Overexpression of REDUCED WALL ACETYLATION C increases xylan acetylation and biomass recalcitrance in Populus

Jin Zhang, Xiaqin Wang, Hsin Tzu Wang, Zhenzhen Qiao, Tao Yao, Meng Xie, Breeanna R. Urbanowicz, Wei Zeng, Sara S. Jawdy, Lee E. Gunter, Xiaohan Yang, Olaf Czarnecki, Sharon Regan, Armand Seguin, William Rottmann, Kimberly A. Winkeler, Robert Sykes, Anna Lipzen, Chris Daum, Kerrie BarryMeng Zhu Lu, Gerald A. Tuskan, Wellington Muchero, Jin Gui Chen

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Plant lignocellulosic biomass, i.e. secondary cell walls of plants, is a vital alternative source for bioenergy. However, the acetylation of xylan in secondary cell walls impedes the conversion of biomass to biofuels. Previous studies have shown that REDUCED WALL ACETYLATION (RWA) proteins are directly involved in the acetylation of xylan but the regulatory mechanism of RWAs is not fully understood. In this study, we demonstrate that overexpression of a Populus trichocarpa PtRWA-C gene increases the level of xylan acetylation and increases the lignin content and S/G ratio, ultimately yielding poplar woody biomass with reduced saccharification efficiency. Furthermore, through gene coexpression network and expression quantitative trait loci (eQTL) analysis, we found that PtRWA-C was regulated not only by the secondary cell wall hierarchical regulatory network but also by an AP2 family transcription factor HARDY (HRD). Specifically, HRD activates PtRWA-C expression by directly binding to the PtRWA-C promoter, which is also the cis-eQTL for PtRWA-C. Taken together, our findings provide insights into the functional roles of PtRWA-C in xylan acetylation and consequently saccharification and shed light on synthetic biology approaches to manipulate this gene and alter cell wall properties. These findings have substantial implications for genetic engineering of woody species, which could be used as a sustainable source of biofuels, valuable biochemicals, and biomaterials.

Original languageEnglish
Pages (from-to)243-257
Number of pages15
JournalPlant Physiology
Volume194
Issue number1
DOIs
StatePublished - Jan 2024

Funding

J.Z. was funded by the Zhejiang Science and Technology Major Program on Agricultural New Variety Breeding (2021C02070-1) and the National Natural Science Foundation of China (32171814). M.X. was supported by the Office of Science of the U.S. Department of Energy, Office of Biological and Environmental Research, as part of the Quantitative Plant Science Initiative (QPSI) at Brookhaven National Laboratory. This research was supported by the Center for Bioenergy Innovation (CBI). CBI is supported by the Office of Biological and Environmental Research (BER) in the Office of Science of the U.S. Department of Energy. Oak Ridge National Laboratory is managed by UT-Battelle, LLC for the U.S. Department of Energy under Contract Number DE-AC05-00OR22725. The work (proposal: 10.46936/10.25585/60000710) conducted by the U.S. Department of Energy Joint Genome Institute (https:/ /ror.org/04xm1d337 ), a DOE Office of Science User Facility, is supported by the Office of Science of the U.S. Department of Energy operated under Contract No. DE-AC02-05CH11231. The activation tagging population was created through a Genome Canada grant to S.R. and A.S.

FundersFunder number
Quantitative Plant Science Initiative
U.S. Department of Energy Joint Genome Institute
Zhejiang Science and Technology Major Program on Agricultural New Variety Breeding2021C02070-1
U.S. Department of Energy
Office of ScienceDE-AC02-05CH11231
Biological and Environmental Research
Oak Ridge National LaboratoryDE-AC05-00OR22725
Center for Bioenergy Innovation
National Natural Science Foundation of China32171814

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