豆科植物结节中叶酸的生物合成得到促进

IF 6 1区 生物学 Q1 PLANT SCIENCES
Sara M Garza-Aguilar, Perla A Ramos-Parra, Rafael Urrea-López, Wendy J Berdeja-Zamudio, Josefina Lozano-Guajardo, Jorge Benavides-Lozano, Mario Ramírez-Yáñez, Rocío I Díaz de la Garza
{"title":"豆科植物结节中叶酸的生物合成得到促进","authors":"Sara M Garza-Aguilar, Perla A Ramos-Parra, Rafael Urrea-López, Wendy J Berdeja-Zamudio, Josefina Lozano-Guajardo, Jorge Benavides-Lozano, Mario Ramírez-Yáñez, Rocío I Díaz de la Garza","doi":"10.1111/pce.15294","DOIUrl":null,"url":null,"abstract":"<p><p>Symbiotic nitrogen fixation (SNF) profoundly alters plant and bacteroid metabolism; however, SNF impact on folates and one-carbon (1C) metabolism are unknown. To explore this, SNF was induced in Phaseolus Vulgaris with Rhizobium etli. Nodules accumulated the highest folate concentration yet reported in a plant tissue (60 nmol/g fresh weight). Folate upregulation was not exclusive of determinate nodules, moderate to high folate contents were also encounter in Medicago truncatula and sativa. Moreover, folates correlated partial and positively with N<sub>2</sub>-fixation. 1C metabolism-associated amino acids (Ser, Gly, Cys, Thr, and Met) accumulated more in nodules than roots. Subcellular profiling of nodule folates revealed that the cytosol fraction primarily contained 5-methyl-tetrahydrofolate, cofactor for Met synthesis. 10-formyl-tetrahydrofolate, required for purine synthesis, was most abundant in nodule plastids, while bacteroids contained low folate levels. Differential transcriptome analysis from nodule legume studies revealed that only a few biosynthetic folate genes expression was increased in nodules whereas several genes for 1C reactions were upregulated. For the first time folates were detected in the xylem sap, with higher concentrations during SNF. We postulate that folates are needed during SNF to sustain purines, thymidylate, and Met synthesis, during both N<sub>2</sub>-fixation and nodule growth; nodule metabolism is then a 1C-unit sink.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.0000,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Folate Biosynthesis is Boosted in Legume Nodules.\",\"authors\":\"Sara M Garza-Aguilar, Perla A Ramos-Parra, Rafael Urrea-López, Wendy J Berdeja-Zamudio, Josefina Lozano-Guajardo, Jorge Benavides-Lozano, Mario Ramírez-Yáñez, Rocío I Díaz de la Garza\",\"doi\":\"10.1111/pce.15294\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Symbiotic nitrogen fixation (SNF) profoundly alters plant and bacteroid metabolism; however, SNF impact on folates and one-carbon (1C) metabolism are unknown. To explore this, SNF was induced in Phaseolus Vulgaris with Rhizobium etli. Nodules accumulated the highest folate concentration yet reported in a plant tissue (60 nmol/g fresh weight). Folate upregulation was not exclusive of determinate nodules, moderate to high folate contents were also encounter in Medicago truncatula and sativa. Moreover, folates correlated partial and positively with N<sub>2</sub>-fixation. 1C metabolism-associated amino acids (Ser, Gly, Cys, Thr, and Met) accumulated more in nodules than roots. Subcellular profiling of nodule folates revealed that the cytosol fraction primarily contained 5-methyl-tetrahydrofolate, cofactor for Met synthesis. 10-formyl-tetrahydrofolate, required for purine synthesis, was most abundant in nodule plastids, while bacteroids contained low folate levels. Differential transcriptome analysis from nodule legume studies revealed that only a few biosynthetic folate genes expression was increased in nodules whereas several genes for 1C reactions were upregulated. For the first time folates were detected in the xylem sap, with higher concentrations during SNF. We postulate that folates are needed during SNF to sustain purines, thymidylate, and Met synthesis, during both N<sub>2</sub>-fixation and nodule growth; nodule metabolism is then a 1C-unit sink.</p>\",\"PeriodicalId\":222,\"journal\":{\"name\":\"Plant, Cell & Environment\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":6.0000,\"publicationDate\":\"2024-11-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant, Cell & Environment\",\"FirstCategoryId\":\"2\",\"ListUrlMain\":\"https://doi.org/10.1111/pce.15294\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant, Cell & Environment","FirstCategoryId":"2","ListUrlMain":"https://doi.org/10.1111/pce.15294","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

