Abstract

Glutamine synthetase (GS) catalyzes the first step at which nitrogen is brought into cellular metabolism and is also involved in the reassimilation of ammonium released by a number of metabolic pathways. Due to its unique position in plant nitrogen metabolism, GS plays essential roles in all aspects of plant development, from germination to senescence, and is a key component of nitrogen use efficiency (NUE) and plant yield. Understanding the mechanisms regulating GS activity is therefore of utmost importance and a great effort has been dedicated to understand how GS is regulated in different plant species. The present review summarizes exciting recent developments concerning the structure and regulation of GS isoenzymes, using the model legume Medicago truncatula. These include the understanding of the structural determinants of both the cytosolic and plastid located isoenzymes, the existence of a seed-specific GS gene unique to M. truncatula and closely related species and the discovery that GS isoenzymes are regulated by nitric oxide at the post-translational level. The data is discussed and integrated with the potential roles of the distinct GS isoenzymes within the whole plant context.

Highlights

  • Glutamine synthetase (GS, E.C. 6.3.1.2) is a tightly controlled enzyme located at the core of nitrogen metabolism

  • We have chosen the model legume Medicago truncatula to try to obtain a holistic view of GS regulation in a single legume species

  • The cytosolic enzymes MtGS1a and MtGS1b are irreversibly inactivated by tyrosine nitration, whereas MtGS2 appears to be reversibly inhibited by cysteine-nitrosylation

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Summary

Introduction

Glutamine synthetase (GS, E.C. 6.3.1.2) is a tightly controlled enzyme located at the core of nitrogen metabolism. GS catalyzes the first step in nitrogen assimilation, the ATP-dependent condensation of ammonium with glutamate. This reaction yields the readily metabolizable glutamine, which is used for the synthesis of all other essential nitrogenous compounds contained in the cells. Besides this key role in primary nitrogen assimilation, GS is crucial for the reassimilation of the NH4+ constantly released in large quantities via processes such as photorespiration, lignin biosynthesis, and protein catabolism (Lea and Miflin, 2010). The GS genes follow a complex pattern of expression, influenced by developmental and environmental cues, and their encoded enzymes

Glutamine synthetase in Medicago truncatula
Concluding Remarks

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