AUTHOR=Rencoret Jorge , Gutiérrez Ana , Marques Gisela , del Río José C. , Tobimatsu Yuki , Lam Pui Ying , Pérez-Boada Marta , Ruiz-Dueñas Francisco Javier , Barrasa José M. , Martínez Angel T. 

TITLE=New Insights on Structures Forming the Lignin-Like Fractions of Ancestral Plants

JOURNAL=Frontiers in Plant Science

VOLUME=12

YEAR=2021

URL=https://www.frontiersin.org/journals/plant-science/articles/10.3389/fpls.2021.740923

DOI=10.3389/fpls.2021.740923

ISSN=1664-462X

ABSTRACT=<p>In the present work, lignin-like fractions were isolated from several ancestral plants –including moss (<italic>Hypnum cupressiforme</italic> and <italic>Polytrichum commune</italic>), lycophyte (<italic>Selaginella kraussiana</italic>), horsetail (<italic>Equisetum palustre</italic>), fern (<italic>Nephrolepis cordifolia</italic> and <italic>Pteridium aquilinum</italic>), cycad (<italic>Cycas revoluta</italic>), and gnetophyte (<italic>Ephedra fragilis</italic>) species– and structurally characterized by pyrolysis-gas chromatography-mass spectrometry (Py-GC/MS) and two-dimensional nuclear magnetic resonance (2D-NMR) spectroscopy. Py-GC/MS yielded marker compounds characteristic of lignin units, except in the <italic>H. cupressiforme</italic>, <italic>P. commune</italic> and <italic>E. palustre</italic> “lignins,” where they were practically absent. Additional structural information on the other five samples was obtained from 2D-NMR experiments displaying intense correlations signals of guaiacyl (G) units in the fern and cycad lignins, along with smaller amounts of <italic>p</italic>-hydroxyphenyl (H) units. Interestingly, the lignins from the lycophyte <italic>S. kraussiana</italic> and the gnetophyte <italic>E. fragilis</italic> were not only composed of G- and H-lignin units but they also incorporated significant amounts of the syringyl (S) units characteristic of angiosperms, which appeared much later in plant evolution, most probably due to convergent evolution. The latter finding is also supported by the abundance of syringol derivatives after the Py-GC/MS analyses of these two samples. Regarding lignin structure, β−<italic>O</italic>−4′ alkyl-aryl ethers were the most abundant substructures, followed by condensed β−5′ phenylcoumarans and β−β′ resinols (and dibenzodioxocins in the fern and cycad lignins). The highest percentages of alkyl-aryl ether structures correlated with the higher S/G ratio in the <italic>S. Kraussiana</italic> and <italic>E. fragilis</italic> lignin-like fractions. More interestingly, apart from the typical monolignol-derived lignin units (H, G and S), other structures, assigned to flavonoid compounds never reported before in natural lignins (such as amentoflavone, apigenin, hypnogenol B, kaempferol, and naringenin), could also be identified in the HSQC spectra of all the lignin-like fractions analyzed. With this purpose, <italic>in vitro</italic> synthesized coniferyl-naringenin and coniferyl-apigenin dehydrogenation polymers were used as standards. These flavonoids were abundant in <italic>H. cupressiforme</italic> appearing as the only constituents of the moss lignin-like fraction (including 84% of dimeric hypnogenol B) and their abundance decreased in those of <italic>S. Kraussiana</italic> (with amentoflavone and naringenin representing 14% of the total aromatic units), and the two ancient gymnosperms (0.4–1.2%) and ferns (0–0.7%).</p>