Method for quickly identifying disease resistance of inoculated in vitro branched to pear fire blight
A technology for branch inoculation and E. amylovora, which is applied in horticultural methods, botany equipment and methods, biochemical equipment and methods, etc., can solve the problem of the lack of a unified and clear evaluation method for disease resistance measurement of E. amylovora. Quantitative statistics on the incidence of disease, rating of disease resistance and other issues, to achieve the same inoculation amount, standard grading standard, and consistent wound size
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Embodiment 1
[0026] Embodiment 1 Determination of pathogenicity of different bacterial strains of E. amylovora
[0027] 1. Preparation of E. amylovora inoculum: the E. amylovora strain E.a 0001, E.a 0017、 E.a 0019, E.a 0033、 E.a 0032 was inoculated on NA+5% sucrose medium, activated at 28.5°C for 48 hours, picked a single colony and inoculated in NA+5% sucrose medium, cultured with shaking at 28.5°C and 160 rpm / min for 12 hours, and measured OD 600 The bacterial solution with a value of about 1.2 was diluted to 10 with sterilized water. 8 as an inoculum.
[0028] 2. Preparation of isolated branches: select the new branches of the high-susceptibility pear fire blight variety Xiangli in the same year as the test branches, cut the stems of the test branches to about 50 cm, disinfect with 75% alcohol, and insert 1 / 3 of them In a Erlenmeyer flask filled with 0.5‰NaCl sterile saline.
[0029] 3. Inoculation: Use a sterilized scalpel to cut a wound of about 5 mm at the leaf axil of...
Embodiment 2
[0036] Embodiment 2 Different pear varieties (germplasm) in vitro branch inoculation E. amylovora Classification of disease resistance
[0037] 1. the preparation of E. amylovora inoculum: according to the measurement result of embodiment 1, will E.a The 0001 strain was identified as a highly pathogenic strain, and this strain was used as the test strain for disease resistance determination. Blight blight E.a 0001 was inoculated on NA + 5% sucrose medium, activated at 28.5°C for 48 hours, picked a single colony and inoculated in NA + 5% sucrose medium, cultured with shaking at 28.5°C and 160 rpm / min for 12 hours, and measured OD 600 The bacterial solution with a value of about 1.2 was diluted to 10 with sterilized water. 8 as an inoculum.
[0038] 2. Preparation of isolated branches: collect the young shoots of the 21 tested pear varieties (germplasm) listed in Table 2 as the inoculation material, cut the stems of the tested branches to about 50 cm, and disinfect them...
Embodiment 3
[0046] Example 3 Different apple varieties (germplasm) in vitro branch inoculation E. amylovora Classification of disease resistance
[0047] 1. Preparation of E. amylovora inoculum: the E. amylovora strain E.a 0001 was inoculated on NA + 5% sucrose medium, activated at 28.5°C for 48 hours, picked a single colony and inoculated in NA + 5% sucrose medium, cultured with shaking at 28.5°C and 160 rpm / min for 12 hours, and measured OD 600 The bacterial solution with a value of about 1.2 was diluted to 10 with sterilized water. 8 as an inoculum.
[0048] 2. Preparation of isolated branches: collect the young shoots of the 19 test apple varieties (germplasm) listed in Table 3 as inoculation materials, cut the test branches to a stem segment of about 50 cm, and disinfect them with 75% alcohol , Insert 1 / 3 of it into the Erlenmeyer flask filled with 0.5‰ NaCl sterilized saline.
[0049] 3. Inoculation: Use a sterilized scalpel to cut a wound of about 5mm at the leaf axil of 3~4...
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