Wu Lan

ORCID: 0000-0002-0677-3085
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About
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Research Areas
  • Lignin and Wood Chemistry
  • Biofuel production and bioconversion
  • Plant Gene Expression Analysis
  • Biochemical and biochemical processes
  • Advanced Cellulose Research Studies
  • Catalysis for Biomass Conversion
  • Fermentation and Sensory Analysis
  • Electrochemical sensors and biosensors
  • Electrochemical Analysis and Applications
  • Enzyme-mediated dye degradation
  • Conducting polymers and applications
  • Phytochemicals and Antioxidant Activities
  • Hydrogels: synthesis, properties, applications
  • Microbial Metabolic Engineering and Bioproduction
  • Advanced Nanomaterials in Catalysis
  • Water Quality Monitoring and Analysis
  • Luminescence Properties of Advanced Materials
  • Analytical Chemistry and Sensors
  • Electrocatalysts for Energy Conversion
  • Advanced Antenna and Metasurface Technologies
  • Pharmacological Effects and Assays
  • Carcinogens and Genotoxicity Assessment
  • Electrospun Nanofibers in Biomedical Applications
  • Gut microbiota and health
  • Electromagnetic wave absorption materials

South China University of Technology
2011-2025

Shandong University
2024-2025

Chinese Academy of Sciences
2025

University of Chinese Academy of Sciences
2025

Beijing Institute of Genomics
2025

University of Wisconsin–Madison
2015-2023

Great Lakes Bioenergy Research Center
2015-2023

State Key Laboratory of Pulp and Paper Engineering
2023

Chinese Academy of Medical Sciences & Peking Union Medical College
2022

Shanghai University of Medicine and Health Sciences
2020-2021

Abstract Tricin was recently discovered in lignin preparations from wheat (Triticum aestivum) straw and subsequently all monocot samples examined. To provide proof that tricin is involved lignification establish the mechanism by which it incorporates into polymer, 4′-O-β-coupling products of with monolignols (p-coumaryl, coniferyl, sinapyl alcohols) were synthesized along trimer would result its alcohol then coniferyl alcohol. also found to cross couple form tricin-(4′-O-β)-linked dimers...

10.1104/pp.114.253757 article EN cc-by PLANT PHYSIOLOGY 2015-02-09

Abstract Protection groups were introduced during biomass pretreatment to stabilize lignin's α,γ‐diol group its extraction and prevent condensation. Acetaldehyde propionaldehyde stabilized the without any aromatic ring alkylation, which significantly increased final product selectivity. The subsequent hydrogenolysis catalyzed by Pd/C generated lignin monomers at near‐theoretical yields based on Klason (48 % from birch, 20 spruce, 70 high‐syringyl transgenic poplar), with high selectivity a...

10.1002/anie.201710838 article EN Angewandte Chemie International Edition 2017-12-06

Lignin is the most abundant aromatic polymer from natural and renewable lignocellulosic biomass resource. Developing highly efficient catalysts for lignin depolymerization to produce valuable monophenols with high yield selectivity remains a desirable but challenging target in this field. Here, we design synergistic catalyst combining atomically dispersed Mo centers Al Lewis acid sites on MgO substrate (Mo1Al/MgO) of Eucalyptus via β-aryl ether bond cleavage. A near-theoretical monophenol...

10.1021/jacs.3c04028 article EN Journal of the American Chemical Society 2023-05-30

Lignocellulose materials are potentially valuable resources for transformation into biofuels and bioproducts. However, their complicated structures make it difficult to fractionate them cellulose, hemicelluloses, lignin, which limits utilization economical conversion value-added products. This study proposes a novel feasible fractionation method based on complete dissolution of bagasse in 1-butyl-3-methylimidazolium chloride ([C(4)mim]Cl) followed by precipitation acetone/water (9:1, v/v)...

10.1021/jf201508g article EN Journal of Agricultural and Food Chemistry 2011-07-12

Tricin [5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-4H-chromen-4-one], a flavone, was recently established as an authentic monomer in grass lignification that likely functions nucleation site. It is linked onto lignin aryl alkyl ether by radical coupling with monolignols or their acylated analogs. However, the level of tricin incorporates into remains unclear. Herein, three characterization methods: acidolysis; thioacidolysis; and derivatization followed reductive cleavage; were applied...

10.1111/tpj.13315 article EN cc-by-nc-nd The Plant Journal 2016-08-24

Lignin oxidation offers a potential sustainable pathway to oxygenated aromatic molecules. However, current methods that use real lignin tend have low selectivity and yield is limited by degradation during its extraction. We developed stoichiometric catalytic using 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) as oxidant/catalyst selectively deprotect the acetal oxidize α-OH into ketone. The oxidized was then depolymerized formic acid/sodium formate system produce monomers with 36 mol % (in...

10.1002/anie.201811630 article EN Angewandte Chemie International Edition 2019-01-02

Lignin is a phenolic heteropolymer that deposited in secondary-thickened cell walls, where it provides mechanical strength. A recent structural characterization of walls from monocot species showed the flavone tricin part native lignin polymer, hypothesized to initiate chains. In this study, we investigated consequences altered levels on structure and wall recalcitrance by profiling, nuclear magnetic resonance, saccharification assays naturally silenced maize (Zea mays) C2-Idf (inhibitor...

10.1104/pp.16.01108 article EN PLANT PHYSIOLOGY 2016-12-09

Lignin is an abundant aromatic plant cell wall polymer consisting of phenylpropanoid units in which the rings display various degrees methoxylation. Tricin [5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-4H-chromen-4-one], a flavone, was recently established as true monomer grass lignins. To elucidate incorporation pathways tricin into lignin, metabolites maize (Zea mays) were extracted from lignifying tissues and profiled using developed 'candidate substrate product pair' algorithm applied...

10.1104/pp.16.02012 article EN PLANT PHYSIOLOGY 2016-04-01

Lignin is the most abundant aromatic polymer in nature and as such an attractive source of molecules. Efficient lignin utilization will also likely play a key role economic success sustainability biomass valorization schemes. However, traditional strategies for isolation depolymerization suffer from repolymerization issues, which result low yield molecular weight fragments. This review summarizes recent progress methods that are able to limit condensation facilitate high production monomers...

10.2533/chimia.2019.591 article EN cc-by-nc CHIMIA International Journal for Chemistry 2019-08-21

10.1631/jzus.2007.b0673 article EN Journal of Zhejiang University SCIENCE B 2007-08-01

Abstract Protection groups were introduced during biomass pretreatment to stabilize lignin's α,γ‐diol group its extraction and prevent condensation. Acetaldehyde propionaldehyde stabilized the without any aromatic ring alkylation, which significantly increased final product selectivity. The subsequent hydrogenolysis catalyzed by Pd/C generated lignin monomers at near‐theoretical yields based on Klason (48 % from birch, 20 spruce, 70 high‐syringyl transgenic poplar), with high selectivity a...

10.1002/ange.201710838 article EN Angewandte Chemie 2017-12-06

Abstract Lignin is a phenylpropanoid polymer produced in the secondary cell walls of vascular plants. Although most eudicot and gymnosperm species generate lignins solely via polymerization p -hydroxycinnamyl alcohols (monolignols), grasses additionally use flavone, tricin, as natural lignin monomer to tricin-incorporated polymers walls. We previously found that disruption rice 5-HYDROXYCONIFERALDEHYDE O -METHYLTRANSFERASE ( OsCAldOMT1 ) reduced extractable tricin-type metabolites vegetative...

10.1038/s41598-019-47957-0 article EN cc-by Scientific Reports 2019-08-12
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