Functional Components and Application of Rue Essential Oil
A technology of volatile oil and rue, which is applied in the field of application of rue volatile oil in inhibiting plant pathogenic bacteria, and can solve problems such as pollution and affecting the quality of edible fungi
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Embodiment 1
[0042] Pathogenic fungi tested: Aspergillus flavus, Rhizopus stolonifer, Mucor racemosus, Trichoderma viride, Colletotrichum lentis, Fusarium oxysporum Fusarium oxysporum and Phytophythora infestans.
[0043]Plants tested: rue (Cymbopogon distans), that is, a plant that is sandwiched in books to make it emit fragrance.
[0044] The preparation method of rue volatile oil is: put rue 250 grams of rue plant into a round bottom flask, add 350 g of distilled water, adopt steam distillation to collect volatile oil, the oil-water mixture collected is extracted with n-hexane, then with anhydrous sulfuric acid Sodium for drying, and finally freeze-drying with a freeze dryer to obtain volatile oil, which was stored in a 4°C refrigerator.
[0045] experimental method:
[0046] The inhibitory effect of rue volatile oil on the mycelial growth of plant pathogenic fungi was determined by the growth rate method in toxic media.
[0047] Weigh 8 mg of rue volatile oil and dissolve it with 10...
Embodiment 2
[0066] Tested fungi: Aspergillus flavus, Rhizopus stolonife, Mucor racemosus, Trichoderma viride, Colletotrichum lentis, Fusarium oxysporum (Fusarium oxysporum) and potato infestans (Phytophythora infestans).
[0067] The method for detecting the antibacterial activity of plant volatile oil and main compounds is as follows:
[0068] The colony diameter of the mycelia of the seven plant pathogenic bacteria under each treatment was tested in a criss-cross manner, and the smaller the value of the diameter, the stronger the inhibitory activity.
[0069] The preparation process of the compound 1-4 for testing is as follows, the obtained rue grass volatile oil is passed through silica gel column chromatography, according to normal hexane and ethyl acetate (volume ratio is successively 100:0, 50:1, 20:1, 10:1, 8:1, 4:1, 2:1, 1:1, 0:1) for gradient elution to obtain Fr.1-Fr.9 fractions respectively.
[0070] Part FR.2 was chromatographed on a silica gel column (petroleum ether and d...
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