Method for recycling hemp strain-containing degumming liquid for degumming hemp
A hemp and degumming technology, applied in the direction of bacterial retting, etc., can solve the problems of low hemp production rate, long degumming cycle, large sewage discharge, etc., and achieve the effect of increasing the hemp production rate, improving the quality of hemp fiber, and saving energy consumption
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specific Embodiment approach 1
[0015] Specific embodiment one: the method that this embodiment marijuana adds bacterium degumming liquid and reuses and carries out hemp degumming realizes by following steps: One, the activation of bacterial classification for hemp degumming: Escherichia coli HDDMG05 and bacillus licheniformis HDDMM02 are respectively in 30 Cultivate on beef extract peptone medium for 24 hours at ℃; 2. First-level seed culture: use an inoculation loop to pick the activated bacteria in step 1 and insert them into 200-500mL industrial expansion medium, at 28-32℃ Cultivate for 20 to 30 hours; 3. Secondary seed cultivation: Inoculate the inoculum of 0.5% to 2% of the inoculum after the primary seed cultivation into 200 to 500L industrial expansion medium, at 28 to 32°C Cultivate under conditions for 20-30 hours; Fourth and third-level seed cultivation: insert the inoculum of 0.5% to 2% of the inoculum of the second-level seed culture into 2-5t industrial expansion medium according to the volume f...
specific Embodiment approach 2
[0021] Specific embodiment 2: The difference between this embodiment and specific embodiment 1 is that in step 2, use the inoculation loop to pick the activated strains of step 1 and insert them into 250-400mL industrial expansion medium, and cultivate them at 30°C for 24h . Other steps and parameters are the same as those in the first embodiment.
specific Embodiment approach 3
[0022] Specific embodiment three: the difference between this embodiment and specific embodiment one is that in step three, the inoculation amount of 1% to 1.5% of the inoculum after the primary seed culture is inserted into 250 ~ 400L industrial expansion medium cultured at 30°C for 24 hours. Other steps and parameters are the same as those in the first embodiment.
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