整合生物学期刊网

应用天然产物 ›› 2024, Vol. 14 ›› Issue (6): 51-51.DOI: 10.1007/s13659-024-00473-9

• ORIGINAL ARTICLES • 上一篇    下一篇

Micro-scale screening of genetically modified Fusarium fujikuroi strain extends the apicidin family

Alica Fischle1,2, Mika Lutsch1, Florian Hübner1, Linda Sch?ker-Hübner3, Lina Schürmann1, Finn K. Hansen3, Svetlana A. Kalinina1,2   

  1. 1. Institute of Food Chemistry, University of Münster, Corrensstra?e 45, 48149 Münster, Germany;
    2. Graduate School of Natural Products, Corrensstra?e 43, 48149 Münster, Germany;
    3. Pharmaceutical Institute, Pharmaceutical and Cell Biological Chemistry, University of Bonn, An Der Immenburg 4, 53121 Bonn, Germany
  • 收稿日期:2024-07-19 出版日期:2024-12-24 发布日期:2024-12-13
  • 通讯作者: Svetlana A. Kalinina,E-mail:s_kali03@uni-muenster.de

Micro-scale screening of genetically modified Fusarium fujikuroi strain extends the apicidin family

Alica Fischle1,2, Mika Lutsch1, Florian Hübner1, Linda Sch?ker-Hübner3, Lina Schürmann1, Finn K. Hansen3, Svetlana A. Kalinina1,2   

  1. 1. Institute of Food Chemistry, University of Münster, Corrensstra?e 45, 48149 Münster, Germany;
    2. Graduate School of Natural Products, Corrensstra?e 43, 48149 Münster, Germany;
    3. Pharmaceutical Institute, Pharmaceutical and Cell Biological Chemistry, University of Bonn, An Der Immenburg 4, 53121 Bonn, Germany
  • Received:2024-07-19 Online:2024-12-24 Published:2024-12-13
  • Contact: Svetlana A. Kalinina,E-mail:s_kali03@uni-muenster.de

摘要: Apicidins are a class of naturally occurring cyclic tetrapeptides produced by few strains within the Fusarium genus. These secondary metabolites have gained significant attention due to their antiprotozoal activity through HDAC inhibition, thereby highlighting their potential for the treatment of malaria. Predominantly, apicidins have been isolated from Fusarium semitectum, offering a deep insight into the biosynthetic pathway responsible for their formation. A similar biosynthetic gene cluster has also been identified in the rice pathogenic fungus F. fujikuroi, leading the discovery of three additional apicidins through genetic manipulation. Routine mass spectrometric screening of these compound-producing strains revealed another metabolite structurally related to previously studied apicidins. By optimizing culture conditions and developing an effective isolation method, we obtained a highly pure substance, whose chemical structure was fully elucidated using NMR and HRMS fragmentation. Further studies were conducted to determine cytotoxicity, antimalarial activity, and HDAC inhibitory activity of this new secondary metabolite alongside the previously known apicidins. This work not only expands the apicidin class with a new member but also provides extensive insights and comparative analysis of apicidin-like substances produced by F. fujikuroi.

关键词: Cyclic tetrapeptides, Apicidins, Cytotoxicity, HDAC inhibition, Tropical diseases

Abstract: Apicidins are a class of naturally occurring cyclic tetrapeptides produced by few strains within the Fusarium genus. These secondary metabolites have gained significant attention due to their antiprotozoal activity through HDAC inhibition, thereby highlighting their potential for the treatment of malaria. Predominantly, apicidins have been isolated from Fusarium semitectum, offering a deep insight into the biosynthetic pathway responsible for their formation. A similar biosynthetic gene cluster has also been identified in the rice pathogenic fungus F. fujikuroi, leading the discovery of three additional apicidins through genetic manipulation. Routine mass spectrometric screening of these compound-producing strains revealed another metabolite structurally related to previously studied apicidins. By optimizing culture conditions and developing an effective isolation method, we obtained a highly pure substance, whose chemical structure was fully elucidated using NMR and HRMS fragmentation. Further studies were conducted to determine cytotoxicity, antimalarial activity, and HDAC inhibitory activity of this new secondary metabolite alongside the previously known apicidins. This work not only expands the apicidin class with a new member but also provides extensive insights and comparative analysis of apicidin-like substances produced by F. fujikuroi.

Key words: Cyclic tetrapeptides, Apicidins, Cytotoxicity, HDAC inhibition, Tropical diseases