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Updated: Mar 6, 2026

Assaying Protein Kinase Activity with Radiolabeled ATP
Published on: May 26, 2017
Assay Methods for ACS Activity and ACS Phosphorylation by MAP Kinases In Vitro and In Vivo
Xiaomin Han1, Guojing Li2, Shuqun Zhang3
1College of Life Sciences, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia, 010018, P. R. China.
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.

