Identification and evaluation method for canker resistance of kiwi fruit
A technology for identification of canker disease and resistance of kiwifruit, applied in the field of level evaluation, can solve the problems of unclear resistance to canker disease, unsatisfactory identification results, large errors, etc., to promote the understanding of canker disease resistance, and the identification method is simple and intuitive Effect
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Embodiment 1
[0028] Adopt the present invention to carry out identification and evaluation to canker disease resistance by in vitro branch inoculation and branch peeling method, comprise the following steps:
[0029] 1. Experimental materials: Hongyang, Walter, Jinkui, Guifei, Yate, Xuxiang, Hayward, Shimei and Qiuxiang; Canker sores is a strong pathogenic type 3 Psa strain isolated in Guangxi.
[0030] 2, adopt the present invention to carry out identification and evaluation to canker disease resistance by in vitro branch inoculation and branch peeling method, comprise the following steps:
[0031] (1) Sample collection: The 1-year-old branches of the above-mentioned kiwifruit after falling leaves were collected in January, and the middle part of the branches was about 30 cm long, and 5 branches were taken for each variety; the high-sensitivity variety "Hongyang" kiwifruit was used as a control (20 branch);
[0032] (2) Pathogen culture: Pick a single clone from the preserved solid mediu...
Embodiment 2
[0037] Use ordinary trays for cultivation, 90% humidity, light at 20°C; dark at 15°C; alternately for 12 h. The disease occurrence was observed and recorded every 7 days, and the disease index was calculated. After 35 days, the disease resistance of each variety was identified and evaluated. Resistance evaluation was performed according to the following criteria. The rest are the same as in Example 1.
[0038]
Embodiment 3
[0040] Take healthy annual branches of different kiwifruit materials in June, take the middle 30cm of the branches, sterilize the surface of the branches with 70% alcohol before inoculation, use an 8mm puncher to punch holes in the middle of the branches, take 15 branches for each material, and use a disposable Inject 100 μL of the suspension of P. kiwifruit canker sores into the syringe, and repeat 3 times. The inoculum concentration was 3×10 8 cfu / mL, placed under constant temperature and humidity at 20°C after inoculation, and the infection rate was investigated every day after 24 hours, until 20 days, the number of infected branches was counted, and the infection rate was calculated. Inoculation identification refers to the method of Ren Xinzheng (1994) (Classification and identification of plant pathogenic bacteria. Beijing: China Agricultural Press). The rest are the same as in Example 1.
[0041] refer to Figure 1-5 , Table 3 shows the identification effects and dif...
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