Method for improving sweetness of stevia sugar
A technology of stevioside and sweetness, which is applied in the field of food additives and sweeteners, and can solve the problems of small sample size and difficult industrial production
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2010-04-07
- Estimated Expiration
- Not applicable · inactive patent
Smart Images
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Abstract
Description
technical field
[0001] The invention relates to a method for separating and purifying a high-quality sweetener component-rebaudioside A or other components in other steviosides by using microorganisms and enzymatic methods, and belongs to the application field of food additives and sweeteners. Background technique
[0002] Steviol glycoside is a white, odorless powder with a melting point of 198-202°C, high temperature resistance, rapid moisture absorption in the air, slightly soluble in ethanol, stable to heat, acid and alkali, and can be heated in a solution in the range of pH 4-10 It does not change or brown at 120°C, and most of it is not metabolized in the human body. It is a non-fermentable sugar, so the heat generated in the body is extremely low. Steviol glycoside (purity above 90%) is a white powder, and subpure product (purity 50%) is light brown. It is easily soluble in water and can quickly absorb moisture in the air. The solubility at room temperature exceeds 4...
Examples
preparation example Construction
[0035] Preparation of bacterial solution:
[0036] Bacillus megaterium J2 (Bacillus megaterium J2) CCTCC NO: M209201 was cultured in a conventional broth liquid medium at 37° C. and 220 rpm for 48 hours to obtain the bacterial liquid.
[0037] Preparation of bacterial powder:
[0038] It includes fermentation culture of bacteria, separation of fermentation liquid, emulsification of bacteria slime and vacuum freeze drying of emulsion. That is, Bacillus megaterium J2 (Bacillus megaterium J2) CCTCC NO: M209201 was cultured in the above liquid based on the bacteria liquid obtained after 48 hours of culture, centrifuged at 8000rpm and 5min to collect the bacteria to obtain the sludge, and the sludge was vacuum-frozen under the condition of a vacuum of 1-5pa After drying for 30 hours, the bacteria powder is obtained.
[0039] Degradation characteristics of SS and RA by degrading bacteria:
[0040] Bacillus megaterium J2 (Bacillus megaterium J2) CCTCC NO: M209201 is cultivated for...
Embodiment 1
[0047] 0.5% (W / W), pH 5.0 stevioside solution (RA purity is about 85%), sterilized and cooled, then added 5% (W / W) Bacillus megaterium J2CCTCC NO: M209201 bacterial solution, cultured at 37°C for 72h, after After conversion, SS was mostly degraded, and RA content remained unchanged. After the transformation, the cells were removed by centrifugation at 5000rpm, and the supernatant was removed by flocculation and sedimentation, adsorbed and separated by macroporous resin, and the purified liquid was crystallized to obtain RA with a purity of about 98%.
Embodiment 2
[0049] 0.01% (W / W), pH 4.5 stevioside solution (RA purity is about 75%), add 2% (W / W) bacteria powder of Bacillus megaterium J2CCTCC NO: M209201, after culturing at 37°C for 36 hours, according to the conventional RA with a purity of about 90% was obtained by separation and purification.