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白头翁中齐墩果酸型皂苷抗白色念珠菌的构效关系及生物膜形成相关基因靶点。

Structure-activity relationship and biofilm formation-related gene targets of oleanolic acid-type saponins from Pulsatilla chinensis against Candida albicans.

机构信息

Institute of Microbial Pharmaceuticals, College of Life and Health Sciences, Northeastern University, Shenyang 110819, China; Key Laboratory of Bioresource Research and Development of Liaoning Province, College of Life and Health Sciences, Northeastern University, Shenyang 110819, China.

Institute of Microbial Pharmaceuticals, College of Life and Health Sciences, Northeastern University, Shenyang 110819, China.

出版信息

Bioorg Chem. 2024 May;146:107311. doi: 10.1016/j.bioorg.2024.107311. Epub 2024 Mar 25.

Abstract

In the course of our investigations of antifungal natural products, the structure-activity relationship and antifungal activities of oleanolic acid-type saponins (1-28) from Pulsatilla chinensis against human and plant pathogenic fungi were elucidated. The analysis of structure-activity relationship of oleanolic acid-type saponins showed that the free carboxyl at C-28 was essential for their antifungal activities; the free hydroxyl group at the C-23 site of oleanolic acid-type saponins played a crucial role in their antifungal activities; the oligosaccharide chain at C-3 oleanolic acid-type saponins showed significant effects on antifungal efficacy and a disaccharide or trisaccharide moiety at position C-3 displayed optimal antifungal activity. The typical saponin pulchinenoside B3 (16, PB3) displayed satisfactory antifungal activity against human and plant pathogenic fungi, especially, C. albicans with an MIC value of 12.5 μg/mL. Furthermore, PB3 could inhibit the biofilm formation of C. albicans through downregulating the expression of the integrated network of biofilm formation-associated transcription factors (Bcr1 Efg1, Ndt80, Brg1, Rob1 and Tec1) and adhesion-related target genes (HWP1, ALS1, and ALS3). Meanwhile, we found that PB3 could effectively destroy the mature biofilm of C. albicans by the oxidative damage and inducing mitochondria-mediated apoptosis in cells.

摘要

在研究抗真菌天然产物的过程中,我们阐明了白头翁中齐墩果酸型皂苷(1-28)对人和植物病原真菌的结构-活性关系和抗真菌活性。齐墩果酸型皂苷的构效关系分析表明,C-28 位的游离羧基是其抗真菌活性所必需的;齐墩果酸型皂苷 C-23 位的游离羟基在其抗真菌活性中起着关键作用;C-3 位的寡糖链对齐墩果酸型皂苷的抗真菌功效有显著影响,C-3 位的二糖或三糖部分显示出最佳的抗真菌活性。典型的皂苷白头翁皂苷 B3(16,PB3)对人和植物病原真菌表现出令人满意的抗真菌活性,特别是对 C. albicans 的 MIC 值为 12.5μg/mL。此外,PB3 可以通过下调生物膜形成相关转录因子(Bcr1 Efg1、Ndt80、Brg1、Rob1 和 Tec1)和粘附相关靶基因(HWP1、ALS1 和 ALS3)的综合网络来抑制 C. albicans 的生物膜形成。同时,我们发现 PB3 可以通过氧化损伤和诱导细胞中线粒体介导的细胞凋亡有效破坏 C. albicans 的成熟生物膜。

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