Saccharomyces cerevisiae for brewing pomegranate fruit wine and pomegranate wine prepared by fermentation
A technology for Saccharomyces cerevisiae and pomegranate wine, which is applied in the field of pomegranate wine, can solve the problems of separation and screening of special yeast for pomegranate fruit wine and the application research has not yet been reported, and achieves the effects of excellent fermentation performance, uniform wine body and long aftertaste.
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Embodiment 1
[0048] Example 1: Isolation, screening and purification of yeast strains
[0049] 1. Collection of yeast isolation sources:
[0050] The principle of random sampling was used to collect fresh pomegranates, rotten pomegranates, pomegranate leaves and their soil from the pomegranate gardens in surrounding cities of Kashgar, Xinjiang. A total of 24 pomegranate samples, 12 pomegranate leaf samples, and 8 pomegranate garden soil samples were collected and packed into sterile paper bags and stored in a refrigerator at 4°C.
[0051] 2. Strain isolation method:
[0052] Yeasts were separated using different medium types, alcohol concentrations, culture temperatures, and pH values to maximize the sample size. Enrichment and separation conditions are as follows:
[0053] A. Take an appropriate amount of samples and add them to sterilized PDA and YPD medium containing 3%, 6%, 9% and 12% ethanol respectively, with a natural pH value, and incubate in a biochemical incubator at 30°C fo...
Embodiment 2
[0086] Embodiment two: the identification of yeast strain
[0087] 1. Morphological identification of yeast
[0088] A. Morphological and cultural characteristics:
[0089] Inoculate the bacteria into PDA liquid medium, culture at 28°C for 3-7 days, observe whether it is fermented, whether the culture medium is turbid, whether it forms rings or islands, the amount of sediment and its tightness, and stain it under a microscope to observe and record the yeast The mode of asexual reproduction and the shape of the cells, the size of the vegetative cells is measured with an eyepiece micrometer, the yeast is streaked on the PDA solid medium, cultured at 30°C for 2-3 days, and the colony shape is observed:
[0090] The SL20 strain was cultured in PDA liquid medium for 3-7 days, the cells were oval, the flask wall had no membrane or web, the cell size was (3.02-7.05)×(1.66-3.17) μm, and the asexual reproduction was budding at one end. The colony grown on PDA solid medium is milky wh...
Embodiment 3
[0103] Embodiment three: the basic brewing performance test of yeast strain
[0104] 1. Fermentation characteristics of self-selected yeast under different temperature conditions (with Angel yeast as the control):
[0105] The screened yeast strains were fermented with pomegranate wine at three temperatures of 20°C, 25°C and 30°C, and Angel active dry yeast was used as a control strain, and each was repeated three times. See attached Figure 1-4 .
[0106] Strain activation: Yeast was shaken and cultivated in 50mL PDA liquid medium for 10h, and then transferred to a 50mL Erlenmeyer flask containing 10°Brix pomegranate juice to continue to expand for 10h. Angel active dry yeast was rehydrated and activated in 2% sugar water at 35°C as required, and then transferred to a 50mL Erlenmeyer flask containing 10°Brix pomegranate juice for 10h of expansion.
[0107] Inoculum volume: 1% of pomegranate juice.
[0108] Processing of pomegranate juice: Sterilization of pomegranate juic...
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