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Molecular characterization of an endophytic Phomopsisliquidambaris CBR-15 from Cryptolepis buchanani Roem. and impact of culture media on biosynthesis of antimicrobial metabolites

机译:来自布氏隐孢子虫(Cryptolepis buchanani Roem)的内生拟南芥液体金龟子CBR-15的分子表征。培养基对抗微生物代谢产物生物合成的影响

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摘要

An endophytic fungus Phomopsis liquidambaris CBR-15, was isolated from Cryptolepis buchanani Roem. (Asclepiadaceae) and identified by its characteristic culture morphology and molecular analysis of the ITS region of rDNA and intervening 5.8S rRNA gene. The impact of different culture media on biosynthesis of antimicrobial metabolites was tested by disc diffusion assay. Polyketide synthase gene (PKS) of the endophytic fungus was investigated using three pairs of degenerate primers LC1–LC2c, LC3–LC5c and KS3–KS4c by PCR. TLC-bioautography method was employed to detect the antimicrobial metabolites. Antimicrobial metabolites fractionated with ethyl acetate extract showed significant antimicrobial activity against the test bacteria and fungi. Biosynthesis of antimicrobial metabolites was optimum as depicted by zone of inhibition from ethyl acetate extract cultured in potato dextrose broth. Strain CBR-15 was identified as Phomopsisliquidambaris and PKS genes of the fungus were amplified with LC3–LC5c and KS3–KS4c sets of degenerate primers. These findings suggest that endophytic P.liquidambaris CBR-15 harbor iterative type I fungal PKS gene domain which indicates the biosynthetic potential of endophytic fungi as producers of natural antimicrobial metabolites. The study also demonstrates the utilization and optimization of different culture media which best supports for the biosynthesis of the antimicrobial metabolites from P.liquidambaris.Electronic supplementary materialThe online version of this article (doi:10.1007/s13205-014-0204-2) contains supplementary material, which is available to authorized users.
机译:从布氏隐孢子虫(Cryptolepis buchanani Roem)中分离出一种内生真菌Phomopsis liquidambaris CBR-15。 (Asclepiadaceae)并通过其特征性的培养形态和对rDNA的ITS区和5.8S rRNA基因的分子分析进行鉴定。通过椎间盘扩散测定法测试了不同培养基对抗微生物代谢产物生物合成的影响。使用三对简并引物LC1-LC2c,LC3-LC5c和KS3-KS4c通过PCR研究了内生真菌的聚酮化合物合酶基因(PKS)。采用薄层色谱-生物自显影技术检测抗菌药物的代谢产物。用乙酸乙酯提取物分级分离的抗微生物代谢产物对测试细菌和真菌具有显着的抗微生物活性。如马铃薯葡萄糖肉汤中培养的乙酸乙酯提取物的抑制区所示,抗微生物代谢产物的生物合成是最佳的。 CBR-15菌株被鉴定为液体枯萎菌,并用LC3-LC5c和KS3-KS4c简并引物扩增了真菌的PKS基因。这些发现表明,内生的P.liquidambaris CBR-15具有I型迭代真菌PKS基因域,这表明内生真菌作为天然抗微生物代谢物的生产者具有生物合成潜力。这项研究还证明了不同培养基的利用和优化,这些培养基最能支持液态拟南芥抗菌素的生物合成。电子补充材料本文的在线版本(doi:10.1007 / s13205-014-0204-2)包含补充剂资料,可供授权用户使用。

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