Gano Marcin, Wójcicki Michał, Janus Ewa
Department of Organic Chemical Technology and Polymer Materials, Faculty of Chemical Technology and Engineering, West Pomeranian University of Technology in Szczecin, Pułaskiego 10 St., 70-322 Szczecin, Poland.
Center for Advanced Materials and Manufacturing Process Engineering (CAMMPE), West Pomeranian University of Technology in Szczecin, 70-310 Szczecin, Poland.
Molecules. 2025 May 15;30(10):2173. doi: 10.3390/molecules30102173.
New chiral salen-based organic salts were synthesised and evaluated for their antibacterial activity against , , and . Their structures and physicochemical properties, namely their specific rotation, melting point, thermal stability, and antibacterial efficacy, including minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC), were determined. The synergy between chiral organic salts and bacteriophages was also demonstrated. [(RR)Sal.5C1.PhIM][Cl], [(RR)Sal.5C1.PhIM][BF], and [(RR)Sal.5C1.Pyr][OTf] had the lowest MIC values (from 500 mg mL for strain KKP 3685 to 2000 mg mL for strain KKP 3692), while the highest MICs (>4000 mg mL) were observed for [(RR)Sal.5C1.Pyr][OTf] and [(RR)Sal.5C1.PhIM][NTf] against strain KKP 3692. The impact of the tested compounds on phage activity was strain-specific. A synergistic effect of [(RR)Sal.5C1.PhIM][BF] at 0.5 mg mL in microcultures with Escherichia phage KKP 3710 (at MOI of 10 and 100) on the complete inhibition of the growth of strain KKP 3688 was observed. The combination of [(RR)Sal.5C1.PhIM])][OTf] at 1 mg mL with the addition of phages (at each MOI) and at 0.5 mg mL and MOI = 100 completely inhibited the growth of strain KKP 3688. Moreover, [(RR)Sal.5C1.PhIM])][OTf] at 1 mg mL and 0.5 mg mL, when combined with Enterobacter phage KKP 3716, inhibited the growth of strain KKP 3692 slightly more effectively than the compound alone at the same concentrations. These results suggest that combining our antibacterial agents can reduce chemical compound concentrations, with effects depending on the bacteria.
合成了新型手性基于萨伦的有机盐,并评估了它们对[具体细菌名称1]、[具体细菌名称2]和[具体细菌名称3]的抗菌活性。测定了它们的结构和物理化学性质,即比旋光度、熔点、热稳定性以及抗菌效力,包括最低抑菌浓度(MIC)和最低杀菌浓度(MBC)。还证明了手性有机盐与噬菌体之间的协同作用。[(RR)Sal.5C1.PhIM][Cl]、[(RR)Sal.5C1.PhIM][BF]和[(RR)Sal.5C1.Pyr][OTf]具有最低的MIC值(对于[细菌名称1]菌株KKP 3685为500毫克/毫升,对于[细菌名称2]菌株KKP 3692为2000毫克/毫升),而对于[(RR)Sal.5C1.Pyr][OTf]和[(RR)Sal.5C1.PhIM][NTf],针对[细菌名称2]菌株KKP 3692观察到最高的MIC值(>4000毫克/毫升)。测试化合物对噬菌体活性的影响具有菌株特异性。在微培养中,[(RR)Sal.5C1.PhIM][BF]在0.5毫克/毫升与大肠杆菌噬菌体KKP 3710(感染复数为10和100)组合时,观察到对[细菌名称1]菌株KKP 3688的生长有完全抑制作用。[(RR)Sal.5C1.PhIM])][OTf]在1毫克/毫升与添加噬菌体(在每个感染复数)以及在0.5毫克/毫升和感染复数 = 100时,完全抑制了[细菌名称1]菌株KKP 3688的生长。此外,[(RR)Sal.5C1.PhIM])][OTf]在1毫克/毫升和0.5毫克/毫升与肠杆菌噬菌体KKP 3716组合时,在相同浓度下比单独的化合物更有效地抑制了[细菌名称2]菌株KKP 3692的生长。这些结果表明,组合我们的抗菌剂可以降低化合物浓度,其效果取决于细菌。