• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

揭示阿月浑子无性系杂种的耐旱策略:渗透调节的作用

Revealing drought tolerance strategies in pistachio clonal hybrids: role of osmotic adjustment.

作者信息

Osku Mozhdeh, Roozban Mahmoud Reza, Sarikhani Saadat, Arab Mohammad Mehdi, Akbari Mohammad, Vahdati Kourosh

机构信息

Department of Horticulture, Faculty of Agricultural Technology (Aburaihan), University of Tehran, Tehran, Iran.

School of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

出版信息

BMC Plant Biol. 2025 May 2;25(1):580. doi: 10.1186/s12870-025-06583-x.

DOI:10.1186/s12870-025-06583-x
PMID:40316914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12049070/
Abstract

BACKGROUND

Pistachio (Pistacia vera L.) growth, yield and quality are affected by abiotic stress especially drought. Understanding the strategies that improve dehydration tolerance is essential for developing resistant pistachio rootstocks. In the experiment, nine-month-old saplings of seven clonal interspecies hybrids of Pistacia atlantica × P. integerrima (C1, C2, C16-1, C8-3, C4-2, C9-4 and UCB1) were assessed for growth and physiological responses to water withholding and recovery.

RESULT

Water deficit negatively impacted growth parameters, including shoot dry weight, root dry weight and leaf area, in all hybrids; however, the C1 demonstrated relatively minor reductions compared to the other hybrids. Glycine betaine content in leaves increased by 49.4% in C9-4 and 47% in C1, while only 7% and 11% increases were found in the most sensitive clones, C8-3 and C4-2. Notably, C9-4, identified as the most tolerant clone, displayed the highest proline levels, with increases of 29.5% in leaves and 41.5% in roots, in contrast to C8-3, which showed minimal increases of 6% and 11% in leaves and roots, respectively. Clones with higher compatible solutes maintained higher relative water content (RWC), lower osmotic potential and smaller reductions in leaf water potential. RWC declined by just 6% in C9-4, whereas it dropped by 88% in C8-3. Osmotic potentials in C9-4 were - 1.61 MPa in leaves and - 0.271 MPa in roots, while in C8-3, they were - 0.93 MPa and - 0.11 MPa in leaves and roots, respectively. Following recovery, evaluations of growth, physiological traits and visual observations indicated that C8-3 had poor recovery ability. Heatmap and PCA analyses categorized the clones into three groups: "tolerant" (C9-4, C1 and C2), "moderately tolerant" (UCB1) and "sensitive" (C8-3, C4-2 and C16-1).

CONCLUSION

The results of this study underscore the significance of osmotic adjustment as a more critical trait compared to growth and stomatal parameters in effectively differentiating tolerant clones from sensitive ones.

摘要

背景

阿月浑子(黄连木)的生长、产量和品质受到非生物胁迫尤其是干旱的影响。了解提高脱水耐受性的策略对于培育抗性阿月浑子砧木至关重要。在该实验中,对大西洋黄连木×全缘黄连木的7个克隆种间杂种(C1、C2、C16 - 1、C8 - 3、C4 - 2、C9 - 4和UCB1)的9月龄幼树进行了水分胁迫和恢复处理后的生长及生理响应评估。

结果

水分亏缺对所有杂种的生长参数均产生负面影响,包括地上部干重、根部干重和叶面积;然而,与其他杂种相比,C1的降幅相对较小。C9 - 4叶片中的甘氨酸甜菜碱含量增加了49.4%,C1增加了47%,而最敏感的克隆C8 - 3和C4 - 2仅分别增加了7%和11%。值得注意的是,被鉴定为最耐受的克隆C9 - 4脯氨酸水平最高,叶片中增加了29.5%,根部增加了41.5%,相比之下,C8 - 3叶片和根部的增幅最小,分别仅为6%和11%。具有较高相容性溶质的克隆保持了较高的相对含水量(RWC)、较低的渗透势以及较小的叶片水势降幅。C9 - 4的RWC仅下降了6%,而C8 - 3下降了88%。C9 - 4叶片的渗透势为 - 1.61MPa,根部为 - 0.271MPa,而C8 - 3叶片和根部的渗透势分别为 - 0.93MPa和 - 0.11MPa。恢复处理后,对生长、生理特性的评估以及外观观察表明,C8 - 3的恢复能力较差。热图和主成分分析将这些克隆分为三组:“耐受型”(C9 - 4、C1和C2)、“中度耐受型”(UCB1)和“敏感型”(C8 - 3、C4 - 2和C16 - 1)。

