Saccharomyces cerevisiae, starter and its application in the preparation of hollow noodles
A technology of Saccharomyces cerevisiae and starter, applied in the field of microorganisms, can solve the problems of shortening the fermentation cycle of hollow noodles, low acid production at fermentation speed, and inability to form hollow noodles, etc., to achieve fast production and reproduction speed, strong fermentation power, and improved production efficiency effect
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Embodiment 1
[0061] The formula of embodiment 1 medium
[0062] 1. YPD liquid medium includes: 2% glucose, 2% peptone, 1% yeast extract and 95% water.
[0063] 2. YPD slant test tubes include: 2% glucose, 2% peptone, 1% yeast extract, 2% agar powder and 93% water.
[0064] 3. YPD plate culture medium includes: 2% glucose, 2% peptone, 1% yeast extract, 2% agar powder and 93% water.
Embodiment 2
[0065] Isolation, screening and identification of embodiment 2 yeast
[0066] 1. Isolation and screening of strains
[0067] Preparation of bacterial suspension: 16 groups of hollow noodle yeast samples were collected from Henan, Shandong, Shaanxi, Sichuan and other places. Wash the samples of each group with sterile water respectively, take 5g of old noodle yeast samples for each group, add them to 45mL of sterile water, take 1mL of the suspension after shaking, and dilute it with a 10-fold gradient until the mass concentration is obtained for 10 -6 diluent; the selected mass concentrations were 10 -4 、10 -5 and 10 -6 Take 100 μL sample dilution for each gradient and evenly spread it on the YPD plate medium, culture it in a biochemical incubator at 28-30°C for 2-3 days, and check the growth of the colony every day.
[0068] After the colony grows, select the target strain according to the growth of the colony and the shape, color, diameter, texture, thickness, and growth...
Embodiment 3
[0096] 1. A starter comprising the above-mentioned Saccharomyces cerevisiae KXMR006.
[0097] 2. the method for preparing above-mentioned leavening agent, comprises the following steps:
[0098] S1. After activating Saccharomyces cerevisiae KXMR006, absorb 10mL of activated Saccharomyces cerevisiae KXMR006 bacterial liquid, inoculate it in 3L of YPD liquid medium, cultivate it in an incubator at 30°C for 24h, and obtain the OD value (620nm) The seed liquid of 2.0;
[0099]S2. Sterilize the 500L fermentor at 121°C for 30min, and sterilize the YPD liquid medium at 121°C for 30min; inoculate 3L of the seed liquid into the sterilized YPD liquid medium, then place it in the fermenter, Cultivate at 30°C for 24 hours, during which the rotation speed of the fermenter is 150r / min, and the ventilation rate is 15CFM, to obtain the culture solution;
[0100] S3. Use a tube centrifuge to centrifuge the culture medium at a speed of 15000r / min, collect the bacteria, mix the bacteria with t...
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Abstract
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