Monascus strain capable of high yielding and enriching Monacolin K and application of monascus strain
A technology of Monascus and Monascus, which is applied in the field of microorganisms, can solve the problems of low cleanliness in the production process, different production processes, and different strains, and achieve excellent lipid-lowering effects and good application prospects
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Embodiment 1
[0026] The isolation and identification of embodiment 1 Aspergillus strain of the present invention
[0027] 1. Separation method
[0028] Add 1ml of pollen honey from different sources to 9ml sterile water, and dilute 10ml -1 to 10 -5 , draw different concentrations of dilutions to the pda plate medium, culture at 32°C for 5 days, streak the suspected Monascus colony observed with the naked eye to a new pda plate to form a single colony, and then pick a single colony to the slant medium superior. If the colony is impure, then isolate and purify according to the above method until pure Monascus colonies appear. figure 1 A and B represent the purified ASP-1 and HOP-1 strains, respectively.
[0029] 2. Identification
[0030] 2.1 Identification of colony characteristics
[0031] Configure standard media for Aspergillus identification: Czapek yeast exatractagar (CYA,), Malt extract agar (MEA), 25% glycerol nitrate agar (25% Glycerol nitrate agar , G25N); the culture temper...
Embodiment 2
[0053] Embodiment 2 adopts Monascus of the present invention to prepare red yeast rice
[0054] Using the strains HOP-1 and ASP-1 isolated in Example 1, prepare functional red yeast rice containing monacolin K:
[0055] First prepare the nutrient solution: add 3g of glycerin, 5g of glucose, 1g of yeast, 1g of soybean peptone, MgSO to 100g of rice 4 0.1g, KH 2 PO 4 0.2g, 0.3g of acetic acid, and then add 50-60g of water to adjust the pH of the nutrient solution to 6, put it into a tray, cook at 105°C for 8 minutes at high temperature. After the first cooking, the water content remains at around 35%. After cooking, the grains of rice are crushed and packed in conical flasks so that the grains of rice are 3-5cm thick in the conical flasks. Finally, seal the Erlenmeyer flask with eight layers of gauze, and sterilize at 121° C. for 20 minutes. After the sterilization, take out the Erlenmeyer flask, you can see that the rice grains are scattered among the rice grains, and afte...
Embodiment 3
[0058] Embodiment 3 adopts Monascus of the present invention to prepare red yeast rice
[0059] Prepare nutrient solution: add 10g bran, 5g glucose, 1g yeast, 1g soybean peptone, MgSO to 100g rice 4 0.1g, KH 2 PO 4 0.2 g, 0.3 g of acetic acid, and then add 50-60 g of water to adjust the pH of the nutrient solution to 6, and the rest of the steps are the same as in Example 2.
[0060] The detection is carried out under the condition of high performance liquid phase, and the detected content of monacolin K is stable at 0.8%-1.1%. The light industry standard (QB / T2847-2007) regards lovastatin as the symbolic functional component of functional red yeast rice, and requires that lovastatin must reach more than 0.4%.
[0061] Experimental results prove that the monacolin K content in the red yeast rice prepared by the method of the present invention is high and has strong application value.
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