Novel tea tree endophytic biocontrol fungus Diamorpha austrialiana and application thereof
A new type of anti-fungal technology, applied in the direction of application, fungi, biocides, etc., can solve the problems of less preventive effect on tea tree diseases, late start of tea tree endophytes, and less research, so as to reduce pollution, improve antagonistic activity, and improve The effect of quality and safety
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Embodiment 1
[0037] Isolation and identification of endophytic strains in embodiment 1
[0038] Take healthy tea tree roots, stems and leaves, wash the surface soil with tap water, soak in 70% alcohol for 1 minute, then soak in 3% sodium hypochlorite solution for 4 minutes, then soak in 70% alcohol for 1 second, and finally use sterile Rinse with water for 5 times, absorb 100uL of sterile water from the last rinse and spread it on the PDA medium to prepare the control medium.
[0039] Tissue separation method: cut the surface-sterilized tea tree tissue into small pieces of 5mm*5mm, stick the cut surface on the PDA medium, culture at a constant temperature of 25°C for 7 days, observe every day, and pick the newly grown hyphae with a transfer ring cultivated alone. figure 1 It is the effect diagram of plate culture of endophytic strains.
[0040] The ITS and 18S gene loci of the isolated endophytic fungi were sequenced, and the sequencing results were compared with BLAST on NCBI to obtain ...
Embodiment 2
[0043] Example 2 Endophyte Antagonism Experiment
[0044] In the present embodiment, the endophytic fungus Diaporthe australiana is used against 5 kinds of plant disease pathogenic bacteria (apple anthracnose pathogenic bacteria Glomerella ciningulaia (Stonem.) Spauld.et Sch.), tea wheel spot disease pathogenic Pseudopestalotiopsis theae, watermelon wilt pathogen Fusarium oxysporum f.sp. Hiveum (E.F.Smith) Wollen., tomato wilt pathogen Fusarium oxysporum f. Fusarium oxysporum f.sp.lycopersici Snyder et Hansen, tobacco black shank pathogen Phylophthora nicotianae (Phylophthora nicotianae)) plate confrontation experiment, and count the diameter of colony growth at different culture time, and calculate the inhibition bacteria rate.
[0045] The specific content is as follows:
[0046] 1. Tablet confrontation method:
[0047] Carve out a bacterium cake with a radius of 5mm from the edge of the pathogenic bacteria colony, and inoculate it on the center point of the PDA medium pl...
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