Microorganism combination solid-state fermentation method for reducing content of butyl isosulfocyanate in rapeseed dregs
An isothiocyanate, solid-state fermentation technology, applied in microorganism-based methods, microorganisms, biochemical equipment and methods, etc., can solve the problems of long fermentation time, excessive fermentation time, complex fermentation process, etc., and reach the fermentation time. Short, high efficiency, the effect of reducing isothiocyanate content
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Embodiment 1
[0016] Embodiment one (laboratory)
[0017] A. Preparation and pretreatment of rapeseed meal raw materials: Rapeseed meal raw materials were purchased from grain, oil and food processing enterprises, and were crushed before sterilization; 50 g of rapeseed meal raw materials were weighed, placed in a 250 mL Erlenmeyer flask, and Add 25mL of water to the Erlenmeyer flask, mix well; adjust the pH to 7.0±0.5, mix well, seal, and sterilize by high pressure steam at 121℃ for 15min;
[0018] B. Preparation of fermented seed liquid: adopt asparagine-glucose medium, lactic acid bacteria medium and potato-glucose-agar medium, three kinds of medium are all liquid medium, adopt shaking flask culture method to be used for cultivating purple red respectively coccus, Pediococcus pentosacea and Pichia montagnis; the medium was sterilized by high-pressure steam at 121°C for 15 minutes, cooled to room temperature, and then inoculated with the corresponding selected strains; The culture tempera...
Embodiment 2
[0024] Embodiment two (pilot test)
[0025] A. Preparation and pretreatment of rapeseed meal raw materials: crush the rapeseed meal raw materials with a pulverizer, weigh 100kg of raw materials, add 50L of water, and mix well; then adjust the pH to 7.0±0.5, mix well, subpackage, seal, Sterilize by high-pressure steam at 121°C for 15 minutes;
[0026] B. Preparation of fermented seed liquid: adopt asparagine-glucose medium, lactic acid bacteria medium and potato-glucose medium, all of which are liquid medium, and use the shake flask culture method to cultivate Rhodococcus rhodochrous and Pediococcus pentosacea respectively and Pichia monteoris; the culture medium was sterilized by high-pressure steam at 121°C for 15 minutes and then cooled to room temperature, and then inoculated with the corresponding selected strains; the culture temperature of Rhodococcus rhodococcus, Pediococcus pentosacea and Pichia mongoliana 28°C, 37°C, and 25-28°C respectively, the shaker speed is 190±...
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