The Narayan lab focuses on identifying and characterizing enzymes from various microorganisms that can catalyze chemical reactions that are challenging to reproduce synthetically. These biocatalysts can be employed to create various chemicals for pharmaceutical or other purposes.[9][13]
Awards and honors
Narayan has received numerous awards and honors including:
Baker Dockrey, S. A. and Narayan, A. R. H. “Flavin-dependent biocatalysts in synthesis” Tetrahedron2019doi:10.1016/j.tet.2019.01.008(Special Issue on Biocatalysis in Organic Synthesis).
Lukowski, A. L.. and Narayan, A. R. H. “Natural voltage-gated sodium channel ligands: Biosynthesis and biology” ChemBioChem2019doi:10.1002/cbic.201800754(Special Issue: New Talent).
Benítez, Attabey Rodríguez; Tweedy, Sara; Dockrey, Summer A. Baker; Lukowski, April L.; Wymore, Troy; Khare, Dheeraj; Brooks L. Charles III; Smith Janet L.; Narayan Alison R.H. (2018): Structural Basis for Selectivity in Flavin-Dependent Monooxygenase-Catalyzed Oxidative Dearomatization. ChemRxiv. Preprint. doi:10.26434/chemrxiv.7297766.v1
Baker Dockrey, S. A.; Doyon, T. J.; Perkins, J. C.; Narayan, A. R. H. “Whole-cell biocatalysis platform for gram-scale oxidative dearomatization of phenols”Chem. Biol. Drug Des.2018doi:10.1111/cbdd.13443
Lukowski, A. L.; Ellinwood, D. C.; Hinze, M. E.; DeLuca, R. J.; Du Bois, J.; Hall, S.; Narayan, A. R. H. "C–H hydroxylation in paralytic shellfish toxin biosynthesis" J. Am. Chem. Soc., 2018, 140 (37), 11863–11869 doi:10.1021/jacs.8b08901
Chun, S. W.; Hinze, M. E.; Skiba, M. A.; Narayan, A. R. H. "Chemistry of a unique polyketide-like synthase" J. Am. Chem. Soc.2018, 140, 2430–2433. doi:10.1021/jacs.7b13297
Baker Dockrey, S. A.; Lukowski, A. L.; Becker, M. R.; Narayan, A. R. H. “Biocatalytic site- and enantioselective oxidative dearomatization of phenols” Nature Chem.2018, 10, 119–125. doi:10.1038/nchem.2879
Mentored Key Publications
“Enzymatic Hydroxylation of an Unactivated Methylene C–H Bond Guided by Molecular Dynamics Simulations” (Nat. Chem. 2015, DOI: 10.1038/nchem.2285)[18]
“Directing Group-Controlled Regioselectivity in an Enzymatic C–H Bond Oxygenation” (J. Am. Chem. Soc. 2014, DOI: 10.1021/ja5016052) [10]
“Indolizinones as Synthetic Scaffolds: Fundamental Reactivity and the Relay of Stereochemical Information” (Org. Biomol. Chem. 2012, DOI: 10.1039/clob06423a)[7]