A kind of enzymatic preparation method of l-xylose
An enzymatic and xylose technology, applied in the field of enzymatic preparation of L-xylose, can solve problems such as affecting extraction process and product quality, unsuitable L-xylose raw materials, increasing environmental protection costs, etc., and achieves low pollution and simple operation. Easy to control and less by-products
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Embodiment 1
[0022] (1) Preparation of pyruvate decarboxylase
[0023] Primers were designed according to the pyruvate decarboxylase gene sequence of Saccharomyces cerevisiae in Genebank, as follows:
[0024] Upstream primer: CATGCCATGGATTCAATTACTTTGGGTAAATATTTGTTCG
[0025] Downstream primer: CCGCTCGAGTTGCTTAGCGTTGGTAGCAGCAGTC
[0026] After the PCR product of pyruvate decarboxylase was inserted into the plasmid pET-22b, the recombinant expression plasmid pET-22b-pdc was constructed.
[0027] Take 0.01g of the recombinant expression plasmid pET-22b-pdc to transform Escherichia coli BL21(DE3) competent cells, culture in 600μL LB medium for 1h, take 100μL of the bacterial liquid and spread it on a solid LB plate containing ampicillin, at 37℃ Cultivate for 10 hours to obtain genetically engineered bacteria capable of highly expressing pyruvate decarboxylase.
[0028] The constructed engineered bacteria were inoculated in TB medium containing ampicillin, and cultured at 37°C until the bact...
Embodiment 2
[0032] Substantially the same as Example 1, the difference is that the buffer is an MES buffer, pH7.5, 5mM magnesium chloride, 1mM thiamine pyrophosphate and 300mM 2-keto-L-gulonic acid, and the conversion rate is similar to that of Example 1 Ratio, increased by 16.9%, that is, 28.0g / L L-xylose was generated.
Embodiment 3
[0034] Basically the same as Example 1, the difference is that the reaction temperature is 45 ° C, 5mM magnesium chloride, 1mM thiamine pyrophosphate, 300mM 2-keto-L-gulonic acid, and the conversion rate is compared with Example 1, which has increased by 24.5 %, that is, 31.4g / L L-xylose was generated.
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