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Heterologous Biosynthesis of the Sterol O-Acyltransferase Inhibitor Helvamide Unveils an α-Ketoglutarate-Dependent Cross-Linking Oxygenase.
Wang, Rui; Liang, Jia-Jing; Yang, Wencong; Vuong, Daniel; Kalaitzis, John A; Lacey, Alastair E; Lacey, Ernest; Piggott, Andrew M; Chooi, Yit-Heng; Li, Hang.
Afiliación
  • Wang R; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China.
  • Liang JJ; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China.
  • Yang W; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China.
  • Vuong D; Microbial Screening Technologies Pty. Ltd., Smithfield, NSW 2164, Australia.
  • Kalaitzis JA; School of Natural Sciences, Macquarie University, Sydney, NSW 2109, Australia.
  • Lacey AE; Microbial Screening Technologies Pty. Ltd., Smithfield, NSW 2164, Australia.
  • Lacey E; Microbial Screening Technologies Pty. Ltd., Smithfield, NSW 2164, Australia.
  • Piggott AM; School of Natural Sciences, Macquarie University, Sydney, NSW 2109, Australia.
  • Chooi YH; School of Molecular Sciences, The University of Western Australia, Perth, WA 6009, Australia.
  • Li H; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China.
Org Lett ; 26(9): 1807-1812, 2024 Mar 08.
Article en En | MEDLINE | ID: mdl-38393343
ABSTRACT
We have identified the biosynthetic gene cluster (hvm) for the sterol O-acyltransferase inhibitor helvamide (1) from the genome of Aspergillus rugulosus MST-FP2007. Heterologous expression of hvm in A. nidulans produced a previously unreported analog helvamide B (5). An α-ketoglutarate-dependent oxygenase Hvm1 was shown to catalyze intramolecular cyclization of 1 to yield 5. The biosynthetic branch to the related hancockiamides and helvamides was found to be controlled by the substrate selectivity of monomodular nonribosomal peptide synthetases.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxigenasas / Ácidos Cetoglutáricos Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxigenasas / Ácidos Cetoglutáricos Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China