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合成植物细胞壁多糖的高尔基体酶:在基因组时代寻找和评估候选酶

Golgi enzymes that synthesize plant cell wall polysaccharides: finding and evaluating candidates in the genomic era.

作者信息

Perrin R, Wilkerson C, Keegstra K

机构信息

Department of Botany and Plant Pathology, MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing 48824, USA.

出版信息

Plant Mol Biol. 2001 Sep;47(1-2):115-30.

Abstract

Although the synthesis of cell wall polysaccharides is a critical process during plant cell growth and differentiation, many of the wall biosynthetic genes have not yet been identified. This review focuses on the synthesis of noncellulosic matrix polysaccharides formed in the Golgi apparatus. Our consideration is limited to two types of plant cell wall biosynthetic enzymes: glycan synthases and glycosyltransferases. Classical means of identifying these enzymes and the genes that encode them rely on biochemical purification of enzyme activity to obtain amino acid sequence data that is then used to identify the corresponding gene. This type of approach is difficult, especially when acceptor substrates for activity assays are unavailable, as is the case for many enzymes. However, bioinformatics and functional genomics provide powerful alternative means of identifying and evaluating candidate genes. Database searches using various strategies and expression profiling can identify candidate genes. The involvement of these genes in wall biosynthesis can be evaluated using genetic, reverse genetic, biochemical, and heterologous expression methods. Recent advances using these methods are considered in this review.

摘要

尽管细胞壁多糖的合成是植物细胞生长和分化过程中的关键环节,但许多细胞壁生物合成基因尚未被鉴定出来。本综述聚焦于在高尔基体中形成的非纤维素基质多糖的合成。我们的讨论仅限于两种植物细胞壁生物合成酶:聚糖合酶和糖基转移酶。鉴定这些酶及其编码基因的传统方法依赖于对酶活性进行生化纯化以获得氨基酸序列数据,然后利用这些数据鉴定相应的基因。这种方法很困难,尤其是当活性测定的受体底物无法获得时,许多酶的情况就是如此。然而,生物信息学和功能基因组学提供了鉴定和评估候选基因的有力替代方法。使用各种策略进行数据库搜索和表达谱分析可以鉴定候选基因。可以使用遗传学、反向遗传学、生物化学和异源表达方法来评估这些基因在细胞壁生物合成中的作用。本综述将探讨使用这些方法取得的最新进展。

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