» Articles » PMID: 17141815

Saponins, Classification and Occurrence in the Plant Kingdom

Overview
Journal Phytochemistry
Publisher Elsevier
Date 2006 Dec 5
PMID 17141815
Citations 127
Authors
Affiliations
Soon will be listed here.
Abstract

Saponins are a structurally diverse class of compounds occurring in many plant species, which are characterized by a skeleton derived of the 30-carbon precursor oxidosqualene to which glycosyl residues are attached. Traditionally, they are subdivided into triterpenoid and steroid glycosides, or into triterpenoid, spirostanol, and furostanol saponins. In this study, the structures of saponins are reviewed and classified based on their carbon skeletons, the formation of which follows the main pathways for the biosynthesis of triterpenes and steroids. In this way, 11 main classes of saponins were distinguished: dammaranes, tirucallanes, lupanes, hopanes, oleananes, taraxasteranes, ursanes, cycloartanes, lanostanes, cucurbitanes, and steroids. The dammaranes, lupanes, hopanes, oleananes, ursanes, and steroids are further divided into 16 subclasses, because their carbon skeletons are subjected to fragmentation, homologation, and degradation reactions. With this systematic classification, the relationship between the type of skeleton and the plant origin was investigated. Up to five main classes of skeletons could exist within one plant order, but the distribution of skeletons in the plant kingdom did not seem to be order- or subclass-specific. The oleanane skeleton was the most common skeleton and is present in most orders of the plant kingdom. For oleanane type saponins, the kind of substituents (e.g. -OH, =O, monosaccharide residues, etc.) and their position of attachment to the skeleton were reviewed. Carbohydrate chains of 18 monosaccharide residues can be attached to the oleanane skeleton, most commonly at the C3 and/or C17 atom. The kind and positions of the substituents did not seem to be plant order-specific.

Citing Articles

Asprecosides A-J, ten new pentacyclic triterpenoid glycosides with cytotoxic activity from the roots of Ilex asprella.

Wu Y, Zhang B, Li W, Peng L, Qiao W, Li W Nat Prod Bioprospect. 2025; 15(1):18.

PMID: 40080319 PMC: 11906957. DOI: 10.1007/s13659-025-00499-7.


Qualitative Phytochemical Profiling and In Vitro Antioxidant Potential Evaluation of South African Momordica Balsamina Linn Fruit Pulp.

Matseke B, Mapfumari S, Mothibe M Life (Basel). 2025; 15(1).

PMID: 39859944 PMC: 11766754. DOI: 10.3390/life15010004.


Immunomodulatory potential of dietary soybean-derived saponins.

White C, Dilger R J Anim Sci. 2024; 102.

PMID: 39529449 PMC: 11630861. DOI: 10.1093/jas/skae349.


Chemical and Transcriptomic Analyses Provide New Insights into Key Genes for Ginsenoside Biosynthesis in the Rhizome of C. A. Meyer.

Yang Q, Xiong C, Zhang J, Ming Y, Zhang S, Wang L Molecules. 2024; 29(20).

PMID: 39459304 PMC: 11510602. DOI: 10.3390/molecules29204936.


Safety and efficacy of a feed additive consisting of a C.Abel seed extract for use in all animal species except fin fish (NOR-FEED SAS).

Villa R, Azimonti G, Bonos E, Christensen H, Durjava M, Dusemund B EFSA J. 2024; 22(10):e9022.

PMID: 39444986 PMC: 11496906. DOI: 10.2903/j.efsa.2024.9022.