Abstract

Wood lignin composition strongly depends on anatomical features and it has been used as a marker for characterizing major plant groups. Wood heterogeneity in Cactaceae is involved in evolutionary and adaptive processes within this group; moreover, it is highly correlated to the species growth form. Here we studied the lignin structure from different types of woods in four Cactaceae species with different stem morphologies (Pereskia lychnidiflora, tree/fibrous wood; Opuntia streptacantha and Pilosocereus chrysacanthus, tree/succulent fibrous wood; Ferocactus hamatacanthus, cylindrical stem/dimorphic wood) in order to determine their relationship with the wood anatomy in an evolutionary-adaptive context. Dioxane lignin was isolated and analyzed by pyrolysis coupled with gas chromatography and mass spectrometry (Py-GC/MS), two-dimensional nuclear magnetic resonance spectroscopy (2D-NMR) and attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR). The main linkages are the β-O−4′ ether (67–85%), the β-β′ resinol (10–26%) and the β-5′ and α-O−4′ linkages of the phenylcoumaran structures (≤7%). Spirodienone structures have a considerable abundance (5%) in the dimorphic wood of F. hamatacanthus. In addition, low contents (≤3%) of α,β-diaryl ether, α-oxidized β-O−4′ ether and dibenzodioxocin structures were found. The sinapyl- and coniferyl acetates are not part of the wood lignin in any of the studied species. The low (≤5%) γ-acetylation in the F. hamatacanthus and P. chrysacanthus wood lignin is here interpreted as an evidence of a high specialization of the wood elements in the conduction/storage of water. The lignin of the studied Cactaceae is composed predominantly of guaiacyl and syringyl units (S/G: 0.9–16.4). High abundance of syringyl units (62–94%) in three of the four species is considered as a defense mechanism against oxidative agents, it is a very conspicuous trait in the most succulent species with dimorphic wood. Furthermore, it is also associated with ferulates and the herein called γ-acetylated guaiacyl-syringaresinol complexes acting as nucleation sites for lignification and as cross-links between lignin and carbohydrates at the wide-band tracheid-fiber junctions.

Highlights

  • Lignin is a phenolic biopolymer derived from hydroxycinnamyl alcohols that differ in their degree of methoxylation: p-coumaryl, coniferyl and sinapyl alcohols, other monolignols have been recently proposed (Lu and Ralph, 2002; del Río et al, 2007; Ralph, 2010; Chen et al, 2013; Carlos Del Río et al, 2017)

  • The Py-GC/MS analysis allowed knowing the predominant units in the Dioxane lignin (DL)

  • The results shown here contrast partially with that fact: in species with contrasting abundances of S units (F. hamatacanthus, 94% and P. chrysacanthus, 46%) very similar abundances of resinol structures (26 and 22%, respectively) were obtained

Read more

Summary

Introduction

Lignin is a phenolic biopolymer derived from hydroxycinnamyl alcohols that differ in their degree of methoxylation: p-coumaryl, coniferyl and sinapyl alcohols, other monolignols have been recently proposed (Lu and Ralph, 2002; del Río et al, 2007; Ralph, 2010; Chen et al, 2013; Carlos Del Río et al, 2017) It is formed under simple chemical control by bimolecular radical coupling reactions and its structure is highly dependent on the nature of monolignols and the cellular characteristics of the lignified tissue (Ralph J. et al, 2004; Bonawitz and Chapple, 2010; Umezawa, 2010; Vanholme et al, 2010). In angiosperms, where the diversity of cell types in wood is higher, lignin is composed by moieties of syringyl (S) units, derived from sinapyl alcohol, and G units (Bonawitz and Chapple, 2010; Barros et al, 2015), with only small amounts of H units

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call