Literature DB >> 35732943

Discovery and Characterization of Oxidative Enzymes Involved in Monoterpenoid Indole Alkaloid Biosynthesis.

Tuan-Anh Minh Nguyen1, Matthew McConnachie1, Trinh-Don Nguyen1, Thu-Thuy T Dang2.   

Abstract

Monoterpene indole alkaloid (MIA) constitutes a structurally diverse plant natural product group with remarkable pharmacological activities. Many MIAs have been routinely used as potent drugs for several diseases, including leukemia (vinblastine), lung cancer (camptothecin), and malaria (quinine). Nevertheless, MIAs are biosynthesized at extremely low abundance in plants and, in many cases, require additional chemical functionalizations before their therapeutic uses. As oxygenations and oxidative rearrangements are critical throughout MIAs' structural scaffolding and modifications, the discovery and engineering of oxidative enzymes play essential roles in understanding and boosting the supplies of MIAs. Recent advances in omics technologies and synthetic biology have provided unprecedented amount of biochemical data and tools, paving a wide pathway for discovering, characterizing, and engineering enzymes involved in MIA biosynthesis. Here, we discuss the latest progress in understanding the roles of oxidative enzymes in MIA metabolism and describe a bioinformatic and biochemical pipeline to identify, characterize, and make use of these plant biocatalysts.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Cytochrome P450; Heterologous expression; Monoterpene indole alkaloids; Oxidative enzymes; Plant-specialized metabolism; Transcriptome analysis; Yeast expression

Mesh:

Substances:

Year:  2022        PMID: 35732943     DOI: 10.1007/978-1-0716-2349-7_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  31 in total

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Journal:  Biochem Cell Biol       Date:  1990-12       Impact factor: 3.626

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Authors:  F Peter Guengerich
Journal:  ACS Catal       Date:  2018-10-18       Impact factor: 13.084

Review 3.  Camptothecin, over four decades of surprising findings.

Authors:  Argelia Lorence; Craig L Nessler
Journal:  Phytochemistry       Date:  2004-10       Impact factor: 4.072

4.  A pair of tabersonine 16-hydroxylases initiates the synthesis of vindoline in an organ-dependent manner in Catharanthus roseus.

Authors:  Sébastien Besseau; Franziska Kellner; Arnaud Lanoue; Antje M K Thamm; Vonny Salim; Bernd Schneider; Fernando Geu-Flores; René Höfer; Grégory Guirimand; Anthony Guihur; Audrey Oudin; Gaëlle Glevarec; Emilien Foureau; Nicolas Papon; Marc Clastre; Nathalie Giglioli-Guivarc'h; Benoit St-Pierre; Danièle Werck-Reichhart; Vincent Burlat; Vincenzo De Luca; Sarah E O'Connor; Vincent Courdavault
Journal:  Plant Physiol       Date:  2013-10-09       Impact factor: 8.340

5.  Solution of the multistep pathway for assembly of corynanthean, strychnos, iboga, and aspidosperma monoterpenoid indole alkaloids from 19E-geissoschizine.

Authors:  Yang Qu; Michael E A M Easson; Razvan Simionescu; Josef Hajicek; Antje M K Thamm; Vonny Salim; Vincenzo De Luca
Journal:  Proc Natl Acad Sci U S A       Date:  2018-03-06       Impact factor: 11.205

6.  Sarpagan bridge enzyme has substrate-controlled cyclization and aromatization modes.

Authors:  Thu-Thuy T Dang; Jakob Franke; Ines Soares Teto Carqueijeiro; Chloe Langley; Vincent Courdavault; Sarah E O'Connor
Journal:  Nat Chem Biol       Date:  2018-06-25       Impact factor: 15.040

7.  Biosynthesis of an Anti-Addiction Agent from the Iboga Plant.

Authors:  Scott C Farrow; Mohamed O Kamileen; Lorenzo Caputi; Kate Bussey; Julia E A Mundy; Rory C McAtee; Corey R J Stephenson; Sarah E O'Connor
Journal:  J Am Chem Soc       Date:  2019-08-06       Impact factor: 15.419

8.  Completion of the seven-step pathway from tabersonine to the anticancer drug precursor vindoline and its assembly in yeast.

Authors:  Yang Qu; Michael L A E Easson; Jordan Froese; Razvan Simionescu; Tomas Hudlicky; Vincenzo De Luca
Journal:  Proc Natl Acad Sci U S A       Date:  2015-04-27       Impact factor: 11.205

9.  A three enzyme system to generate the Strychnos alkaloid scaffold from a central biosynthetic intermediate.

Authors:  Evangelos C Tatsis; Inês Carqueijeiro; Thomas Dugé de Bernonville; Jakob Franke; Thu-Thuy T Dang; Audrey Oudin; Arnaud Lanoue; Florent Lafontaine; Anna K Stavrinides; Marc Clastre; Vincent Courdavault; Sarah E O'Connor
Journal:  Nat Commun       Date:  2017-08-22       Impact factor: 17.694

10.  Structural basis of cycloaddition in biosynthesis of iboga and aspidosperma alkaloids.

Authors:  Lorenzo Caputi; Jakob Franke; Kate Bussey; Scott C Farrow; Ivo Jose Curcino Vieira; Clare E M Stevenson; David M Lawson; Sarah E O'Connor
Journal:  Nat Chem Biol       Date:  2020-02-17       Impact factor: 15.040

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