Nitrogen‐assimilating enzymes in land plants and algae: phylogenic and physiological perspectives
Abstract
An important biochemical feature of autotrophs, land plants and algae, is their incorporation of inorganic nitrogen, nitrate and ammonium, into the carbon skeleton. Nitrate and ammonium are converted into glutamine and glutamate to produce organic nitrogen compounds, for example proteins and nucleic acids. Ammonium is not only a preferred nitrogen source but also a key metabolite, situated at the junction between carbon metabolism and nitrogen assimilation, because nitrogen compounds can choose an alternative pathway according to the stages of their growth and environmental conditions. The enzymes involved in the reactions are nitrate reductase (EC 1.6.6.1‐2), nitrite reductase (EC 1.7.7.1), glutamine synthetase (EC 6.3.1.2), glutamate synthase (EC 1.4.1.13‐14, 1.4.7.1), glutamate dehydrogenase (EC 1.4.1.2‐4), aspartate aminotransferase (EC 2.6.1.1), asparagine synthase (EC 6.3.5.4), and phosphoenolpyruvate carboxylase (EC 4.1.1.31). Many of these enzymes exist in multiple forms in different subcellular compartments within different organs and tissues, and play sometimes overlapping and sometimes distinctive roles. Here, we summarize the biochemical characteristics and the physiological roles of these enzymes. We also analyse the molecular evolution of glutamine synthetase, glutamate synthase and glutamate dehydrogenase, and discuss the evolutionary relationships of these three enzymes.
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Some cyanobacteria can fix nitrogen, while almost all algal species identified to date require an exogenous source of fixed nitrogen, and most prefer ammonia.
“Some cyanobacteria also have the ability to fix nitrogen, while almost all algal species identified to date require an exogenous source of fixed nitrogen, and most prefer ammonia, as it is less energetically demanding than nitrate or nitrite [45].”
From Biofuels from algae: Challenges and potential (2010) · cites this paper as [45]
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References 46 · Cited by 93
- Authors
- Inokuchi, R., Kuma, K., Miyata, T., & Okada, M.
- Affiliations
- Toho University (JP)
- Kyoto University (JP)
- Corresponding author
- Inokuchi, Ritsuko
- ORCID
- Miyata, Takashi
- Venue
- Physiologia Plantarum
- Publisher
- Wiley
- Published
- 2002-09
- Volume
- 116
- Issue
- 1
- Pages
- 1-11
- ISSN
- 0031-9317 (ISSN-L)
- 1399-3054
- OpenAlex
- W2024713266
- Cited by
- 93
- References
- 46
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 5 · 2023: 4 · 2021: 3 · 2020: 6 · 2019: 2 · 2018: 4 · 2017: 6 · 2016: 10 · 2015: 4 · 2014: 7 · 2012: 5
- FWCI
- 4.22
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Physiologia Plantarum (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant nutrient uptake and metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nitrogen and Sulfur Effects on Brassica
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Legume Nitrogen Fixing Symbiosis
- Keywords
- nitrogen assimilation, nitrate reductase, nitrite reductase, glutamine synthetase, glutamate synthase, glutamate dehydrogenase, aspartate aminotransferase, phosphoenolpyruvate carboxylase, molecular evolution, enzyme phylogeny, land plants, algae, ammonium assimilation, glutamine and glutamate metabolism
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