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1. Szwalbe  AJ, Williams  K, Song  Z, de Mattos-Shipley  K, Vincent  JL, Bailey  AM, Willis  CL, Cox  RJ, Simpson  TJ,     ( 2019 )

Characterisation of the biosynthetic pathway to agnestins A and B reveals the reductive route to chrysophanol in fungi.

Chemical science 10 (1)
PMID : 30746079  :   DOI  :   10.1039/c8sc03778g     PMC  :   PMC6335632    
Abstract >>
Two new dihydroxy-xanthone metabolites, agnestins A and B, were isolated from Paecilomyces variotii along with a number of related benzophenones and xanthones including monodictyphenone. The structures were elucidated by NMR analyses and X-ray crystallography. The agnestin (agn) biosynthetic gene cluster was identified and targeted gene disruptions of the PKS, Baeyer-Villiger monooxygenase, and other oxido-reductase genes revealed new details of fungal xanthone biosynthesis. In particular, identification of a reductase responsible for in vivo anthraquinone to anthrol conversion confirms a previously postulated essential step in aromatic deoxygenation of anthraquinones, e.g. emodin to chrysophanol.
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2. Williams  K, Szwalbe  AJ, Dickson  C, Desson  TR, Mulholland  NP, Vincent  JL, Clough  JM, Bailey  AM, Butts  CP, Willis  CL, Simpson  TJ, Cox  RJ,     ( 2017 )

Genetic and chemical characterisation of the cornexistin pathway provides further insight into maleidride biosynthesis.

Chemical communications (Cambridge, England) 53 (56)
PMID : 28660939  :   DOI  :   10.1039/c7cc03303f    
Abstract >>
The biosynthesis of the herbicide cornexistin in the fungus Paecilomyces variotii was investigated by full sequencing of its genome, knockout of key genes within its biosynthetic gene cluster and isolation and identification of intermediate compounds. The general biosynthetic pathway resembles that of byssochlamic acid and other nonadrides in the early stages, but differs in requiring fewer enzymes in the key nonadride dimerisation step, and in the removal of one maleic anhydride moiety.
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