Antioxidant activity of alcohol extract of endophytic fungal mycelium of hosta ventricosa and application of alcohol extract of endophytic fungal mycelium
A technology of endophytic fungi and purple flower hosta, applied in the field of microorganisms, can solve problems such as unreported research
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example 1
[0023] Example 1: Typical isolation of endophytic fungi HoV1, HoV4, and HoV8 from Hosta japonica
[0024] 1. Collection of plant samples: Fresh and healthy rhizomes of Hosta japonica were collected from Chengdu Campus of Sichuan Agricultural University, rinsed under running water for 12 h, rinsed with 6% sodium hypochlorite for 25 s, blotted the surface liquid with sterile filter paper, rinsed with sterile water for 3 times, absorbed Dry surface liquid for surface disinfection. After surface disinfection, check the cleanliness of the ultra-clean workbench, check the rinsing solution, and screen the sterile tissue blocks with the plant tissue imprinting method.
[0025] 2. Isolation and purification of endophytic fungi: Cut the above-mentioned sterile tissue into small pieces with a diameter of about 0.5 cm on a sterile workbench, place them in PDA medium, and culture them upside down in a constant temperature fungal incubator at 25 °C. When the hyphae of endophytic fungi grow...
Embodiment 2
[0034] Example 2: Antioxidant activity test of endophytic fungi HoV1, HoV4, HoV8 mycelia of Hosta violet
[0035] 1. Resuscitation and activation of strains: Inoculate the fungi stored in the 4°C refrigerator into PDA medium, place them in a 25°C fungal constant temperature incubator and cultivate them for 7 days, activate them, pick mycelia around the activated colonies and inoculate them into In PDA medium, cultured in a fungal incubator at 25°C for 7 days to restore the normal growth of the fungus.
[0036]2. Preparation of fermentation products of endophytic fungi HoV1, HoV4, and HoV8 of Hosta violet: Inoculate the strains on PDA plates and culture at 25 °C for 7 days. On the workbench, use a hole puncher to punch a 6 mm diameter bacterial cake along the edge of the colony, and inoculate it into a 250 mL Erlenmeyer flask containing 100 mL of LPDB medium; incubate at 25 °C, 170 r / min for 15 days, until the mycelium After the liquid surface of the culture liquid was complet...
Embodiment 3
[0053] Embodiment 3: preparation test:
[0054] The product contains 5% alcohol extract of HoV1, HoV4, HoV8 mycelium, 2% sodium soap is added as emulsifier, and 1% fragrance is added to prepare antioxidant cream.
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