Abstract

BackgroundThe recalcitrance of lignocellulosic biomass provided technical and economic challenges in the current biomass conversion processes. Lignin is considered as a crucial recalcitrance component in biomass utilization. An in-depth understanding of lignin biosynthesis can provide clues to overcoming the recalcitrance. Laccases are believed to play a role in the oxidation of lignin monomers, leading to the formation of higher-order lignin. In plants, functions of only a few laccases have been evaluated, so little is known about the effect of laccases on cell wall structure and biomass saccharification.ResultsIn this study, we screened a gain-of-function mutant with a significant increase in lignin content from Arabidopsis mutant lines overexpressing a full-length poplar cDNA library. Further analysis confirmed that a Chinese white poplar (Populus tomentosa) laccase gene PtoLAC14 was inserted into the mutant, and PtoLAC14 could functionally complement the Arabidopsis lac4 mutant. Overexpression of PtoLAC14 promoted the lignification of poplar and reduced the proportion of syringyl/guaiacyl. In contrast, the CRISPR/Cas9-generated mutation of PtLAC14 results in increased the syringyl/guaiacyl ratios, which led to integrated enhancement on biomass enzymatic saccharification. Notably, the recombinant PtoLAC14 protein showed higher oxidized efficiency to coniferyl alcohol (precursor of guaiacyl unit) in vitro.ConclusionsThis study shows that PtoLAC14 plays an important role in the oxidation of guaiacyl deposition on cell wall. The reduced recalcitrance of the PtoLAC14-KO lines suggests that PtoLAC14 is an elite target for cell wall engineering, and genetic manipulation of this gene will facilitate the utilization of lignocellulose.

Highlights

  • The recalcitrance of lignocellulosic biomass provided technical and economic challenges in the current biomass conversion processes

  • Lignocellulose recalcitrance is principally determined by cell wall composition, wall polymer feature, and network among cell wall polymer [4, 5]

  • Morphological characterization of df1 mutant To identify genes involved in cell wall formation, we constructed a full-length cDNA library from various tissues in P. tomentosa and performed full-length cDNA overexpressor (FOX) gene hunting in Arabidopsis [29, 30]

Read more

Summary

Introduction

The recalcitrance of lignocellulosic biomass provided technical and economic challenges in the current biomass conversion processes. Functions of only a few laccases have been evaluated, so little is known about the effect of laccases on cell wall structure and biomass saccharification. The plant cell wall represents an enormous renewable biomass resource for biochemical, biofuels and materials production on the earth [1, 2]. For effective utilization of these carbohydrates, it is necessary to overcome the recalcitrance of cell wall. Lignocellulose recalcitrance is principally determined by cell wall composition, wall polymer feature (such as cellulose crystalline index, degree of polymerization, monomer proportions of lignin), and network among cell wall polymer [4, 5]. During the biological conversion processes, lignin does act as a physical barrier

Methods
Results
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