Production of L-allose and D-talose from L-psicose and D-tagatose by L-ribose isomerase

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Abstract

L-ribose isomerase (L-RI) from Cellulomonas parahominis MB426 can convert L-psicose and D-tagatose to L-allose and D-talose, respectively. Partially purified recombinant L-RI from Escherichia coli JM109 was immobilized on DIAION HPA25L resin and then utilized to produce L-allose and D-talose. Conversion reaction was performed with the reaction mixture containing 10% L-psicose or D-tagatose and immobilized L-RI at 40 °C. At equilibrium state, the yield of L-allose and D-talose was 35.0% and 13.0%, respectively. Immobilized enzyme could convert L-psicose to L-allose without remarkable decrease in the enzyme activity over 7 times use and D-tagatose to D-talose over 37 times use. After separation and concentration, the mixture solution of L-allose and D-talose was concentrated up to 70% and crystallized by keeping at 4 °C. L-Allose and D-talose crystals were collected from the syrup by filtration. The final yield was 23.0% L-allose and 7.30% D-talose that were obtained from L-psicose and D-tagatose, respectively.

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Terami, Y., Uechi, K., Nomura, S., Okamoto, N., Morimoto, K., & Takata, G. (2015). Production of L-allose and D-talose from L-psicose and D-tagatose by L-ribose isomerase. Bioscience, Biotechnology and Biochemistry, 79(10), 1725–1729. https://doi.org/10.1080/09168451.2015.1038215

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