| Literature DB >> 35087923 |
Nicholas R Moody1, Chatawal Phansopal1, James D Reid1.
Abstract
Phosphoenolpyruvate carboxylase (PEPC) catalyzes a critical step in carbon metabolism in plants and bacteria, the irreversible reaction between bicarbonate and phosphoenolpyruvate to produce the C4 compound oxaloacetate. This enzyme is particularly important in the context of C4 photosynthesis, where it is the initial carbon-fixing enzyme. Many studies have used kinetic approaches to characterize the properties of PEPCs from different species, different post-translational states, and after mutagenesis. Most of these studies have worked at a fixed saturating concentration of bicarbonate. Controlling the concentration of bicarbonate is difficult at low concentrations because of equilibration with atmospheric CO2. We describe here a simple, repeatable, and gas-tight assay system for PEPC that allows bicarbonate concentrations to be controlled above ca. 50 µM.Entities:
Keywords: C4; Bicarbonate assay; Gas-controlled assay; Malate dehydrogenase coupled assay; PEPC
Year: 2021 PMID: 35087923 PMCID: PMC8720526 DOI: 10.21769/BioProtoc.4264
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325