A kind of method and dha to prepare dha by using bean dregs
A technology of enzymatic hydrolysis of bean dregs and bean dregs, which is applied in the field of DHA, can solve the problems of low DHA content, low utilization rate of bean dregs, and high production costs, and achieve the effects of increasing DHA content, realizing resource recycling, and increasing production
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Embodiment 1
[0069] A kind of method utilizing bean dregs to prepare DHA, comprises the steps:
[0070] (1) Okara pretreatment
[0071] First dehydrate and dry the bean dregs until the water content of the bean dregs is about 20%, then crush them, pass through a 60-mesh sieve, and then expand them;
[0072] (2) Enzymatic hydrolysis of bean dregs
[0073] Weigh 40g of puffed dried okara to make okara homogenate at a solid-to-liquid mass ratio of 1:20, add a compound enzyme preparation with a mass content of not more than 0.3% to the okara homogenate, adjust pH to 4.0, and enzymatically hydrolyze for 24 hours at a temperature of 55°C , to obtain an enzymolysis mixture; the enzymolysis mixture is centrifuged to obtain sediment and bean dregs enzymolysis supernatant, and all bean dregs enzymolysis supernatants are collected for the next step of the fermentation production of Schizochytrium; the compound enzyme preparation is a volume ratio 1:1 cellulase and pectinase with enzyme activity rea...
Embodiment 2
[0082] The difference between this embodiment and embodiment 1 is that the concentration of bean dregs is 20g / L.
Embodiment 3
[0084] The difference between this embodiment and embodiment 1 is that the concentration of bean dregs is 60g / L.
[0085] The dry powders of Schizochytrium obtained in Examples 1-3 were respectively subjected to the following experimental determinations: take an appropriate amount of dry powder of Schizochytrium and add concentrated HCl to break the wall in a water bath at 60-70°C, extract the oil with n-hexane, and put it in a water bath at 55°C. Rotary evaporation to constant weight, measure its total oil yield; take appropriate amount of oil and internal standard (eicosanoic acid), according to the conventional BF 3 -Ether catalyst for KOH-CH 3 OH methyl esterification, and the DHA production in the bacteria was determined by gas chromatography.
[0086] The experimental results are shown in Table 1, figure 2 with image 3 shown.
[0087] Table 1 Fatty acid composition of Schizochytrium cultured at different concentrations of okara in the late stage of fermentation
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