Conformational Dynamics and Exchange Kinetics of N‑Formyl and N‑Acetyl Groups Substituting 3‑Amino-3,6-dideoxy-α‑d‑galactopyranose, a Sugar Found in Bacterial O‑Antigen Polysaccharides

• Published in: The journal of physical chemistry. B Vol. 121; no. 41; pp. 9487 - 9497
• Main Authors: Engström, Olof, Mobarak, Hani, Ståhle, Jonas, Widmalm, Göran
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 19-10-2017
• Subjects: Organic Chemistry; organisk kemi
• ISSN: 1520-6106; 1520-5207; 1520-5207
• DOI: 10.1021/acs.jpcb.7b05611

Three dimensional shape and conformation of carbohydrates are important factors in molecular recognition events and the N-acetyl group of a monosaccharide residue can function as a conformational gatekeeper whereby it influences the overall shape of the oligosaccharide. NMR spectroscopy and quantum mechanics (QM) calculations are used herein to investigate both the conformational preferences and the dynamic behavior of N-acetyl and N-formyl substituents of 3-amino-3,6-dideoxy-α-d-galactopyranose, a sugar and substitution pattern found in bacterial O-antigen polysaccharides. QM calculations suggest that the amide oxygen can be involved in hydrogen bonding with the axial OH4 group primarily but also with the equatorial OH2 group. However, an NMR J coupling analysis indicates that the θ1 torsion angle, adjacent to the sugar ring, prefers an ap conformation where conformations <180° also are accessible, but does not allow for intramolecular hydrogen bonding. In the formyl-substituted compound 4 J HH coupling constants to the exo-cyclic group were detected and analyzed. A van’t Hoff analysis revealed that the trans conformation at the amide bond is favored by ΔG° ≈ – 0.8 kcal·mol–1 in the formyl-containing compound and with ΔG° ≈ – 2.5 kcal·mol–1 when the N-acetyl group is the substituent. In both cases the enthalpic term dominates to the free energy, irrespective of water or DMSO as solvent, with only a small contribution from the entropic term. The cis–trans isomerization of the θ2 torsion angle, centered at the amide bond, was also investigated by employing 1H NMR line shape analysis and 13C NMR saturation transfer experiments. The extracted transition rate constants were utilized to calculate transition energy barriers that were found to be about 20 kcal·mol–1 in both DMSO-d 6 and D2O. Enthalpy had a higher contribution to the energy barriers in DMSO-d 6 compared to in D2O, where entropy compensated for the loss of enthalpy.