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铜绿假单胞菌中抑制蛋白质合成的天然产物化合物的发现与分析

Discovery and Analysis of Natural-Product Compounds Inhibiting Protein Synthesis in Pseudomonas aeruginosa.

作者信息

Hu Yanmei, Keniry Megan, Palmer Stephanie O, Bullard James M

机构信息

Chemistry Department, The University of Texas-RGV, Edinburg, Texas, USA.

Biology Department, The University of Texas-RGV, Edinburg, Texas, USA.

出版信息

Antimicrob Agents Chemother. 2016 Jul 22;60(8):4820-9. doi: 10.1128/AAC.00800-16. Print 2016 Aug.

Abstract

Bacterial protein synthesis is the target for numerous natural and synthetic antibacterial agents. We have developed a poly(U) mRNA-directed aminoacylation/translation (A/T) protein synthesis system composed of phenylalanyl-tRNA synthetases (PheRS), ribosomes, and ribosomal factors from Pseudomonas aeruginosa This system has been used for high-throughput screening of a natural-compound library. Assays were developed for each component of the system to ascertain the specific target of inhibitory compounds. In high-throughput screens, 13 compounds were identified that inhibit protein synthesis with 50% inhibitory concentrations ranging from 0.3 to >80 μM. MICs were determined for the compounds against the growth of a panel of pathogenic organisms, including Enterococcus faecalis, Escherichia coli, Haemophilus influenzae, Moraxella catarrhalis, P. aeruginosa, Staphylococcus aureus, and Streptococcus pneumoniae Three of the compounds were observed to have broad-spectrum activity and inhibited a hypersensitive strain of P. aeruginosa with MICs of 8 to 16 μg/ml. The molecular target of each of the three compounds was determined to be PheRS. One compound was found to be bacteriostatic, and one compound was bactericidal against both Gram-positive and Gram-negative pathogens. The third compound was observed to be bacteriostatic against Gram-positive and bactericidal against Gram-negative bacteria. All three compounds were competitive with the substrate ATP; however, one compound was competitive, one was uncompetitive, and one noncompetitive with the amino acid substrate. Macromolecular synthesis assays confirm the compounds inhibit protein synthesis. The compounds were shown to be more than 25,000-fold less active than the control staurosporine in cytotoxicity MTT testing in human cell lines.

摘要

细菌蛋白质合成是众多天然和合成抗菌剂的作用靶点。我们开发了一种由来自铜绿假单胞菌的苯丙氨酰 - tRNA合成酶(PheRS)、核糖体和核糖体因子组成的聚(U)mRNA指导的氨酰化/翻译(A/T)蛋白质合成系统。该系统已用于天然化合物文库的高通量筛选。针对系统的每个组分开发了检测方法,以确定抑制性化合物的具体靶点。在高通量筛选中,鉴定出13种化合物可抑制蛋白质合成,其50%抑制浓度范围为0.3至>80μM。测定了这些化合物对一组致病生物生长的最低抑菌浓度(MIC),这些致病生物包括粪肠球菌、大肠杆菌、流感嗜血杆菌、卡他莫拉菌、铜绿假单胞菌、金黄色葡萄球菌和肺炎链球菌。观察到其中三种化合物具有广谱活性,对铜绿假单胞菌的一个超敏菌株有抑制作用,MIC为8至16μg/ml。确定这三种化合物各自的分子靶点均为PheRS。发现一种化合物具有抑菌作用,一种化合物对革兰氏阳性和革兰氏阴性病原体均有杀菌作用。观察到第三种化合物对革兰氏阳性菌有抑菌作用,对革兰氏阴性菌有杀菌作用。所有三种化合物都与底物ATP竞争;然而,一种化合物是竞争性的,一种是非竞争性的,一种与氨基酸底物是反竞争性的。大分子合成检测证实这些化合物抑制蛋白质合成。在人细胞系的细胞毒性MTT检测中,这些化合物的活性比对照星形孢菌素低25000倍以上。

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