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红树林内生真菌 Phomopsis asparagi DHS-48 与Pestalotiopsis sp. HHL-101 共培养次级代谢产物研究

Investigation of Secondary Metabolites from the Co-cultivation of the Mangrove Endophytic Fungi Phomopsis asparagi DHS-48 and Pestalotiopsis sp. HHL-101

  • 摘要:目的】研究来源于海南红树林植物大红树(Rhizophora mangle)内生真菌 Phomopsis asparagi DHS-48 与红海榄(Rhizophora stylosa)内生真菌 Pestalotiopsis sp. HHL-101 共培养体系的次级代谢产物。【方法】通过平板对峙实验与扫描电镜(SEM)观察菌株间的竞争性相互作用及微观形态变化;利用HPLC图谱分析单一培养与共培养发酵粗提物的代谢差异;采用正相硅胶柱层析、反相 ODS 柱层析、Sephadex LH-20 凝胶柱层析及半制备高效液相色谱等多种色谱技术,对其共培养发酵产物的乙酸乙酯提取物进行分离纯化;运用核磁共振波谱、质谱等波谱学方法,并结合文献数据比对,鉴定化合物的结构。【结果】平板对峙实验与 SEM 结果显示,两菌在接触区形成色素带,且菌丝致密缠绕在交界处两者细胞膜相融合,表明在共培养体系中存在激烈的竞争性相互作用。代谢分析显示,共培养体系的 HPLC 图谱发生变化,其特征色谱峰的强度明显增强,且色谱峰数量增多,表明共培养提升了代谢产物的丰度与多样性。从该共培养体系中分离得到 12 个化合物,分别鉴定为:2-苯乙基-β-D-吡喃葡萄糖苷(1)、对羟基苯乙醇(2)、4-羟基苯乙基乙酸酯(3)、对羟基苯甲醛(4)、对羟基苯甲酸(5)、3-氯龙胆醇(6)、2'-O-甲基尿苷(7)、2'-脱氧胸腺嘧啶核苷(8)、胸腺嘧啶(9)、cyclo(L-Hyp-L-Ala)(10)、(1R,2R,4R)-三羟基薄荷烷(11)和麦角甾醇(12)。其中,经文献比对确认,化合物 6和11 为首次从拟茎点霉属(Phomopsis)与拟盘多毛孢属(Pestalotiopsis)真菌中分离得到。【结论】从 Phomopsis asparagi DHS-48 与 Pestalotiopsis sp. HHL-101 的共培养体系中成功分离并鉴定了 12 个次级代谢产物,为芳香族类、核苷类、单萜、环二肽类及甾体等多种结构类型,并发现 2 个化合物为该两属真菌的首次分离报道,丰富了上述属真菌次级代谢产物的结构多样性。

     

    Abstract:Objective】To investigate the secondary metabolites produced by the co-culture system of two mangrove endophytic fungi: Phomopsis asparagi DHS-48 (isolated from Rhizophora mangle) and Pestalotiopsis sp. HHL-101 (isolated from Rhizophora stylosa). 【Methods】Interspecific competitive interactions and micromorphological changes were observed using plate confrontation assays and scanning electron microscopy (SEM). Metabolic differences between the crude extracts of mono-cultures and the co-culture were analyzed using HPLC profiling. The ethyl acetate extract from the co-culture fermentation was isolated and purified using various chromatographic techniques, including normal-phase silica gel column chromatography, reversed-phase ODS column chromatography, Sephadex LH-20 gel column chromatography, and semi-preparative high-performance liquid chromatography (HPLC). The structures of the isolated compounds were identified using spectroscopic methods, including NMR and MS, in combination with literature data comparison. 【Results】Plate confrontation assays and SEM results revealed the formation of a pigmented line in the contact zone, accompanied by dense mycelial coiling and cell membrane fusion at the interface, indicating intense competitive interactions within the co-culture system. Metabolic analysis demonstrated changes in the HPLC profile of the co-culture, characterized by significantly enhanced intensity of characteristic peaks and an increased number of peaks, suggesting that co-cultivation improved both the abundance and diversity of metabolic products. Twelve compounds were isolated from the co-culture system and identified as: 2-phenylethyl-β-D-glucopyranoside (1), tyrosol (2), 4-hydroxyphenethyl acetate (3), 4-hydroxybenzaldehyde (4), 4-hydroxybenzoic acid (5), 3-chlorogentisyl alcohol (6), 2'-O-methyluridine (7), 2'-deoxythymidine (8), thymine (9), cyclo(L-Hyp-L-Ala) (10), (1R,2R,4R)-trihydroxymenthane (11), and ergosterol (12). Notably, compounds 6, 9, and 11 were isolated from the genera Phomopsis and Pestalotiopsis for the first time. 【Conclusion】Twelve secondary metabolites were successfully isolated and identified from the co-culture of Phomopsis asparagi DHS-48 and Pestalotiopsis sp. HHL-101, encompassing diverse structural types such as aromatic derivatives, nucleosides, monoterpenes, cyclic dipeptides, and sterols. The discovery of three compounds reported for the first time from these two genera enriches the structural diversity of secondary metabolites known to be produced by them.

     

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