Microbial preparation for treating tobacco stems and preparation method thereof
A microbial preparation and microbial technology, applied in the field of tobacco additives, can solve unseen problems and achieve the effects of simple operation, convenient large-scale industrial production, and strong controllability
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Embodiment 1
[0031] The strain source of microorganism Aureobasidium OF-01 of the present invention:
[0032] The invention provides a microbial preparation for improving the quality of tobacco stems. The preparation of the microorganism is obtained by the following method: pulverize a sample of Honghua Dajinyuan tobacco leaves aged in storage for 3 years, and take 5 grams of pulverized tobacco powder Put it into a triangular flask with 100ml of sterile water, shake it on a shaker at 100-250rpm for 30 minutes, filter to remove the smoke dust, and apply the suspension to MYP medium (malt extract 7g, yeast extract 0.5g, peptone 2.5 g, agar 20g, water 1L, pH7.0) plate, 200 microliters / dish, a total of 50 dishes, cultured in an incubator at 28°C for 5-7 days to purify a single microorganism with MYP medium, from the surface of the purified tobacco leaves The OF-01 strain with aroma-producing properties was screened from microorganisms, which was identified as Aureobasidium pullulans.
[0033]...
Embodiment 2
[0037] Microorganism preparation of the present invention adopts following steps to prepare:
[0038] 1. The liquid strain of the mold OF-01 isolated from the flue-cured tobacco leaves in Example 1 was cultured on a test tube slant: inoculate the thalli of the bacterial strain OF-01 into the MYP medium (7 g of malt extract, 0.5 g of yeast extract , peptone 2.5g, agar 20g, water 1L, pH7.0) on a slant, cultured at 20-30°C for 4-10 days to obtain seeds cultured on the slant, the suitable culture condition is 26-32°C, the best is at Cultured at 28°C for 7 days.
[0039] 2. Liquid seed culture:
[0040] Seeds cultivated on slant planes are inoculated into MYP liquid medium in Erlenmeyer flasks and cultured on a shaker at 15-30° C. and 50-300 rpm for 3-7 days. The optimum culture condition is 28°C, 200rpm for 4 days.
[0041] 3. Mass cultivation in fermenter:
[0042] Put the seeds after liquid seed culture into the MYP liquid medium in the fermenter at a ratio of 1-5% (V / V), an...
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