» Articles » PMID: 18393951

Mixed-linkage (1-->3,1-->4)-beta-D-glucan is a Major Hemicellulose of Equisetum (horsetail) Cell Walls

Overview
Journal New Phytol
Specialty Biology
Date 2008 Apr 9
PMID 18393951
Citations 69
Authors
Affiliations
Soon will be listed here.
Abstract

Mixed-linkage (1-->3,1-->4)-beta-d-glucan (MLG) is a hemicellulose reputedly confined to certain Poales. Here, the taxonomic distribution of MLG, and xyloglucan, especially in early-diverging pteridophytes, has been re-investigated. Polysaccharides were digested with lichenase and xyloglucan endoglucanase (XEG), which specifically hydrolyse MLG and xyloglucan, respectively. The oligosaccharides produced were analysed by thin-layer chromatography (TLC), high-pressure liquid chromatography (HPLC) and alkaline peeling. Lichenase yielded oligo-beta-glucans from all Equisetum species tested (Equisetum arvense, Equisetum fluviatile, Equisetum scirpoides, Equisetum sylvaticum and Equisetum xtrachyodon). The major product was the tetrasaccharide beta-glucosyl-(1-->4)-beta-glucosyl-(1-->4)-beta-glucosyl-(1-->3)-glucose (G4G4G3G), which was converted to cellotriose by alkali, confirming its structure. Minor products included G3G, G4G3G and a nonasaccharide. By contrast, poalean MLGs yielded G4G3G > G4G4G3G > nonasaccharide > dodecasaccharide. No other pteridophytes tested contained MLG, including Psilotum and eusporangiate ferns. No MLG was found in lycopodiophytes, bryophytes, Chara or Nitella. XEG digestion showed that Equisetum xyloglucan has unusual repeat units. Equisetum, an exceedingly isolated genus whose closest living relatives diverged > 380 million years ago, has evolved MLG independently of the Poales. Equisetum and poalean MLGs share basic structural motifs but also exhibit clear-cut differences. Equisetum MLG is firmly wall-bound, and may tether neighbouring microfibrils. It is also suggested that MLG acts as a template for silica deposition, characteristic of grasses and horsetails.

Citing Articles

Subcritical water extraction of Equisetum arvense biomass withdraws cell wall fractions that trigger plant immune responses and disease resistance.

Rebaque D, Lopez G, Sanz Y, Vilaplana F, Brunner F, Melida H Plant Mol Biol. 2023; 113(6):401-414.

PMID: 37129736 PMC: 10730674. DOI: 10.1007/s11103-023-01345-5.


Silica deposition in plants: scaffolding the mineralization.

Zexer N, Kumar S, Elbaum R Ann Bot. 2023; 131(6):897-908.

PMID: 37094329 PMC: 10332400. DOI: 10.1093/aob/mcad056.


Evolution of p-coumaroylated lignin in eudicots provides new tools for cell wall engineering.

Mottiar Y, Smith R, Karlen S, Ralph J, Mansfield S New Phytol. 2022; 237(1):251-264.

PMID: 36196006 PMC: 10099755. DOI: 10.1111/nph.18518.


From Cancer Therapy to Winemaking: The Molecular Structure and Applications of β-Glucans and β-1, 3-Glucanases.

Caseiro C, Dias J, de Andrade Fontes C, Bule P Int J Mol Sci. 2022; 23(6).

PMID: 35328577 PMC: 8949617. DOI: 10.3390/ijms23063156.


Search for evolutionary roots of land plant arabinogalactan-proteins in charophytes: presence of a rhamnogalactan-protein in Spirogyra pratensis (Zygnematophyceae).

Pfeifer L, Utermohlen J, Happ K, Permann C, Holzinger A, von Schwartzenberg K Plant J. 2021; 109(3):568-584.

PMID: 34767672 PMC: 7612518. DOI: 10.1111/tpj.15577.