Suppr超能文献

从温泉中分离出的嗜热细菌产生的抗菌肽的纯化与鉴定

Purification and Identification of Antimicrobial Peptides Produced by Thermophilic Bacteria Isolated from Hot Springs.

作者信息

Abdulsalam Latifat, Ganiyu Saheed Adewale, Khalil Amjad Bajes

机构信息

Department of Bioengineering, King Fahd University of Petroleum and Minerals (KFUPM), Dhahran, 31261, Saudi Arabia.

Chemistry Department, King Fahd University of Petroleum and Minerals (KFUPM), Dhahran, 31261, Saudi Arabia.

出版信息

Probiotics Antimicrob Proteins. 2025 Sep 26. doi: 10.1007/s12602-025-10772-3.

Abstract

Every year, bacterial infections lead to over 7.7 million deaths, with 4.95 million of these caused by drug-resistant organisms. This growing resistance emphasizes the urgent need for a different approach to combat bacterial infections. Antimicrobial peptides (AMPs) offer a promising solution due to their unique mechanisms of action. However, their clinical application is often limited by their instability under extreme physiological conditions like high temperatures. To address this limitation, this study focuses on extracting and characterizing AMPs from thermophilic bacteria, specifically Bacillus licheniformis, Geobacillus stearothermophilus, Brevibacillus borstelensis AK1, and Anoxybacillus flavithermus AK1. These strains exhibited strong antimicrobial activity against Staphylococcus aureus and Escherichia coli. The antimicrobial peptides (AMPs) were purified using C18 reverse-phase column chromatography and characterized through multiple spectrometric techniques. UPLC revealed strong absorption peaks between 210 and 298 nm, while FTIR spectra showed characteristic peptide bands, including Amide A and B (3100-3500 cm), Amide I (1600-1700 cm), Amide II (1480-1600 cm), and Amide III-VI (500-1300 cm), confirming their proteinaceous nature. Complementary NMR analysis further supported these findings, with H signals for alkyl amines (3-4 ppm), aliphatic groups (1-2 ppm), and amide protons (7-10 ppm), as well as C resonances characteristic of amide compounds. Bioactive fractions displayed molecular masses ranging from 500 to 2000 Da. In silico genome mining of Brevibacillus borstelensis AK1 and Anoxybacillus flavithermus AK1 revealed gene clusters encoding ribosomally synthesized and post-translationally modified peptides (RiPPs), nonribosomal peptides (NRPs), and a terpene. Despite some thermal sensitivity, the compounds retained substantial activity at elevated temperatures; notably, AMPs from B. borstelensis AK1 preserved over 84% inhibition even after exposure to 70 °C. These results highlight thermophilic bacteria from Saudi Arabian hot springs as a promising source of AMPs with potential applications in medicine, food preservation, and agriculture.

摘要

每年,细菌感染导致超过770万人死亡,其中495万例是由耐药生物引起的。这种日益增长的耐药性凸显了采用不同方法对抗细菌感染的迫切需求。抗菌肽(AMPs)因其独特的作用机制提供了一个有前景的解决方案。然而,它们的临床应用常常受到在高温等极端生理条件下不稳定的限制。为了解决这一限制,本研究聚焦于从嗜热细菌中提取和鉴定抗菌肽,具体为地衣芽孢杆菌、嗜热栖热放线菌、博斯德短芽孢杆菌AK1和嗜热栖热嗜酸芽孢杆菌AK1。这些菌株对金黄色葡萄球菌和大肠杆菌表现出强大的抗菌活性。抗菌肽(AMPs)通过C18反相柱色谱法进行纯化,并通过多种光谱技术进行鉴定。超高效液相色谱显示在210至298纳米之间有强烈的吸收峰,而傅里叶变换红外光谱显示出特征性的肽带,包括酰胺A和B(3100 - 3500厘米)、酰胺I(1600 - 1700厘米)、酰胺II(1480 - 1600厘米)以及酰胺III - VI(500 - 1300厘米),证实了它们的蛋白质性质。互补的核磁共振分析进一步支持了这些发现,其显示了烷基胺(3 - 4 ppm)、脂肪族基团(1 - 2 ppm)和酰胺质子(7 - 10 ppm)的H信号,以及酰胺化合物特有的C共振。生物活性组分的分子量范围为500至2000道尔顿。对博斯德短芽孢杆菌AK1和嗜热栖热嗜酸芽孢杆菌AK1的计算机基因组挖掘揭示了编码核糖体合成及翻译后修饰肽(RiPPs)、非核糖体肽(NRPs)和一种萜烯的基因簇。尽管有一定的热敏感性,但这些化合物在升高的温度下仍保留了相当的活性;值得注意的是,来自博斯德短芽孢杆菌AK1的抗菌肽即使在暴露于70°C后仍保留超过84%的抑制活性。这些结果突出了沙特阿拉伯温泉中的嗜热细菌作为抗菌肽的一个有前景的来源,在医学、食品保鲜和农业中具有潜在应用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验