Journal of the American Chemical Society · 2021 · 70 citations · 56 references
Life SciencesBiochemistryMicrobiologyEnzymologyMycologyNatural Product Biosynthesis5-Enolpyruvylshikimate-3-phosphate Synthase InhibitionAcetolactate Synthase InhibitionAmino Acid Biosynthesis InhibitionEnzyme InhibitionFungal Natural Product BiosynthesisPhenylpropanoid BiosynthesisAcetolactate Synthase Inhibition ResistanceAcetolactate Synthase Inhibitor ResistanceAcetolactate Synthase Inhibitor ToleranceBranched-chain Amino Acid MetabolismBranched-chain Amino AcidsFungal Enzyme InhibitorsFungicide TreatmentsInhibitors Of Acetolactate Synthase
Acetohydroxyacid synthase (AHAS) is the first enzyme in the branched-chain amino acid biosynthetic pathway and is a validated target for herbicide and fungicide development. Here we report harzianic acid (HA, 1) produced by the biocontrol fungus Trichoderma afroharzianum t-22 (Tht22) as a natural product inhibitor of AHAS. The biosynthetic pathway of HA was elucidated with heterologous reconstitution. Guided by a putative self-resistance enzyme in the genome, HA was biochemically demonstrated to be a selective inhibitor of fungal AHAS, including those from phytopathogenic fungi. In addition, HA can inhibit a common resistant variant of AHAS in which the active site proline is mutated. Structural analysis of AHAS complexed with HA revealed the molecular basis of competitive inhibition, which differs from all known commercial AHAS inhibitors. The alternative binding mode also rationalizes the selectivity of HA, as well as effectiveness toward resistant mutants. A proposed role of HA biosynthesis by Tht22 in the rhizosphere is discussed based on the data.
56
The genome portal of the Department of Energy Joint Genome Institute: 2014 updates
Henrik Nordberg, Michael Cantor, Serge Dusheyko et al. · Nucleic Acids Research · 2013 · 852 citations · Full text
Francisco Javier Gutiérrez‐Mañero, Beatriz Ramos‐Solano, A. Probanza et al. · Physiologia Plantarum · 2001 · 614 citations