肉桂(Cinnamomum Cassia)和黑孜然籽(Nigella Sativa)不同提取物对茄丝核生长及其胞外水解酶的抑制作用

seham abd el aziz, A. abo-shady, Mervat A. R. Ibrahim, Maha Helmy
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引用次数: 1

摘要

茄核菌、肉桂、奈杰尔拉、果胶酶和蛋白酶、羧甲基纤维素酶、对接摘要:本研究评估了肉桂和黑孜然种子的不同提取物对植物病原真菌茄核菌及其细胞外细胞壁降解酶生长的抑制能力。在25±1°C的体外培养72小时后,浓度为300和450ppm的二氯甲烷和己烷肉桂提取物完全抑制了龙葵的生长。4000ppm的黑孜然种子的二氯甲烷或己烷提取物在72小时后分别抑制了37%和39%的龙葵生长。此外,2000ppm的黑孜然籽己烷提取物对果胶裂解酶(PL)和多聚半乳糖醛酸酶(PG)的活性分别抑制了55%和38%。此外,2000ppm的黑孜然种子甲醇提取物表现出显著的外显蛋白酶活性降低(74.8%)。GC-MS分析结果表明,亚油酸是黑孜然籽己烷提取物固定油分的主要成分,而(E)-肉桂醛是肉桂己烷和二氯甲烷提取物的主要成分。高效液相色谱-质谱联用技术对黑孜然种子甲醇提取物进行分析,结果表明,其主要成分为核黄素。对接用于鉴定与果胶裂解酶A和外显蛋白酶的主要成分相互作用。
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Inhibition Of Rhizoctonia Solani Growth and Its Extracellular Hydrolytic Enzymes by Different Extracts of Cinnamon (Cinnamomum Cassia) and Black Cumin Seeds (Nigella Sativa)
Rhizoctonia solani, Cinnamomum cassia, Nigella sativa, Pectinases and protease, Carboxymethyl cellulase, Docking Abstract: The present study evaluated the ability of different extracts of cinnamon and black cumin seeds to inhibit the growth of the phytopathogenic fungus Rhizoctonia solani and its extracellular cell wall degrading enzymes. Concentrations of 300 and 450 ppm of methylene chloride and hexane extracts of cinnamon completely inhibited the growth of R. solani after 72 hours of incubation at 25±1°C in vitro. Methylene chloride or hexane extracts of black cumin seeds at 4000 ppm after 72 hours inhibited the growth of R. solani by 37 and 39% respectively. Moreover, black cumin seed hexane extract at 2000 ppm inhibited 55% and 38% of the activity of pectin lyase (PL) and polygalacturonase (PG) respectively. In addition, the methanolic extract of black cumin seeds at 2000 ppm exhibited a significant reduction of exo-protease activity (74.8%). GC-MS analysis results showed that linoleic acid is the main component of the fixed oil fraction of black cumin seed hexane extract while (E)-cinnamaldehyde is the main component in both hexane and methylene chloride extracts of cinnamon. HPLC-MS analysis of black cumin seeds methanolic extract showed that amentoflavone, was the main component. Docking was used to identify the major component interaction with pectin lyase A and exo-protease.
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