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体外和体内通过丝裂原活化蛋白激酶检测ACS活性及ACS磷酸化的方法

Assay Methods for ACS Activity and ACS Phosphorylation by MAP Kinases In Vitro and In Vivo.

作者信息

Han Xiaomin, Li Guojing, Zhang Shuqun

机构信息

College of Life Sciences, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia, 010018, P. R. China.

Division of Biochemistry, Interdisciplinary Plant Group, and Bond Life Sciences Center, University of Missouri, 371G Bond Life Sciences Center, 117 Schweitzer Hall, Columbia, MO, 65211, USA.

出版信息

Methods Mol Biol. 2017;1573:59-71. doi: 10.1007/978-1-4939-6854-1_6.

Abstract

Ethylene, a gaseous phytohormone, has profound effects on plant growth, development, and adaptation to the environment. Ethylene-regulated processes begin with the induction of ethylene biosynthesis. There are two key steps in ethylene biosynthesis. The first is the biosynthesis of 1-aminocyclopropane-1-carboxylic acid (ACC) from S-Adenosyl-Methionine (SAM), a common precursor in many metabolic pathways, which is catalyzed by ACC synthase (ACS). The second is the oxidative cleavage of ACC to form ethylene under the action of ACC oxidase (ACO). ACC biosynthesis is the committing and generally the rate-limiting step in ethylene biosynthesis. As a result, characterizing the cellular ACS activity and understanding its regulation are important. In this chapter, we detail the methods used to measure, (1) the enzymatic activity of both recombinant and native ACS proteins, and (2) the phosphorylation of ACS protein by mitogen-activated protein kinases (MAPKs) in vivo and in vitro.

摘要

乙烯是一种气态植物激素,对植物的生长、发育以及环境适应性有着深远影响。乙烯调控的过程始于乙烯生物合成的诱导。乙烯生物合成有两个关键步骤。第一步是由1-氨基环丙烷-1-羧酸合酶(ACS)催化,从许多代谢途径中的常见前体S-腺苷甲硫氨酸(SAM)合成1-氨基环丙烷-1-羧酸(ACC)。第二步是在ACC氧化酶(ACO)的作用下,ACC发生氧化裂解形成乙烯。ACC生物合成是乙烯生物合成中的关键步骤,通常也是限速步骤。因此,表征细胞ACS活性并了解其调控机制很重要。在本章中,我们详细介绍了用于测量以下两项的方法:(1)重组和天然ACS蛋白的酶活性,以及(2)体内和体外丝裂原活化蛋白激酶(MAPK)对ACS蛋白的磷酸化作用。

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