Literature DB >> 32696567

Total Synthesis and Structural Revision of Kasumigamide, and Identification of a New Analogue.

Takefumi Kuranaga1, Kenichi Matsuda1, Masachika Takaoka1, Chisato Tachikawa1, Ayae Sano1, Kosei Itoh1, Ayumu Enomoto1, Kei Fujita1, Ikuro Abe2,3, Toshiyuki Wakimoto1.   

Abstract

Kasumigamide is an antialgal hybrid peptide-polyketide isolated from the freshwater cyanobacterium Microcystis aeruginosa (NIES-87). The biosynthetic gene cluster was identified from not only the cyanobacterium but also Candidatus "Entotheonella", associated with the Japanese marine sponge Discodermia calyx. Therefore, kasumigamide is considered to play a key role in microbial ecology, regardless of the terrestrial and marine habitats. We now report synthetic studies on this intriguing natural product that have led to a structural revision and the first total synthesis. During this study, a new analogue, deoxykasumigamide, was also isolated and structurally validated. This study confirmed the presence of the unusual pathway in the biosynthesis of a hybrid peptide-polyketide natural product.
© 2020 Wiley-VCH GmbH.

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Keywords:  biosynthesis; kasumigamide; natural products; peptides; total synthesis

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Year:  2020        PMID: 32696567     DOI: 10.1002/cbic.202000409

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  1 in total

1.  Direct and Asymmetric Aldol Reactions of N-Azidoacetyl-1,3-thiazolidine-2-thione Catalyzed by Chiral Nickel(II) Complexes. A New Approach to the Synthesis of β-Hydroxy-α-Amino Acids.

Authors:  Saul F Teloxa; Miguel Mellado-Hidalgo; Stuart C D Kennington; Pedro Romea; Fèlix Urpí; Gabriel Aullón; Mercè Font-Bardia
Journal:  Chemistry       Date:  2022-05-26       Impact factor: 5.020

  1 in total

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