudomonads can protect plants from soilborne fungal pathogens through production of the antifungal secondary metabolite 2,4-diacetylphloroglucinol (Phl). One of the phl biosynthetic genes, phlD , encodes a polyketide synthase similar to plant chalcone synthases. Here, restriction analysis of phlD from 39 Phl+ biocontrol fluorescent pseudomonads yielded seven different banding patterns. The gene was sequenced in seven strains, representing the different restriction patterns. Cluster analysis of phlD restriction data or phlD sequences indicated that phlD polymorphism was high, and two main clusters were obtained when predicted PhlD sequences were compared. When the seven PhlD sequences were studied with those of other procaryotic polyketide synthases (gram-positive bacteria) and plant chalcone synthases, however, Phl+ pseudomonads, gram-positive bacteria, and plants clustered separately. Yet, sequence analysis of active site regions for PhlD and plant chalcone synthases revealed that PhlD can be considered a member of the chalcone synthase family, which may be interpreted as convergent evolution of key enzymes involved in secondary metabolism. For the 39 Phl+ pseudomonads, a relationship was found among phlD restriction patterns, phylogenetic groups defined by 16S rDNA restriction analysis (confirmed by 16S rDNA sequencing), and production levels of Phl in vitro.
机译:许多生物防治荧光假单胞菌可以通过产生抗真菌次生代谢物2,4-二乙酰基间苯三酚(Phl)保护植物免受土壤传播的真菌病原体的侵害。 phl生物合成基因之一phlD编码类似于植物查耳酮合酶的聚酮化合物合酶。在这里,对39个Phl + 生防荧光假单胞菌对phlD的限制性酶切分析产生了7种不同的谱带模式。该基因在代表不同限制模式的七个菌株中测序。对phlD限制性数据或phlD序列的聚类分析表明,phlD多态性很高,并且当比较预测的PhlD序列时获得了两个主要的聚类。当与其他原核聚酮化合物合酶(革兰氏阳性细菌)和植物查尔酮合酶一起研究七个PhlD序列时,Phl + 假单胞菌,革兰氏阳性细菌和植物分别聚集。然而,对PhlD和植物查耳酮合酶的活性位点区域的序列分析显示,PhlD可以被认为是查耳酮合酶家族的成员,这可以解释为参与次级代谢的关键酶的趋同进化。对于39个Phl + 假单胞菌,发现了phlD限制模式,通过16S rDNA限制分析(通过16S rDNA测序确认)定义的系统发育基团和体外Phl的生产水平之间的关系。

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