TY - JOUR A2 - Cooper, Arthur AU - Vidal, Laetitia AU - Thuault, Véronique AU - Mangas, Arturo AU - Coveñas, Rafael AU - Thienpont, Anne AU - Geffard, Michel PY - 2014 DA - 2014/02/23 TI - Lauryl-poly-L-lysine: A New Antimicrobial Agent? SP - 672367 VL - 2014 AB - The development of multiple antibiotic resistance is a global problem. It is necessary to find new tools whose mechanisms of action differ from those of currently used antibiotics. It is known that fatty acids and cationic polypeptides are able to fight bacteria. Here, we describe the synthesis of fatty acids linked to a polypeptide with antibacterial activity. The linkage of fatty acids to a polypeptide is reported to increase the antibacterial effect of the linked fatty acid in comparison with free fatty acids (FA) or free poly-L-lysine (PLL) or a mixture of both (FA free + PLL free). A number of C6–C18 fatty acids were linked to PLL to obtain new synthetic products. These compounds were assessed in vitro to evaluate their antibacterial activity. Some fatty acid-PLLs showed a good ability to fight bacteria. Their bactericidal activity was evaluated, and, lauryl linked to PLL was found to be the most active product against both Gram-positive and Gram-negative bacteria. This new active component showed a good degree of specificity and reproducibility and its minimum inhibitory concentration (MIC) was comparatively good. The antibacterial activity of the lauryl-PLL compound suggests that it is a new and promising antimicrobial agent. SN - 2090-0104 UR - https://doi.org/10.1155/2014/672367 DO - 10.1155/2014/672367 JF - Journal of Amino Acids PB - Hindawi Publishing Corporation KW - ER -