Laver fermented material and application of laver fermented material in preparation of antioxidant
A technology of antioxidants and fermented products, which is applied in the field of laver fermented products and its application in the preparation of antioxidants, can solve the problem of less detection of laver antioxidants, and achieve good antioxidant activity
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Embodiment 1
[0029] Embodiment 1: selection and activation of bacterial classification
[0030] In this experiment, lactic acid bacteria (Lactobacillus plantarum, commercially available strain) and yeast (wine yeast, commercially available strain) were selected for fermentation comparison.
[0031] Gently scrape a ring of yeast and Lactobacillus plantarum from the slant and inoculate them on YPD and MRS liquid medium respectively, culture at 37°C for 24 hours, quantitatively inoculate into laver fermentation broth, pass 2-3 times until viable bacteria Count to over 1×108.
Embodiment 2
[0032] Embodiment 2: Different strains are to the mensuration of DPPH scavenging rate in laver fermented product
[0033] Crush the laver, pass through a 40-mesh sieve, add 100ml of distilled water, and sterilize at 121°C for 20 minutes. The activated Lactobacillus plantarum was inoculated with yeast, the inoculation amount was 4%, the fermentation temperature was 37° C., the fermentation time was 48 hours, the rotation speed was 120 r / min, and the pH was natural. At the end of the fermentation, the fermentation broth was centrifuged at 5000r / min for 10min, and the supernatant was taken to measure DPPH. Three parallels were set for each group. Experimental results such as figure 1 shown.
[0034] Depend on figure 1 It can be seen that the scavenging rate of yeast and Lactobacillus plantarum to DPPH in laver fermented product is generally on the rise. When the seaweed fermentation time is 24-60h, the scavenging rate of yeast to DPPH free radicals in the seaweed fermented pr...
Embodiment 3
[0035] Embodiment 3: the mensuration of DPPH scavenging rate in laver fermented product with different solid-liquid ratio
[0036] Weigh 5g, 4g, 3g, 2g, and 1g of laver respectively, and place them in a 250ml Erlenmeyer flask filled with 100% distilled water, and successively obtain a solid-liquid ratio of 1:20, 1:30, 1:40, 1:50, 1: 60 broth. Select the best strain, the inoculation amount is 4%, the fermentation temperature is 37°C, and the fermentation time is 48h. After the fermentation, the fermentation broth is centrifuged to take the supernatant to measure DPPH, and three parallels are set for each group. Experimental results such as figure 2 shown.
[0037] Depend on figure 2 It can be seen that with the gradual decrease of the laver material-to-liquid ratio, the scavenging rate of DPPH free radicals by the laver fermented product shows a downward trend, and the maximum DPPH scavenging rate is 86% when the laver-solid-liquid ratio is 1:20, which is significantly hig...
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