Profile for John May

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John May
Pronouns: He/Him/His
Associate Professor
Chemistry & Biochemistry
University of Wisconsin-La Crosse
John May Pronouns: He/Him/His
Associate Professor
Chemistry & Biochemistry
Specialty area(s)
Biochemistry, Molecular Biology, Molecular Genetics and Physiology of Salmonella, Structural Biology
Current courses at UWL
CHM 103: General Chemistry I
CHM 103L: General Chemistry I Lab
CHM 419: Advanced Biochemistry Lab
CHM 445: Biochemistry of Antimicrobials
Education
NIH Postdoctoral Fellowship, Department of Microbial Pathogenesis, Yale School of Medicine
Ph.D. Biochemistry (2009) University of Wisconsin–Madison
B.S. Chemistry with concentration in Biochemistry (2003) Duke University
Career
Teaching history
CHM 103: General Chemistry I
CHM 103L: General Chemistry I Lab
CHM 417L: Biochemistry I: Macromolecules Lab
CHM 419: Advanced Biochemistry Lab
CHM 445: Biochemistry of Antimicrobials
Research and publishing
Peer-reviewed Publications from Research at UWL
*UWL undergraduate
May, J.F. and *Gonske, S.J. (2025) Insights into mechanisms and significance of domain swapping from emerging examples in the Mog1p/PsbP-like fold. Biochemical and Biophysical Research Communications. https://doi.org/10.1016/j.bbrc.2025.151570
Schwan, W.R., Moore, M., Zank, A., *Cannarella, S., Gebhardt, K., May, J.F. (2024) SK-03-92 Treatment Causes Release of a Lethal Factor Protein That Kills Staphylococcus aureus Cells. Targets. 2: 80–92. https://doi.org/10.3390/targets2020005
*Thielen, M.K., *Vaneerd, C.K., Goswami, M., Carlson, E.E., and May, J.F. (2020) 2-Aminobenzothiazoles inhibit virulence gene expression and block polymyxin resistance in Salmonella enterica. ChemBioChem. 21: 3500–3503. https://doi.org/10.1002/cbic.202000422
*Stuttgen, G. M., *Grosskopf, J.D., *Berger, C.R., May, J.F., Bhattacharyya, B., and Weaver, T.M. (2020) Closed fumarase C active site structures reveal SS Loop
residue contribution in catalysis. FEBS Letters. 594: 337–357. https://doi.org/10.1002/1873-3468.13603
*Rasmussen, D.M., *Soens, R.W., *Davie, T.J., *Vaneerd, C.K., Bhattacharyya, B., and May, J.F. (2018) The structure of DcrB, a lipoprotein from Salmonella enterica,
reveals flexibility in the N-terminal segment of the Mog1p/PsbP-like fold.
Journal of Structural Biology. 204: 513–518. https://doi.org/10.1016/j.jsb.2018.10.005
Protein Structures Deposited in the Protein Data Bank from Research at UWL
https://doi.org/10.2210/pdb6P3C/pdb
https://doi.org/10.2210/pdb6OS7/pdb
https://doi.org/10.2210/pdb6NZC/pdb
https://doi.org/10.2210/pdb6NZB/pdb
https://doi.org/10.2210/pdb6NZA/pdb
https://doi.org/10.2210/pdb6NZ9/pdb
https://doi.org/10.2210/pdb6E8A/pdb
Peer-reviewed Publications from Postdoctoral, Graduate, and Undergraduate Research
May, J.F. and Groisman, E.A. (2013) Conflicting roles for a cell surface modification in Salmonella. Molecular Microbiology. 88: 970–983. https://doi.org/10.1111/mmi.12236
Wesener, D.A., May, J.F., Huffman, E.M., and Kiessling, L.L. (2013) UDP-galactopyranose mutase in nematodes. Biochemistry. 52: 4391–4398. https://doi.org/10.1021/bi400264d
May, J.F., Levengood, M.R., Splain, R.A., Brown, C.D., and Kiessling, L.L. (2012) A processive carbohydrate polymerase that mediates bifunctional catalysis using a single active site. Biochemistry. 51: 1148–1159. https://doi.org/10.1021/bi201820p
May, J.F., Splain, R.A., Brotschi, C., and Kiessling, L.L. (2009) A tethering mechanism for length control in a processive carbohydrate polymerization. Proceedings of the National Academy of Sciences of the United States of America. 106: 11851–11856. https://doi.org/10.1073/pnas.0901407106
Dykhuizen, E.C., May, J.F., Tongpenyai, A., and Kiessling, L.L. (2008) Inhibitors of UDP-galactopyranose mutase thwart mycobacterial growth. Journal of the American Chemical Society. 130: 6706–6707. https://doi.org/10.1021/ja8018687
Carlson, E.E., May, J.F., and Kiessling, L.L. (2006) Chemical probes of UDP-galactopyranose mutase. Chemistry & Biology. 13: 825–837. https://doi.org/10.1016/j.chembiol.2006.06.007
Pirrung, M.C., Liu, Y., Deng, L., Halstead, D.K., Li, Z., May, J.F., Wedel, M., Austin, D.A., and Webster, N.J. (2005) Methyl scanning: total synthesis of demethylasterriquinone B1 and derivatives for identification of sites of interaction with and isolation of its receptor(s). Journal of the American Chemical Society. 127: 4609–4624. https://doi.org/10.1021/ja044325h
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