Burkholderia cepacia SD7 and culturing method and application thereof
A technology of Burkholderia and onion, applied in the field of Burkholderia cepacia SD7 and its cultivation, can solve the problems of large side effects of chemical agents for plant disease prevention and control, lack of biological control drugs, etc., which is not easy to achieve. The effect of producing resistance, strong inhibitory effect, and broad application prospects
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Embodiment 1
[0019] Example 1 Screening and Identification of Burkholderia cepacia SD7
[0020] 1. Screening of bacterial strains
[0021] (1) Collection of soil samples
[0022] In this experiment, soil samples were collected from the farm orchard of South China Agricultural University. According to the topography of the collection site, five points were used for sampling. The sampling depth was 15 cm below the plow layer or the surface, and the sampling volume was 200-250 g. The five samples collected at each site were evenly distributed. Mix them, put them into sterilized sealed polyethylene bags, and bring them back to the laboratory for immediate separation.
[0023] (2) Preparation of sample suspension
[0024] Add the soil sample into sterile water and shake vigorously. Sample: water = 1:9 (mass to volume ratio), such as: 10 g of soil is added to a conical flask filled with 90 mL of sterilized water to obtain a suspension concentration of 10 -1 . Prepare 5 test tubes co...
Embodiment 2
[0040] Example 2 Inhibitory effect of Burkholderia cepacia SD7 on plant pathogenic bacteria
[0041] 1. Control effect of Burkholderia cepacia SD7 on banana fruit anthracnose
[0042] (1) Tested banana anthracnose strains
[0043] Banana anthracnose bacteria used for inoculation ( C. musae ) was isolated and purified from the diseased banana fruit, and was preserved by our laboratory.
[0044] (2) Control effect of Burkholderia cepacia SD7 on banana fruit anthracnose
[0045] For every 100 mL of 2-day-old seeds of Burkholderia cepacia SD7 strain (yeast extract powder 5 g, tryptone 10 g, NaCl 10 g, agar powder 15-18 g, water 1000 mL, pH 7.0- 7.2) Inoculate 1 mL of seeds at a ratio of inoculation to expand the culture. The culture conditions are: rotation speed 180 r / min, 25°C, after 3 days of culture, collect the supernatant after centrifugation, and filter with a bacterial filter to obtain a sterile filtrate. Select seven or eight mature bananas, disinfect the surface w...
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