Pathway from N‐Alkylglycine to Alkylisonitrile Catalyzed by Iron(II) and 2‐Oxoglutarate‐Dependent Oxygenases. Issue 19 (10th March 2020)

• Record Type: Journal Article
• Authors: Chen, Tzu‐Yu; Chen, Jinfeng; Tang, Yijie; Zhou, Jiahai; Guo, Yisong; Chang, Wei‐chen
• Is Part Of: Angewandte Chemie international edition. Volume 59:Issue 19(2020)
• Page Start: 7367
• Page End: 7371
• Publication Date: 2020-03-10
• Subjects: catalysis -- decarboxylation -- enzymes -- iron -- reaction mechanisms; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.201914896
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: N‐alkylisonitrile, a precursor to isonitrile‐containing lipopeptides, is biosynthesized by decarboxylation‐assisted ‐N≡C group (isonitrile) formation by using N‐alkylglycine as the substrate. This reaction is catalyzed by iron(II) and 2‐oxoglutarate (Fe/2OG) dependent enzymes. Distinct from typical oxygenation or halogenation reactions catalyzed by this class of enzymes, installation of the isonitrile group represents a novel reaction type for Fe/2OG enzymes that involves a four‐electron oxidative process. Reported here is a plausible mechanism of three Fe/2OG enzymes, Sav607, ScoE and SfaA, which catalyze isonitrile formation. The X‐ray structures of iron‐loaded ScoE in complex with its substrate and the intermediate, along with biochemical and biophysical data reveal that ‐N≡C bond formation involves two cycles of Fe/2OG enzyme catalysis. The reaction starts with an Fe IV ‐oxo‐catalyzed hydroxylation. It is likely followed by decarboxylation‐assisted desaturation to complete isonitrile installation. Abstract : CN installation : A subclass of Fe/2OG (2‐oxoglutarate) enzymes catalyze decarboxylation‐assisted desaturation of N‐alkylglycine to install the isonitrile functionality. By using a complementary approach, including structure determination, NMR spectroscopy, and Mössbauer analyses, the reaction intermediate and a plausible reaction mechanism are established.