Suppr超能文献

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.

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。

相似文献

4
Myo-inositol hexakisphosphate degradation by Bifidobacterium infantis ATCC 15697.婴儿双歧杆菌ATCC 15697对肌醇六磷酸的降解
Int J Food Microbiol. 2007 Jun 10;117(1):76-84. doi: 10.1016/j.ijfoodmicro.2007.02.021. Epub 2007 Mar 30.
5
The pathway for the production of inositol hexakisphosphate in human cells.人体细胞中肌醇六磷酸的产生途径。
J Biol Chem. 2005 Jan 21;280(3):1911-20. doi: 10.1074/jbc.M411528200. Epub 2004 Nov 5.

引用本文的文献

本文引用的文献

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.
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.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验