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Professor John D. Buynak
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John D. Buynak
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Professor |
Office: |
311
Fondren Science |
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Department of Chemistry |
Phone: |
(214) 768-2484 |
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Southern Methodist University |
Fax: |
(214) 768-4089 |
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PO Box 750314 |
e-mail: |
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Dallas, TX 75275-0314 |
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Prof. Buynak's
Home Page | |
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Education & Experience:
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NIH Postdoctoral Fellow,
Yale University, 1980-1981
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Ph.D. Rice University, 1980
Research Interests:
Bioorganic chemistry, medicinal chemistry, design of enzyme
inhibitors, synthesis of beta-lactam antibiotics and beta-lactamase
inhibitors.
Selected Publications:
Ganta, S. R.; Perumal, S.; Pagadala, S.
R. R.; Samuelsen, O.; Spencer, J.; Pratt, R. F.; Buynak, J. D. “Approaches
to the simultaneous inactivation of metallo- and serine-b-lactamases”
Bioorg. Med. Chem. Lett. 2009, 19, 1618-1622.
Kalp, M.; Totir, M. A.; Buynak, J. D.;
Carey, P. R. "Different intermediate populations formed by tazobactam,
sulbactam, and clavulanate reacting with SHV-1 b-lactamases: Raman crystallographic evidence"
J. Am. Chem. Soc. 2009, 131, 2338-2347.
Pattanaik, P.; Bethel, C. R.; Hujer, A.
M.; Hujer, K. M.; Distler, A. M.; Taracila, M.; Anderson, V. E.; Fritsche,
T. R.; Jones, R. N.; Pagadala, S. R. R.; van den Akker, F.; Buynak, J. D.;
Bonomo, R. A. "Strategic Design of an Effective b-Lactamase Inhibitor:
LN-1-255, A 6-alkylidene--2'-substituted penicillin sulfone." J. Biol.
Chem. 2009, 284, 945-953.
Totir, M. A.; Cha, J.; Ishiwata, A.;
Wang, B.; Sheri, A.; Anderson, V. E.; Buynak, J.; Mobashery, S.; Carey, P.
R. "Why Clinically Used Tazobactam and Sulbactam Are Poor Inhibitors of
OXA-10 b-Lactamase: Raman Crystallographic Evidence." Biochemistry
2008, 47, 4094-4101.
Buynak, J. D. "Cutting and
Stitching: the Cross-Linking of Peptidoglycan in the Assembly of the
Bacterial Cell Wall." ACS Chem. Biol. 2007, 2,
602-605.
Kalp, M.; Sheri, A.;
Buynak, J. D.; Bethel, C. R.; Bonomo, R. A. Carey, P. R. "Efficient
Inhibition of Class A and Class D
b-Lactamases
by Michaelis Complexes." J. Biol.
Chem. 2007,
282, 21588-21591.
Buynak, J. D.; Chen, H.
"Cephalosporin-derived mercaptans as inhibitors of serine and metallo-b-lactamases."
U. S. Patent 2006, US 2006178357 A1 200660810.
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Padayatti, P. S.; Sheri,
A.; Totir, M. A.; Helfand, M. S.; Carey, M. P.; Anderson, V. E.; Carey, P.
R.; Bethel, C. R.; Bonomo, R. A.; Buynak, J. D.; van den Akker, F. "Rational
Design of a b-Lactamase
Inhibitor Achieved via Stabilization of the trans-Enamine Intermediate: 1.28
Å Crystal Structure of wt SHV-1 with a Penam Sulfone. J. Am. Chem.
Soc. 2006, 128, 13235-13242.
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Buynak, John D.
“Understanding the longevity of the
b-lactam
antibiotics and of antibiotic/b-lactamase
inhibitor combinations.” Biochemical Pharmacology
2006,
71, 930-940.
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Zhu, D.; Yang, Y.; Buynak,
J. D.; Hua, L. "Stereoselective ketone reduction by a carbonyl reductase
from Sporobolomyces salmonicolor. Substrate specificity,
enantioselectivity and enzyme-substrate docking studies." Organic and
Biomolecular Chemistry 2006, 4, 2690-2695.
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Buynak, John D.;
Ghadhachanda, Venkat R; Vogeti, Lakshminarayana; Zhang, H.; Chen, H.
"Synthesis and Evaluation of 3-(Carboxymethylidene)- and
3-(Carboxymethyl)penicillinates as Inhibitors of
b-Lactamase"
Journal of Organic Chemistry 2005, 70, 4510-4513.
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Hujer, A. M.; Kania, M.;
Gerken, T.; Anderson, V. E.; Buynak, J.; Ge, X.; Caspers, P.; Page, M. G.
P.; Rice, L. B.; Bonomo, R. A. "Structure-Activity Relationships of
Different b-Lactam
Antibiotics against a Soluble Form of Enterococcus faecium PBP5, a
Type II Bacterial Transpeptidase" Antimicrobial Agents and Chemotherapy
2005, 49, 612-618.
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Buynak, J. D.; Chen H.,
Vogeti, L.; Gadhachanda, V. R.; Buchanan, C. A.; Palzkill, T.; Shaw, R. W.;
Spencer, J.; Walsh, T. R. "Penicillin-derived Inhibitors that simultaneously
target both metallo- and serine-b-Lactamases"
Bioorganic & Medicinal Chemistry Letters 2004, 14,
1299-1304.
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Buynak, John D. "The
discovery and development of modified penicillin- and cephalosporin-derived
b-Lactamase
inhibitors." Current Medicinal Chemistry
2004, 11,
1951-1964.
Courses Taught:
- Advanced Organic Chemistry (CHEM 5393)
- Medicinal Chemistry (CHEM 5398)
- Introduction to Bioorganic and Medicinal Chemistry (CHEM
6116)
- Synthetic Strategies (CHEM 6119)
- Chemical Mechanisms (CHEM 6130)
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