Solid fermentation process for preparing bacillus natto microecological preparation
A technology of Bacillus natto and probiotics, applied in the field of probiotics, can solve the problems of low number of viable bacteria and affecting the growth of Bacillus natto, and achieve low production cost, stable and efficient product quality, and high spore rate Effect
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Embodiment 1
[0035] Embodiment 1: the solid-state fermentation method of bacillus natto probiotics
[0036]Bacillus natto CCTCC M207147 was inoculated on the slant of broth medium and cultured at 37°C for 24h. Pick 1 ring of slant seeds and inoculate them in liquid seed medium (1% peptone, 0.5% beef extract, 0.5% NaCl, pH 7.0-7.2), culture in a rotary shaker at 200r.p.m, 37°C for 16h, and obtain the first grade seed liquid. Put 35L of liquid seed medium into a 50L seed fermenter, sterilize at 121°C for 15 minutes, cool to 37°C, inoculate with 1.5% primary seed liquid, and incubate at 37°C for 10 hours to obtain secondary seed liquid. 6.5 parts of bran, 2 parts of bean cake powder, and 1.5 parts of cornstarch are mixed evenly, and the inorganic salt solution is added according to the ratio of solid-liquid weight ratio of 1: 1.2 (the solution contains K 2 HPO 4 ·3H 2 O 1.0%, MgSO 4 ·7H 2 O 0.1%), mix well, sterilize at 121° C. for 30 minutes, and cool to 37° C. to obtain a solid-state ...
Embodiment 2
[0037] Example 2: Tolerance of Bacillus natto CCTCC M207147 to temperature
[0038] The spore liquid and vegetative bacterial liquid of Bacillus natto CCTCC M207147 were kept in water baths at 100°C and 80°C for a period of time, respectively, and then counted live bacteria, and the number of live bacteria before the water bath was used as a control to calculate the relative survival rate . see results figure 2 , 3.
Embodiment 3
[0039] Example 3: Tolerance of Bacillus natto CCTCC M207147 to acid and alkali
[0040] The vegetative bacterial liquid of Bacillus natto CCTCC M207147 was incubated at 37°C at different pH for 45 minutes, and then the viable bacteria were counted, and the untreated vegetative bacterial liquid was used as a control to calculate the relative survival rate. see results Figure 4 .
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