Savoini A, Marzari R, Dolzani L, Serranò D, Graziosi G, Gennaro R, Romeo D
Antimicrob Agents Chemother. 1984 Sep;26(3):405-7. doi: 10.1128/AAC.26.3.405.
The antibiotic activity of a polypeptide fraction purified from bovine granulocyte granules was tested against Escherichia coli, Pseudomonas aeruginosa, Salmonella typhimurium, Bacillus subtilis, Bacillus stearothermophilus, Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus faecalis, Streptococcus pyogenes, and clinical isolates of Staphylococcus and Enterobacter spp. All of these bacterial species were susceptible to the antibiotic polypeptide(s), with MICs ranging from 3 to 100 micrograms of protein per ml. The antimicrobial activity was resistant to boiling and abolished by proteinase treatment. Saccharomyces cerevisiae and human fibroblasts grew normally in the presence of 100 and 50 micrograms of antibiotic polypeptide(s) per ml, respectively. [3H]thymidine incorporation into bacterial, but not fibroblast, DNA was efficiently and promptly inhibited by the antimicrobial polypeptide preparation. This suggests that its main target is a component of the system, which catalyzes and regulates the biosynthesis of bacterial DNA.
对从牛粒细胞颗粒中纯化得到的一种多肽组分的抗菌活性进行了测试,受试菌株包括大肠杆菌、铜绿假单胞菌、鼠伤寒沙门氏菌、枯草芽孢杆菌、嗜热脂肪芽孢杆菌、金黄色葡萄球菌、表皮葡萄球菌、粪肠球菌、化脓性链球菌以及葡萄球菌属和肠杆菌属的临床分离株。所有这些细菌对该抗菌多肽均敏感,最低抑菌浓度(MIC)范围为每毫升3至100微克蛋白质。该抗菌活性耐热,经蛋白酶处理后被消除。酿酒酵母和人成纤维细胞分别在每毫升含有100微克和50微克抗菌多肽的情况下正常生长。抗菌多肽制剂能有效且迅速地抑制[3H]胸腺嘧啶掺入细菌DNA,但不抑制成纤维细胞DNA。这表明其主要作用靶点是催化和调节细菌DNA生物合成的系统中的一个组分。