首页> 外文期刊>International Journal of Medicinal Mushrooms >Free-Radical Scavenging Activities of Cultured Mycelia of Paecilomyces hepiali (Ascomycetes) Extracts and Structural Characterization of Bioactive Components by Nuclear Magnetic Resonance Spectroscopy
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Free-Radical Scavenging Activities of Cultured Mycelia of Paecilomyces hepiali (Ascomycetes) Extracts and Structural Characterization of Bioactive Components by Nuclear Magnetic Resonance Spectroscopy

机译:肝拟青霉(Ascomycetes)提取物的菌丝体的自由基清除活性和生物活性成分的核磁共振谱结构表征

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摘要

Current research is focused on testing the cultivation of Paecilomyces hepiali mycelia on various plant substrates and producing fungus or mycelial biomass with qualitatively interesting substances. P. hepiali mycelia was cultivated using solid-state fermentation of different substrates. Mycelial biomass was then analyzed, and antioxidant activity was evaluated using the DPPH radical scavenging method for different ethanolic extracts based on a millet substrate (extract 1) or a chickpea substrate (extract 2). Extract 1 corresponds to a half-maximal DPPH radical inhibitory concentration of 1.73 mg/mL; the inhibitory concentration of ethanol extract 2 was almost 4.5 times higher at 7.92 mg/mL. Extracts 1 and 2 were separated into fractions by column chromatography and the chemical structures were determined for the substances that formed the most effective fraction of sample 1. The chemical structures of all compounds in the most active fraction of sample 1 were analyzed by H-1, C-13, distortionless enhancement by polarization transfer, correlation spectroscopy, heteronuclear single-quantum correlation spectroscopy, and heteronuclear multiple-bond correlation spectra.
机译:当前的研究集中在测试各种植物基质上的拟青霉菌丝体的培养,以及产生具有定性有趣物质的真菌或菌丝生物质。使用不同底物的固态发酵培养肝假单胞菌菌丝体。然后分析菌丝的生物量,并使用DPPH自由基清除方法针对基于谷子底物(提取物1)或鹰嘴豆底物(提取物2)的不同乙醇提取物评估抗氧化活性。提取物1对应于DPPH自由基抑制半数最大浓度为1.73 mg / mL;乙醇提取物2的抑制浓度为7.92 mg / mL,几乎提高了4.5倍。通过柱色谱法将提取物1和2分离成馏分,并确定形成样品1最有效馏分的物质的化学结构。用H-1分析样品1活性最高的馏分中所有化合物的化学结构。 ,C-13,通过极化转移进行的无畸变增强,相关光谱,异核单量子相关光谱和异核多键相关光谱。

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