A method for separating gamma-aminobutyric acid and glutamic acid by chromatography
An aminobutyric acid and chromatographic separation technology, applied in the field of biochemical separation, can solve the problems of large loss rate of GABA, increase of GABA dissociation, increase of escape rate, etc., and achieve the effects of high selectivity, high degree of separation and simple process
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Embodiment 1
[0033] The GABA feed solution produced by the enzymatic conversion of glutamic acid is filtered through membrane, concentrated to 20% (w / w) concentration using nanofiltration membrane, and adjusted to pH 7.5 with ammonia water; 1:1 filled calcium-type cationic chromatographic resin, controlled column temperature at 10°C, feed volume at 0.05BV, constant temperature chromatographic separation; using deionized water as eluent, controlled temperature at 10°C and flow rate at 1.0BV / h Carry out eluting under the following conditions; collect eluent and residual liquid respectively, obtain the aqueous solution of two kinds of products of decolorized GABA and glutamic acid respectively, the separation rate of two substances reaches more than 98% (w / w), and the decolorization rate of GABA reaches 96% above.
Embodiment 2
[0035] The GABA feed solution produced by enzymatic conversion of glutamic acid is filtered through the plate frame, concentrated to 80% (w / w) concentration by using heat, and adjusted to pH 8 with NaOH; according to the volume specification of the chromatographic column, the ratio of diameter to height is 1 : 30 filled lithium-type cationic chromatographic resin, control the column temperature at 40°C, the feed volume is 0.1BV, constant temperature chromatographic separation; use deionized water to adjust the pH to 8 as eluent, control the temperature at 40°C and the flow rate is 2.0BV Elution is carried out under the condition of 1 / h; the eluent and residual liquid are collected respectively to obtain the aqueous solution of two products of decolorized GABA and glutamic acid respectively, the separation rate of the two substances reaches more than 99%, and the decolorization rate of GABA reaches more than 98%.
Embodiment 3
[0037] The GABA feed solution produced by enzymatic conversion of glutamic acid is filtered through the plate frame, concentrated to 60% (w / w) concentration by using heat, and adjusted to pH 10 with KOH; according to the volume specification of the chromatographic column, the ratio of diameter to height is 1 : 40 filled with ammonia-type cationic chromatographic resin, control the column temperature at 50°C, the feed rate is 0.3BV, constant temperature chromatographic separation; use deionized water to adjust the pH to 7 as eluent, control the temperature at 50°C and the flow rate is 0.5BV Elution is carried out under the condition of / h; the eluent and residual liquid are collected respectively, and the aqueous solutions of two products of decolorized GABA and glutamic acid are respectively obtained. The separation rate of the two substances reaches more than 90%, and the decolorization rate of GABA reaches more than 81%.
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