A culture method of Burkholderia cepacia and its application in catalytic synthesis of liquor flavor esters and degradation of liquor harmful esters
A Holderia catalyzed ester technology, applied in the field of microorganisms, can solve the problems of low yield of high-quality wine, long aroma production cycle, slow ester production and aroma production, etc.
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Embodiment 1
[0023] Example 1 Burkholderia cepacia CGMCC 1.3055 Catalyzes Ester Synthesis and Nitrogen Source and Carbon Source Optimization for Fermentation Culture under the Condition of Simulated Liquor Fermentation Water Phase System
[0024]This example is carried out in order to optimize the cultivation method of Burkholderia polyphage CGMCC 1.3829 to obtain better production of liquor flavor esters.
[0025] 1. Strain activation: Under aseptic conditions, inoculate Burkholderia cepacia CGMCC 1.3055 into a 30mL test tube containing 5mL fermentation medium, and culture on a shaker at 30±2°C and 150±50r / min for 1– 2 days.
[0026] 2. Nitrogen source optimization fermentation culture: under aseptic conditions, inoculate activated Burkholderia cepacia CGMCC1.3055 into a 300mL Erlenmeyer flask containing 100mL fermentation medium, shaker at 30±2°C, 150±50r / min, cultured for 2–5 days. The fermented broth after cultivation is prepared according to the following point 4 to prepare the cru...
Embodiment 2
[0038] Degradation of DMP, DEP, DBP and DEHP by Example 2 Burkholderia cepacia CGMCC 1.3055
[0039] 1, the cultivation method of Burkholderia cepacia CGMCC 1.3055, it is characterized in that, medium composition comprises: yeast powder 5.0g / L, (NH 4 ) 2 SO 4 2.0g / L, MgSO 4 ·7H 2 O, CaCl 2 2H 2 O 0.01g / L, FeSO 4 ·7H 2 O0.001g / L, Na 2 HPO 4 12H 2 O 1.5g / L, KH 2 PO 4 1.5g / L, sterilized at 115°C for 20min, and added DEP, DBP and DEHP with a final concentration of 200mg / L. Put 10mL of medium into a 100mL Erlenmeyer flask, and inoculate 1–3%. The culture conditions are: 30±2°C, 150±50r / min, culture for 3-7 days.
[0040] After culturing, transfer 10 mL of fermentation broth into a 50 mL centrifuge tube, add 2 mL of n-hexane, shake and mix vigorously for 30 seconds, centrifuge, take the supernatant, filter and centrifuge for quantitative detection by gas chromatography internal standard method.
[0041] 2. Quantitative detection by gas chromatography:
[0042] The ...
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