结论

本研究结果强调了渗透调节作为一个比生长和气孔参数更关键的性状在有效区分耐受型克隆和敏感型克隆方面的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/a26f6b762eef/12870_2025_6583_Fig17_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/801ce0a2b321/12870_2025_6583_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/b9a2d90fe83f/12870_2025_6583_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/99abeac86ae4/12870_2025_6583_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/bbeeea31c2fe/12870_2025_6583_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/d6bba844c5ef/12870_2025_6583_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/6006906a9015/12870_2025_6583_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/ce54c4fa4560/12870_2025_6583_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/0874b74af206/12870_2025_6583_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/2b943f05d37a/12870_2025_6583_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/8cdfeb857b68/12870_2025_6583_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/b6f68bb4f777/12870_2025_6583_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/2e178e9f8389/12870_2025_6583_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/55afc631badc/12870_2025_6583_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/f6ed2895b445/12870_2025_6583_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/6e22051438fc/12870_2025_6583_Fig15_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/ee159b8744bc/12870_2025_6583_Fig16_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/a26f6b762eef/12870_2025_6583_Fig17_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/801ce0a2b321/12870_2025_6583_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/b9a2d90fe83f/12870_2025_6583_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/99abeac86ae4/12870_2025_6583_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/bbeeea31c2fe/12870_2025_6583_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/d6bba844c5ef/12870_2025_6583_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/6006906a9015/12870_2025_6583_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/ce54c4fa4560/12870_2025_6583_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/0874b74af206/12870_2025_6583_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/2b943f05d37a/12870_2025_6583_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/8cdfeb857b68/12870_2025_6583_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/b6f68bb4f777/12870_2025_6583_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/2e178e9f8389/12870_2025_6583_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/55afc631badc/12870_2025_6583_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/f6ed2895b445/12870_2025_6583_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/6e22051438fc/12870_2025_6583_Fig15_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/ee159b8744bc/12870_2025_6583_Fig16_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65e/12049070/a26f6b762eef/12870_2025_6583_Fig17_HTML.jpg

相似文献

1
Revealing drought tolerance strategies in pistachio clonal hybrids: role of osmotic adjustment.揭示阿月浑子无性系杂种的耐旱策略:渗透调节的作用
BMC Plant Biol. 2025 May 2;25(1):580. doi: 10.1186/s12870-025-06583-x.
2
Tolerance of Mycorrhiza infected pistachio (Pistacia vera L.) seedling to drought stress under glasshouse conditions.温室条件下菌根感染的巴旦木(Pistacia vera L.)幼苗对干旱胁迫的耐受性。
J Plant Physiol. 2012 May 1;169(7):704-9. doi: 10.1016/j.jplph.2012.01.014. Epub 2012 Mar 13.
3
Ion homeostasis, osmoregulation, and physiological changes in the roots and leaves of pistachio rootstocks in response to salinity.阿月浑子砧木根和叶中离子稳态、渗透调节及响应盐分的生理变化
Protoplasma. 2018 Sep;255(5):1349-1362. doi: 10.1007/s00709-018-1235-z. Epub 2018 Mar 12.
4
How does drought tolerance compare between two improved hybrids of balsam poplar and an unimproved native species?两个改良的银白杨杂种与一个未改良的本地种之间的耐旱性有何不同?
Tree Physiol. 2011 Mar;31(3):240-9. doi: 10.1093/treephys/tpr011. Epub 2011 Mar 28.
5
Foliar application of glycinebetaine regulates soluble sugars and modulates physiological adaptations in sweet potato (Ipomoea batatas) under water deficit.叶面喷施甜菜碱调节甘薯(Ipomoea batatas)水分亏缺下的可溶性糖并调节生理适应性。
Protoplasma. 2020 Jan;257(1):197-211. doi: 10.1007/s00709-019-01429-4. Epub 2019 Aug 12.
6
Physiological, biochemical and molecular responses in four Prunus rootstocks submitted to drought stress.四种桃砧木在干旱胁迫下的生理、生化和分子响应。
Tree Physiol. 2013 Oct;33(10):1061-75. doi: 10.1093/treephys/tpt074. Epub 2013 Oct 25.
7
Identification and development of drought-tolerant cocoa hybrids: physiological insights for enhanced water use efficiency under water stress conditions.耐旱可可杂交种的鉴定与培育:水分胁迫条件下提高水分利用效率的生理学见解
BMC Plant Biol. 2025 Apr 21;25(1):501. doi: 10.1186/s12870-025-06448-3.
8
Clonal differences in ecophysiological responses to imposed drought in selected Eucalyptus grandis × E. urophylla hybrids.在选定的巨桉×尾叶桉杂交种中,对人工施加干旱的生态生理响应的克隆差异。
Tree Physiol. 2025 Jan 25;45(1). doi: 10.1093/treephys/tpae160.
9
Osmotic regulation in leaves and roots of olive trees during a water deficit and rewatering.水分亏缺和复水期间橄榄树叶片和根系的渗透调节
Tree Physiol. 2006 Feb;26(2):179-85. doi: 10.1093/treephys/26.2.179.
10
Seasonal changes of whole root system conductance by a drought-tolerant grape root system.耐旱葡萄根系对整个根系传导性的季节性变化。
J Exp Bot. 2011 Jan;62(1):99-109. doi: 10.1093/jxb/erq247. Epub 2010 Sep 17.

