Saccharomyces cerevisiae and application of the same in dry red wine brewing
A technology of Saccharomyces cerevisiae and red wine, applied in the preparation of wine, the preparation of alcoholic beverages, methods based on microorganisms, etc., can solve the problems of flavor and aroma substances disappearing, affecting biodiversity, lacking regional characteristics, etc., and achieve strong aroma , good clarity and high alcohol production
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Embodiment 1
[0016] Example 1 Separation, purification and screening of Saccharomyces cerevisiae WR1104
[0017] 1. Selection of starting strains
[0018] (1) Isolation of fruit surface yeast aseptically weigh 10g ripe grapes, put them into a 90ml sterile water Erlenmeyer flask, shake culture for 30min, make a bacterial suspension, accurately suck 50ul into YPD solid medium, and sterile scrape Shovel and scrape well, incubate at 25℃ for 24-28h;
[0019] (2) Isolation of natural fermentation yeast aseptically weigh about 100g of fresh grapes with good ripeness, put them into a sterile 500ml Erlenmeyer flask, break them with a sterile hammer, culture at 27°C, take 1ml of fermentation broth every 24h and add Stepwise dilution in 9ml sterile water to 10 -7 , Take 50ul of the diluted bacterial solution into YPD solid medium, scrape it with a sterile spatula, and incubate at 25°C for 24-28h;
[0020] (3) For the yeast strains cultured in YPD for 48 hours in (1) and (2), pick the macroscopic fungal colo...
Embodiment 2
[0038] Example 2 Identification of Saccharomyces cerevisiae WR1104 strain
[0039] 1. Identification of lysine medium (Saccharomyces cerevisiae cannot use lysine as a nitrogen source and therefore cannot grow on this medium)
[0040] Yeast strain WR1104 was inoculated into YPD liquid medium and activated for 24 hours, and then inoculated into 5mL sterile water according to the inoculation amount of 1% for starvation treatment. After 7 days, it was inoculated into lysine medium. After 5 days of cultivation at 27°C, no yeast growth was observed. And observation, the aseptic colony grew after 15 days, indicating that the strain is Saccharomyces cerevisiae.
[0041] 2. Physiological and biochemical identification
[0042] The yeast strain WR1104 was respectively inoculated on each medium for sugar fermentation (glucose, sucrose, maltose, lactose, galactose, ribose, inulin), carbon source assimilation (rhamnose, L-arabinose, inositol, cellobiose) Pond, soluble starch, inulin, methanol, D-...
Embodiment 3
[0060] Example 3 Application of Saccharomyces cerevisiae WR1104 in the brewing of special high-quality dry red wine
[0061] (With commercial active dry yeast RC212 as control, 4L small test)
[0062] 1. Dry red wine brewing process
[0063] SO 2 Sugar, pectinase, activated yeast seeds
[0064] ↓ ↓
[0065] Fresh wine red grapes→stemmed and broken→skinned grape pulp fermentation liquid→dipping tank→main fermentation (20-28℃)→5-7d main fermentation completed→grape wine→post-fermentation (20-25℃)→after about 30d End of fermentation
[0066] ↓ ↑ ↑
[0067] Dregs Lactobacillus SO 2
[0068] →Storage and aging →Completion of aging →Gluing, separation of wine feet →bottling
[0069] 2. Preparation of Saccharomyces cerevisiae WR1104 seed solution
[0070] Transfer the WR1104 strain stored on the slope of the YPD test tube to liquid grape juice medium with natural sugar content (about 16%) and natural pH. Incubate at 27°C for 12-1...
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