Wang Yang, Desai Janish, Zhang Yonghui, Malwal Satish R, Shin Christopher J, Feng Xinxin, Sun Hong, Liu Guizhi, Guo Rey-Ting, Oldfield Eric
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.
ChemMedChem. 2016 Oct 19;11(20):2311-2319. doi: 10.1002/cmdc.201600342. Epub 2016 Aug 31.
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.
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。