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1
Dialkylamino-2,4-dihydroxybenzoic acids as easily synthesized analogues of platensimycin and platencin with comparable antibacterial properties.二烷基氨基-2,4-二羟基苯甲酸作为易于合成的藤黄紫霉素和藤黄绿菌素类似物,具有相当的抗菌特性。
Chemistry. 2011 Mar 14;17(12):3352-7. doi: 10.1002/chem.201002410. Epub 2011 Feb 14.
2
The kalimantacin/batumin biosynthesis operon encodes a self-resistance isoform of the FabI bacterial target.卡里曼他星/巴图霉素生物合成操纵子编码细菌靶标FabI的一种自身抗性异构体。
Chem Biol. 2010 Oct 29;17(10):1067-71. doi: 10.1016/j.chembiol.2010.07.015.
3
Discovery and syntheses of "superbug challengers"-platensimycin and platencin.发现并合成“超级细菌挑战者”-普拉地霉素和普拉替尼。
Chem Asian J. 2010 Apr 1;5(4):668-703. doi: 10.1002/asia.200900423.
4
Essentiality of FASII pathway for Staphylococcus aureus.金黄色葡萄球菌 FASII 途径的必需性。
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5
Aquastatin A, a new inhibitor of enoyl-acyl carrier protein reductase from Sporothrix sp. FN611.水瓜柳抑酶肽 A,来自申克氏孢子丝菌 FN611 的一种新型烯酰基辅酶 A 还原酶抑制剂。
Biol Pharm Bull. 2009 Dec;32(12):2061-4. doi: 10.1248/bpb.32.2061.
6
Waves of resistance: Staphylococcus aureus in the antibiotic era.耐药浪潮:抗生素时代的金黄色葡萄球菌
Nat Rev Microbiol. 2009 Sep;7(9):629-41. doi: 10.1038/nrmicro2200.
7
AFN-1252, a FabI inhibitor, demonstrates a Staphylococcus-specific spectrum of activity.AFN-1252是一种FabI抑制剂,具有针对葡萄球菌的特异性活性谱。
Antimicrob Agents Chemother. 2009 Aug;53(8):3544-8. doi: 10.1128/AAC.00400-09. Epub 2009 Jun 1.
8
Acyl-Acyl carrier protein regulates transcription of fatty acid biosynthetic genes via the FabT repressor in Streptococcus pneumoniae.酰基-酰基载体蛋白通过肺炎链球菌中的FabT阻遏物调节脂肪酸生物合成基因的转录。
J Biol Chem. 2009 Jun 5;284(23):15364-8. doi: 10.1074/jbc.C109.002410. Epub 2009 Apr 17.
9
Vinaxanthone, a new FabI inhibitor from Penicillium sp.来自青霉菌的新型FabI抑制剂——紫黄双醌
J Antimicrob Chemother. 2009 May;63(5):949-53. doi: 10.1093/jac/dkp058. Epub 2009 Mar 12.
10
Type II fatty acid synthesis is not a suitable antibiotic target for Gram-positive pathogens.II型脂肪酸合成不是革兰氏阳性病原体合适的抗生素靶点。
Nature. 2009 Mar 5;458(7234):83-6. doi: 10.1038/nature07772.

细菌脂肪酸合成是否是抗菌药物发现的有效靶点?

Is bacterial fatty acid synthesis a valid target for antibacterial drug discovery?

机构信息

Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, United States.

出版信息

Curr Opin Microbiol. 2011 Oct;14(5):544-9. doi: 10.1016/j.mib.2011.07.029. Epub 2011 Aug 20.

DOI:10.1016/j.mib.2011.07.029
PMID:21862391
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3193581/
Abstract

The emergence of resistance against most current drugs emphasizes the need to develop new approaches to control bacterial pathogens, particularly Staphylococcus aureus. Bacterial fatty acid synthesis is one such target that is being actively pursued by several research groups to develop anti-Staphylococcal agents. Recently, the wisdom of this approach has been challenged based on the ability of a Gram-positive bacterium to incorporate extracellular fatty acids and thus circumvent the inhibition of de novo fatty acid synthesis. The generality of this conclusion has been challenged, and there is enough diversity in the enzymes and regulation of fatty acid synthesis in bacteria to conclude that there is not a single organism that can be considered typical and representative of bacteria as a whole. We are left without a clear resolution to this ongoing debate and await new basic research to define the pathways for fatty acid uptake and that determine the biochemical and genetic mechanisms for the regulation of fatty acid synthesis in Gram-positive bacteria. These crucial experiments will determine whether diversity in the control of this important pathway accounts for the apparently different responses of Gram-positive bacteria to the inhibition of de novo fatty acid synthesis in presence of extracellular fatty acid supplements.

摘要

耐药性的出现凸显了开发新方法来控制细菌病原体(尤其是金黄色葡萄球菌)的必要性。细菌脂肪酸合成是一个备受关注的目标,多个研究小组正在积极研究开发抗金葡菌药物。最近,由于革兰氏阳性菌能够摄取细胞外脂肪酸并因此规避从头合成脂肪酸的抑制,这种方法的有效性受到了质疑。这一结论的普遍性受到了挑战,而且细菌脂肪酸合成的酶和调控存在足够的多样性,足以得出没有一种细菌可以被视为整个细菌的典型代表的结论。对于这一持续存在的争论,我们没有明确的解决方案,只能等待新的基础研究来确定脂肪酸摄取途径,并确定革兰氏阳性菌脂肪酸合成调控的生化和遗传机制。这些关键实验将决定对这条重要途径的控制的多样性是否可以解释革兰氏阳性菌在存在细胞外脂肪酸补充时对从头合成脂肪酸抑制的反应为何不同。