Disruption of aldehyde dehydrogenase decreases cell wall‐bound p‐hydroxycinnamates and improves cell wall digestibility in rice

细胞壁 木质素 阿魏酸 生物化学 化学 细胞 次生细胞壁 醛脱氢酶 突变体 纤维素 阿拉伯木聚糖 基因 有机化学
作者
Senri Yamamoto,Osama Ahmed Afifi,Pui Ying Lam,Yuri Takeda,Yuriko Osakabe,Keishi Osakabe,Laura Bartley,Toshiaki Umezawa,Yuki Tobimatsu
出处
期刊:Plant Journal [Wiley]
卷期号:120 (6): 2828-2845 被引量:6
标识
DOI:10.1111/tpj.17148
摘要

SUMMARY In grass cell walls, ferulic acid (FA) serves as an important cross‐linker between cell wall polymers, such as arabinoxylan (AX) and lignin, affecting the physicochemical properties of the cell walls as well as the utilization properties of grass lignocellulose for biorefinering. Here, we demonstrate that hydroxycinnamaldehyde dehydrogenase (HCALDH) plays a crucial role in the biosynthesis of the FA used for cell wall feruloylation in rice ( Oryza sativa ). Bioinformatic and gene expression analyses of aldehyde dehydrogenases (ALDHs) identified two rice ALDH subfamily 2C members, OsHCALDH2 (OsALDH2C2) and OsHCALDH3 (OsALDH2C3), potentially involved in cell wall feruloylation in major vegetative tissues of rice. CRISPR‐Cas9 genome editing of OsHCALDH2 and OsHCALDH3 revealed that the contents of AX‐bound ferulate were reduced by up to ~45% in the cell walls of the HCALDH ‐edited mutants, demonstrating their roles in cell wall feruloylation. The abundance of hemicellulosic sugars including arabinosyl units on AX was notably reduced in the cell walls of the HCALDH ‐edited mutants, whereas cellulose and lignin contents remained unaffected. In addition to reducing cell wall‐bound ferulate, the loss of OsHCALDH2 and/or OsHCALDH3 also partially reduced cell wall‐bound p ‐coumarate and sinapate in the vegetative tissues of rice, whereas it did not cause detectable changes in the amount of γ‐oryzanol (feruloyl sterols) in rice seeds. Furthermore, the HCALDH ‐edited mutants exhibited improved cell wall saccharification efficiency, both with and without alkaline pretreatment, plausibly due to the reduction in cell wall cross‐linking FA. Overall, HCALDH appears to present a potent bioengineering target for enhancing utilization properties of grass lignocellulose.
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