Literature DB >> 29318245

Chemicals from lignin: an interplay of lignocellulose fractionation, depolymerisation, and upgrading.

W Schutyser1, T Renders, S Van den Bosch, S-F Koelewijn, G T Beckham, B F Sels.   

Abstract

In pursuit of more sustainable and competitive biorefineries, the effective valorisation of lignin is key. An alluring opportunity is the exploitation of lignin as a resource for chemicals. Three technological biorefinery aspects will determine the realisation of a successful lignin-to-chemicals valorisation chain, namely (i) lignocellulose fractionation, (ii) lignin depolymerisation, and (iii) upgrading towards targeted chemicals. This review provides a summary and perspective of the extensive research that has been devoted to each of these three interconnected biorefinery aspects, ranging from industrially well-established techniques to the latest cutting edge innovations. To navigate the reader through the overwhelming collection of literature on each topic, distinct strategies/topics were delineated and summarised in comprehensive overview figures. Upon closer inspection, conceptual principles arise that rationalise the success of certain methodologies, and more importantly, can guide future research to further expand the portfolio of promising technologies. When targeting chemicals, a key objective during the fractionation and depolymerisation stage is to minimise lignin condensation (i.e. formation of resistive carbon-carbon linkages). During fractionation, this can be achieved by either (i) preserving the (native) lignin structure or (ii) by tolerating depolymerisation of the lignin polymer but preventing condensation through chemical quenching or physical removal of reactive intermediates. The latter strategy is also commonly applied in the lignin depolymerisation stage, while an alternative approach is to augment the relative rate of depolymerisation vs. condensation by enhancing the reactivity of the lignin structure towards depolymerisation. Finally, because depolymerised lignins often consist of a complex mixture of various compounds, upgrading of the raw product mixture through convergent transformations embodies a promising approach to decrease the complexity. This particular upgrading approach is termed funneling, and includes both chemocatalytic and biological strategies.

Entities:  

Year:  2018        PMID: 29318245     DOI: 10.1039/c7cs00566k

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  121 in total

1.  Electrochemical Aminoxyl-Mediated Oxidation of Primary Alcohols in Lignin to Carboxylic Acids: Polymer Modification and Depolymerization.

Authors:  Mohammad Rafiee; Manar Alherech; Steven D Karlen; Shannon S Stahl
Journal:  J Am Chem Soc       Date:  2019-09-16       Impact factor: 15.419

2.  Intracellular pathways for lignin catabolism in white-rot fungi.

Authors:  Carlos Del Cerro; Erika Erickson; Tao Dong; Allison R Wong; Elizabeth K Eder; Samuel O Purvine; Hugh D Mitchell; Karl K Weitz; Lye Meng Markillie; Meagan C Burnet; David W Hoyt; Rosalie K Chu; Jan-Fang Cheng; Kelsey J Ramirez; Rui Katahira; Wei Xiong; Michael E Himmel; Venkataramanan Subramanian; Jeffrey G Linger; Davinia Salvachúa
Journal:  Proc Natl Acad Sci U S A       Date:  2021-03-02       Impact factor: 11.205

3.  Characterization of alkylguaiacol-degrading cytochromes P450 for the biocatalytic valorization of lignin.

Authors:  Morgan M Fetherolf; David J Levy-Booth; Laura E Navas; Jie Liu; Jason C Grigg; Andrew Wilson; Rui Katahira; Gregg T Beckham; William W Mohn; Lindsay D Eltis
Journal:  Proc Natl Acad Sci U S A       Date:  2020-09-28       Impact factor: 11.205

4.  Selective molecular separation of lignin model compounds by reduced graphene oxide membranes from solvent-water mixture.

Authors:  Ashish Aher; Rupam Sarma; Mark Crocker; Dibakar Bhattacharyya
Journal:  Sep Purif Technol       Date:  2019-07-27       Impact factor: 7.312

5.  A multi-omics approach to lignocellulolytic enzyme discovery reveals a new ligninase activity from Parascedosporium putredinis NO1.

Authors:  Nicola C Oates; Amira Abood; Alexandra M Schirmacher; Anna M Alessi; Susannah M Bird; Joseph P Bennett; Daniel R Leadbeater; Yi Li; Adam A Dowle; Sarah Liu; Vitaliy I Tymokhin; John Ralph; Simon J McQueen-Mason; Neil C Bruce
Journal:  Proc Natl Acad Sci U S A       Date:  2021-05-04       Impact factor: 11.205

6.  Oxalohydrazide Ligands for Copper-Catalyzed C-O Coupling Reactions with High Turnover Numbers.

Authors:  Ritwika Ray; John F Hartwig
Journal:  Angew Chem Int Ed Engl       Date:  2021-03-03       Impact factor: 15.336

7.  Structural and functional analysis of lignostilbene dioxygenases from Sphingobium sp. SYK-6.

Authors:  Eugene Kuatsjah; Anson C K Chan; Rui Katahira; Stefan J Haugen; Gregg T Beckham; Michael E P Murphy; Lindsay D Eltis
Journal:  J Biol Chem       Date:  2021-05-06       Impact factor: 5.157

8.  Highly Efficient Semi-Continuous Extraction and In-Line Purification of High β-O-4 Butanosolv Lignin.

Authors:  Douwe Sjirk Zijlstra; Joren de Korte; Ernst P C de Vries; Lisanne Hameleers; Erwin Wilbers; Edita Jurak; Peter Joseph Deuss
Journal:  Front Chem       Date:  2021-05-10       Impact factor: 5.221

9.  Synthesis of thioethers, arenes and arylated benzoxazoles by transformation of the C(aryl)-C bond of aryl alcohols.

Authors:  Mingyang Liu; Zhanrong Zhang; Bingfeng Chen; Qinglei Meng; Pei Zhang; Jinliang Song; Buxing Han
Journal:  Chem Sci       Date:  2020-04-15       Impact factor: 9.825

10.  Reductive catalytic fractionation of pine wood: elucidating and quantifying the molecular structures in the lignin oil.

Authors:  K Van Aelst; E Van Sinay; T Vangeel; E Cooreman; G Van den Bossche; T Renders; J Van Aelst; S Van den Bosch; B F Sels
Journal:  Chem Sci       Date:  2020-09-26       Impact factor: 9.825

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