Design and synthesis of anti-biofilm derivatives from phospholipid amides.

IF 3.8 2区 化学 Q2 CHEMISTRY, APPLIED
Song Bai, Suran Wan, Yi Chen, Miao Li, Rong Wu, Shouying Tang, Lijun Chen, Yazhen Chen, Xiaokang Lv
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引用次数: 0

Abstract

Bacterial biofilms serve as a natural barrier, enabling bacteria residing within them to exist and potentially amplify bacterial resistance by shielding themselves from bactericide exposure. Despite considerable efforts directed toward inhibiting bacterial growth, research has overlooked bacterial biofilms to a significant extent, leading to the frequent deficiency of traditional antimicrobials in inhibiting such biofilms. This necessitates the development of antimicrobials capable of inhibiting biofilms for effective antibacterial intervention. Herein, we have developed a new bacteriostatic agent, A6, which has demonstrated the capability of inhibiting biofilm formation. It achieved a biofilm inhibition rate of 72.76% at a concentration of 47.94 μg/mL (2.0 EC50). Mechanistic studies revealed that A6 inhibits extracellular polymeric substances (EPS) production and bacterial motility, both critical for bacterial virulence, biofilm formation, maturation, or plant cell wall degradation. Additionally, the conductivity and protein leakage experiments demonstrated that compound A6 significantly affected various physiological processes of Xoc. In summary, A6 presents a promising antimicrobial solution by simultaneously inhibiting biofilms, addressing a crucial aspect of bacterial plant diseases.

磷脂酰胺类抗生物膜衍生物的设计与合成。
细菌生物膜作为一种天然屏障,使居住在其中的细菌能够生存,并通过屏蔽杀菌剂来潜在地增强细菌耐药性。尽管在抑制细菌生长方面做出了相当大的努力,但研究在很大程度上忽视了细菌生物膜,导致传统抗菌剂在抑制这种生物膜方面经常不足。这就需要开发能够抑制生物膜的抗菌剂来进行有效的抗菌干预。在此,我们开发了一种新的抑菌剂A6,它已经证明了抑制生物膜形成的能力。在47.94 μg/mL (2.0 EC50)浓度下,生物膜抑制率为72.76%。机制研究表明,A6抑制细胞外聚合物质(EPS)的产生和细菌的运动,这对细菌的毒力、生物膜的形成、成熟或植物细胞壁的降解都至关重要。此外,电导率和蛋白质渗漏实验表明,化合物A6显著影响了Xoc的各种生理过程。综上所述,A6通过同时抑制生物膜,解决植物细菌性病害的一个关键方面,是一种很有前途的抗菌解决方案。
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来源期刊
Molecular Diversity
Molecular Diversity 化学-化学综合
CiteScore
7.30
自引率
7.90%
发文量
219
审稿时长
2.7 months
期刊介绍: Molecular Diversity is a new publication forum for the rapid publication of refereed papers dedicated to describing the development, application and theory of molecular diversity and combinatorial chemistry in basic and applied research and drug discovery. The journal publishes both short and full papers, perspectives, news and reviews dealing with all aspects of the generation of molecular diversity, application of diversity for screening against alternative targets of all types (biological, biophysical, technological), analysis of results obtained and their application in various scientific disciplines/approaches including: combinatorial chemistry and parallel synthesis; small molecule libraries; microwave synthesis; flow synthesis; fluorous synthesis; diversity oriented synthesis (DOS); nanoreactors; click chemistry; multiplex technologies; fragment- and ligand-based design; structure/function/SAR; computational chemistry and molecular design; chemoinformatics; screening techniques and screening interfaces; analytical and purification methods; robotics, automation and miniaturization; targeted libraries; display libraries; peptides and peptoids; proteins; oligonucleotides; carbohydrates; natural diversity; new methods of library formulation and deconvolution; directed evolution, origin of life and recombination; search techniques, landscapes, random chemistry and more;
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