Abstract
Recently, we reported on the construction of a whole-cell biotransformation system in Escherichia coli for the production of d-mannitol from d-fructose (Kaup B, Bringer-Meyer S, Sahm H (2004) Metabolic engineering of Escherichia coli: construction of an efficient biocatalyst for d-mannitol formation in a whole-cell biotransformation. Appl Microbiol Biotechnol 64:333–339). Supplementation of this strain with extracellular glucose isomerase resulted in the formation of 800 mM d-mannitol from 1,000 mM d-glucose. Co-expression of the xylA gene of E. coli in the biotransformation strain resulted in a d-mannitol concentration of 420 mM from 1,000 mM d-glucose. This is the first example of conversion of d-glucose to d-mannitol with direct coupling of a glucose isomerase to the biotransformation system.
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Acknowledgements
We wish to thank N. Esaki for plasmid pMcFDH, G.A. Sprenger for plasmid pZY507glf. This work was supported by the InnoSweet GmbH, Braunschweig, Germany and the Fonds der Chemischen Industrie.
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Kaup, B., Bringer-Meyer, S. & Sahm, H. d-Mannitol formation from d-glucose in a whole-cell biotransformation with recombinant Escherichia coli . Appl Microbiol Biotechnol 69, 397–403 (2005). https://doi.org/10.1007/s00253-005-1996-0
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DOI: https://doi.org/10.1007/s00253-005-1996-0