Dual stress (waterlogging and salinity) resilience in Arabidopsis thaliana conferred by overexpression of a putative daylily (Hemerocallis spp.) betaine aldehyde dehydrogenase gene.

IF 2.2 3区 生物学 Q2 PLANT SCIENCES
Journal of Plant Research Pub Date : 2026-03-01 Epub Date: 2026-02-13 DOI:10.1007/s10265-026-01692-6
Meiqing Pan, Anqi Zhao, Min Fan, Xiang Liu, Yanpeng Wang, Qiaoping Qin, Dongmei Yin, Di-An Ni
{"title":"Dual stress (waterlogging and salinity) resilience in Arabidopsis thaliana conferred by overexpression of a putative daylily (Hemerocallis spp.) betaine aldehyde dehydrogenase gene.","authors":"Meiqing Pan, Anqi Zhao, Min Fan, Xiang Liu, Yanpeng Wang, Qiaoping Qin, Dongmei Yin, Di-An Ni","doi":"10.1007/s10265-026-01692-6","DOIUrl":null,"url":null,"abstract":"<p><p>Glycine betaine (GB), a key osmoprotectant in plants, alleviates abiotic stress through osmotic adjustment and reactive oxygen species (ROS) scavenging. Although betaine aldehyde dehydrogenase (BADH) catalyzes GB biosynthesis and enhances salinity tolerance in crops such as rice and maize, its role in waterlogging adaptation remains unclear. A putative BADH gene, HfBADH1, was cloned from waterlogging-treated daylily (Hemerocallis spp.) 'Autumn Red'. HfBADH1 expression increased 6.8-fold under waterlogging and 8.9-fold under salinity. Notably, HfBADH1 expression was repressed by abscisic acid (ABA), in contrast with typical stress-responsive genes. In addition, the activities of BADH and aldehyde dehydrogenase (ALDH) correlated with waterlogging tolerance among different daylily cultivars. Overexpression of HfBADH1 in Arabidopsis thaliana under the CaMV35S promoter resulted in 2.4-fold higher BADH activity and twofold higher ALDH activity than in wild-type plants. The transgenic lines exhibited enhanced tolerance to both salinity and waterlogging. Stress responses were evaluated by antioxidant and anaerobic respiration enzyme activities, and physiological indices including malondialdehyde (MDA) levels and chlorophyll content. The observed stress tolerance in transgenic A.thaliana suggested that BADH overexpression helps stabilize cellular structures and scavenges ROS. The increase in ALDH activity indicated that HfBADH1 overexpression may facilitate aldehyde oxidation, supporting adaptation to hypoxic conditions induced by waterlogging. This study is the first to link BADH overexpression to dual stress resilience, highlighting its combined enzymatic roles in GB biosynthesis and aldehyde detoxification. The ABA-independent regulatory pattern provides insight into noncanonical stress adaptation and suggests new strategies for engineering crops tolerant to saline and flood-prone environments.</p>","PeriodicalId":16813,"journal":{"name":"Journal of Plant Research","volume":" ","pages":"267-281"},"PeriodicalIF":2.2000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Plant Research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s10265-026-01692-6","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/13 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Glycine betaine (GB), a key osmoprotectant in plants, alleviates abiotic stress through osmotic adjustment and reactive oxygen species (ROS) scavenging. Although betaine aldehyde dehydrogenase (BADH) catalyzes GB biosynthesis and enhances salinity tolerance in crops such as rice and maize, its role in waterlogging adaptation remains unclear. A putative BADH gene, HfBADH1, was cloned from waterlogging-treated daylily (Hemerocallis spp.) 'Autumn Red'. HfBADH1 expression increased 6.8-fold under waterlogging and 8.9-fold under salinity. Notably, HfBADH1 expression was repressed by abscisic acid (ABA), in contrast with typical stress-responsive genes. In addition, the activities of BADH and aldehyde dehydrogenase (ALDH) correlated with waterlogging tolerance among different daylily cultivars. Overexpression of HfBADH1 in Arabidopsis thaliana under the CaMV35S promoter resulted in 2.4-fold higher BADH activity and twofold higher ALDH activity than in wild-type plants. The transgenic lines exhibited enhanced tolerance to both salinity and waterlogging. Stress responses were evaluated by antioxidant and anaerobic respiration enzyme activities, and physiological indices including malondialdehyde (MDA) levels and chlorophyll content. The observed stress tolerance in transgenic A.thaliana suggested that BADH overexpression helps stabilize cellular structures and scavenges ROS. The increase in ALDH activity indicated that HfBADH1 overexpression may facilitate aldehyde oxidation, supporting adaptation to hypoxic conditions induced by waterlogging. This study is the first to link BADH overexpression to dual stress resilience, highlighting its combined enzymatic roles in GB biosynthesis and aldehyde detoxification. The ABA-independent regulatory pattern provides insight into noncanonical stress adaptation and suggests new strategies for engineering crops tolerant to saline and flood-prone environments.

甜菜碱醛脱氢酶基因的过度表达对拟南芥(拟南芥)双重胁迫(涝渍和盐度)抗性的影响。
甜菜碱(Glycine betaine, GB)是植物体内重要的渗透保护剂,通过渗透调节和清除活性氧(reactive oxygen species, ROS)来缓解非生物胁迫。虽然甜菜碱醛脱氢酶(BADH)在水稻和玉米等作物中催化GB生物合成并增强耐盐性,但其在涝渍适应中的作用尚不清楚。从经涝渍处理的黄花菜“秋红”中克隆出一个推测的BADH基因HfBADH1。涝渍处理下HfBADH1表达量增加6.8倍,盐度处理下增加8.9倍。值得注意的是,与典型的应激反应基因相比,HfBADH1的表达被脱落酸(ABA)抑制。此外,不同黄花菜品种BADH和醛脱氢酶(ALDH)活性与耐涝性相关。CaMV35S启动子下的HfBADH1在拟南芥中过表达,导致BADH活性比野生型高2.4倍,ALDH活性高2倍。转基因品系对盐渍和涝渍的耐受性均有增强。通过测定抗氧化酶和厌氧呼吸酶活性以及丙二醛(MDA)水平和叶绿素含量等生理指标来评价胁迫反应。转基因拟蓝藻的抗逆性表明,BADH过表达有助于稳定细胞结构和清除ROS。ALDH活性的增加表明HfBADH1过表达可能促进醛氧化,支持对内涝引起的缺氧条件的适应。这项研究首次将BADH过表达与双重应激恢复联系起来,强调了其在GB生物合成和醛解毒中的联合酶作用。aba独立的调控模式提供了对非规范胁迫适应的见解,并为工程作物耐盐和易涝环境提供了新的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Plant Research
Journal of Plant Research 生物-植物科学
CiteScore
5.40
自引率
3.60%
发文量
59
审稿时长
1 months
期刊介绍: The Journal of Plant Research is an international publication that gathers and disseminates fundamental knowledge in all areas of plant sciences. Coverage extends to every corner of the field, including such topics as evolutionary biology, phylogeography, phylogeny, taxonomy, genetics, ecology, morphology, physiology, developmental biology, cell biology, molecular biology, biochemistry, biophysics, bioinformatics, and systems biology. The journal presents full-length research articles that describe original and fundamental findings of significance that contribute to understanding of plants, as well as shorter communications reporting significant new findings, technical notes on new methodology, and invited review articles.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书