High-salinity fermentation monascus yellow pigment preparation method
A monascus yellow pigment and high-salt technology, applied in biochemical equipment and methods, fermentation, microorganism-based methods, etc., can solve problems such as limited increase in amount, and achieve the effects of low production cost, increased yield, and high yield
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Embodiment 1
[0024] Activation of strains: Get Monascus ruber (CGMCC 10910) strains and spread them on the plate medium for cultivation, wherein the components of the plate medium are glucose, potato, agar and water respectively, and the concentration of glucose is 20g / L , the concentration of potato is 200g / L, the concentration of agar is 20g / L, and its culture condition is: culture temperature 25-35 ℃, preferably 30 ℃; plate culture time 4-7d, preferably 6d, after the strain activation will be on the plate Bacterial colonies were formed.
[0025] Preparation of seed bacterial liquid: take 20g glucose, 3g yeast extract powder, 10g fish meal peptone, 0.5g KCl, 0.01g FeSO 4 ·7H 2 O and 4g KH 2 PO 4 Dissolve in 500mL of water, then add water to make up to 1L to obtain seed culture medium, take 80mL of seed culture medium to sterilize and cool, inoculate 13 colonies taken from the plate, and then cultivate in a constant temperature shaker at a temperature of 25 ~ 35°C, the oscillation fre...
Embodiment 2
[0027] Take 50g glucose, 5g (NH 4 ) 2 SO 4 , 5g KH 2 PO 4 , 0.5g MgSO 4 ·7H 2 O, 0.5g KCl, 0.01g FeSO 4 ·7H 2 O, 0.01g ZnSO 4 ·7H 2 O, 0.03g MnSO 4 ·H 2 O and 20g NaCl were dissolved in deionized water and made up to 1L with deionized water, followed by sterilization at 115°C for 20min. Then inoculate 80mL of the seed bacteria liquid prepared in Example 1 and carry out shaker culture, wherein the temperature of shaker culture is 30°C, the oscillation frequency is 180rpm, and the fermentation culture time is 6d; after the cultivation is completed, the fermented liquid is centrifuged (8000r / min, 5min), and the supernatant and precipitate were collected respectively, wherein the supernatant was used to obtain extracellular monascus yellow, and the precipitate was used to extract intracellular monascus yellow.
Embodiment 3
[0029] With embodiment 2, its difference is, described NaCl consumption is 35g.
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