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Synthesis Characterization and Antimicrobial Properties of Peptides Mimicking Copolymers of Maleic Anhydride and 4-Methyl-1-pentene

机译:模仿马来酸酐和4-甲基-1-戊烯共聚物的肽的合成表征和抗菌性能

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摘要

Synthetic amphiphilic copolymers with strong antimicrobial properties mimicking natural antimicrobial peptides were obtained via synthesis of an alternating copolymer of maleic anhydride and 4-methyl-1-pentene. The obtained copolymer was modified by grafting with 3-(dimethylamino)-1-propylamine (DMAPA) and imidized in a one-pot synthesis. The obtained copolymer was modified further to yield polycationic copolymers by means of quaternization with methyl iodide and dodecyl iodide, as well as by being sequentially quaternized with both of them. The antimicrobial properties of obtained copolymers were tested against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus epidermidis, and Staphylococcus aureus. Both tested quaternized copolymers were more active against the Gram-negative E. coli than against the Gram-positive S. aureus. The copolymer modified with both iodides was best when tested against E. coli and, comparing all three copolymers, also exhibited the best effect against S. aureus. Moreover, it shows (limited) selectivity to differentiate between mammalian cells and bacterial cell walls. Comparing the minimum inhibitory concentration (MIC) of Nisin against the Gram-positive bacteria on the molar basis instead on the weight basis, the difference between the effect of Nisin and the copolymer is significantly lower.
机译:通过合成顺丁烯二酸酐和4-甲基-1-戊烯的交替共聚物,可制得具有模仿天然抗菌肽的强抗菌特性的两亲共聚物。通过用3-(二甲基氨基)-1-丙胺(DMAPA)接枝改性所得共聚物,并在一锅合成中将其酰亚胺化。通过用甲基碘和十二烷基碘进行季铵化,以及依次将它们同时进行季铵化,将所得共聚物进一步改性以产生聚阳离子共聚物。测试了所得共聚物对大肠杆菌,铜绿假单胞菌,表皮葡萄球菌和金黄色葡萄球菌的抗菌性能。两种测试的季铵化共聚物对革兰氏阴性大肠杆菌的活性均大于对革兰氏阳性金黄色葡萄球菌的活性。用两种碘化物改性的共聚物对大肠杆菌进行测试时效果最好,并且将所有三种共聚物进行比较,对金黄色葡萄球菌也表现出最佳效果。而且,它显示出(有限的)区分哺乳动物细胞和细菌细胞壁的选择性。以摩尔为基准,而不是以重量为基础,比较乳链菌肽对革兰氏阳性菌的最低抑菌浓度(MIC),乳链菌肽和共聚物的作用之间的差异明显较小。

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