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The mechanism of phloem loading in rice (Oryza sativa).水稻韧皮部装载的机制。
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本文引用的文献

1
Antisense suppression of the rice transporter gene, OsSUT1, leads to impaired grain filling and germination but does not affect photosynthesis.对水稻转运蛋白基因OsSUT1进行反义抑制会导致籽粒灌浆和萌发受损,但不影响光合作用。
Funct Plant Biol. 2002 Jul;29(7):815-826. doi: 10.1071/PP01204.
2
Leaf structure in relation to solute transport and phloem loading in Zea mays L.玉米叶片结构与溶质运输及韧皮部装载的关系
Planta. 1978 Jan;138(3):279-94. doi: 10.1007/BF00386823.
3
Evolution of plant sucrose uptake transporters.植物蔗糖摄取转运蛋白的进化。
Front Plant Sci. 2012 Feb 15;3:22. doi: 10.3389/fpls.2012.00022. eCollection 2012.
4
Sucrose efflux mediated by SWEET proteins as a key step for phloem transport.SWEET 蛋白介导的蔗糖外排是韧皮部运输的关键步骤。
Science. 2012 Jan 13;335(6065):207-11. doi: 10.1126/science.1213351. Epub 2011 Dec 8.
5
Vacuoles release sucrose via tonoplast-localised SUC4-type transporters.液泡通过液泡膜定位的 SUC4 型转运蛋白释放蔗糖。
Plant Biol (Stuttg). 2012 Mar;14(2):325-36. doi: 10.1111/j.1438-8677.2011.00506.x. Epub 2011 Sep 13.
6
Impaired function of the tonoplast-localized sucrose transporter in rice, OsSUT2, limits the transport of vacuolar reserve sucrose and affects plant growth.定位于液泡膜的蔗糖转运蛋白 OsSUT2 功能受损,限制了液泡内贮藏蔗糖的转运,从而影响植物生长。
Plant Physiol. 2011 Sep;157(1):109-19. doi: 10.1104/pp.111.176982. Epub 2011 Jul 19.
7
Proton-driven sucrose symport and antiport are provided by the vacuolar transporters SUC4 and TMT1/2.质子驱动的蔗糖协同运输和反向运输由液泡转运蛋白 SUC4 和 TMT1/2 提供。
Plant J. 2011 Oct;68(1):129-36. doi: 10.1111/j.1365-313X.2011.04672.x. Epub 2011 Jul 27.
8
Membrane-transport systems for sucrose in relation to whole-plant carbon partitioning.与植物整体碳分配有关的蔗糖膜转运系统。
Mol Plant. 2011 May;4(3):377-94. doi: 10.1093/mp/ssr014. Epub 2011 Apr 18.
9
The sucrose transporter family in Populus: the importance of a tonoplast PtaSUT4 to biomass and carbon partitioning.杨树蔗糖转运蛋白家族:液泡膜 PtaSUT4 对生物量和碳分配的重要性。
Plant J. 2011 Mar;65(5):757-70. doi: 10.1111/j.1365-313X.2010.04463.x. Epub 2011 Jan 24.
10
Interaction between sieve element and companion cell and the consequences for photoassimilate distribution. Two structural hardware frames with associated physiological software packages in dicotyledons?筛管分子与伴胞之间的相互作用以及对光合产物分配的影响。双子叶植物中两个带有相关生理软件包的结构硬件框架?
J Exp Bot. 1996 Aug;47 Spec No:1129-40. doi: 10.1093/jxb/47.Special_Issue.1129.

水稻韧皮部装载的机制。

The mechanism of phloem loading in rice (Oryza sativa).

机构信息

Graduate School of Biotechnology and Crop Biotech Institute, Kyung Hee University, Yongin 446-701, Korea.

出版信息

Mol Cells. 2012 May;33(5):431-8. doi: 10.1007/s10059-012-0071-9. Epub 2012 Mar 26.

DOI:10.1007/s10059-012-0071-9
PMID:22453778
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3887736/
Abstract

Carbohydrates, mainly sucrose, that are synthesized in source organs are transported to sink organs to support growth and development. Phloem loading of sucrose is a crucial step that drives long-distance transport by elevating hydrostatic pressure in the phloem. Three phloem loading strategies have been identified, two active mechanisms, apoplastic loading via sucrose transporters and symplastic polymer trapping, and one passive mechanism. The first two active loading mechanisms require metabolic energy, carbohydrate is loaded into the phloem against a concentration gradient. The passive process, diffusion, involves equilibration of sucrose and other metabolites between cells through plasmodesmata. Many higher plant species including Arabidopsis utilize the active loading mechanisms to increase carbohydrate in the phloem to higher concentrations than that in mesophyll cells. In contrast, recent data revealed that a large number of plants, especially woody species, load sucrose passively by maintaining a high concentration in mesophyll cells. However, it still remains to be determined how the worldwide important cereal crop, rice, loads sucrose into the phloem in source organs. Based on the literature and our results, we propose a potential strategy of phloem loading in rice. Elucidation of the phloem loading mechanism should improve our understanding of rice development and facilitate its manipulation towards the increase of crop productivity.

摘要

碳水化合物,主要是蔗糖,在源器官中合成,然后运输到汇器官,以支持生长和发育。韧皮部装载蔗糖是一个关键步骤,它通过提高韧皮部中的静水压力来驱动长距离运输。已经确定了三种韧皮部装载策略,两种主动机制,通过蔗糖转运蛋白进行质外体装载和共质体聚合物捕获,以及一种被动机制。前两种主动装载机制需要代谢能量,碳水化合物逆浓度梯度装载到韧皮部中。被动过程,扩散,涉及通过胞间连丝在细胞之间平衡蔗糖和其他代谢物。许多高等植物物种,包括拟南芥,利用主动装载机制将碳水化合物增加到韧皮部中的浓度高于叶肉细胞中的浓度。相比之下,最近的数据显示,大量植物,特别是木本植物,通过在叶肉细胞中维持高浓度来被动地装载蔗糖。然而,仍有待确定世界重要的谷类作物水稻如何将蔗糖装载到源器官的韧皮部中。基于文献和我们的结果,我们提出了水稻韧皮部装载的一种潜在策略。阐明韧皮部装载机制应该有助于我们理解水稻的发育,并促进对其进行操作以提高作物生产力。