Bacillus pumilus preparation for processing tobacco stems
A technology for microbial preparations and bacteria, applied in the field of microbial preparations, can solve the problems that have not yet been discovered, and achieve the effects of reducing irritation, reducing the concentration and energy of smoke, and increasing the amount of aroma.
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Embodiment 1
[0025] ——Test tube slant culture
[0026] A Luria-Bertani (LB) medium was used, and the formula was: 10 g of peptone, 10 g of sodium chloride, 5 g of yeast extract, 20 g of agar, and distilled water to a volume of 1000 ml. Sterilize at 121°C for 25 minutes and place on a slope. Inoculate Van35, culture at 28°C for 24 hours, and obtain test tube seeds.
Embodiment 2
[0028] - Seed cultivation
[0029] A Luria-Bertani (LB) medium was used, and the formula was: 10 g of peptone, 10 g of sodium chloride, 5 g of yeast extract, and distilled water to a volume of 1000 ml. Sterilize at 121°C for 25 minutes. Inoculate the Van35 test tube species and culture at 28°C for 12 hours to obtain liquid strains.
Embodiment 3
[0031] - Preparation of microbial preparations
[0032] Take the liquid strain, inoculate it into 200ml of LB liquid medium according to the inoculum amount of 0.1%, and cultivate it in a shaker at 37°C with a rotation speed of 180r / min until the OD value = 2.0. Centrifuge at 3500rpm / min for 10min, wash with sterile water Precipitate, centrifuge, and finally shake evenly with 20mL sterile water, and dilute 10 times before use to obtain the bacterial agent.
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