Phosphorylation of Arabidopsis transketolase at Ser <sup>428</sup> provides a potential paradigm for the metabolic control of chloroplast carbon metabolism

Author(s)
Agostinho G Rocha, Norbert Mehlmer, Simon Stael, Andrea Mair, Nargis Parvin, Fatima Chigri, Markus Teige, Ute C Vothknecht
Abstract

Calcium is an important second messenger in eukaryotic cells that regulates many different cellular processes. To elucidate calcium regulation in chloroplasts, we identified the targets of calcium-dependent phosphorylation within the stromal proteome. A 73 kDa protein was identified as one of the most dominant proteins undergoing phosphorylation in a calcium-dependent manner in the stromal extracts of both Arabidopsis and Pisum. It was identified as TKL (transketolase), an essential enzyme of both the Calvin-Benson-Bassham cycle and the oxidative pentose phosphate pathway. Calcium-dependent phosphorylation of both Arabidopsis isoforms (AtTKL1 and AtTKL2) could be confirmed in vitro using recombinant proteins. The phosphorylation is catalysed by a stroma-localized protein kinase, which cannot utilize GTP. Phosphorylation of AtTKL1, the dominant isoform in most tissues, occurs at a serine residue that is conserved in TKLs of vascular plants. By contrast, an aspartate residue is present in this position in cyanobacteria, algae and mosses. Characterization of a phosphomimetic mutant (S428D) indicated that Ser428 phosphorylation exerts significant effects on the enzyme's substrate saturation kinetics at specific physiological pH values. The results of the present study point to a role for TKL phosphorylation in the regulation of carbon allocation.

Organisation(s)
Department of Biochemistry and Cell Biology
External organisation(s)
Ludwig-Maximilians-Universität München
Journal
Biochemical Journal
Volume
458
Pages
313-322
No. of pages
10
ISSN
0264-6021
DOI
https://doi.org/10.1042/BJ20130631
Publication date
12-2013
Peer reviewed
Yes
Austrian Fields of Science 2012
106002 Biochemistry, 106052 Cell biology
Keywords
ASJC Scopus subject areas
Molecular Biology, Biochemistry, Cell Biology
Portal url
https://ucris.univie.ac.at/portal/en/publications/phosphorylation-of-arabidopsis-transketolase-at-ser-428-provides-a-potential-paradigm-for-the-metabolic-control-of-chloroplast-carbon-metabolism(8f519e68-0186-4919-8a48-6f1fc97cbb15).html