Application of trichoderma koningii SMF2 in prevention and treatment of plant bacterial diseases
A trichoderma pseudocorning, bacterial technology, applied in the field of plant disease biological control, can solve problems such as lack of application of plant bacterial diseases, achieve significant control effects, reduce residues, and reduce dosage effects
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Embodiment 1
[0042] Example 1 Cultivation of Trichoderma pseudocorning SMF2
[0043] The culturing method of Trichoderma pseudocanning SMF2 strain, the concrete steps are as follows:
[0044] (1) inoculate the Trichoderma quaternum SMF2 strain with the strain preservation number of CCTCC NO: M209031 on the PDA solid medium, and cultivate at 28° C. for 48 hours to obtain the activated Trichoderma quasicornis SMF2;
[0045] (2) The activated Trichoderma quasiformis SMF2 was transferred into a PDA liquid medium, and cultured at 28° C. and 180 rpm for 12 days to obtain a Trichoderma quasiformis SMF2 seed culture solution.
[0046] The components of the PDA solid medium are as follows: 200 parts of potatoes, 20 parts of glucose, 1000 parts of ionized water, and 1.5 parts of agarose, all of which are parts by weight. The components of the PDA liquid culture medium are as follows: 200 parts of potatoes, 20 parts of glucose, and 1000 parts of ionized water, all of which are parts by weight.
Embodiment 2
[0047] Example 2 Trichoderma pseudocanning SMF2 inhibits the growth of Xoo and Xoc
[0048] The activated Trichoderma quasicornin SMF2 in Example 1 was transferred to the NB solid medium containing Xoo and the NB solid medium containing Xoc (OD of Xoo and Xoc) respectively. 600 Both were 0.01), cultured at 28°C for 6 days, to observe the situation that Trichoderma pseudocorning SMF2 produced a bacteriostatic zone on Xoo or Xoc, and the NB solid medium containing only Xoo or Xoc was used as a control group. The results are as follows figure 1 shown.
[0049] The activated Trichoderma pseudocanning SMF2 in Example 1 was transferred to the NB liquid medium containing Xoo and the NB solid medium containing Xoc (OD of Xoo and Xoc) 600 Both were 0.01), cultured at 28°C and 180rpm for 48h, and the number of Xoo or Xoc cells was determined. The NB liquid medium containing only Xoo or Xoc was used as the control group. The results are as follows figure 2 shown.
[0050] The compone...
Embodiment 3
[0054] Example 3 Extraction of Trichoderma pseudocanning SMF2 secondary metabolite kangningmycin
[0055] The extraction method of the secondary metabolite kangningmycin of Trichoderma pseudocanning SMF2 is as follows:
[0056] a, liquid extraction method
[0057] (1) by the Trichoderma pseudocorning SMF2 seed culture liquid among the embodiment 1, filter through three layers of lens paper, remove mycelium, keep filtrate;
[0058] (2) centrifuge the filtrate at 10000rpm for 10min, and get the supernatant;
[0059] (3) Take 20 mL of the centrifuged supernatant, add it to the SPE C18 adsorption column, and stand to filter;
[0060] (4) Add 2 mL of methanol solution to the SPE C18 adsorption column to dissolve the adsorbed substances, and finally filter the solution through a 0.22 μm organic filter to obtain a crude extract of metabolites, which is stored at 4°C for later use.
[0061] b. Solid extraction method
[0062] (1) Using a circular hole punch with a diameter of 0.5 ...
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