Penicillium oxalicum as well as preparation method and application thereof
A technology of Penicillium oxalate and Penicillium oxalate, applied in the field of microorganisms, can solve problems such as unreported prevention research and application, and achieve the effects of less pollution, wide antibacterial spectrum and less dosage
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Embodiment 1
[0045] The recheck identification of embodiment 1 Penicillium oxalicum
[0046] 1. Morphological identification
[0047] The colonies were inoculated on carboxymethylcellulose sodium (CMC-Na) differential solid medium for colony morphology observation and microscopic examination. After the strain was cultured on carboxymethylcellulose sodium (CMC-Na) differential solid medium, the colonies were grayish green at first, evenly distributed on the surface of the medium, in the shape of rings, the edges were colorless and translucent, and the back of the colonies was turquoise or dark green. Under the microscope, it can be seen that the hyphae are colorless, and the conidiophores are scattered, growing vertically from the mycelium, the conidiophores are long columnar, and the lower part of the conidiophores is not branched; there is a diaphragm, and the tops of the conidiophores are arranged in broom-like Interbranches, the top layer of interbranches is a small stalk, the small s...
Embodiment 2
[0067] The medium screening of embodiment 2 Penicillium oxalicum
[0068] Penicillium oxalicum uses an 8mm hole puncher under aseptic operation conditions, selects a single and neat place to punch holes, and obtains 5 bacteria cakes of the same size, which are added to 100mL flavored PDA liquid medium, and 180r / m at 25°C. Cultivate on a shaker for 7 days, transfer it to the next batch of flavored PDA liquid medium at a 10% inoculum size, continue to cultivate for 7 days, and then transfer it to the next batch of flavored PDA at a 10% inoculum size In the culture medium, continue to cultivate for 7 days. After transferring 5 times according to this method, take 0.1 mL of the culture solution and transfer it to a flavored PDA solid culture dish, spread the plate, and place it in a constant temperature incubator at 25°C for 48 hours. Select a single colony Neat single colonies were inoculated on flavored PDA solid medium.
[0069] At the same time, repeat the above operation wit...
Embodiment 3
[0070] Embodiment 3: Penicillium oxalicum and multiple phytopathogenic bacterium plate confrontation test (common PDA medium)
[0071] Prepare pathogenic bacteria cakes and Penicillium oxalicum cakes with a diameter of 8 mm, and place the pathogenic bacteria cakes (8 mm) and antagonistic bacteria cakes (8 mm) equidistantly on both sides of the center of the ordinary PDA medium medium to form a straight line; no antagonistic bacteria are used as blank controls . Each treatment was repeated 5 times, and cultured in a constant temperature incubator at 25°C. After 5 days, the size of the inhibition zone was observed, and the diameter of the colony was measured by the cross method. The results are shown in Table 1. The results showed that the antagonism of Penicillium oxalicum on peach brown rot, apple ring rot, potato dry rot and bacterial perforator was between 35-52%, which was significantly lower than the inhibition rate of medium plus pine pollen.
[0072] Table 1 The confro...
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