figshare
Browse
ppat.1009425.s001.tif (1006.84 kB)

Biochemical basis of AQ biosynthesis.

Download (1006.84 kB)
figure
posted on 2021-08-30, 17:38 authored by Eliza Ye-Chen Soh, Frances Smith, Maxime Rémi Gimenez, Liang Yang, Rebecca Munk Vejborg, Matthew Fletcher, Nigel Halliday, Sophie Bleves, Stephan Heeb, Miguel Cámara, Michael Givskov, Kim R. Hardie, Tim Tolker-Nielsen, Bérengère Ize, Paul Williams

PqsA catalyses the formation of anthraniloyl-CoA that is condensed with malonyl-CoA by PqsD to form 2-aminobenzoylacetyl-CoA (2-ABA-CoA). The latter is converted to 2-aminobenzoylacetate (2-ABA) via the thioesterase functionality of PqsE. The PqsBC heterodimer condenses 2-ABA with octanoyl-CoA to generate HHQ. PQS is formed through the oxidation of HHQ by PqsH. For AQ N-oxides such as 2-heptyl-4-hydroxyquinoline N-oxide (HQNO), 2-ABA is oxidized to 2-HABA by the alternative mono-oxygenase PqsL and then condensed with octanoyl-CoA by PqsBC to form HQNO. PqsBC can accept acyl-CoAs of different acyl chain lengths to generate diverse AQs and AQ N-oxides.

(TIF)

History