Method of quantitatively evaluating cucumber green mottle mosaic virus resisting ability of Lagenaria leucantha
A quantitative evaluation, gourd technology, applied in the fields of botanical equipment and methods, measuring devices, instruments, etc., can solve the problems of hidden disease manifestations, complex CGMMV symptoms of gourd, inability to classify and describe, etc., to achieve system disease resistance, Accurate identification results and the effect of avoiding grading uncertainty
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Embodiment 1
[0021] Analysis of the inoculation effect of different concentrations of invasive cloning bacteria:
[0022] (1) Plant material: Hangzhou long melon, CGMMV in the field.
[0023] (2) Inoculation identification: The seeds of Hangzhou long melon are sown in a nutrient bowl and grown in a glass greenhouse. The light time is 16 hours, and the temperature is controlled at 25-30°C during the day and 20-25°C at night. Inoculation working solution is OD 600 =1 Bacterial liquid diluted 10, 100, 1000, 10000 times, namely OD 600 =0.1, 0.01, 0.001, 0.0001 four concentrations. After the seedlings grow to the one-leaf-one-heart stage, they are inoculated by the cotyledon pressure contact method. Each individual plant produces 2 inoculation points, and 4 plants are inoculated at each concentration. At the same time, 4 plants are selected for inoculation buffer (Agrobacterium carrying empty vector) as a control (ck). Sampling was taken 15 days and 25 days after inoculation. The selection criteri...
Embodiment 2
[0028] Identification of germplasm resources of gourd gourd resistant to CGMMV
[0029] (1) Plant material: 173 germplasm resources of gourd gourd.
[0030] (2) Inoculation identification: All materials are uniformly sown in a nutrient bowl, with 6-10 plants for each material, arranged in 2 rows, and grown in a glass greenhouse. Use OD 600 =0.01 concentration of the bacterial liquid, after the cotyledons of each material are flattened to the one-leaf one-heart stage inoculation, press the back of the cotyledons with a 1ml syringe until the bacterial liquid penetrates into the leaves evenly. After inoculation, control the temperature at 25-30℃ during the day and 20- 25°C. All materials were sampled for the first time 15 days after inoculation. The selection criterion was the first flat leaf under the apical bud. Each material and each row of plants were sampled and mixed together to form 2 samples, which were grinded by liquid nitrogen and weighed. Add 15ml of the extraction solut...
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