Department of Chemical and Biomolecular Engineering, University of Illinois Urbana-Champaign, Urbana, Illinois 61801, United States.
Carl R. Woese Institute for Genomic Biology, University of Illinois Urbana-Champaign, Urbana, Illinois 61801, United States.
ACS Synth Biol. 2024 Nov 15;13(11):3746-3753. doi: 10.1021/acssynbio.4c00594. Epub 2024 Oct 31.
Ribosomally synthesized lanthionine-containing peptides (lanthipeptides) have emerged as a promising source of antimicrobials against multidrug resistance pathogens. An effective way to discover and engineer lanthipeptides is through heterologous expression of their biosynthetic gene clusters (BGCs) in a host of choice. Here we report a plug-and-play pathway refactoring strategy for rapid evaluation of lanthipeptide BGCs in based on the T7 expression system. As a proof of concept, we used this strategy to not only observe the successful production of a known lanthipeptide haloduracin β but also discover two new human-microbiota-derived lanthipeptides that previously failed to be produced in . The resulting plug-and-play T7 expression system should enable the genome mining of new lanthipeptides in a high-throughput manner.
核糖体合成的含硫肽(lanthipeptides)已成为对抗多药耐药病原体的有前途的抗菌药物来源。发现和工程化硫肽的一种有效方法是在宿主中异源表达其生物合成基因簇(BGCs)。在这里,我们报告了一种基于 T7 表达系统的快速评估 中硫肽 BGCs 的即插即用途径重构策略。作为概念验证,我们不仅使用这种策略观察到已知硫肽卤二孢菌素 β 的成功生产,还发现了两种以前无法在 中生产的新的人类微生物群衍生硫肽。由此产生的即插即用 T7 表达系统应该能够以高通量的方式对新的硫肽进行基因组挖掘。