Literature DB >> 23109283

Synthesis and characterization of new 5-linked pinoresinol lignin models.

Fengxia Yue1, Fachuang Lu, Runcang Sun, John Ralph.   

Abstract

Pinoresinol structures, featuring a β-β'-linkage between lignin monomer units, are important in softwood lignins and in dicots and monocots, particularly those that are downregulated in syringyl-specific genes. Although readily detected by NMR spectroscopy, pinoresinol structures largely escaped detection by β-ether-cleaving degradation analyses presumably due to the presence of the linkages at the 5 positions, in 5-5'- or 5-O-4'-structures. In this study, which is aimed at helping better understand 5-linked pinoresinol structures by providing the required data for NMR characterization, new lignin model compounds were synthesized through biomimetic peroxidase-mediated oxidative coupling reactions between pre-formed (free-phenolic) coniferyl alcohol 5-5'- or 5-O-4'-linked dimers and a coniferyl alcohol monomer. It was found that such dimers containing free-phenolic coniferyl alcohol moieties can cross-couple with the coniferyl alcohol producing pinoresinol-containing trimers (and higher oligomers) in addition to other homo- and cross-coupled products. Eight new lignin model compounds were obtained and characterized by NMR spectroscopy, and one tentatively identified cross-coupled β-O-4'-product was formed from a coniferyl alcohol 5-O-4'-linked dimer. It was demonstrated that the 5-5'- and 5-O-4'-linked pinoresinol structures could be readily differentiated by using heteronuclear multiple-bond correlation (HMBC) NMR spectroscopy. With appropriate modification (etherification or acetylation) to the newly obtained model compounds, it would be possible to identify the 5-5'- or 5-O-4'-linked pinoresinol structures in softwood lignins by 2D HMBC NMR spectroscopic methods. Identification of the cross-coupled dibenzodioxocin from a coniferyl alcohol 5-5'-linked moiety suggested that thioacidolysis or derivatization followed by reductive cleavage (DFRC) could be used to detect and identify whether the coniferyl alcohol itself undergoes 5-5'-cross-linking during lignification.
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2012        PMID: 23109283     DOI: 10.1002/chem.201201506

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  5 in total

1.  Coexistence but independent biosynthesis of catechyl and guaiacyl/syringyl lignin polymers in seed coats.

Authors:  Yuki Tobimatsu; Fang Chen; Jin Nakashima; Luis L Escamilla-Treviño; Lisa Jackson; Richard A Dixon; John Ralph
Journal:  Plant Cell       Date:  2013-07-31       Impact factor: 11.277

2.  Enantioselective Synthesis of Dilignol Model Compounds and Their Stereodiscrimination Study with a Dye-Decolorizing Peroxidase.

Authors:  Gaochao Huang; Ruben Shrestha; Kaimin Jia; Brian V Geisbrecht; Ping Li
Journal:  Org Lett       Date:  2017-03-22       Impact factor: 6.005

3.  Lignin-Derived Thioacidolysis Dimers: Reevaluation, New Products, Authentication, and Quantification.

Authors:  Fengxia Yue; Fachuang Lu; Matt Regner; Runcang Sun; John Ralph
Journal:  ChemSusChem       Date:  2017-02-15       Impact factor: 8.928

4.  Promising and efficient lignin degradation versatile strategy based on DFT calculations.

Authors:  Zichen Wang; Mingtian Hao; Xiaoyu Li; Beibei Zhang; Mingyang Jiao; Bo-Zhen Chen
Journal:  iScience       Date:  2022-01-10

Review 5.  An Introduction to Model Compounds of Lignin Linking Motifs; Synthesis and Selection Considerations for Reactivity Studies.

Authors:  Ciaran W Lahive; Paul C J Kamer; Christopher S Lancefield; Peter J Deuss
Journal:  ChemSusChem       Date:  2020-07-09       Impact factor: 8.928

  5 in total

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