Monascus strain and application thereof in preparing functional monascus
A technology of Monascus pilosa and Monascus, which is applied in the field of Monascus pilosa, can solve the problems of unstable passage, difficulty in obtaining high-yield MK Monascus strains, and poor purpose, and achieve the effect of broad application prospects
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Embodiment 1
[0024] The identification of embodiment 1 Monascus MS-1
[0025] A Monascus strain isolated from Monascus that can produce MK but not citrinin was identified by morphology and ITS sequence analysis.
[0026] 1. Morphological identification of Monascus MS-1
[0027] 1. Medium
[0028] (1) Malt juice agar medium (MA): 1000mL of 10°Bx wort juice, 15g of agar.
[0029] (2) Saccharomyces tsarzia extract agar medium (CYA): NaNO 3 3.0g, K 2 HPO 4 1.0g, KCl0.5g, MgSO 4 ·7H 2 O0.5g, FeSO 4 ·7H 2 O0.01g, yeast extract 5.0g, glucose 20g, agar 15g, add distilled water to 1000mL.
[0030] (3) Glycerol nitrate agar medium (G25N): Add 25% glycerol (w / w) to CYA medium.
[0031] (4) Potato Dextrose Agar (PDA) Medium: Peel 200g of potatoes, cut into small pieces, add 1000mL of distilled water and boil for 20min, after filtering, add 20g of glucose, 15g of agar powder, and dilute to 1000mL with distilled water.
[0032] All the above four media were sterilized by moist heat at 121°C f...
Embodiment 2
[0050] Example 2 Preparation of solid-state fermentation product of Monascus pilosa strain MS-1 and detection of MK and citrinin
[0051] 1. Culture medium
[0052] 1. PDB medium: PDA medium without adding agar powder is PDB medium.
[0053] 2. Yeast extract sucrose (YES) medium: Yeast extract 40g / L, sucrose 160g / L, dilute to 1000mL with distilled water.
[0054] Two, the preparation of Monascus pilosa strain MS-1 seed solution
[0055] Same as the content of the invention.
[0056] 3. Preparation of solid-state fermentation products of Monascus pilosa strain MS-1
[0057] Crush the rice (20 mesh), adjust the water content to 20%, sterilize at 121°C for 20 minutes and break up while hot, inoculate the activated liquid seed solution with 10% (v / w) inoculum and use sterile water Adjust the water content and culture at 28°C for 14 days. The fermented red yeast rice flour was dried at 55°C for 12 hours, and the amount of MK and citrinin was extracted and analyzed.
[0058] 4...
Embodiment 3
[0066] Example 3 Analysis of Synthetic Related Genes of Monascus Placiferus Strain MS-1 Citrinin
[0067] Using molecular biology methods, the citrinin high-yielding strain Monascus ruber (M. ruber) M-7 (CCAM070120) was used as a positive control (Li L., Shao Y.C., Li Q. et al.. Identification of Mga1, a G-protein α-subunit gene involved in regulating citrinin and pigment production in Monascus ruber M-7.FEMS Microbiology Letters.2010,308:108-114.), its citrinin synthesis-related genes (ctnA, ctnE, ctnR, pks CT) analysis, Monascus genome extraction method is the same as ITS sequence analysis, the reaction system is 25 μL, including Monascus genome DNA 1 μL, 10 μmol / L forward and reverse primers 1 μL, dNTP 1 μL, 10×buffer 2.5 μL, 2.5mmol / LTaq plus DNA Polymerase0.2μL, ddH 2 O18.3 μL. The PCR reaction program was pre-denaturation at 95°C for 5min, denaturation at 95°C for 30s, annealing at 55°C for 30s, extension at 72°C for 1min, a total of 30 cycles, and a final extension at...
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