Separation and purification method of mannosylerythritol lipids (MELs)
A technology of separation and purification, erythromycin sugar, applied in the field of separation and purification, to achieve the effect of high product recovery rate and purity, efficient separation and purification, and low solvent toxicity
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Embodiment 1
[0032] Take the fermentation broth rich in MELs, filter it with filter paper, and dissolve the semi-solid filter residue with enough methanol to obtain a methanol solution of MELs. Then according to the ratio of methanol: water: n-hexane=4:1:1, water and n-hexane of corresponding volume are added thereto, and the pH of the control water phase is 2, 5, 7, 9, 11, fully Mix for 2 minutes, then centrifuge at 4000 rpm for 2 minutes, and remove the lower methanol phase. The results are shown in Table 1 below. This method can achieve the purpose of separating and purifying MELs, and the acidic pH of the aqueous phase is better.
[0033] Table 1
[0034] pH of aqueous phase
Embodiment 2
[0036] Take the fermentation broth rich in MELs, filter it with filter paper, and dissolve the semi-solid filter residue with enough methanol to obtain a methanol solution of MELs. According to the ratio of methanol: water: n-hexane=2:1:1, 3:1:1, 4:1:1, 5:1:1, water and n-hexane of corresponding volume are added thereto, and the pH of the water phase is adjusted to 2. Mix well for 2 minutes on the suspension apparatus, then centrifuge at 4000rpm for 2 minutes, and take out the lower methanol phase. The results are shown in Table 2 below. This method can achieve the purpose of separating MELs.
[0037] Table 2
[0038]
Embodiment 3
[0040] Take the fermentation broth rich in MELs, filter it with filter paper, and dissolve the semi-solid filter residue with enough methanol to obtain a methanol solution of MELs. According to the ratio of methanol: water: n-hexane=2:1:0.5, 2:1:1.5, 2:1:2, 2:1:2.5, water and n-hexane of corresponding volume are added thereto, and the pH of the water phase is adjusted to 2. Mix well for 2 minutes on the suspension apparatus, then centrifuge at 4000rpm for 2 minutes, and take out the lower methanol phase. The results are shown in Table 3 below. This method can achieve the purpose of separating MELs.
[0041] table 3
[0042]
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