Department of Chemistry, Simon Fraser University, 8888 University Drive, Burnaby, British Columbia, V5A 1S2, Canada.
ACS Infect Dis. 2021 Jan 8;7(1):153-161. doi: 10.1021/acsinfecdis.0c00687. Epub 2020 Dec 8.
A solid-phase platform for the precise and sequential synthesis of enterobactin analogues is described. This chemistry unites the power of solid-phase peptide synthesis with the unique opportunities and applications offered by siderophore chemistry. Here, a series of hybrid enterobactin hydroxamate/catecholate (HEHC) analogues were synthesized using both catechols and amino acid derived hydroxmate chelators. The HEHC analogues were evaluated for their ability to bind free iron and to promote growth in siderophore-auxotrophic mutant bacteria. We find that, in contrast to or , a number of HEHC analogues promote growth in and structure-activity relationships (SARs) exist for the growth promotion via HEHC analogues in this organism.
本文描述了一种用于精确和顺序合成依泊菌素类似物的固相平台。这种化学方法结合了固相肽合成的优势以及铁载体化学所提供的独特机会和应用。在这里,使用儿茶酚和氨基酸衍生的羟肟酸螯合剂合成了一系列混合依泊菌素羟肟酸/儿茶酚(HEHC)类似物。评估了 HEHC 类似物结合游离铁和促进铁载体缺陷型突变细菌生长的能力。我们发现,与 或 相比,许多 HEHC 类似物能够促进 和 的生长,并且在该生物体中通过 HEHC 类似物促进生长存在构效关系(SARs)。