Method for preparing optical pure (R)-2-octanol by immobilized microorganism
A technology of immobilized microorganisms and immobilized cells, which is applied in the field of preparing optically pure (R)-2-octanol from immobilized microorganisms, can solve the problems of product separation being too complicated and cells not being reusable, and achieve the goal of reducing toxicity and durability The effect of strong acceptance and easy separation of products
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Embodiment 1
[0014] Wash the D-101 non-polar macroporous adsorption resin with deionized water for several times, soak it in 0.5% NaOH for 48 hours, wash it with deionized water until it is neutral, and dry it;
[0015] Insert baker's yeast into the culture medium for routine culture. The composition of the medium is that the components contained in each L of culture solution are in g: glucose 20.0, yeast extract 1.0, peptone 5.0, K 2 HPO 4 1.0, KH 2 PO 4 1.0, MgSO 4 0.2, prepare the bacterial liquid, soak the D-101 non-polar macroporous adsorption resin in the bacterial liquid, the temperature of the bacterial liquid is 30°C, the pH value is 6.5, the rotation speed of the shaking flask is 150rpm, the bacteria are fixed for 28 hours, and the bacteria are filtered out. solution, washed with saline, and heat-treated the immobilized cells for 15 min to prepare baker's yeast cells immobilized by non-polar macroporous adsorption resin.
[0016] Dissolve baker's yeast cells immobilized by D-...
Embodiment 2
[0018] Wash the H103 type non-polar macroporous adsorption resin with deionized water several times, soak it in 2.0% NaOH for 30 hours, wash it with deionized water until it is neutral, and dry it;
[0019] Insert baker's yeast into the culture medium for routine culture. The composition of the medium is that the components contained in each L of culture solution are in g: glucose 60.0, yeast extract 8.0, peptone 1.0, K 2 HPO 4 2.0, KH 2 PO 4 2.0, MgSO 4 0.5, to prepare the bacterial liquid, soak the H103 non-polar macroporous adsorption resin in the bacterial liquid, the temperature of the bacterial liquid is 28°C, the pH value is 7.0, the rotation speed of the shaking flask is 200rpm, the bacterial strain is fixed for 40h, the bacterial liquid is filtered off, and used After washing with physiological saline, the immobilized cells were heat-treated for 60 minutes to prepare baker's yeast cells immobilized by non-polar macroporous adsorption resin.
[0020] Dissolve baker...
Embodiment 3
[0022] Wash the HPD-300 non-polar macroporous adsorption resin with deionized water for several times, soak it in 4.0% NaOH for 24 hours, wash it with deionized water until it is neutral, and dry it;
[0023] Insert baker's yeast into the culture medium for routine culture. The composition of the medium is that the components contained in each L of culture solution are in g: glucose 30.0, yeast extract 4.0, peptone 6.0, K 2 HPO 4 1.0, KH 2 PO 4 2.0, MgSO 4 0.5, to prepare the bacterial liquid, soak the HPD-300 non-polar macroporous adsorption resin in the bacterial liquid, the temperature of the bacterial liquid is 28°C, the pH value is 7.0, the rotation speed of the shaking flask is 180rpm, the bacteria are fixed for 48 hours, and the bacteria are filtered out. solution, washed with saline, and heat-treated the immobilized cells for 55 minutes to prepare baker's yeast cells immobilized by non-polar macroporous adsorption resin.
[0024]Dissolve baker's yeast cells immobil...
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