Flexizyme-aminoacylated shortened tRNAs demonstrate that only the aminoacylated acceptor arms of the two tRNA substrates are required for cyclodipeptide synthase activity

• Published in: Nucleic acids research Vol. 48; no. 20; pp. 11615 - 11625
• Main Authors: Canu, Nicolas, Tellier, Carine, Babin, Morgan, Thai, Robert, Ajel, Inès, Seguin, Jérôme, Cinquin, Olivier, Vinck, Robin, Moutiez, Mireille, Belin, Pascal, Cintrat, Jean-Christophe, Gondry, Muriel
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 18.11.2020
• Subjects: Enzyme Assays; Nucleic Acid Enzymes; Peptide Synthases - metabolism; RNA, Transfer - chemistry; RNA, Transfer - metabolism; RNA, Transfer, Amino Acyl - metabolism; Transfer RNA Aminoacylation
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gkaa903

Abstract Cyclodipeptide synthases (CDPSs) use two aminoacyl-tRNAs (AA-tRNAs) to catalyse cyclodipeptide formation in a ping-pong mechanism. Despite intense studies of these enzymes in past years, the tRNA regions of the two substrates required for CDPS activity are poorly documented, mainly because of two limitations. First, previously studied CDPSs use two identical AA-tRNAs to produce homocyclodipeptides, thus preventing the discriminative study of the binding of the two substrates. Second, the range of tRNA analogues that can be aminoacylated by aminoacyl-tRNA synthetases is limited. To overcome the limitations, we studied a new model CDPS that uses two different AA-tRNAs to produce an heterocyclodipeptide. We also developed a production pipeline for the production of purified shortened AA-tRNA analogues (AA-minitRNAs). This method combines the use of flexizymes to aminoacylate a diversity of minitRNAs and their subsequent purifications by anion-exchange chromatography. Finally, we were able to show that aminoacylated molecules mimicking the entire acceptor arms of tRNAs were as effective a substrate as entire AA-tRNAs, thereby demonstrating that the acceptor arms of the two substrates are the only parts of the tRNAs required for CDPS activity. The method developed in this study should greatly facilitate future investigations of the specificity of CDPSs and of other AA-tRNAs-utilizing enzymes.