Journal
APPLIED BIOCHEMISTRY AND MICROBIOLOGY
Volume 52, Issue 2, Pages 222-225Publisher
MAIK NAUKA/INTERPERIODICA/SPRINGER
DOI: 10.1134/S0003683816020149
Keywords
low-molecular weight chitosan; chitosan hydrolysis; quaternized chitosan derivatives; chitosan acylated derivatives; antibacterial activity
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Funding
- Russian Foundation for Basic Research [14-04-00687a, 15-29-05858 ofi_M]
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A number of alkylated (quaternized) and acylated derivatives of low-molecular weight chitosan were obtained. The structure and composition of the compounds were confirmed by the results of IR and PMR spectroscopy, as well as conductometric titration. The effect of the acyl substituent and the degree of substitution of N-(2-hydroxy-3-trimethylammonium) propyl fragment appended to amino groups of the C-2 atom of polymer chains on antibacterial activity against typical representatives of gram-positive and gram-negative microorganisms (Staphylococcus epidermidis and Escherichia coli) was studied. The highest activity was in the case of N-[(2-hydroxy-3-trimethylammonium) propyl] chitosan chloride (HTCC) with the maximal substitution (98%). The minimal inhibitory concentration of the derivative was 0.48 mu g/mL and 3.90 mu g/mL for S. epidermis and E. coli, respectively.
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