共生固氮(SNF)会极大地改变植物和细菌的新陈代谢;然而,SNF 对叶酸和一碳(1C)代谢的影响尚不清楚。为了探究这一问题,我们用根瘤菌诱导了普通相思豆(Phaseolus Vulgaris)的SNF。结节中积累的叶酸浓度是迄今所报道的植物组织中最高的(60 nmol/g鲜重)。叶酸的上调并不局限于决定性球茎,在Medicago truncatula和sativa中也发现了中等到较高的叶酸含量。此外,叶酸与 N2 固定量部分正相关。1C 代谢相关氨基酸(Ser、Gly、Cys、Thr 和 Met)在结核中的积累多于根。对结核叶酸的亚细胞分析表明,细胞质部分主要含有 5-甲基-四氢叶酸,这是合成 Met 的辅助因子。嘌呤合成所需的 10-甲酰基四氢叶酸在结核质粒中含量最高,而菌体中叶酸含量较低。对豆科植物结核研究的差异转录组分析表明,只有少数生物合成叶酸的基因在结核中表达增加,而几个 1C 反应的基因则上调。我们首次在木质部汁液中检测到叶酸盐,SNF 期间叶酸盐浓度更高。我们推测,在氮固定和结核生长过程中,需要叶酸盐来维持嘌呤、胸腺嘧啶酸和金属元素的合成;因此,结核代谢是一个 1C 单位汇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Folate Biosynthesis is Boosted in Legume Nodules.

Symbiotic nitrogen fixation (SNF) profoundly alters plant and bacteroid metabolism; however, SNF impact on folates and one-carbon (1C) metabolism are unknown. To explore this, SNF was induced in Phaseolus Vulgaris with Rhizobium etli. Nodules accumulated the highest folate concentration yet reported in a plant tissue (60 nmol/g fresh weight). Folate upregulation was not exclusive of determinate nodules, moderate to high folate contents were also encounter in Medicago truncatula and sativa. Moreover, folates correlated partial and positively with N2-fixation. 1C metabolism-associated amino acids (Ser, Gly, Cys, Thr, and Met) accumulated more in nodules than roots. Subcellular profiling of nodule folates revealed that the cytosol fraction primarily contained 5-methyl-tetrahydrofolate, cofactor for Met synthesis. 10-formyl-tetrahydrofolate, required for purine synthesis, was most abundant in nodule plastids, while bacteroids contained low folate levels. Differential transcriptome analysis from nodule legume studies revealed that only a few biosynthetic folate genes expression was increased in nodules whereas several genes for 1C reactions were upregulated. For the first time folates were detected in the xylem sap, with higher concentrations during SNF. We postulate that folates are needed during SNF to sustain purines, thymidylate, and Met synthesis, during both N2-fixation and nodule growth; nodule metabolism is then a 1C-unit sink.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Plant, Cell & Environment
Plant, Cell & Environment 生物-植物科学
CiteScore
13.30
自引率
4.10%
发文量
253
审稿时长
1.8 months
期刊介绍: Plant, Cell & Environment is a premier plant science journal, offering valuable insights into plant responses to their environment. Committed to publishing high-quality theoretical and experimental research, the journal covers a broad spectrum of factors, spanning from molecular to community levels. Researchers exploring various aspects of plant biology, physiology, and ecology contribute to the journal's comprehensive understanding of plant-environment interactions.
×
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:481959085
Book学术官方微信