Bariae fabreidii, microbial preparations containing it and applications thereof
A microbial preparation and yeast technology, applied in the application of tea fermentation, Barley Fabry, the field of microbial preparations containing the yeast, can solve the problem of poor taste of Pu-erh tea, the fermentation effect is not as good as natural fermentation, and the content is reduced, etc. To achieve obvious antioxidant effect, beneficial to human health, and the effect of improving antioxidant capacity
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Embodiment 1
[0074] Example 1 Screening and identification of P. fabridii strains
[0075] 1.1 Sample collection and data collection
[0076] 100g of raw Pu-erh tea from Lincang, Yunnan Province was fermented at room temperature. The whole process of Pu-erh raw tea fermentation was followed, and fermented tea samples were collected in stages, and the collection time was recorded (3 days (3d), 15 days (15d) after stacking. ), 21 days (21d), 29 days (29d)), samples were stored in sterile sample collection tubes after collection. Store samples immediately after collection at -80°C to terminate microbial activity.
[0077] 1.2 Sample processing and DNA extraction
[0078] Within 24 hours after the termination of microbial activity, use Bioteke automatic nucleic acid extractor and soil genomic DNA extraction kit (Beijing Bioteke Biotechnology Co., Ltd.) to extract DNA from the collected fermented tea samples. This operation can eliminate DNA caused by human error Extraction quality is incons...
Embodiment 2
[0085] The preparation of embodiment 2 Fabre Debari yeast agent
[0086] The P. fabreidii D-1 isolated in Example 1 was prepared into a freeze-dried bacterial preparation (dry powder). The specific process is as follows:
[0087] (1) Inoculate the P. fabrierii strain D-1 strain into 200mL of YPD liquid medium at 2v / v%, and cultivate it at 30°C and 200rpm for 12h to obtain the seed culture solution;
[0088] (2) Inoculate the above-mentioned seed culture solution at 2v / v% into a 20L fermenter containing 20L sterilized YPD liquid medium, the pH of the fermentation solution is 6.5, and continuously cultivate at 30°C and 200rpm for 24h, Obtain the culture fluid of P. fabreidii strain D-1;
[0089] (3) Centrifuge the above-mentioned culture solution at 8000 rpm and 4°C for 10 minutes to collect the bacteria sludge. According to the volume ratio of the bacteria sludge and the freeze-drying protective agent (trehalose and glycerol, the volume ratio is 1:1), the volume ratio is 1:3 ...
Embodiment 3
[0090] Example 3 Fermented Pu'er Tea Prepared by Fabrid's Barley Yeast
[0091] The P.fabridii yeast D-1 obtained in Example 1 is used to make fermented Pu'er tea, and the specific process is as follows:
[0092] 1) Preparation of seed liquid: Inoculate the preserved yeast culture liquid into 100mL PDB liquid medium (as seed medium) at 2v / v% after recovery, cultivate at 30°C and 200rpm for 18h, and inoculate the obtained yeast culture medium with PDB liquid medium The culture medium was adjusted to a viable count of about 1×10 8 CFU / mL, ready to use.
[0093] 2) Fermentation of Pu'er raw tea: Add sterile water to the raw Pu'er raw tea (50g) until the content of water is 30wt% compared to the total weight of the tea leaves, take 5mL of the above bacteria solution and inoculate it into Pu'er raw tea, and mix well; After the inoculated tea leaves were sealed with a parafilm, they were placed in an incubator at 30°C and incubated for 52 hours.
[0094] 3) Drying the Pu'er tea f...
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