Abstract

BackgroundThe genetic modification of plant cell walls has been considered to reduce lignocellulose recalcitrance in bioenergy crops. As a result, it is important to develop a precise and rapid assay for the major wall polymer features that affect biomass saccharification in a large population of transgenic plants. In this study, we collected a total of 246 transgenic rice plants that, respectively, over-expressed and RNAi silenced 12 genes of the OsGH9 and OsGH10 family that are closely associated with cellulose and hemicellulose modification. We examined the wall polymer features and biomass saccharification among 246 transgenic plants and one wild-type plant. The samples presented a normal distribution applicable for statistical analysis and NIRS modeling.ResultsAmong the 246 transgenic rice plants, we determined largely varied wall polymer features and the biomass enzymatic saccharification after alkali pretreatment in rice straws, particularly for the fermentable hexoses, ranging from 52.8 to 95.9%. Correlation analysis indicated that crystalline cellulose and lignin levels negatively affected the hexose and total sugar yields released from pretreatment and enzymatic hydrolysis in the transgenic rice plants, whereas the arabinose levels and arabinose substitution degree (reverse xylose/arabinose ratio) exhibited positive impacts on the hexose and total sugars yields. Notably, near-infrared spectroscopy (NIRS) was applied to obtain ten equations for predicting biomass enzymatic saccharification and seven equations for distinguishing major wall polymer features. Most of the equations exhibited high R2/R2cv/R2ev and RPD values for a perfect prediction capacity.ConclusionsDue to large generated populations of transgenic rice lines, this study has not only examined the key wall polymer features that distinctively affect biomass enzymatic saccharification in rice but has also established optimal NIRS models for a rapid and precise screening of major wall polymer features and lignocellulose saccharification in biomass samples. Importantly, this study has briefly explored the potential roles of a total of 12 OsGH9 and OsGH10 genes in cellulose and hemicellulose modification and cell wall remodeling in transgenic rice lines. Hence, it provides a strategy for genetic modification of plant cell walls by expressing the desired OsGH9 and OsGH10 genes that could greatly improve biomass enzymatic digestibility in rice.

Highlights

  • The genetic modification of plant cell walls has been considered to reduce lignocellulose recalcitrance in bioenergy crops

  • Our study provides a strategy for the genetic modification of plant cell walls by over-expressing or RNAi knockingdown OsGH9 and OsGH10 genes and demonstrated a precise and rapid near-infrared spectroscopy (NIRS) assay, which may be applicable for large-scale screening of target traits in bioenergy crops and beyond

  • A total of 246 transgenic rice plants were selected by overexpressing and RNAi silencing 12 representative genes for cellulose and hemicellulose modification from the OsGH9 and OsGH10 families

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Summary

Introduction

The genetic modification of plant cell walls has been considered to reduce lignocellulose recalcitrance in bioenergy crops. It is important to develop a precise and rapid assay for the major wall polymer features that affect biomass saccharification in a large population of transgenic plants. We examined the wall polymer features and biomass saccharification among 246 transgenic plants and one wild-type plant. The genetic modification of plant cell walls has been proposed as a promising solution by selecting transgenic plants that over-express the key genes associated with cell wall biosynthesis and modification [4, 5]. It becomes essential to distinguish, among the transgenic plants, the major wall polymer features that basically determine biomass enzymatic saccharification

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