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靶向十一异戊二烯二磷酸合酶和十一异戊二烯二磷酸磷酸酶的细菌细胞生长抑制剂

Bacterial Cell Growth Inhibitors Targeting Undecaprenyl Diphosphate Synthase and Undecaprenyl Diphosphate Phosphatase.

作者信息

Wang Yang, Desai Janish, Zhang Yonghui, Malwal Satish R, Shin Christopher J, Feng Xinxin, Sun Hong, Liu Guizhi, Guo Rey-Ting, Oldfield Eric

机构信息

Department of Chemistry, University of Illinois at Urbana-Champaign, 600 South Mathews Avenue, Urbana, IL, 61801, USA.

Center for Biophysics and Quantitative Biology, University of Illinois at Urbana-Champaign, 1110 West Green Street, Urbana, IL, 61801, USA.

出版信息

ChemMedChem. 2016 Oct 19;11(20):2311-2319. doi: 10.1002/cmdc.201600342. Epub 2016 Aug 31.

Abstract

We synthesized a series of benzoic acids and phenylphosphonic acids and investigated their effects on the growth of Staphylococcus aureus and Bacillus subtilis. One of the most active compounds, 5-fluoro-2-(3-(octyloxy)benzamido)benzoic acid (7, ED ∼0.15 μg mL ) acted synergistically with seven antibiotics known to target bacterial cell-wall biosynthesis (a fractional inhibitory concentration index (FICI) of ∼0.35, on average) but had indifferent effects in combinations with six non-cell-wall biosynthesis inhibitors (average FICI∼1.45). The most active compounds were found to inhibit two enzymes involved in isoprenoid/bacterial cell-wall biosynthesis: undecaprenyl diphosphate synthase (UPPS) and undecaprenyl diphosphate phosphatase (UPPP), but not farnesyl diphosphate synthase, and there were good correlations between bacterial cell growth inhibition, UPPS inhibition, and UPPP inhibition.

摘要

我们合成了一系列苯甲酸和苯基膦酸,并研究了它们对金黄色葡萄球菌和枯草芽孢杆菌生长的影响。其中活性最强的一种化合物,5-氟-2-(3-(辛氧基)苯甲酰胺基)苯甲酸(7,ED~0.15μg mL)与七种已知靶向细菌细胞壁生物合成的抗生素具有协同作用(平均分数抑制浓度指数(FICI)约为0.35),但与六种非细胞壁生物合成抑制剂联合使用时效果不明显(平均FICI~1.45)。研究发现,活性最强的化合物可抑制类异戊二烯/细菌细胞壁生物合成过程中的两种酶:十一异戊烯二磷酸合酶(UPPS)和十一异戊烯二磷酸磷酸酶(UPPP),但对法尼基二磷酸合酶没有抑制作用,并且在细菌细胞生长抑制、UPPS抑制和UPPP抑制之间存在良好的相关性。

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本文引用的文献

1
A Small-Molecule Screening Platform for the Discovery of Inhibitors of Undecaprenyl Diphosphate Synthase.
ACS Infect Dis. 2016 Jul 8;2(7):489-99. doi: 10.1021/acsinfecdis.6b00044. Epub 2016 May 24.
2
Antiinfectives targeting enzymes and the proton motive force.
Proc Natl Acad Sci U S A. 2015 Dec 22;112(51):E7073-82. doi: 10.1073/pnas.1521988112. Epub 2015 Dec 7.
3
Proposed carrier lipid-binding site of undecaprenyl pyrophosphate phosphatase from Escherichia coli.
J Biol Chem. 2014 Jul 4;289(27):18719-35. doi: 10.1074/jbc.M114.575076. Epub 2014 May 22.
5
Antibacterial drug leads targeting isoprenoid biosynthesis.
Proc Natl Acad Sci U S A. 2013 Jan 2;110(1):123-8. doi: 10.1073/pnas.1219899110. Epub 2012 Dec 17.
6
Allosteric non-bisphosphonate FPPS inhibitors identified by fragment-based discovery.
Nat Chem Biol. 2010 Sep;6(9):660-6. doi: 10.1038/nchembio.421. Epub 2010 Aug 15.
9
European Committee on Antimicrobial Susceptibility Testing (EUCAST) Technical Notes on antimicrobial susceptibility testing.
Clin Microbiol Infect. 2006 Jun;12(6):501-3. doi: 10.1111/j.1469-0691.2006.01454.x.
10
Synergistic and additive killing by antimicrobial factors found in human airway surface liquid.
Am J Physiol Lung Cell Mol Physiol. 2000 Nov;279(5):L799-805. doi: 10.1152/ajplung.2000.279.5.L799.

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