Method for improving resistance of sunflowers to parasitic weed sunflower orobanche Cumana by utilizing 5-aminolevulinic acid
An aminolevulinic acid, sunflower technology, applied in the directions of botanical equipment and methods, application, seed and rhizome treatment, etc., to achieve the effect of reducing use and protecting the ecological environment
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Embodiment 1
[0038] 1 Preparation of different concentrations of 5-aminolevulinic acid
[0039] Weigh 5-aminolevulinic acid in the dark, and prepare 0, 5, 10, 15, 20 mg / L ALA mediation solution with distilled water.
[0040] Table 1 Concentration gradient of 5-aminolevulinic acid
[0041]
[0042] Note: The recommended concentration refers to the optimal concentration obtained after passing the test, that is, the ALA content added per 1L of water.
[0043] 2 Materials and methods
[0044] 2.1 Pretreatment and germination of sunflower seeds
[0045] Select plump and healthy sunflower TK0409 seeds to peel off the exocarp, sterilize in 70% absolute ethanol solution for 2 minutes, rinse with sterile water several times, put the seeds in different concentrations of ALA solution and soak for 18 hours; after fully absorbing the ALA solution After the seeds were washed twice with distilled water, they were put into a petri dish with two layers of filter paper containing distilled water, and ...
Embodiment 2
[0056] Example 2 Determination of antioxidant enzymes
[0057] Antioxidant enzyme activity includes ascorbate peroxidase (APX), catalase (CAT), peroxidase (POD), superoxide dismutase (SOD), and glutathione reductase (GR) , the antioxidant enzyme activity was measured with a Muti-ModeReader (SYNERGY HTX) instrument according to the following method.
[0058] 1. Determination of APX enzyme
[0059] The APX activity assay method was improved according to the method of Nakano and Asada (1981). The reaction system was 3 mL, including 2.9 mL of 100 mM potassium phosphate buffer (pH 7.0, containing 0.1 mM EDTA-Na 2 , 0.3mM Ascorbic Acid, 0.06mM H 2 o 2 ) and 100 μl enzyme extract. Measure the absorbance change of the reaction mixture within 1min at 290 nm, and the extinction coefficient is 2.8mM -1 cm -1 .
[0060] 2. Determination of CAT enzyme
[0061] CAT activity through H 2 o 2 Determination of consumption (the extinction coefficient is 39.4mM -1 cm -1 ). The react...
Embodiment 3
[0074] The measurement of embodiment 3 MDA and ROS
[0075] MDA and ROS were measured with a spectrophotometer (UV-5500, METASH).
[0076] 1. Determination of MDA
[0077] The content of MDA was determined according to Zhou and Leul (1999) with modified thiobarbituric acid colorimetric method. Add 5 mL of 0.5% thiobarbituric acid (TBA, prepared with 10% trichloroacetic acid) solution to 2 mL of the supernatant enzyme solution, react in a water bath at 95 ° C for 30 min, and immediately put it in an ice bath; Colorimetric at the place, the difference is used to calculate the MDA content, the extinction coefficient is 155mM -1 cm -1 .
[0078] 2. Determination of ROS
[0079] Reactive oxygen species (ROS) including hydrogen peroxide (H 2 o 2 ), superoxide anion (O 2 - ),Hydroxyl radicals( - OH).
[0080] 2.1H 2 o 2 Determination of
[0081] h 2 o 2 According to the method of Velikova et al. (2000), the reaction system was 2 mL, containing 0.5 mL of supernatant, 0...
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