Recombinant Pseudomonas plecoglossicida for producing L-xylose and application thereof
AssigneeLinkchem Co. Ltd.
InventorXi Lu
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AssigneeLinkchem Co. Ltd.
InventorXi Lu
Estimating the term…
The disclosure discloses recombinant Pseudomonas plecoglossicida for producing L-xylose and application thereof, and belongs to the technical field of bioengineering. According to the disclosure, a synthesized 2-ketogluconate reductase gene and a 2,5-diketogluconate reductase gene derived from Corynebaterium ATCC 31090 and a pyruvate decarboxylase gene derived from Saccharomyces cerevisiae are successfully expressed in a host P. plecoglossicida by a double plasmid system, and an obtained genetically engineered strain is fermented for 56 h in a shake flask, where the yield of L-xylose reaches 16.2 g/L, and the transformation rate reaches 20.3%; the obtained genetically engineered strain is fermented for 48 h and 44 h in 3 L and 15 L fermentors, respectively, where the yields of L-xylose reach 37.6 g/L and 45.8 g/L, respectively, and the glucose transformation rates are 47.0% and 57.3%, respectively. The method has the advantages of low raw material cost, no pollution to the environment, simple operation, and important economic and social benefits.
A recombinant strain for producing L-xylose, comprising nucleic acid sequences for expressing a 2-ketogluconate dehydrogenase gene, a 2,5-diketogluconate reductase gene, and a pyruvate decarboxylase gene, wherein the recombinant strain uses Pseudomonas plecoglossicida as a host strain, wherein the 2-ketogluconate dehydrogenase gene comprises nucleic acid sequences for three subunits, which are set forth in SEQ ID NO:
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