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对西加云杉(Picea sitchensis)树枝中压缩木和非压缩木发育中的木质部蛋白质进行比较,发现一种差异表达的漆酶。

A comparison of proteins from the developing xylem of compression and non-compression wood of branches of sitka spruce (Picea sitchensis) reveals a differentially expressed laccase.

作者信息

McDougall G J

机构信息

Unit of Plant Biochemistry, Biochemistry and Cell Biology Division, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, Scotland, UK.

出版信息

J Exp Bot. 2000 Aug;51(349):1395-401.

Abstract

Soluble and cell wall-associated proteins were extracted from the developing xylem of the compression and non-compression sides of branches of Sitka spruce (Picea sitchensis (Bong) Carr.) by an identical procedure. Equal amounts of proteins were separated by SDS-PAGE, and polypeptides were identified that were more abundant in soluble and cell wall-associated extracts from the developing xylem of either compression or non-compression wood. Two polypeptides (at apparent M(r)s of 48 kDa and 120 kDa) that were more abundant in cell wall-associated extracts of the developing xylem of the compression tissues were selected for amino-terminal protein sequencing. The 48 kDa polypeptide yielded an amino-terminal sequence that had no homology with known protein, gene or EST database sequences. The amino-terminal sequence of the 120 kDa polypeptide was homologous to a number of laccase-type polyphenol oxidases (EC 1.10.3.2) thought to be involved in lignin biosynthesis in trees. Using non-denaturing SDS-PAGE, the 120 kDa laccase was confirmed as a major oxidase activity in extracts of lignifying compression xylem but it was barely detectable in the non-compression extracts where an 85 kDa oxidase was the predominant activity. The differential expression of oxidases in compression and non-compression xylem is discussed.

摘要

采用相同的方法,从西加云杉(Picea sitchensis (Bong) Carr.)枝条受挤压侧和非挤压侧正在发育的木质部中提取可溶性蛋白和细胞壁相关蛋白。等量的蛋白质通过SDS-PAGE进行分离,鉴定出在受挤压木材或非受挤压木材正在发育的木质部的可溶性提取物和细胞壁相关提取物中含量更高的多肽。选择了在受挤压组织正在发育的木质部的细胞壁相关提取物中含量更高的两种多肽(表观分子量分别为48 kDa和120 kDa)进行氨基末端蛋白质测序。48 kDa的多肽产生的氨基末端序列与已知的蛋白质、基因或EST数据库序列没有同源性。120 kDa多肽的氨基末端序列与许多漆酶型多酚氧化酶(EC 1.10.3.2)同源,这些酶被认为参与树木木质素的生物合成。使用非变性SDS-PAGE,证实120 kDa漆酶是正在木质化的受挤压木质部提取物中的主要氧化酶活性,但在非受挤压提取物中几乎检测不到,在非受挤压提取物中85 kDa氧化酶是主要活性。本文讨论了氧化酶在受挤压和非受挤压木质部中的差异表达。

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