Nakagawa Y, Tawaratani T, Kourai H, Horie T, Shibasaki I
Appl Environ Microbiol. 1984 Jan;47(1):88-93. doi: 10.1128/aem.47.1.88-93.1984.
Insoluble lauryl pyridinium iodide [C12(50)] was synthesized as an antimicrobial agent. Escherichia coli cells were not killed by C12(50) but only adsorbed onto it. Though cells on C12(50) could not grow in nutrient agar, they possessed the ability to develop once they were liberated from C12(50). The adsorption of cells onto C12(50) was inhibited by iodide anions released from C12(50) itself. The ability of C12(50) to adsorb was decreased by the adsorbed cells, but C12(50) could be reactivated by washing with alkaline solutions. It was, therefore, suggested that this adsorption was mainly due to the electrostatic interaction between cells and C12(50). The adsorption of cells onto C12(50) was confirmed by scanning electron microscopy.
不溶性月桂基碘化吡啶鎓[C12(50)]被合成为一种抗菌剂。大肠杆菌细胞不会被C12(50)杀死,而是仅吸附在其上。虽然吸附在C12(50)上的细胞不能在营养琼脂中生长,但一旦它们从C12(50)上释放出来,就具备生长的能力。细胞对C12(50)的吸附受到C12(50)自身释放的碘离子的抑制。吸附的细胞会降低C12(50)的吸附能力,但用碱性溶液洗涤可使C12(50)重新活化。因此,表明这种吸附主要是由于细胞与C12(50)之间的静电相互作用。通过扫描电子显微镜证实了细胞对C12(50)的吸附。