陈东升, 汪钰, 于志国. 埃勒斯致病杆菌SN22发酵液中Xenorhabic acid的分离[J]. 农药学学报, 2017, 19(1): 32-36. DOI: 10.16801/j.issn.1008-7303.2017.0005
    引用本文: 陈东升, 汪钰, 于志国. 埃勒斯致病杆菌SN22发酵液中Xenorhabic acid的分离[J]. 农药学学报, 2017, 19(1): 32-36. DOI: 10.16801/j.issn.1008-7303.2017.0005
    CHEN Dongsheng, WANG Yu, YU Zhiguo. Separation of Xenorhabic acid from fermented broth of Xenorhabdus ehlersii SN22[J]. Chinese Journal of Pesticide Science, 2017, 19(1): 32-36. DOI: 10.16801/j.issn.1008-7303.2017.0005
    Citation: CHEN Dongsheng, WANG Yu, YU Zhiguo. Separation of Xenorhabic acid from fermented broth of Xenorhabdus ehlersii SN22[J]. Chinese Journal of Pesticide Science, 2017, 19(1): 32-36. DOI: 10.16801/j.issn.1008-7303.2017.0005

    埃勒斯致病杆菌SN22发酵液中Xenorhabic acid的分离

    Separation of Xenorhabic acid from fermented broth of Xenorhabdus ehlersii SN22

    • 摘要: 从土壤中分离得到一株抗菌活性菌株,通过16SrDNA基因序列相似性和系统发育分析,发现该菌株为埃勒斯致病杆菌,并将其命名为埃勒斯致病杆菌SN22(Xenorhabdus ehlersii SN22)。利用硅胶柱层析结合凝胶柱层析技术,从埃勒斯致病杆菌SN22(X.ehlersii SN22)发酵液中分离得到化合物 1 ,通过核磁共振波谱、质谱及X-光单晶衍射技术分析,鉴定其为3-(环己-2-烯)丙烯酸。文献调研发现,该化合物为新的天然产物,命名为Xenorhabic acid。采用菌丝生长速率法测定了该化合物对植物病原真菌的抑菌活性;采用微量稀释法测定了其对病原细菌的最小抑制浓度。结果表明:其对向日葵菌核病菌Sclerotinia sclerotiorum和瓜果腐霉病菌Pythium aphanidermatum菌丝生长具有明显抑制作用,其EC50值分别为27.99和29.55 μg/mL;对大肠埃希杆菌Escherichia coli的最小抑制浓度(MIC)为62.5 μg/mL。

       

      Abstract: 16SrDNA gene sequence similarity and phylogentic analysis indicated that the strain of antimicrobial activity obtained from soil belonged to the genus Xenorhabdus ehlersii and named Xenorhabdus ehlersii SN22. Xenorhabic acid (compound 1 ) was isolated from fermented broth of X. ehlersii SN22 by silica gel column chromatography and Sephadex LH-20 chromatography. Characterized by X-ray crystal diffraction, 1HNMR and 13C NMR, and ESI-MS spectral analysis, the chemical structure of 1 was confirmed to be 3-(cyclohex-2-en) acrylic acid which was a new natural product. The antifungal activity of Xenorhabic acid against phytopathogenic fungi was determined by mycelium growth rate method. The results showed Xenorhabic acid could effectively inhibit the mycelium growth of Sclerotinia sclerotiorum and Pythium aphanidermatum, and the EC50 values were 27.99 and 29.55 μg/mL respectively. In addition, Xenorhabic acid also showed antibacterial activity against Escherichia coli, with the minimum inhibitory concentration (MIC) value of 62.5 μg/mL.

       

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