4.8 Article

Divergent Biosynthesis of Fungal Dioxafenestrane Sesquiterpenes by the Cooperation of Distinctive Baeyer-Villiger Monooxygenases and α-Ketoglutarate-Dependent Dioxygenases

Journal

ACS CATALYSIS
Volume 11, Issue 2, Pages 948-957

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.0c05319

Keywords

divergent biosynthesis; terpene; Baeyer-Villiger monooxygenase; alpha-ketoglutarate-dependent dioxygenase; enzyme evolution

Funding

  1. National Key RAMP
  2. D Program of China [2020YFA0907700]
  3. National Natural Science Foundation of China [31870022]
  4. Chongqing Science Funds for Distinguished Young Scientists [cstc2020jcyj-jqX0005]
  5. Scientific Research Starting Foundation of Southwest University [SWU117034]
  6. Innovation Research Group at higher Education Institutions in Chongqing, Chongqing Education Committee [CQXT20006]
  7. Venture AMP
  8. Innovation Support Program for Chongqing Overseas Returnees [cx2018006]
  9. Thousand Young Talents Program of China

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This study identified two parallel and complex pathways of fungal dioxafenestrane sesquiterpenes from terrestrial and marine-derived fungi, revealing their differences in late-stage tailoring steps. It also discovered important enzymes and catalytic steps, providing valuable insights for natural product generation and metabolic enzymes.
Divergent biosynthesis is widely employed in nature to promote chemical diversity, usually depending on multifunctional enzymes from different environments, for the generation of diverse biologically active compounds. In this work, we identified two parallel and complex pathways (peni and aspe) of fungal dioxafenestrane sesquiterpenes from terrestrial fungus and marine-derived fungus, respectively. These two pathways share a common intermediate but are different in late-stage tailoring steps such as Baeyer-Villiger oxidation in delta-lactone formation and hydroxylation carried on nonactivated carbons. It is important that a distinctive Baeyer-Villiger monooxygenase (BVMO) AspeB from a marine-derived fungus source and a large number of substrate-tolerant alpha-ketoglutarate-dependent dioxygenases (alpha-KGDs, AspeC/D, and PeniD/F) and their artificial mutants used for structural diversity are discovered. Moreover, an acetylation step catalyzed by the acetyltransferase PeniE in the peni pathway was also identified. Our work not only reveals a representative example of the evolutionary relationship between natural product generation and corresponding metabolic enzymes from different environments but also provides valuable biocatalysts for nonactivated carbon oxidation modification.

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