Literature DB >> 32118354

Enzyme evolution in fungal indole alkaloid biosynthesis.

Amy E Fraley1,2, David H Sherman1,2,3,4.   

Abstract

The class of fungal indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring is comprised of diverse molecules that display a range of biological activities. While much interest has been garnered due to their therapeutic potential, this class of molecules also displays unique chemical functionality, making them intriguing synthetic targets. Many elegant and intricate total syntheses have been developed to generate these alkaloids, but the selectivity required to produce them in high yield presents great barriers. Alternatively, if we can understand the molecular mechanisms behind how fungi make these complex molecules, we can leverage the power of nature to perform these chemical transformations. Here, we describe the various studies regarding the evolutionary development of enzymes involved in fungal indole alkaloid biosynthesis.
© 2020 Federation of European Biochemical Societies.

Entities:  

Keywords:  Diels-Alderase; biosynthesis; monooxygenase; natural products; nonribosomal peptides

Mesh:

Substances:

Year:  2020        PMID: 32118354      PMCID: PMC7317620          DOI: 10.1111/febs.15270

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  60 in total

1.  Studies on the Biosynthesis of Paraherquamide: Synthesis and Incorporation of a Hexacyclic Indole Derivative as an Advanced Metabolite This work was supported by the National Institutes of Health (Grant no. CA70375 to R.M.W.). We wish to acknowledge the American Chemical Society Division of Organic Chemistry Fellowship (sponsored by SmithKline Beecham) and the Pharmacia-Upjohn Company for financial support (to E.M.S.). Mass spectra were obtained on instruments supported by the National Institutes of Health Shared Instrumentation Grant (No. GM49631). We also wish to thank Professor Dean Crick of the Department of Microbiology at Colorado State University for helpful discussions. J.F.S.-C. thanks the DGICYT of Spain for a research grant (project no. PB98-1438).

Authors:  Emily M. Stocking; Juan F. Sanz-Cervera; Robert M. Williams
Journal:  Angew Chem Int Ed Engl       Date:  2001-04-01       Impact factor: 15.336

2.  Biosynthesis of 4-methylproline in cyanobacteria: cloning of nosE and nosF genes and biochemical characterization of the encoded dehydrogenase and reductase activities.

Authors:  Hendrik Luesch; Dietmar Hoffmann; Joan M Hevel; Julia E Becker; Trimurtulu Golakoti; Richard E Moore
Journal:  J Org Chem       Date:  2003-01-10       Impact factor: 4.354

3.  A concise total synthesis of the notoamides C and D.

Authors:  Alan W Grubbs; Gerald D Artman; Sachiko Tsukamoto; Robert M Williams
Journal:  Angew Chem Int Ed Engl       Date:  2007       Impact factor: 15.336

4.  Utilizing DART mass spectrometry to pinpoint halogenated metabolites from a marine invertebrate-derived fungus.

Authors:  Katharine R Watts; Steven T Loveridge; Karen Tenney; Joseph Media; Frederick A Valeriote; Phillip Crews
Journal:  J Org Chem       Date:  2011-06-29       Impact factor: 4.354

5.  Studies on the biosynthesis of paraherquamide A and VM99955. A theoretical study of intramolecular Diels-Alder cycloaddition.

Authors:  Luis R Domingo; Ramón J Zaragozá; Robert M Williams
Journal:  J Org Chem       Date:  2003-04-04       Impact factor: 4.354

6.  Insecticidal activity of Paraherquamides, including paraherquamide H and paraherquamide I, two new alkaloids isolated from Penicillium cluniae.

Authors:  M Pilar López-Gresa; M Carmen González; Letizia Ciavatta; Ildefonso Ayala; Pilar Moya; Jaime Primo
Journal:  J Agric Food Chem       Date:  2006-04-19       Impact factor: 5.279

7.  Biomimetic Diels-Alder cyclizations for the construction of the brevianamide, paraherquamide, sclerotamide, asperparaline and VM55599 ring systems.

Authors:  R M Williams; J F Sanz-Cervera; F Sancenón; J A Marco; K M Halligan
Journal:  Bioorg Med Chem       Date:  1998-08       Impact factor: 3.641

Review 8.  Structural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi.

Authors:  Kimberly R Klas; Hikaru Kato; Jens C Frisvad; Fengan Yu; Sean A Newmister; Amy E Fraley; David H Sherman; Sachiko Tsukamoto; Robert M Williams
Journal:  Nat Prod Rep       Date:  2018-06-20       Impact factor: 13.423

9.  Enzyme-catalysed [4+2] cycloaddition is a key step in the biosynthesis of spinosyn A.

Authors:  Hak Joong Kim; Mark W Ruszczycky; Sei-hyun Choi; Yung-nan Liu; Hung-wen Liu
Journal:  Nature       Date:  2011-05-05       Impact factor: 49.962

Review 10.  Medium- and short-chain dehydrogenase/reductase gene and protein families : the SDR superfamily: functional and structural diversity within a family of metabolic and regulatory enzymes.

Authors:  K L Kavanagh; H Jörnvall; B Persson; U Oppermann
Journal:  Cell Mol Life Sci       Date:  2008-12       Impact factor: 9.261

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  3 in total

Review 1.  Halogenation in Fungi: What Do We Know and What Remains to Be Discovered?

Authors:  Bastien Cochereau; Laurence Meslet-Cladière; Yves François Pouchus; Olivier Grovel; Catherine Roullier
Journal:  Molecules       Date:  2022-05-14       Impact factor: 4.927

2.  Structural basis of the stereoselective formation of the spirooxindole ring in the biosynthesis of citrinadins.

Authors:  Zhiwen Liu; Fanglong Zhao; Boyang Zhao; Jie Yang; Joseph Ferrara; Banumathi Sankaran; B V Venkataram Prasad; Biki Bapi Kundu; George N Phillips; Yang Gao; Liya Hu; Tong Zhu; Xue Gao
Journal:  Nat Commun       Date:  2021-07-06       Impact factor: 14.919

3.  A unified strategy to reverse-prenylated indole alkaloids: total syntheses of preparaherquamide, premalbrancheamide, and (+)-VM-55599.

Authors:  Jose B Roque; Eduardo V Mercado-Marin; Sven C Richter; Danilo Pereira de Sant'Ana; Ken Mukai; Yingda Ye; Richmond Sarpong
Journal:  Chem Sci       Date:  2020-05-28       Impact factor: 9.825

  3 in total

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