{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Stadler KA"],"funding":["Austrian Science Fund FWF","FWF","Land Steiermark","Land Steiermark, City of Graz","University of Graz"],"pagination":["1041-1053"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9217835"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["54(7)"],"pubmed_abstract":["Vibrio natriegens is the fastest growing organism identified so far. The minimum doubling time of only 9.4 min, the ability to utilize over 60 different carbon sources and its non-pathogenic properties make it an interesting alternative to E. coli as a new production host for recombinant proteins. We investigated the ability of the engineered V. natriegens strain, Vmax™ Express, to incorporate the non-canonical amino acid (ncAA) p-azido-L-phenylalanine (AzF) into recombinant proteins for NMR applications. AzF was incorporated into enhanced yellow fluorescent protein (EYFP) and MlaC, an intermembrane transport protein, by stop codon suppression. AzF incorporation into EYFP resulted in an improved suppression efficiency (SE) of up to 35.5 ± 0.8% and a protein titer of 26.7 ± 0.7 mg/L. The ex"],"journal":["Amino acids"],"pubmed_title":["Overexpression of recombinant proteins containing non-canonical amino acids in Vibrio natriegens: p-azido-L-phenylalanine as coupling site for <sup>19</sup>F-tags."],"pmcid":["PMC9217835"],"funding_grant_id":["Frontier NMR","DOC 50","Initiative BioHealth","doc.fund MOBILES (DOC 50)"],"pubmed_authors":["Stadler KA","Zangger K","Darnhofer B","Becker W","Birner-Gruenberger R"],"additional_accession":[]},"is_claimable":false,"name":"Overexpression of recombinant proteins containing non-canonical amino acids in Vibrio natriegens: p-azido-L-phenylalanine as coupling site for <sup>19</sup>F-tags.","description":"Vibrio natriegens is the fastest growing organism identified so far. The minimum doubling time of only 9.4 min, the ability to utilize over 60 different carbon sources and its non-pathogenic properties make it an interesting alternative to E. coli as a new production host for recombinant proteins. We investigated the ability of the engineered V. natriegens strain, Vmax™ Express, to incorporate the non-canonical amino acid (ncAA) p-azido-L-phenylalanine (AzF) into recombinant proteins for NMR applications. AzF was incorporated into enhanced yellow fluorescent protein (EYFP) and MlaC, an intermembrane transport protein, by stop codon suppression. AzF incorporation into EYFP resulted in an improved suppression efficiency (SE) of up to 35.5 ± 0.8% and a protein titer of 26.7 ± 0.7 mg/L. The ex","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Jul","modification":"2026-05-09T14:35:32.751Z","creation":"2024-11-21T05:02:01.756Z"},"accession":"S-EPMC9217835","cross_references":{"pubmed":["35419750"],"doi":["10.1007/s00726-022-03148-2"]}}