引用本文的文献

1
Improved root architecture and seedling performance in pistachio (Pistacia vera L.) via radicle-tip excision.通过胚根尖端切除改善阿月浑子(Pistacia vera L.)的根系结构和幼苗性能。
BMC Plant Biol. 2025 Aug 2;25(1):1020. doi: 10.1186/s12870-025-07069-6.

本文引用的文献

1
Cadmium transport characteristics in the phloem of sweet potato.甘薯韧皮部中镉的运输特性
Plant Physiol Biochem. 2025 Jul;224:109932. doi: 10.1016/j.plaphy.2025.109932. Epub 2025 Apr 16.
2
Glycine betaine enhances tolerance of low temperature combined with low light in pepper (Capsicum annuum L.) by improving the antioxidant capacity and regulating GB metabolism.甜菜碱通过提高抗氧化能力和调节甜菜碱代谢增强辣椒对低温弱光的耐受性。
Plant Physiol Biochem. 2025 May;222:109705. doi: 10.1016/j.plaphy.2025.109705. Epub 2025 Feb 24.
3
Rootstocks affect the vulnerability to embolism and pit membrane thickness in Citrus scions.
砧木影响柑橘接穗中栓塞的脆弱性和纹孔膜厚度。
Plant Cell Environ. 2024 Aug;47(8):3063-3075. doi: 10.1111/pce.14924. Epub 2024 Apr 25.
4
Update on stomata development and action under abiotic stress.非生物胁迫下气孔发育与功能的研究进展
Front Plant Sci. 2023 Oct 2;14:1270180. doi: 10.3389/fpls.2023.1270180. eCollection 2023.
5
Drought responsiveness in six wheat genotypes: identification of stress resistance indicators.六种小麦基因型的干旱响应:抗逆指标的鉴定
Front Plant Sci. 2023 Sep 13;14:1232583. doi: 10.3389/fpls.2023.1232583. eCollection 2023.
6
Natural variation in photosynthesis and water use efficiency of locally adapted Persian walnut populations under drought stress and recovery.在干旱胁迫和恢复条件下,适应本地环境的波斯核桃群体光合作用和水分利用效率的自然变异。
Plant Physiol Biochem. 2023 Aug;201:107859. doi: 10.1016/j.plaphy.2023.107859. Epub 2023 Jun 29.
7
Modeling the response of Japanese quail to arginine intake.模拟日本鹌鹑对精氨酸摄入的反应。
PeerJ. 2022 Dec 21;10:e14337. doi: 10.7717/peerj.14337. eCollection 2022.
8
Metabolic adjustment and regulation of gene expression are essential for increased resistance to severe water deficit and resilience post-stress in soybean.代谢调节和基因表达调控对于提高大豆对严重水分亏缺的抗性和应激后恢复能力至关重要。
PeerJ. 2022 Mar 18;10:e13118. doi: 10.7717/peerj.13118. eCollection 2022.
9
Genome Wide Association Study Uncovers the QTLome for Osmotic Adjustment and Related Drought Adaptive Traits in Durum Wheat.全基因组关联研究揭示了硬粒小麦渗透调节和相关耐旱适应性状的 QTLome。
Genes (Basel). 2022 Feb 2;13(2):293. doi: 10.3390/genes13020293.
10
Author Correction: Comparison of cognitive performance between patients with Parkinson's disease and dystonia using an intraoperative recognition memory test.作者更正:使用术中识别记忆测试比较帕金森病患者和肌张力障碍患者的认知表现。
Sci Rep. 2021 Dec 27;11(1):24525. doi: 10.1038/s41598-021-04332-2.