The vancomycin group of antibiotics kill Gram-positive bacteria by binding
to nascent bacterial cell-wall peptidoglycan bearing the C-terminal sequenc
e -D-Ala-D-Ala. In this paper, affinity adsorbents for the vancomycin group
of antibiotics were prepared by immobilizing the peptidoglycan analogues -
D-Ala-D-Ala, -succinyl-D-Ala and -succinyl-Gly on to crosslinked poly(N,N-d
imethylacrylamide). The adsorption capacities of the three adsorbents for d
emethyl-vancomycin were 0.59, 0.35 and 0.29 mmol/g, respectively. The adsor
ption capacity of the adsorbent with -D-Ala-D-Ala for vancomycin was 0.53 m
mol/g. In contrast, the adsorbent bearing -succinyl-L-Ala hardly adsorbed d
emethylvancomycin. Aqueous sodium carbonate (0.4 M)/acetonitrile (7/3, v/v)
completely desorbed demethylvancomycin adsorbed on the adsorbents.