2015
DOI: 10.1080/09168451.2015.1012148
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Reactivity of sorbose dehydrogenase from Sinorhizobium sp. 97507 for 1,5-anhydro-d-glucitol

Abstract: Purified recombinant sorbose dehydrogenase from Sinorhizobium sp. 97507 exhibited high reactivity for 1,5-anhydro-d-glucitol (1,5-AG) and l-sorbose, but little activity for the other sugars or sugar alcohols tested. Kinetic analysis revealed that its catalytic efficiency (kcat/Km) for l-sorbose and 1,5-AG is 1.8 × 102 and 1.5 × 102 s−1·M−1, respectively.

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Cited by 2 publications
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“…Among them, the A551N and A551L mutants were less active towards glucose and more specific for 1,5-AG, relative to WT. Although their catalytic efficiency was decreased significantly and may be too low for clinical application, 22) we believe that they should be useful as leads for further optimization to obtain more active and 1,5-AG-specific enzymes by means of random mutagenesis 23) 24) 25) and high-throughput screening, 26) 27) paving the way for clinical application.…”
Section: Resultsmentioning
confidence: 97%
“…Among them, the A551N and A551L mutants were less active towards glucose and more specific for 1,5-AG, relative to WT. Although their catalytic efficiency was decreased significantly and may be too low for clinical application, 22) we believe that they should be useful as leads for further optimization to obtain more active and 1,5-AG-specific enzymes by means of random mutagenesis 23) 24) 25) and high-throughput screening, 26) 27) paving the way for clinical application.…”
Section: Resultsmentioning
confidence: 97%