Phytochemical targeting of SASP2-mediated DNA protection to impair spore resilience in Bacillus cereus: A Computational Investigation.

IF 3.8 2区 化学 Q2 CHEMISTRY, APPLIED
Rajaram Abhirami, Chandrabose Selvaraj, Sanjeev Kumar Singh
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引用次数: 0

Abstract

Spore-forming bacteria such as Bacillus cereus pose a significant public health challenge due to their ability to survive harsh environmental conditions, resist conventional decontamination strategies, and cause recurrent infections in clinical and food-associated environments. This persistence is primarily associated with sporulation, a tightly regulated developmental process in which long-term survival depends on maintaining genome integrity while cellular metabolism remains largely inactive. DNA-binding proteins are therefore central to sporulation, as effective DNA condensation and protection are essential for sporulation progression and cyst wall maturation. Among these, α/β-class small acid-soluble proteins (SASPs), particularly SASP2, bind to the DNA minor groove and stabilize the genome during dormancy. In this study, a structural model of the B. cereus SASP2-DNA complex was constructed and analyzed through an integrated computational approach to identify compounds targeting this interaction. Phytochemicals derived from Garcinia mangostana, Garcinia cowa, Ficus exasperata, and Entada abyssinica, previously reported for antimicrobial activity, were evaluated for their potential to interact with the SASP2-DNA interface, a mechanism not previously explored. Several compounds showed strong binding affinity at the SASP2-DNA minor-groove interface and were predicted to influence key interactions under simulated stress conditions, leading to DNA compaction stability and stress tolerance, which may subsequently affect cyst wall formation and spore viability. Notably, the identification of plant-derived compounds capable of targeting the SASP2-DNA interface represents a novel observation. Overall, these findings provide a promising computational basis for exploring strategies to limit the persistence and transmission of B. cereus infections.

植物化学靶向sasp2介导的DNA保护损害蜡样芽孢杆菌孢子弹性:一项计算研究。
蜡样芽孢杆菌等孢子形成细菌由于能够在恶劣的环境条件下生存,抵抗传统的去污策略,并在临床和与食物相关的环境中引起反复感染,因此对公共卫生构成了重大挑战。这种持久性主要与孢子形成有关,这是一个受到严格调控的发育过程,在这个过程中,长期生存依赖于维持基因组的完整性,而细胞代谢在很大程度上是不活跃的。因此,DNA结合蛋白是孢子形成的核心,因为有效的DNA凝聚和保护是孢子形成和囊壁成熟所必需的。其中,α/β类酸溶性小蛋白(SASP2)与DNA小槽结合,在休眠期间稳定基因组。本研究构建了蜡样芽孢杆菌SASP2-DNA复合物的结构模型,并通过综合计算方法对其进行分析,以确定靶向这种相互作用的化合物。先前报道的从山竹藤黄、藤黄、梧树和深草中提取的植物化学物质具有抗菌活性,我们评估了它们与SASP2-DNA界面相互作用的潜力,这是一种以前没有探索过的机制。一些化合物在SASP2-DNA小凹槽界面上显示出很强的结合亲和力,并被预测在模拟应力条件下影响关键的相互作用,从而导致DNA压实稳定性和耐受性,这可能随后影响囊肿壁的形成和孢子的活力。值得注意的是,能够靶向SASP2-DNA界面的植物源化合物的鉴定代表了一种新的观察结果。总的来说,这些发现为探索限制蜡样芽孢杆菌感染的持久性和传播的策略提供了有希望的计算基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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