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植物胼胝质合成酶复合体

Plant callose synthase complexes.

作者信息

Verma D P, Hong Z

机构信息

Department of Molecular Genetics and Plant Biotechnology Center, Ohio State University, Columbus 43210, USA.

出版信息

Plant Mol Biol. 2001 Dec;47(6):693-701. doi: 10.1023/a:1013679111111.

Abstract

Synthesis of callose (beta-1,3-glucan) in plants has been a topic of much debate over the past several decades. Callose synthase could not be purified to homogeneity and most partially purified cellulose synthase preparations yielded beta-1,3-glucan in vitro, leading to the interpretation that cellulose synthase might be able to synthesize callose. While a rapid progress has been made on the genes involved in cellulose synthesis in the past five years, identification of genes for callose synthases has proven difficult because cognate genes had not been identified in other organisms. An Arabidopsis gene encoding a putative cell plate-specific callose synthase catalytic subunit (CalS1) was recently cloned. CalS1 shares high sequence homology with the well-characterized yeast beta-1,3-glucan synthase and transgenic plant cells over-expressing CalS1 display higher callose synthase activity and accumulate more callose. The callose synthase complex exists in at least two distinct forms in different tissues and interacts with phragmoplastin. UDP-glucose transferase, Rop1 and, possibly, annexin. There are 12 CalS isozymes in Arabidopsis, and each may be tissue-specific and/or regulated under different physiological conditions responding to biotic and abiotic stresses.

摘要

在过去几十年里,植物中胼胝质(β-1,3-葡聚糖)的合成一直是一个备受争议的话题。胼胝质合酶无法纯化至同质状态,并且大多数部分纯化的纤维素合酶制剂在体外产生β-1,3-葡聚糖,这导致有人认为纤维素合酶可能能够合成胼胝质。尽管在过去五年中,参与纤维素合成的基因研究取得了快速进展,但胼胝质合酶基因的鉴定却很困难,因为在其他生物体中尚未鉴定出同源基因。最近克隆了拟南芥中一个编码假定的细胞板特异性胼胝质合酶催化亚基(CalS1)的基因。CalS1与已充分表征的酵母β-1,3-葡聚糖合酶具有高度序列同源性,过表达CalS1的转基因植物细胞表现出更高的胼胝质合酶活性并积累更多的胼胝质。胼胝质合酶复合物在不同组织中至少以两种不同形式存在,并与成膜体、UDP-葡萄糖转移酶、Rop1以及可能的膜联蛋白相互作用。拟南芥中有12种CalS同工酶,每种同工酶可能具有组织特异性和/或在不同生理条件下受生物和非生物胁迫的调控。

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