A tale of four kingdoms – isoxazolin-5-one- and 3-nitropropanoic acid-derived natural products. Issue 4 (8th March 2017)
- Record Type:
- Journal Article
- Title:
- A tale of four kingdoms – isoxazolin-5-one- and 3-nitropropanoic acid-derived natural products. Issue 4 (8th March 2017)
- Main Title:
- A tale of four kingdoms – isoxazolin-5-one- and 3-nitropropanoic acid-derived natural products
- Authors:
- Becker, Tobias
Pasteels, Jacques
Weigel, Christiane
Dahse, Hans-Martin
Voigt, Kerstin
Boland, Wilhelm - Abstract:
- Abstract : The occurrence, structural diversity, (bio-)synthesis, properties and detoxification mechanisms of isoxazolinone- and 3-nitropropanoic acid-derived natural compounds are reviewed. Abstract : Covering up to September 2016 This review reports on natural compounds that derive from the isoxazolinone ring as well as the 3-nitropropanoic acid (3-NPA) moiety. These structural elements occur in compounds that have been identified in plants, insects, bacteria and fungi. In particular, plants belonging to the family of legumes produce such compounds. In the case of insects, isoxazolin-5-one and 3-NPA derivatives were found in leaf beetles of the subtribe Chrysomelina. A number of these natural products have been synthesized so far. In the case of the single compound 3-NPA, several synthetic strategies have been reported and some of the most efficient routes are reviewed. The toxicity of 3-NPA results from its ability to bind covalently to the catalytic center of succinate dehydrogenase causing irreversible inhibition of mitochondrial respiration. As a motif that is produced by many species of plants, leaf beetles and fungi, different detoxification mechanisms for 3-NPA have evolved in different species. These mechanisms are based on amide formation of 3-NPA with amino acids, reduction to β-alanine, ester formation or oxidation to malonic acid semialdehyde. The biosynthetic pathways of 3-NPA and isoxazolin-5-one moieties have been studied in fungi, plants and leaf beetles.Abstract : The occurrence, structural diversity, (bio-)synthesis, properties and detoxification mechanisms of isoxazolinone- and 3-nitropropanoic acid-derived natural compounds are reviewed. Abstract : Covering up to September 2016 This review reports on natural compounds that derive from the isoxazolinone ring as well as the 3-nitropropanoic acid (3-NPA) moiety. These structural elements occur in compounds that have been identified in plants, insects, bacteria and fungi. In particular, plants belonging to the family of legumes produce such compounds. In the case of insects, isoxazolin-5-one and 3-NPA derivatives were found in leaf beetles of the subtribe Chrysomelina. A number of these natural products have been synthesized so far. In the case of the single compound 3-NPA, several synthetic strategies have been reported and some of the most efficient routes are reviewed. The toxicity of 3-NPA results from its ability to bind covalently to the catalytic center of succinate dehydrogenase causing irreversible inhibition of mitochondrial respiration. As a motif that is produced by many species of plants, leaf beetles and fungi, different detoxification mechanisms for 3-NPA have evolved in different species. These mechanisms are based on amide formation of 3-NPA with amino acids, reduction to β-alanine, ester formation or oxidation to malonic acid semialdehyde. The biosynthetic pathways of 3-NPA and isoxazolin-5-one moieties have been studied in fungi, plants and leaf beetles. In the case of fungi, 3-NPA derives from aspartate, while leaf beetles use essential amino acids such as valine as ultimate precursors. In the case of plants, it is supposed that malonate serves as a precursor of 3-NPA, as indicated by feeding of 14 C-labeled precursors to Indigofera spicata . In other leguminous plants it is suggested that asparagine is incorporated into compounds that derive from isoxazolin-5-one, which was indicated by 14 C-labeled compounds as well. In the case of leaf beetles it was demonstrated that detection of radioactivity after 14 C-labeling from a few precursors is not sufficient to unravel biosynthetic pathways. … (more)
- Is Part Of:
- Natural product reports. Volume 34:Issue 4(2017)
- Journal:
- Natural product reports
- Issue:
- Volume 34:Issue 4(2017)
- Issue Display:
- Volume 34, Issue 4 (2017)
- Year:
- 2017
- Volume:
- 34
- Issue:
- 4
- Issue Sort Value:
- 2017-0034-0004-0000
- Page Start:
- 343
- Page End:
- 360
- Publication Date:
- 2017-03-08
- Subjects:
- Natural products -- Periodicals
Produits naturels -- Périodiques
547.7 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/np#!issueid=np031010&type=current&issnprint=0265-0568 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6np00122j ↗
- Languages:
- English
- ISSNs:
- 0265-0568
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6040.738000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 770.xml