Monascus purpureus induced strain and water-soluble functional monascus as well as preparation method and application of water-soluble functional monascus
A technology of Monascus purple and mutagenic strains, applied in the biological field, can solve the problems of solid-state fermentation products such as severe bitterness, difficult product, and difficult secretion of intracellular and extracellular metabolites, and achieve easy large-scale production, increased application range, and good water solubility Effect
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[0064] Example 1
[0065] (1) Preparation of seed liquid
[0066] Preparation of first-level seed liquid:
[0067] A mutagenic strain of Monascus purpureus Went was used as the production seed. Inoculate the seed culture medium (glucose 5%, peptone 2.0%, corn steep liquor 0.5%, NaNO) with shake flask seed solution at 5% inoculation amount (V / V) 3 0.1 %, MgSO4•7H 2 O 0.05%, K 2 HPO 4 • 3H 2 O 0.05%, the components are calculated by weight-volume ratio, the unit is kg / m 3 ; PH value (natural) for culture and propagation, 30°C, 150 rpm, ventilation ratio 1:1.5, tank pressure 0.04Mpa, culture for 36 hours, so that the bacteria are in the logarithmic growth phase.
[0068] Preparation of secondary seed liquid:
[0069] The first-level seed solution in the logarithmic growth phase is inoculated into a sterilized and cooled seed medium (glucose 6%, peptone 2.5%, corn steep liquor 0.8%, NaNO) at a 6% inoculum amount (V / V) 3 0.12 %, MgSO 4 • 7H 2 O 0.05%, K 2 HPO 4 • 3H 2 O0.05%, the componen...
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[0073] Example 2
[0074] (1) Preparation of seed liquid
[0075] Preparation of first-level seed liquid:
[0076] A mutagenic strain of Monascus purpureus Went was used as the production seed. Inoculate the seed medium (glucose 6%, peptone 2.5%, corn steep liquor 0.8%, NaNO 3 0.15 %, MgSO4•7H 2 O 0.08%, K 2 HPO 4 • 3H 2 O 0.08%, the components are calculated by weight to volume ratio, the unit is kg / m 3 ;PH value (natural) culture and proliferation, 31℃, 180 rpm, ventilation ratio 1:1.6, tank pressure 0.04Mpa, culture for 32h, make the bacteria in the logarithmic growth phase.
[0077] Preparation of secondary seed liquid:
[0078] The first-level seed solution in the logarithmic growth phase was inoculated into sterilized and cooled seed medium (glucose 6.5 %, peptone 2.8%, corn steep liquor 1.0%, NaNO) at 8% inoculum amount (V / V) 3 0.2 %, MgSO 4 • 7H 2 O 0.08%, K 2 HPO 4 • 3H 2 O 0.08%, the components are calculated by weight to volume ratio, the unit is kg / m 3 ;PH value (natural) ...
Example Embodiment
[0082] Example 3
[0083] (1) Preparation of seed liquid
[0084] Preparation of first-level seed liquid:
[0085] A mutagenic strain of Monascus purpureus Went was used as the production seed. Inoculate the seed medium (glucose 8%, peptone 2.8%, corn steep liquor 1.0%, NaNO) with 8% inoculum amount (V / V) of shake flask seed solution 3 0.2 %, MgSO4•7H 2 O 0.1%, K 2 HPO 4 • 3H 2 O 0.1%, the components are calculated by weight-volume ratio, the unit is kg / m 3 ;PH value (natural) culture and proliferation, 32 ℃, 200 rpm, ventilation ratio of 1:1.8, tank pressure of 0.05Mpa, culture for 24h, so that the bacteria in the logarithmic growth phase.
[0086] Preparation of secondary seed liquid:
[0087] The first-level seed solution in the logarithmic growth phase was inoculated into sterile and cooled seed culture medium (glucose 8.5%, peptone 3.0%, corn steep liquor 1.2%, NaNO) at 10% inoculum amount (V / V) 3 0.25 %, MgSO 4 • 7H 2 O 0.12%, K 2 HPO 4 • 3H 2 O 0.12%, the components are calcul...
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