Abstract

BackgroundThe development of bioenergy crops with reduced recalcitrance to enzymatic degradation represents an important challenge to enable the sustainable production of advanced biofuels and bioproducts. Biomass recalcitrance is partly attributed to the complex structure of plant cell walls inside which cellulose microfibrils are protected by a network of hemicellulosic xylan chains that crosslink with each other or with lignin via ferulate (FA) bridges. Overexpression of the rice acyltransferase OsAT10 is an effective bioengineering strategy to lower the amount of FA involved in the formation of cell wall crosslinks and thereby reduce cell wall recalcitrance. The annual crop sorghum represents an attractive feedstock for bioenergy purposes considering its high biomass yields and low input requirements. Although we previously validated the OsAT10 engineering approach in the perennial bioenergy crop switchgrass, the effect of OsAT10 expression on biomass composition and digestibility in sorghum remains to be explored.ResultsWe obtained eight independent sorghum (Sorghum bicolor (L.) Moench) transgenic lines with a single copy of a construct designed for OsAT10 expression. Consistent with the proposed role of OsAT10 in acylating arabinosyl residues on xylan with p-coumarate (pCA), a higher amount of p-coumaroyl-arabinose was released from the cell walls of these lines upon hydrolysis with trifluoroacetic acid. However, no major changes were observed regarding the total amount of pCA or FA esters released from cell walls upon mild alkaline hydrolysis. Certain diferulate (diFA) isomers identified in alkaline hydrolysates were increased in some transgenic lines. The amount of the main cell wall monosaccharides glucose, xylose, and arabinose was unaffected. The transgenic lines showed reduced lignin content and their biomass released higher yields of sugars after ionic liquid pretreatment followed by enzymatic saccharification.ConclusionsExpression of OsAT10 in sorghum leads to an increase of xylan-bound pCA without reducing the overall content of cell wall FA esters. Nevertheless, the amount of total cell wall pCA remains unchanged indicating that most pCA is ester-linked to lignin. Unlike other engineered plants overexpressing OsAT10 or a phylogenetically related acyltransferase with similar putative function, the improvements of biomass saccharification efficiency in sorghum OsAT10 lines are likely the result of lignin reductions rather than reductions of cell wall-bound FA. These results also suggest a relationship between xylan-bound pCA and lignification in cell walls.

Highlights

  • The development of bioenergy crops with reduced recalcitrance to enzymatic degradation represents an important challenge to enable the sustainable production of advanced biofuels and bioproducts

  • Generation of sorghum pSbUbi:AT10 lines expressing OsAT10 A construct consisting of an OsAT10 open reading frame codon-optimized for expression in sorghum and placed downstream of the promoter of a sorghum polyubiquitin gene was built for Agrobacterium-mediated sorghum transformation (Fig. 2a)

  • Measurements of growth parameters including the number of days to panicle emergence, number of flowering tillers, height of the main tiller, stover dry weight, and estimated seeds dry weight did not reveal any consistent differences between wild type and the transgenic lines, showing that OsAT10 expression has little impact on development in plants grown under controlled conditions (Additional file 1: Table S1)

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Summary

Introduction

The development of bioenergy crops with reduced recalcitrance to enzymatic degradation represents an important challenge to enable the sustainable production of advanced biofuels and bioproducts. Feruloyl-arabinose (FA-Ara) residues are typically more frequent than coumaroyl-arabinose (pCA-Ara) residues, and substitution patterns vary depending on grass species and plant organs [7, 8]. These grass-specific FA and pCA esters have been implicated in GAX crosslinks that reinforce cell walls [9]. PCA is predominantly found ester-linked to lignin in grass cell walls, and it may assist lignin formation by providing a transfer mechanism to optimize the radical coupling of monolignols [15, 16]

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