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替代碳源用于异戊二烯排放。

Alternative Carbon Sources for Isoprene Emission.

机构信息

Laboratory of Plant Physiology and Biochemistry, National Institute for Amazonian Research (INPA), Manaus, AM 69011-970, Brazil; University of Amazonas State, Manaus, AM 69050-010, Brazil.

Department of Crop Science and Plant Biology, Estonian University of Life Sciences, Tartu 51006, Estonia; Estonian Academy of Sciences, 10130 Tallinn, Estonia.

出版信息

Trends Plant Sci. 2018 Dec;23(12):1081-1101. doi: 10.1016/j.tplants.2018.09.012. Epub 2018 Oct 25.

DOI:10.1016/j.tplants.2018.09.012
PMID:30472998
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6354897/
Abstract

Isoprene and other plastidial isoprenoids are produced primarily from recently assimilated photosynthates via the 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway. However, when environmental conditions limit photosynthesis, a fraction of carbon for MEP pathway can come from extrachloroplastic sources. The flow of extrachloroplastic carbon depends on the species and on leaf developmental and environmental conditions. The exchange of common phosphorylated intermediates between the MEP pathway and other metabolic pathways can occur via plastidic phosphate translocators. C and C carbon intermediates can contribute to chloroplastic metabolism, including photosynthesis and isoprenoid synthesis. Integration of these metabolic processes provide an example of metabolic flexibility, and results in the synthesis of primary metabolites for plant growth and secondary metabolites for plant defense, allowing effective use of environmental resources under multiple stresses.

摘要

异戊二烯和其他质体类异戊二烯主要通过 2-C-甲基-D-赤藓醇 4-磷酸(MEP)途径,由最近同化的光合产物产生。然而,当环境条件限制光合作用时,部分 MEP 途径的碳可以来自于质外体来源。质外体碳的流动取决于物种以及叶片发育和环境条件。MEP 途径和其他代谢途径之间的常见磷酸化中间产物的交换可以通过质体磷酸转运蛋白发生。C3 和 C4 碳中间产物可以为质体代谢做出贡献,包括光合作用和类异戊二烯合成。这些代谢过程的整合提供了代谢灵活性的一个例子,并导致为植物生长合成初级代谢物和为植物防御合成次生代谢物,从而在多种胁迫下有效利用环境资源。

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Interactions between leaf phenological type and functional traits drive variation in isoprene emissions in central Amazon forest trees.亚马逊中部森林树木中,叶片物候类型与功能性状之间的相互作用驱动异戊二烯排放的变化。
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本文引用的文献

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Xylem-transported glucose as an additional carbon source for leaf isoprene formation in Quercus robur.木质部运输的葡萄糖作为欧洲栓皮栎叶片异戊二烯形成的额外碳源。
New Phytol. 2002 Nov;156(2):171-178. doi: 10.1046/j.1469-8137.2002.00516.x.
2
Malate transported from chloroplast to mitochondrion triggers production of ROS and PCD in Arabidopsis thaliana.苹果酸从叶绿体转运到线粒体引发拟南芥 ROS 和 PCD 的产生。
Cell Res. 2018 Apr;28(4):448-461. doi: 10.1038/s41422-018-0024-8. Epub 2018 Mar 14.
3
Evidence That Isoprene Emission Is Not Limited by Cytosolic Metabolites. Exogenous Malate Does Not Invert the Reverse Sensitivity of Isoprene Emission to High [CO].
Limitations of Plant Stress Tolerance upon Heat and CO Exposure in Black Poplar: Assessment of Photosynthetic Traits and Stress Volatile Emissions.
黑杨在热胁迫和一氧化碳暴露下植物胁迫耐受性的局限性:光合特性和胁迫挥发性排放的评估
Plants (Basel). 2024 Apr 22;13(8):1165. doi: 10.3390/plants13081165.
4
Leaf-level metabolic changes in response to drought affect daytime CO2 emission and isoprenoid synthesis pathways.叶片代谢对干旱的响应变化会影响日间 CO2 排放和类异戊二烯合成途径。
Tree Physiol. 2023 Nov 13;43(11):1917-1932. doi: 10.1093/treephys/tpad094.
5
Age effects of Moso bamboo on leaf isoprene emission characteristics.毛竹年龄对叶片异戊二烯排放特征的影响。
Front Plant Sci. 2023 Mar 7;14:1132717. doi: 10.3389/fpls.2023.1132717. eCollection 2023.
6
Short-term severe drought influences root volatile biosynthesis in eastern white pine .短期严重干旱影响东部白松根系挥发性物质的生物合成。
Front Plant Sci. 2022 Oct 26;13:1030140. doi: 10.3389/fpls.2022.1030140. eCollection 2022.
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Improved plant heat shock resistance is introduced differently by heat and insect infestation: the role of volatile emission traits.热胁迫和虫害以不同的方式提高植物的抗热性:挥发物排放特性的作用。
Oecologia. 2022 May;199(1):53-68. doi: 10.1007/s00442-022-05168-x. Epub 2022 Apr 26.
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Responses of isoprene emission and photochemical efficiency to severe drought combined with prolonged hot weather in hybrid Populus.杂种杨中异戊二烯排放和光化学效率对严重干旱并伴有长期炎热天气的响应。
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证据表明异戊二烯排放不受细胞质代谢物的限制。外源苹果酸不会逆转异戊二烯排放对高[CO]的反向敏感性。
Plant Physiol. 2018 Feb;176(2):1573-1586. doi: 10.1104/pp.17.01463. Epub 2017 Dec 12.
4
Nutrient-rich plants emit a less intense blend of volatile isoprenoids.营养丰富的植物会散发出挥发性异戊二烯混合物,其强度较低。
New Phytol. 2018 Nov;220(3):773-784. doi: 10.1111/nph.14889. Epub 2017 Nov 9.
5
Integration of C₁ and C₂ Metabolism in Trees.树木中 C₁ 和 C₂ 代谢的整合。
Int J Mol Sci. 2017 Sep 23;18(10):2045. doi: 10.3390/ijms18102045.
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Isoprene Responses and Functions in Plants Challenged by Environmental Pressures Associated to Climate Change.异戊二烯在受气候变化相关环境压力挑战的植物中的响应与功能。
Front Plant Sci. 2017 Jul 26;8:1281. doi: 10.3389/fpls.2017.01281. eCollection 2017.
7
In Planta Recapitulation of Isoprene Synthase Evolution from Ocimene Synthases.罗勒烯合酶在植物中异戊二烯合酶进化的重演
Mol Biol Evol. 2017 Oct 1;34(10):2583-2599. doi: 10.1093/molbev/msx178.
8
Trade-Off Between Dimethyl Sulfide and Isoprene Emissions from Marine Phytoplankton.海洋浮游植物中二甲基硫与异戊二烯排放的权衡。
Trends Plant Sci. 2017 May;22(5):361-372. doi: 10.1016/j.tplants.2017.01.006. Epub 2017 Feb 24.
9
Isoprene research - 60 years later, the biology is still enigmatic.异戊二烯研究——60 年后,生物学仍然扑朔迷离。
Plant Cell Environ. 2017 Sep;40(9):1671-1678. doi: 10.1111/pce.12930. Epub 2017 Mar 30.
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The Methylerythritol Phosphate Pathway to Isoprenoids.异戊烯焦磷酸途径。
Chem Rev. 2017 Apr 26;117(8):5675-5703. doi: 10.1021/acs.chemrev.6b00537. Epub 2016 Dec 20.