Bactericide for suppressing growth of neurospora and preparation method thereof
A bactericide, Alternaria technology, applied in the field of microorganisms, can solve the problems of weak bactericidal effect of Alternaria, pollute the environment, economic losses, etc., and achieve the effects of preventing and controlling Alternaria pollution, good bactericidal effect, and convenient use.
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Embodiment 1
[0028] Example 1 Preparation of Neurospora fungicide 1 and detection of fungicidal activity
[0029] Prepare liquid medium: beef extract 3 g, peptone 10 g, NaC 15 g, agar 20 g, water 1000 mL, pH 7.0-7.2; put Pseudomonas putida into the liquid medium according to the inoculum size of 5%, put Cultivate in a constant temperature shaker at 37°C, with a rotation speed of 120rmp / min, and shake for 4 days; centrifuge the cultured bacterial solution at 4000rmp / min for 15 minutes, and take the supernatant. After repeating 3 times, take the supernatant and vacuum filter it. As a fungicide 1. Store in a sealed container at 4°C.
[0030] Streak fungicide 1 on both sides of a 90mm LB plate 2cm away from the center, inoculate a white Neurospora plate and a red Neurospora plate in the center respectively, culture at 28°C for 3 days, observe the growth of Neurospora, and compare with the blank Control comparison.
Embodiment 2
[0031] Example 2 Preparation of Neurospora fungicide 2 and detection of its fungicidal activity
[0032] The Neurospora fungicide 1 prepared in Example 1 was filtered through a 0.22 μm microporous membrane, sealed and stored at 4° C., and used as fungicide 2.
[0033] After dissolving 100ml PDA, add 11ml of fungicide 2 (10%); each 100ml of PDA was poured into six dishes, and inoculated with Neurospora rubrum, Neurospora albicans, and blank control respectively; PDA plates without any treatment were inoculated with Neurospora rubrum (R) and Neurospora albicans (W).
Embodiment 3
[0034] Example 3 Preparation of Neurospora fungicide 3 and detection of its fungicidal activity
[0035] Filter the Neurospora fungicide 1 prepared in Example 1 with a 10 μm microporous membrane, concentrate it with a 45° C. rotary evaporator until the OD value of the bacterial solution is 0.1, filter it with a 0.22 μm microporous membrane, and store it in a sealed container at 4° C. Agent 3.
[0036] After dissolving 80ml of PDA, add 20ml of fungicide 3 (20%); each 100ml of PDA was poured into six dishes, and inoculated with Neurospora rubrum, Neurospora albicans, and blank control respectively; PDA plates without any treatment were inoculated with Neurospora rubrum (R) and Neurospora albicans (W).
[0037] The fungicides in Example 1, Example 2 and Example 3 can all effectively kill Neurospora, and their bactericidal rates to Neurospora rubrum and Neurospora albicans are shown in the table below.
[0038]
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