大麦(Hordeum vulgare L.)对低温胁迫的生理和广泛靶向代谢组学分析

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Mingzhai Yu, Zhaxi Luobu, Deqing Zhuoga, Xiaohong Wei, Yawei Tang
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引用次数: 0

摘要

大麦作为一种重要的粮食作物,在生长发育过程中经常遭受低温胁迫,对大麦的产量和品质造成重大影响。因此,深入研究大麦在低温胁迫下的代谢响应,对提高大麦的耐寒性具有重要意义。本研究采用超高效液相色谱-串联质谱法(UPLC-MS/MS)对不同低温胁迫时间下大麦叶片的代谢物进行分析,并结合生理数据进行分析。结果:低温胁迫降低了大麦叶片的Pn、Gs、Tr和SPAD,导致ROS含量增加,通过代谢组分析共鉴定出800种代谢物,分别为氨基酸及其衍生物、酚酸、核苷酸及其衍生物、黄酮类、香豆素、生物碱、有机酸和游离脂肪酸。在0 h-vs-12 h、0 h-vs-48 h、12 h-vs-48 h和0 h-vs- re24 h共鉴定出92、91、40和101个差异显著的代谢物,主要参与代谢途径、次生代谢物、abc等代谢物的生物合成。这些差异代谢物主要涉及代谢途径、次生代谢物的生物合成、ABC转运体、氨基酸的生物合成、苯丙素的生物合成、色氨酸的生物合成、类黄酮的生物合成、甘氨酸、丝氨酸和苏氨酸的代谢、组氨酸的代谢和亚油酸的代谢。其中,低温胁迫下主要上调代谢物为4-羟基苯乙酮、o -乙酰丝氨酸、Sinapoylagmatine和sinapoyl腐胺,主要下调代谢物为儿茶素没食子酸酯、D-Melezitose和表没食子儿茶素-3-没食子酸酯,差异代谢物富集程度最高的途径为甘氨酸、丝氨酸、苏氨酸代谢和亚油酸代谢。结论:通过对生理和代谢组学数据的综合分析,初步揭示了低温胁迫下大麦的代谢网络,确定了与抗寒相关的关键代谢物和代谢途径。该研究不仅为研究大麦抗寒分子机制提供了新的视角,也为大麦抗寒育种提供了重要的理论依据。未来,我们将继续研究这些关键代谢物的调控机制和代谢途径,通过基因工程和分子育种,培育出抗寒性更强的大麦新品种。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Physiological and broadly targeted metabolomic analyses of barley (Hordeum vulgare L.) in response to low-temperature stress.

Barley, as an important grain crop, often suffers from low-temperature stress during growth and development, which constitutes a significant impact on the yield and quality of barley. Therefore, an in-depth study of the metabolic response of barley under low-temperature stress is of great significance to improve the cold tolerance of barley. In this study, metabolites in barley leaves under different times of low-temperature stress were analyzed by ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), together with physiological data analysis. Result: Low-temperature stress decreased Pn, Gs, Tr, and SPAD in barley leaves, leading to an increase in ROS content, and a total of 800 metabolites were identified by metabolome analysis, belonging to amino acids and their derivatives, phenolic acids, nucleotides, and their derivatives, flavonoids, coumarins, alkaloids, organic acids, and free fatty acids. A total of 92, 91, 40, and 101 significantly different metabolites were identified at 0 h-vs-12 h, 0 h-vs-48 h, 12 h-vs-48 h, and 0 h-vs-Re24h, which were mainly involved in metabolic pathways, biosynthesis of secondary metabolites, ABCs and other metabolites. These differential metabolites were mainly involved in Metabolic pathways, Biosynthesis of secondary metabolites, ABC transporters, Biosynthesis of amino acids, Phenylpropanoid biosynthesis, Tryptophan metabolism, Flavonoid biosynthesis, Glycine, serine and threonine metabolism, Histidine metabolism, and Linoleic acid metabolism. Among them, the main up-regulated metabolites under low-temperature stress were 4-Hydroxyacetophenone, O-Acetylserine, Sinapoylagmatine, and Sinapoylputrescine, and the main down-regulated metabolites were Catechin gallate, D-Melezitose and Epigallocatechin-3-gallate, and the pathways with the highest enrichment of differential metabolites were Glycine, serine and threonine metabolism and Linoleic acid metabolism. Conclusion: Through the comprehensive analysis of physiological and metabolomic data, we initially revealed the metabolic network of barley under low-temperature stress and identified the key metabolites and metabolic pathways related to cold resistance. This study not only provides a new perspective on the molecular mechanism of cold resistance in barley but also provides an important theoretical basis for breeding barley for cold resistance. In the future, we will continue to study the regulatory mechanisms of these key metabolites and metabolic pathways, to produce new barley varieties with stronger cold resistance through genetic engineering and molecular breeding.

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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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