School of Interdisciplinary Bioscience and Bioengineering (I-Bio), Pohang University of Science and Technology, Pohang 37673, Republic of Korea.
Department of Chemical Engineering, Pohang University of Science and Technology, Pohang 37673, Republic of Korea.
Int J Mol Sci. 2024 Aug 22;25(16):9109. doi: 10.3390/ijms25169109.
Peptide-based antibiotics (PBAs), including antimicrobial peptides (AMPs) and their synthetic mimics, have received significant interest due to their diverse and unique bioactivities. The integration of high-throughput sequencing and bioinformatics tools has dramatically enhanced the discovery of enzymes, allowing researchers to identify specific genes and metabolic pathways responsible for producing novel PBAs more precisely. Cell-free systems (CFSs) that allow precise control over transcription and translation in vitro are being adapted, which accelerate the identification, characterization, selection, and production of novel PBAs. Furthermore, these platforms offer an ideal solution for overcoming the limitations of small-molecule antibiotics, which often lack efficacy against a broad spectrum of pathogens and contribute to the development of antibiotic resistance. In this review, we highlight recent examples of how CFSs streamline these processes while expanding our ability to access new antimicrobial agents that are effective against antibiotic-resistant infections.
基于肽的抗生素(PBAs),包括抗菌肽(AMPs)及其合成模拟物,由于其多样且独特的生物活性而受到广泛关注。高通量测序和生物信息学工具的整合极大地促进了酶的发现,使研究人员能够更准确地识别产生新型 PBA 的特定基因和代谢途径。允许体外精确控制转录和翻译的无细胞系统(CFS)正在被采用,这加速了新型 PBA 的鉴定、表征、选择和生产。此外,这些平台为克服小分子抗生素的局限性提供了理想的解决方案,小分子抗生素通常对广谱病原体的疗效不佳,并且导致抗生素耐药性的发展。在这篇综述中,我们强调了最近的一些例子,说明了 CFS 如何简化这些过程,同时扩大我们获得有效对抗抗生素耐药性感染的新型抗菌剂的能力。