Method for biosynthesis of organic selenium by using Hypsizygus marmoreus
A seafood mushroom and organic selenium technology, applied in the field of microbiology, can solve the problems of no MeSeCys and other problems, achieve the effect of controllable selenium addition, controllable cultivation conditions, and increase yield
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Embodiment 1
[0032] Embodiment 1 strain breeding and the acquisition of selenium-enriched carrier
[0033] The seafood mushroom strain H023 preserved in the Edible Mushroom Research Office of China Agricultural University was cultured on PDA medium for 14 days, and 5 mm of bacterial cakes were taken from the growth edge of the colony to inoculate sodium selenate and sodium selenite at 1.0 mg / kg respectively. , 5.0mg / kg and 20.0mg / kg plates, cultivated at 21°C for 10 days, and measured the colony diameter. The results showed that H023 colony growth was significantly inhibited under the treatment of 5.0mg / kg sodium selenite; at 25.0mg / kg Sodium selenate treatment significantly inhibited the growth of H023 mycelia ( figure 2 ).
[0034] Cultivate the seafood mushroom strain H023 preserved in the Edible Mushroom Research Office of China Agricultural University on PDA medium for 14 days, take 5mm fungus cakes from the growth edge of the colony and inoculate them on 10 PDA plates and culture t...
Embodiment 2
[0036] Embodiment 2 sodium selenate treatment selenium-enriched cultivation
[0037] The weight ratio of Douglas fir sawdust, corn cobs, soybean hulls, and wheat bran with uniform particle size is 40:30:15:15, the pH is adjusted to 8 with lime powder, the moisture content is 80%, and the selenate concentration gradient is set to 0.5, 1.0, 2.5, 5.0, 10.0, 20.0, 40.0mg / kg, each culture bag is filled with 2.0kg of mixed material, 121 ℃ high temperature, autoclave for 2 hours. After cooling to room temperature, the bacteria were inoculated. Take 5mm uniform bacterium cake from the test tube for preserving the strain and inoculate it into a 500mL Erlenmeyer shaker flask filled with 150mL liquid PDA medium, and shake it at 170-180r / min at 21-23°C for 4 days to become the first-grade bacteria kind. Use a sterile pipette to draw 5mL of bacteria from the first-level strain shake flask covered with mycelium balls and transfer it to a 500mL shake flask containing 150mL of PDA liquid me...
Embodiment 3
[0038] Embodiment 3 Sodium Selenite Treatment Selenium-enriched Cultivation
[0039] Use Douglas fir sawdust, corn cobs, soybean hulls, and wheat bran with a weight ratio of 40:30:15:15, use lime powder to adjust the pH to 8, the moisture content is 80%, and the selenite concentration gradient is set 0.5, 1.0, 2.5, 5.0, 10.0, 20.0, 40.0 mg / kg, each culture bag is loaded with 2.0 kg of mixed material, and sterilized in a high temperature and high pressure autoclave at 121 °C for 2 hours. After cooling to room temperature, the bacteria were inoculated. Take a 5mm uniform bacterium cake from the test tube for preserving the strain and inoculate it into a 500mL Erlenmeyer shaker flask filled with 150mL liquid PDA medium, and culture it with shaking at 170-180r / min at 21-23°C for 4 days as the first-grade bacteria kind. Use a sterile pipette to draw 5mL of bacteria from the first-level strain shake flask covered with mycelium balls and transfer it to a 500mL shake flask containin...
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