Gliocladium spp. strain for suppressing botrytis cinerea pers
A technology for tomato botrytis cinerea and Slime mold, which is applied in the direction of chemicals, fungi and fungicides for biological control, and can solve problems such as endangering the safety and health of humans and animals, shortage, pollution of agricultural products and the environment, etc.
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specific Embodiment approach 1
[0022] Embodiment 1: The Gliococcus strain that suppresses Botrytis cinerea in this embodiment is Bionectria ochroleuca WY-1 (Bionectria ochroleuca WY-1), which is preserved in the General Microorganism Center of China Microbiological Culture Collection Management Committee, and the preservation number is CGMCC No. 1977.
[0023] G. pink WY-1 of the present invention can be very good on potato dextrose agar (PDA) medium, oatmeal agar medium, Gao's No. 1 medium, cornmeal peptone medium, carrot medium or sporulation medium. Good growth and sporulation, the most suitable medium is PDA medium. Wherein the corn meal peptone medium (1000ml) is made up of 30g corn meal, 20g peptone, 20g sucrose, 18g agar and the distilled water of remainder. Carrot culture medium (1000ml) consists of 200g carrots, 20g glucose, 18g agar and the balance of distilled water. Sporulation medium (1000ml) is made of 1.0g yeast extract, 1.0g beef extract, 2.0g tryptone, 10.0g glucose, 0.1g ferrous sulfate ...
specific Embodiment approach 2
[0065] Specific embodiment 2: The β-1,3-glucanase gene fragment in Gliococcus pinkum WY-1, which inhibits Botrytis cinerea in this embodiment, is shown in SEQ ID NO: 1.
[0066] In this embodiment, G. pink WY-1 is activated with PDA solid medium, and then transferred to the enzyme-producing medium for culture. Take 100 mg of G. pink WY-1 mycelium to extract RNA and transcribe it into cDNA, and pass GenBank Compared with the β-1,3-glucanase genes of other known fungi, the homology was compared with the Clustalw method, and then the most conserved amino acid sequence was found, and two pairs of degenerate primers were designed according to the conserved region, The β-1,3-glucanase gene fragment was amplified by RT-PCR and sequenced, and the GenBank accession number was DQ975304.
[0067] It was found that M. rosea WY-1 of this embodiment contains the β-1,3-glucanase gene. 100ml of the enzyme-producing medium consists of 3g laminarin, 0.3g NaNO 3 , 0.1g K 2 HPO 4 , 0.05g KCl,...
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