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Acyl-lipid metabolism.酰基脂质代谢
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The Arabidopsis DSO/ABCG11 transporter affects cutin metabolism in reproductive organs and suberin in roots.拟南芥 DSO/ABCG11 转运蛋白影响生殖器官的角质代谢和根部的栓质化。
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本文引用的文献

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Lipases: Interfacial Enzymes with Attractive Applications.脂肪酶:具有诱人应用前景的界面酶。
Angew Chem Int Ed Engl. 1998 Jul 3;37(12):1608-1633. doi: 10.1002/(SICI)1521-3773(19980703)37:12<1608::AID-ANIE1608>3.0.CO;2-V.
2
Composition, ultrastructure and function of the cutin- and suberin-containing layers in the leaf, fruit peel, juice-sac and inner seed coat of grapefruit (Citrus paradisi Macfed.).柚皮(Citrus paradisi Macfed.)叶、果皮、汁囊和内种皮中含角质层和栓质层的组成、超微结构和功能。
Planta. 1980 Oct;149(5):498-511. doi: 10.1007/BF00385755.
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Mini-review: what nuclear magnetic resonance can tell us about protective tissues.综述:磁共振能告诉我们关于保护组织的什么信息。
Plant Sci. 2012 Oct;195:120-4. doi: 10.1016/j.plantsci.2012.06.013. Epub 2012 Jun 29.
4
A land-plant-specific glycerol-3-phosphate acyltransferase family in Arabidopsis: substrate specificity, sn-2 preference, and evolution.拟南芥中一种陆生植物特异性甘油-3-磷酸酰基转移酶家族:底物特异性、sn-2 偏好性和进化。
Plant Physiol. 2012 Oct;160(2):638-52. doi: 10.1104/pp.112.201996. Epub 2012 Aug 3.
5
Tomato GDSL1 is required for cutin deposition in the fruit cuticle.番茄 GDSL1 是果实角质层中角质沉积所必需的。
Plant Cell. 2012 Jul;24(7):3119-34. doi: 10.1105/tpc.112.101055. Epub 2012 Jul 17.
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Plants: Knitting a polyester skin.植物:编织聚酯外皮。
Nat Chem Biol. 2012 Jun 18;8(7):603-4. doi: 10.1038/nchembio.1004.
7
Arabidopsis ECERIFERUM9 involvement in cuticle formation and maintenance of plant water status.拟南芥 ECERIFERUM9 参与角质层形成和植物水分状况维持。
Plant Physiol. 2012 Jul;159(3):930-44. doi: 10.1104/pp.112.198697. Epub 2012 May 25.
8
The identification of cutin synthase: formation of the plant polyester cutin.角质合成酶的鉴定:植物聚酯角质的形成。
Nat Chem Biol. 2012 Jul;8(7):609-11. doi: 10.1038/nchembio.960. Epub 2012 May 20.
9
TGD1, -2, and -3 proteins involved in lipid trafficking form ATP-binding cassette (ABC) transporter with multiple substrate-binding proteins.TGD1、-2 和 -3 蛋白参与脂质转运,形成具有多种底物结合蛋白的三磷酸腺苷结合盒(ABC)转运体。
J Biol Chem. 2012 Jun 15;287(25):21406-15. doi: 10.1074/jbc.M112.370213. Epub 2012 Apr 27.
10
The acyl-acyl carrier protein synthetase from Synechocystis sp. PCC 6803 mediates fatty acid import.集胞藻 PCC 6803 的酰基辅酶 A-酰基载体蛋白合成酶介导脂肪酸导入。
Plant Physiol. 2012 Jun;159(2):606-17. doi: 10.1104/pp.112.195263. Epub 2012 Apr 24.

酰基脂质代谢

Acyl-lipid metabolism.

作者信息

Li-Beisson Yonghua, Shorrosh Basil, Beisson Fred, Andersson Mats X, Arondel Vincent, Bates Philip D, Baud Sébastien, Bird David, Debono Allan, Durrett Timothy P, Franke Rochus B, Graham Ian A, Katayama Kenta, Kelly Amélie A, Larson Tony, Markham Jonathan E, Miquel Martine, Molina Isabel, Nishida Ikuo, Rowland Owen, Samuels Lacey, Schmid Katherine M, Wada Hajime, Welti Ruth, Xu Changcheng, Zallot Rémi, Ohlrogge John

出版信息

Arabidopsis Book. 2013;11:e0161. doi: 10.1199/tab.0161. Epub 2013 Jan 29.

DOI:10.1199/tab.0161
PMID:23505340
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3563272/
Abstract

Acyl lipids in Arabidopsis and all other plants have a myriad of diverse functions. These include providing the core diffusion barrier of the membranes that separates cells and subcellular organelles. This function alone involves more than 10 membrane lipid classes, including the phospholipids, galactolipids, and sphingolipids, and within each class the variations in acyl chain composition expand the number of structures to several hundred possible molecular species. Acyl lipids in the form of triacylglycerol account for 35% of the weight of Arabidopsis seeds and represent their major form of carbon and energy storage. A layer of cutin and cuticular waxes that restricts the loss of water and provides protection from invasions by pathogens and other stresses covers the entire aerial surface of Arabidopsis. Similar functions are provided by suberin and its associated waxes that are localized in roots, seed coats, and abscission zones and are produced in response to wounding. This chapter focuses on the metabolic pathways that are associated with the biosynthesis and degradation of the acyl lipids mentioned above. These pathways, enzymes, and genes are also presented in detail in an associated website (ARALIP: http://aralip.plantbiology.msu.edu/). Protocols and methods used for analysis of Arabidopsis lipids are provided. Finally, a detailed summary of the composition of Arabidopsis lipids is provided in three figures and 15 tables.

摘要

拟南芥和所有其他植物中的酰基脂质具有多种不同的功能。这些功能包括提供分隔细胞和亚细胞细胞器的膜的核心扩散屏障。仅这一功能就涉及10多种膜脂类别,包括磷脂、半乳糖脂和鞘脂,并且在每一类中,酰基链组成的变化将结构数量扩展到数百种可能的分子种类。三酰甘油形式的酰基脂质占拟南芥种子重量的35%,是其碳和能量储存的主要形式。一层角质和角质层蜡覆盖了拟南芥的整个地上表面,限制水分流失并提供抵御病原体入侵和其他胁迫的保护。栓质及其相关蜡质也具有类似功能,它们位于根、种皮和脱落区,并在受伤时产生。本章重点介绍与上述酰基脂质生物合成和降解相关的代谢途径。这些途径、酶和基因也在相关网站(ARALIP:http://aralip.plantbiology.msu.edu/)中详细介绍。提供了用于分析拟南芥脂质的实验方案和方法。最后,在三个图和15个表中提供了拟南芥脂质组成的详细总结。