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Protonation of kanamycin A: detailing of thermodynamics and protonation sites assignment

Authors :
Carolina Godoy-Alcántar
Yanet Fuentes-Martínez
Anatoly K. Yatsimirsky
Alexander Dikiy
Felipe Medrano
Source :
Bioorganic chemistry. 38(4)
Publication Year :
2010

Abstract

Protonation of an aminoglycoside antibiotic kanamycin A sulfate was studied by potentiometric titrations at variable ionic strength, sulfate concentration and temperature. From these results the association constants of differently protonated forms of kanamycin A with sulfate and enthalpy changes for protonation of each amino group were determined. The protonation of all amino groups of kanamycin A is exothermic, but the protonation enthalpy does not correlate with basicity as in a case of simple polyamines. The sites of stepwise protonation of kanamycin A have been assigned by analysis of 1 H– 13 C–HSQC spectra at variable pH in D 2 O. Plots of chemical shifts for each H and C atom of kanamycin A vs. pH were fitted to the theoretical equation relating them to p K a values of ionogenic groups and it was observed that changes in chemical shifts of all atoms in ring C were controlled by ionization of a single amino group with p K a 7.98, in ring B by ionization of two amino groups with p K a 6.61 and 8.54, but in ring A all atoms felt ionization of one group with p K a 9.19 and some atoms felt ionization of a second group with p K a 6.51, which therefore should belong to amino group at C3 in ring B positioned closer to the ring A while higher p K a 8.54 can be assigned to the group at C1. This resolves the previously existed uncertainty in assignment of protonation sites in rings B and C.

Details

ISSN :
10902120
Volume :
38
Issue :
4
Database :
OpenAIRE
Journal :
Bioorganic chemistry
Accession number :
edsair.doi.dedup.....e45cb6bb94845581ce5a6a9bce7913b5