An unusual Burkholderia gladioli double chain-initiating nonribosomal peptide synthetase assembles ‘fungal’ icosalide antibiotics

Matt Jenner, Xinyun Jian, Yousef Dashti, Joleen Masschelein, Christian Hobson, Doug Roberts, Cerith Jones, Simon Harris, Julian Parkhill, Huzefa Raja, Nicholas Oberlies, Cedric Pearce, Eshwar Mahenthiralingam, Gregory L Challis

    Allbwn ymchwil: Cyfraniad at gyfnodolynErthygladolygiad gan gymheiriaid

    12 Wedi eu Llwytho i Lawr (Pure)

    Crynodeb

    Burkholderia is a multi-talented genus of Gram-negative bacteria, which in recent years has become increasingly recognised as a promising source of bioactive natural products. Metabolite profiling of Burkholderia gladioli BCC0238 showed that it produces the asymmetric lipopeptidiolide antibiotic icosalide A1, originally isolated from a fungus. Genome sequencing of several B. gladioli isolates identified a gene encoding a nonribosomal peptide synthase (NRPS) with an unsual architecture that was predicted to be responsible for icosalide biosynthesis. Inactivation of this gene in B. gladioli BCC0238 abolished icosalide production. PCR analysis and sequencing of total DNA from the orginal fungal icosalide A1 producer revealed it has a B. gladioli strain associated with it that harbours an NRPS with an identical arcitecture to that responsible for icosalide A1 assembly in B. gladioli BCC0238. Sequence analysis of the icosalide NRPS indicated that it contains two chain-initiating condensation (CI) domains. One of these is appended to the N-terminus of module 1 – a common archictecture for NRPSs involved in lipopeptide assembly. The other is embedded in module 3, immediately downstream of a putative chain-elongating condensation domain. Analysis of the reactions catalysed by a tridomain construct from module 3 of the NRPS using intact protein mass spectometry showed that the embedded CI domain initiates assembly of a second lipopetide chain, providing key insights into the mechanism for asymmetric diolide assembly.
    Iaith wreiddiolSaesneg
    Nifer y tudalennau6
    CyfnodolynChemical Science
    Dyddiad ar-lein cynnar25 Ebr 2019
    Dynodwyr Gwrthrych Digidol (DOIs)
    StatwsE-gyhoeddi cyn argraffu - 25 Ebr 2019

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