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甜菜中蔗糖裂解酶的发育及器官特异性表达表明,在主根中,质外体和共质体韧皮部卸载之间存在转变。

The developmental and organ specific expression of sucrose cleaving enzymes in sugar beet suggests a transition between apoplasmic and symplasmic phloem unloading in the tap roots.

作者信息

Godt D, Roitsch T

机构信息

Lehrstuhl für Pharmazeutische Biologie, Universität Würzburg, Julius-von-Sachs-Platz 2, 97082 Würzburg, Germany.

出版信息

Plant Physiol Biochem. 2006 Nov-Dec;44(11-12):656-65. doi: 10.1016/j.plaphy.2006.09.019. Epub 2006 Oct 11.

Abstract

Sucrose utilisation in sink tissues depend on its cleavage and is mediated by two different classes of enzymes, invertase and sucrose synthase, which determine the mechanism of phloem unloading. Cloning of two extracellular (BIN35 and BIN46) and one vacuolar invertase (BIN44) provided the basis for a detailed molecular analysis of the relative contribution of the sucrose cleaving enzymes to the sink metabolism of sugar beets (Beta vulgaris) during development. The determination of the steady state levels of mRNAs has been complemented by the analysis of the corresponding enzyme activities. The present study demonstrates an inverse regulation of extracellular invertase and sucrose synthase during tap root development indicating a transition between functional unloading pathways. Extracellular cleavage by invertase is the dominating mechanism to supply hexoses via an apoplasmic pathway at early stages of storage root development. Only at later stages sucrose synthase takes over the function of the key sink enzyme to contribute to the sink strength of the tap root via symplasmic phloem unloading. Whereas mRNAs for both extracellular invertase BIN35 and sucrose synthase were shown to be induced by mechanical wounding of mature leaves of adult plants, only sucrose synthase mRNA was metabolically induced by glucose in this source organ supporting the metabolic flexibility of this species.

摘要

库组织中蔗糖的利用取决于其裂解,由两类不同的酶介导,即转化酶和蔗糖合酶,它们决定了韧皮部卸载的机制。两种胞外转化酶(BIN35和BIN46)和一种液泡转化酶(BIN44)的克隆为详细分子分析蔗糖裂解酶在甜菜(Beta vulgaris)发育过程中对库代谢的相对贡献提供了基础。mRNA稳态水平的测定通过相应酶活性的分析得到了补充。本研究表明,在主根发育过程中,胞外转化酶和蔗糖合酶存在反向调节,这表明功能卸载途径之间发生了转变。在贮藏根发育早期,转化酶的胞外裂解是通过质外体途径供应己糖的主要机制。只有在后期,蔗糖合酶才接管关键库酶的功能,通过共质体韧皮部卸载来促进主根的库强度。虽然成年植株成熟叶片受到机械损伤可诱导胞外转化酶BIN35和蔗糖合酶的mRNA表达,但在这个源器官中,只有蔗糖合酶的mRNA受到葡萄糖的代谢诱导,这支持了该物种的代谢灵活性。

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