| Literature DB >> 33497199 |
Simon J Moore1,2,3, Hung-En Lai1,2, Soo-Mei Chee2,4, Ming Toh1,2, Seth Coode3, Kameshwari Chengan3, Patrick Capel5, Christophe Corre5, Emmanuel Lc de Los Santos5, Paul S Freemont1,2,4,6.
Abstract
Prokaryotic cell-free coupled transcription-translation (TX-TL) systems are emerging as a powerful tool to examine natural product biosynthetic pathways in a test tube. The key advantages of this approach are the reduced experimental time scales and controlled reaction conditions. To realize this potential, it is essential to develop specialized cell-free systems in organisms enriched for biosynthetic gene clusters. This requires strong protein production and well-characterized synthetic biology tools. The Streptomyces genus is a major source of natural products. To study enzymes and pathways from Streptomyces, we originally developed a homologous Streptomyces cell-free system to provide a native protein folding environment, a high G+C (%) tRNA pool, and an active background metabolism. However, our initial yields were low (36 μg/mL) and showed a high level of batch-to-batch variation. Here, we present an updated high-yield and robust Streptomyces TX-TL protocol, reaching up to yields of 266 μg/mL of expressed recombinant protein. To complement this, we rapidly characterize a range of DNA parts with different reporters, express high G+C (%) biosynthetic genes, and demonstrate an initial proof of concept for combined transcription, translation, and biosynthesis of Streptomyces metabolic pathways in a single "one-pot" reaction.Entities:
Keywords: Streptomyces; cell-free protein synthesis; cell-free synthetic biology; in vitro transcription−translation; natural products
Year: 2021 PMID: 33497199 PMCID: PMC7901020 DOI: 10.1021/acssynbio.0c00581
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110