Biological control bacillus subtilis for crop bacterial wilt
A technology of Bacillus subtilis and bacterial wilt, which is applied in the direction of plant growth regulators, bacteria, biocides, etc., can solve the problems that the physiological and biochemical characteristics of biological control bacteria and disease prevention mechanisms have not been studied in depth, and achieve dark green leaf color and strong growth. Good, the effect of leaf color hypertrophy
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Embodiment 1
[0064] 1.1 Screening of antagonistic bacteria SH7 for the control of tobacco bacterial wilt, greenhouse pot plant disease control experiment and growth promotion effect
[0065] Evenly add 100 μl of Ralstonia solanacearum (Ralstonia solanacearum) bacterial suspension with a concentration of 1×107 cfu / ml into a sterilized petri dish, pour into 20 ml of molten NA medium cooled to about 50° C. and mix well. After the culture medium is completely solidified, use an inoculation loop to inoculate the antagonistic bacteria to be tested, spot 8-10 bacterial strains to be tested in each dish, and culture them in a 30°C incubator for 48 hours to detect the presence and size of the inhibition zone. The strains with antagonistic effect in the initial test were streaked and purified, and the test was repeated. The basic method was the same as above. Three strains were spotted on each plate, and each was repeated three times. From the antibacterial effect of the plate, the indoor plate of t...
Embodiment 2
[0091] Example 2 SH7 antagonistic protein and its properties
[0092] Extraction of crude protein and detection of its activity: inoculate the activated SH7 strain in NB medium, culture at a constant temperature of 30°C, shake at 150rpm for 48 hours, centrifuge at 4°C for 10 minutes, remove bacteria, and make extracellular metabolites for fermentation Serum. Slowly add a certain amount of (NH4)2SO4 to the fermentation broth to reach a saturation of 70%, stir evenly, and place it at 4°C overnight.
[0093] Centrifuge the salting-out solution at low temperature for 20 minutes (12000r / min), pour off the supernatant, suspend the precipitated substance with 1 / 15 volume of PBS buffer solution (pH7.6), and put the suspension into the pretreated dialysis bag (Cut-off molecular weight is 5kD), the two ends of the dialysis bag are clamped with dialysis clips, placed in 100 times the volume of PBS buffer (pH7.6), dialyzed on a magnetic stirrer at 4°C for 24 hours, and then dialyzed for ...
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