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本文引用的文献

1
Subcellular distribution of phytin in the endosperm of developing castor bean: a possibility for its synthesis in the cytoplasm prior to deposition within protein bodies.在发育中的蓖麻胚乳中植酸的亚细胞分布:在其沉积在蛋白体之前于细胞质中合成的可能性。
Planta. 1984 Feb;160(2):113-20. doi: 10.1007/BF00392859.
2
Effect of phosphorus and zinc nutrition on soybean seed phytic Acid and zinc.磷、锌营养对大豆种子植酸和锌的影响。
Plant Physiol. 1984 Aug;75(4):1094-8. doi: 10.1104/pp.75.4.1094.
3
Cytoplasmic inositol hexakisphosphate production is sufficient for mediating the Gle1-mRNA export pathway.细胞质肌醇六磷酸的产生足以介导Gle1 - mRNA输出途径。
J Biol Chem. 2004 Dec 3;279(49):51022-32. doi: 10.1074/jbc.M409394200. Epub 2004 Sep 30.
4
Isolation of intact vacuoles and proteomic analysis of tonoplast from suspension-cultured cells of Arabidopsis thaliana.拟南芥悬浮培养细胞中完整液泡的分离及液泡膜的蛋白质组学分析。
Plant Cell Physiol. 2004 Jun;45(6):672-83. doi: 10.1093/pcp/pch099.
5
myo-Inositol-1,2,3,4,5,6-hexakisphosphate.肌醇-1,2,3,4,5,6-六磷酸
Phytochemistry. 2003 Nov;64(6):1033-43. doi: 10.1016/s0031-9422(03)00446-1.
6
Phenotypic, genetic and molecular characterization of a maize low phytic acid mutant (lpa241).一个玉米低植酸突变体(lpa241)的表型、遗传和分子特征
Theor Appl Genet. 2003 Oct;107(6):980-7. doi: 10.1007/s00122-003-1316-y. Epub 2003 Oct 2.
7
Expression of 1L-myoinositol-1-phosphate synthase in organelles.1L-肌醇-1-磷酸合酶在细胞器中的表达。
Plant Physiol. 2003 Aug;132(4):2240-7. doi: 10.1104/pp.103.020610.
8
Inositol hexakisphosphate mobilizes an endomembrane store of calcium in guard cells.肌醇六磷酸动员保卫细胞内膜系统中的钙库。
Proc Natl Acad Sci U S A. 2003 Aug 19;100(17):10091-5. doi: 10.1073/pnas.1133289100. Epub 2003 Aug 11.
9
Seed phosphorus and inositol phosphate phenotype of barley low phytic acid genotypes.大麦低植酸基因型的种子磷和肌醇磷酸表型
Phytochemistry. 2003 Mar;62(5):691-706. doi: 10.1016/s0031-9422(02)00610-6.
10
The maize low-phytic acid mutant lpa2 is caused by mutation in an inositol phosphate kinase gene.玉米低植酸突变体lpa2是由肌醇磷酸激酶基因突变引起的。
Plant Physiol. 2003 Feb;131(2):507-15. doi: 10.1104/pp.014258.

高浓度无机磷酸盐和阳离子诱导长春花悬浮培养细胞中植酸的合成与液泡积累

Phytic acid synthesis and vacuolar accumulation in suspension-cultured cells of Catharanthus roseus induced by high concentration of inorganic phosphate and cations.

作者信息

Mitsuhashi Naoto, Ohnishi Miwa, Sekiguchi Yoko, Kwon Yong-Uk, Chang Young-Tae, Chung Sung-Kee, Inoue Yoshinori, Reid Robert J, Yagisawa Hitoshi, Mimura Tetsuro

机构信息

Japan Society for the Promotion of Science, Tokyo 102-8471, Japan.

出版信息

Plant Physiol. 2005 Jul;138(3):1607-14. doi: 10.1104/pp.105.060269. Epub 2005 Jun 17.

DOI:10.1104/pp.105.060269
PMID:15965017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1176430/
Abstract

We have established a new system for studying phytic acid, myo-inositol hexakisphosphate (InsP(6)) synthesis in suspension-cultured cells of Catharanthus. InsP(6) and other intermediates of myo-inositol (Ins) phosphate metabolism were measured using an ion chromatography method. The detection limit for InsP(6) was less than 50 nM, which was sufficient to analyze Ins phosphates in living cells. Synthesis of Ins phosphates was induced by incubation in high inorganic phosphate medium. InsP(6) was mainly accumulated in vacuoles and was enhanced when cells were grown in high concentration of inorganic phosphates with the cations K(+), Ca(2+), or Zn(2+). However, there was a strong tendency for InsP(6) to accumulate in the vacuole in the presence of Ca(2+) and in nonvacuolar compartments when supplied with Zn(2+), possibly due to precipitation of InsP(6) with Zn(2+) in the cytosol. A vesicle transport inhibitor, brefeldin A, stimulated InsP(6) accumulation. The amounts of both Ins(3)P(1) myo-inositol monophosphate synthase, a key enzyme for InsP(6) synthesis, and Ins(1,4,5)P(3) kinase were unrelated to the level of accumulation of InsP(6). The mechanisms for InsP(6) synthesis and localization into vacuoles in plant cells are discussed.

摘要

我们建立了一个新系统,用于研究长春花悬浮培养细胞中植酸(即肌醇六磷酸,InsP(6))的合成。采用离子色谱法测定InsP(6)和肌醇(Ins)磷酸代谢的其他中间产物。InsP(6)的检测限低于50 nM,这足以分析活细胞中的肌醇磷酸盐。在高无机磷酸盐培养基中培养可诱导肌醇磷酸盐的合成。InsP(6)主要积累在液泡中,当细胞在含有阳离子K(+)、Ca(2+)或Zn(2+)的高浓度无机磷酸盐中生长时,其积累量会增加。然而,在Ca(2+)存在的情况下,InsP(6)有强烈的积累在液泡中的趋势,而在供应Zn(2+)时则积累在非液泡区室中,这可能是由于InsP(6)与细胞质中的Zn(2+)沉淀所致。囊泡运输抑制剂布雷菲德菌素A刺激了InsP(6)的积累。Ins(3)P(1)(肌醇单磷酸合成酶,InsP(6)合成的关键酶)和Ins(1,4,5)P(3)激酶的量与InsP(6)的积累水平无关。本文讨论了植物细胞中InsP(6)的合成机制及其在液泡中的定位。