Fungus capable of producing fragrant substances
A technology for aroma substances and fungi, applied in the field of fungal biology, can solve the problems of lack of microbial aroma production resources and other problems
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Embodiment 1
[0017] The present embodiment is the culture condition of bacterial strain TapuXJ14C02 of the present invention
[0018] A flavor-producing fungus proposed by the present invention, said flavor-producing fungus is Talaromyces purpureogenus (Talaromyces purpureogenus) bacterial strain TapuXJ14C02; ℃ constant temperature culture; wherein, the PDA medium formula is: 200g of potatoes, 20g of agar powder, 20g of glucose and 1000mL of water.
Embodiment 2
[0020] The present embodiment is the morphological identification of bacterial strain TapuXJ14C02 of the present invention
[0021] The morphological identification experiment of the strain TapuXJ14C02 was as follows: the strain TapuXJ14C02 was inoculated on PDA medium and cultured at a constant temperature of 28°C. After the strain TapuXJ14C02 was cultured on MEA medium at 25°C for 7 days, the diameter of the colony reached 9-14mm, the colony was white at the initial stage, with few conidia in the early stage, and a large number of sporulation in the later stage was blue green, with more aerial hyphae, and the back was yellowish brown , specifically as figure 1 shown. A large number of conidia and sporulation structures, bristle-like branches are mostly in double whorls, smooth, 150–250×2.5–3.5 μm; 3 to 5 stem bases per round, 12–14.5×2.5–4 μm; phialides lanceolate Shaped, 12–13.5×2–3 μm, 3 to 6 phialides per peduncle; conidia smooth, elliptic, 3–3.5×2–2.5 μm, as figure 2...
Embodiment 3
[0023] The present embodiment is the molecular biological identification of bacterial strain TapuXJ14C02 of the present invention
[0024] The molecular identification experiment of described bacterial strain TapuXJ14C02 comprises the following steps:
[0025] 1. Extraction of bacterial strain DNA:
[0026] 1. Genomic DNA was extracted using a kit to extract fungal DNA, and stored in a -20°C refrigerator for later use;
[0027] 2. Ribosomal rDNA-ITS segment amplification: PCR amplification was performed using fungal genome rDNA as a template, primers were synthesized by Shanghai Sangon Bioengineering Co., Ltd., and the amplification cycle reaction conditions were: 94°C pre-denaturation for 3 minutes; 94°C denaturation 30s, annealing at 55°C for 30s, extension at 72°C for 1min, a total of 33 cycles; extension at 72°C for 10min; ITS-PCR amplification reaction was carried out in a 50μL reaction system (see the table below):
[0028] Primer: ITS15′-TCCGTAGGTGAACCTGCGG-3′
[002...
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