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海洋放线菌Y12-26中抗真菌活性代谢产物的分离纯化与结构鉴定 被引量:11

Purification and structure elucidation of antifungal bioactive metabolites from marine actinomycete Y12-26
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摘要 目的研究海洋放线菌Y12-26发酵液中对几种植物病原真菌具有抑制作用的次生代谢活性物质。方法发酵离心上清液用等体积正丁醇萃取,得到发酵液浸膏。浸膏采用正相硅胶柱色谱、制备TLC和半制备HPLC等方法进行分离纯化该菌株活性次级代谢产物,并运用MS、~1H NMR和^(13)C NMR等波谱技术并结合文献比对鉴定所分离的单体化合物。结果从28g正丁醇萃取物中分离纯化并鉴定了3个单体活性化合物,分别为:salicylamide(1)、iturin A-2(2)、daidzein-4',7-di-α-L-rhamnoside(3)。结论海洋放线菌Y12-26能代谢产生具有多种生物活性的化合物。化合物1对Botriytis cinerea和Pyricularia oryzae的最低抑菌浓度(minimal inhibitory concentration,MIC)为125μg/mL,化合物2有强烈的抗真菌活性,其对Rhizoctonia solani的MIC为12.5μg/mL,化合物3对Botriytis cinerea的MIC为125μg/mL。本文首次报道大豆素类化合物3抗植物病原真菌活性。 Objective To study the antifungal constituents of a marine actinomycete Y12-26. Methods The fermentation centrifugal supernatant was extracted with an equal volume of butanol. The extracts was isolated and repeatedly purified by column chromatography on silica gel, preparative TLC arid semi-preparative HPLC. Their structures were elucidated by MS, ^1H-NMR, ^13C-NMR spectral analysis and compared with the data of literature. Results Three compounds were isolated and identified as salicylamide (1), iturin A-2 (2), daidzein-4',7-di-α-L-rhamnoside (3) from 28g butanol extracts. Conclusion The marine actinomycete Y12-26 can produce the compounds with many biological activities. The MIC of compound 1 against Botrytis cinerea and Pyricularia oryzae is 125μg/mL, compound 2 shows significant antifungal bioactivity against Rhizoctonia solaniis 12.5μg/mL, compound 3 against Botrytis cinereais 125μg/mL. Compound 3 is reported firstly for the inhibitory activities against plant-pathogenic fungus.
出处 《中国抗生素杂志》 CAS CSCD 北大核心 2017年第8期631-638,共8页 Chinese Journal of Antibiotics
基金 国家科技支撑项目(No.2011BAE06B04-1)
关键词 海洋放线菌 分离纯化 结构鉴定 抗真菌活性 Marine actinomycete Purification Structural elucidation Antifungal bioactivity
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  • 1Zhu F. Chapter 6: The metabolites of marine actinomycetes [A]. In: Lin Y C. Marine microorganisms and the metabolites[M]. Beijing: Chemical Industry press, 2003: 169
  • 2He H Y, Ding W D, Beman V S, et al. Lomaiviticins A and B, potent antitumor antibiotics from Micromonospora lomaivitiensis [J]. J Am Chem Soc , 2001,123(22): 5362
  • 3Kuznetsova T A, Dmitrenok A S, Sobolevskaya M P, et al. Ubiquinone Q(9) from a marine isolate of an actinobacterium Nocardia sp. [J]. Russ Chem Bull, 2002,51 (10): 1951
  • 4Maskey R P, Helmke E, Fiebig H H, et al. Parimycin: Isolation and structure elucidation of a novel cytotoxic 2,3-dihydroquinizarin analogue of gamma-indomyclnone from a marine streptomycete isolate [J]. d Antibiot, 2002,55 (12): 1031
  • 5Maskey R P, Pusecker K, Speitling M, et al. On marine bacteria, article 18. 2"-chartreusin-monoacetate, a new natural product with unusual anisotropy effects from the marine isolate Streptornyces sp. B5525, and its 4"-isomer [J]. Zeit Fur Nat Section B, 2002,57(7):823
  • 6Furumai T, Igarashi Y, Higuchi H, et al. Kosinostatin, a quinocycline antibiotic with antitumor activity from Micromonospora sp. TP-A0468 [J]. J Antibiot,2002,55(2): 128
  • 7Igarashi Y, Higuchi H, Oki T, et al. NMR analysis of quinocycline antibiotic: Structure determination of kosinostatin, an antitumor substance from Micromonospora sp. TP-A0468 [J]. J Antibiot,2002,55(2): 134
  • 8Kalaitzis J A, Hamano Y, Nilsen G, et al. Biosynthesis and structural revision of neomarinone [J]. Org Lett,2003,5(23):4449
  • 9Malet-Cascon L, Romero F, Espliego-Vazquez F, et al. IB-00208, a new cyctotoxic polycyclic xanthone produced by a marinederived Actinomadura I. Isolation of the strain, taxonomy and biological activities [J]. J Antibiot,2003,56(3): 219
  • 10Rodrlguez J C, Puents J L F, Baz J P, et al. IB-00208, a new cyctotoxlc polycyclic xanthone produced by a marine-derived Actinomadura I. Isolation, physico-chemical properties and structure determination [J]. J Antibiot, 2003,56(3):318

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