Bioorganic and Medicinal Chemistry Letters p. 65 - 68 (1999)
Update date:2022-08-23
Topics:
Velonia, Kelly
Tsigos, Iason
Bouriotis, Vassilis
Smonou, Ioulia
Investigation of the stereochemistry of the hydride transfer in reactions catalyzed by the recently isolated NAD+-linked alcohol dehydrogenase from the Antarctic psychrophile Moraxella sp. TAE123 was accomplished by using 1H NMR spectroscopy of the deuterated coenzyme. It was found that this new psychrophilic enzyme is a type A dehydrogenase. Moraxella sp. ADH reduces stereospecifically 2-butanone to produce (S)-2-butanol.
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