Jack E. Richman, Ph.D.

Affiliations: 
Biochemistry, Molecular Biology, and Biophysics University of Minnesota, Twin Cities, Minneapolis, MN 
Area:
organic chemistry
Website:
http://cbs.umn.edu/contacts/jack-e-richman
Google:
"Jack Richman"
Mean distance: 7.31
 
SNBCP

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Stephan Mary Cameron collaborator 2005-2013
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Publications

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Robinson SL, Christenson JK, Richman JE, et al. (2019) Mechanism of a Standalone β-Lactone Synthetase: New Continuous Assay for a Widespread ANL Superfamily Enzyme. Chembiochem : a European Journal of Chemical Biology
Christenson JK, Robinson SL, Engel TA, et al. (2017) OleB from bacterial hydrocarbon biosynthesis is a β-lactone decarboxylase sharing key features with haloalkane dehalogenases. Biochemistry
Christenson JK, Richman JE, Jensen MR, et al. (2016) β-Lactone Synthetase Found in Olefin Biosynthesis Pathway. Biochemistry
Aukema KG, Makris TM, Stoian SA, et al. (2013) Cyanobacterial aldehyde deformylase oxygenation of aldehydes yields n-1 aldehydes and alcohols in addition to alkanes. Acs Catalysis. 3: 2228-2238
Seffernick JL, Erickson JS, Cameron SM, et al. (2012) Defining sequence space and reaction products within the cyanuric acid hydrolase (AtzD)/barbiturase protein family. Journal of Bacteriology. 194: 4579-88
Cameron SM, Durchschein K, Richman JE, et al. (2011) A New Family of Biuret Hydrolases Involved in S-Triazine Ring Metabolism. Acs Catalysis. 2011: 1075-1082
Frias JA, Richman JE, Erickson JS, et al. (2011) Purification and characterization of OleA from Xanthomonas campestris and demonstration of a non-decarboxylative Claisen condensation reaction. The Journal of Biological Chemistry. 286: 10930-8
Sukovich DJ, Seffernick JL, Richman JE, et al. (2010) Structure, function, and insights into the biosynthesis of a head-to-head hydrocarbon in Shewanella oneidensis strain MR-1. Applied and Environmental Microbiology. 76: 3842-9
Sukovich DJ, Seffernick JL, Richman JE, et al. (2010) Widespread head-to-head hydrocarbon biosynthesis in bacteria and role of OleA. Applied and Environmental Microbiology. 76: 3850-62
Richman JE. (2010) Salts of Mosher's thioacid: agents for determining the enantiomer excess of SN2 substrates Tetrahedron Letters. 51: 2793-2796
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