Polin A N, Bulgakova V G, Silaev A B
Mikrobiologiia. 1979 Jul-Aug;48(4):699-704.
Gramicidin S derivatives with the substituted amino groups of ornithines (carbamoylgramicidin and diacetylgramicidin) possess nearly the same level of the lytic activity when acting on Micrococcus lysodeikticus protoplasts in a 1 M sucrose solution as the original antibiotic. The lytic activity of gramicidin S and these derivatives considerably increases in a solution of sucrose in phosphate buffer. The dependence of the lytic activity of gramicidin on its concentration is of a complex character: two "peaks" of activity and a region of "nonlyzing" concentrations. The lytic activity of gramicidin derivatives with substituted amino groups directly depends on the concentration. When gramicidin S acts upon the intact cells of M. lysodeikticus, it impair with the permeability of their membranes and causes a loss of compounds absorbing at 260 nm; the derivatives with the substituted amino groups change the permeability of the cellular membranes only to a slight extent.
带有鸟氨酸取代氨基的短杆菌肽 S 衍生物(氨甲酰短杆菌肽和二乙酰短杆菌肽)在 1 M 蔗糖溶液中作用于溶壁微球菌原生质体时,其溶菌活性水平与原始抗生素几乎相同。短杆菌肽 S 及其这些衍生物在磷酸盐缓冲液中的蔗糖溶液中的溶菌活性显著增加。短杆菌肽的溶菌活性对其浓度的依赖性具有复杂的特征:有两个活性“峰”和一个“非裂解”浓度区域。带有取代氨基的短杆菌肽衍生物的溶菌活性直接取决于浓度。当短杆菌肽 S 作用于溶壁微球菌的完整细胞时,它会损害其细胞膜的通透性,并导致在 260 nm 处有吸收的化合物损失;带有取代氨基的衍生物仅在很小程度上改变细胞膜的通透性。