Acremonium persicae MR-47 and application thereof
A technology of Acremonium peach, MR-47, applied in application, climate change adaptation, chemicals for biological control, etc., can solve the problems of human health threats, ecological balance destruction, pesticide residues, etc.
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Embodiment 1
[0028] Example 1 Separation, purification and screening of Acremonium peach MR-47
[0029] experimental method:
[0030] 1. The soil samples tested were collected by the five-point sampling method from the artificially cultivated windbreak rhizosphere soil collected from the Medicinal Botanical Garden of Jilin Agricultural University (43°48′23″N, 125°24′57″) in July 2019. Store in a sterile ziplock bag and store in a 4°C refrigerator for later use.
[0031] 2. Use the dilution coating method to separate the fungi in the soil, weigh 10 g of the wind-dried rhizosphere soil sample and put it into a conical flask containing 90 mL of sterile physiological saline, shake it for 30 minutes, and make the soil sample evenly dispersed It becomes soil suspension in the dilution solution; after the soil samples are dispersed, they are successively diluted by 10-fold gradient to obtain soil dilution solutions of various concentrations; respectively, take the dilution gradient as 10 -3 , 1...
Embodiment 2
[0035] Example 2 Identification of Acremonium peach MR-47
[0036] experimental method:
[0037] 1. Select the purified strain MR-47 and inoculate it on the PDA medium, cultivate it in the dark at 25°C for 14 days, and carry out morphological identification according to its colony morphology, hyphal diameter, spore size, morphology and implantation method, and refer to " The "Handbook of Fungal Identification" preliminarily determines the taxonomic status of strains.
[0038] 2. Use the kit TaKaRa MiniBEST Universal Genomic DNA Extraction Kit Ver.5.0 to extract the total genomic DNA of strain MR-47. The ITS rDNA of strain MR-47 was PCR amplified and sequenced using fungal universal primers ITS1 (5'-TCCGTAGGTGAACCTGCGG-3') and ITS4 (5'-TCCTCCGCTTATTGATATGC-3'). PCR reaction system: Master Mix 12.5 μL, ITS 11 μL, ITS 41 μL, rDNA 2 μL, ddH 2 O 8.5 μL, the amplification program was 94°C for 3 min; 94°C for 30s, 55°C for 30s, 72°C for 1min, 30 cycles; 72°C for 5min. PCR amplifi...
Embodiment 3
[0043] Embodiment 3 The antibacterial spectrum of Acremonium peach MR-47
[0044] experimental method:
[0045] Determination of Acremonium persicinum MR-47 against Fusarium oxysporum, Fusarium solani, Phytophthora cactorum, Botrytis cinerea, Rhizoctonia solani by plate confrontation method , the antibacterial spectrum of Alternaria tenuissima, Alternaria liriodendra, Sclerotinia sclerotiorum, Cylindrocarpon destructans, the specific operation steps are the same as step 3 in Example 1.
[0046] Experimental results:
[0047] Acremonium persicinum MR-47 has strong antibacterial effect on 9 pathogenic fungi, among which the inhibitory effect on Phytophthora mala and Cylindrosporium is the strongest, reaching more than 70%, 72.22% and 72.22% respectively. 74.07%; the bacteriostatic effect against Rhizoctonia solani is weak, only 40.74%; the bacteriostatic rate against several other fungi is 62-70%, indicating that Acremonium persicinum MR-47 has a relatively wide range of The ...
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