Structure and Engineering of l-Arabinitol 4-Dehydrogenase from Neurospora crassa |
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Authors: | Brian Bae Ryan P. Sullivan Huimin Zhao Satish K. Nair |
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Affiliation: | 1 Department of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA2 Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA3 Department of Chemistry and Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA |
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Abstract: | l-Arabinitol 4-dehydrogenase (LAD) catalyzes the conversion of l-arabinitol into l-xylulose with concomitant NAD+ reduction. It is an essential enzyme in the development of recombinant organisms that convert l-arabinose into fuels and chemicals using the fungal l-arabinose catabolic pathway. Here we report the crystal structure of LAD from the filamentous fungus Neurospora crassa at 2.6 Å resolution. In addition, we created a number of site-directed variants of N. crassa LAD that are capable of utilizing NADP+ as cofactor, yielding the first example of LAD with an almost completely switched cofactor specificity. This work represents the first structural data on any LAD and provides a molecular basis for understanding the existing literature on the substrate specificity and cofactor specificity of this enzyme. The engineered LAD mutants with altered cofactor specificity should be useful for applications in industrial biotechnology. |
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Keywords: | LAD, l-arabinitol 4-dehydrogenase ncLAD, Neurospora crassa LAD PDB, Protein Data Bank ncLAD-S, D211S ncLAD-SR, D211S/I212R ncLAD-SRN, D211S/I212R/D213N ncLAD-3x, D211S/I212R/S348T psXDH, Pichia stipitis xylitol dehydrogenase |
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