Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Jun 21:7:870.
doi: 10.3389/fpls.2016.00870. eCollection 2016.

Cadaverine's Functional Role in Plant Development and Environmental Response

Affiliations
Review

Cadaverine's Functional Role in Plant Development and Environmental Response

Amy L Jancewicz et al. Front Plant Sci. .

Abstract

Cadaverine derives from lysine in a pathway that is distinct from that of the other well-characterized ornithine- or arginine-derived polyamines. Despite a multitude of studies in bacterial systems, cadaverine has garnered little attention in plant research. Nonetheless, many plants have been found to synthesize it. For instance, the Leguminosae have been shown to produce cadaverine and use it as a precursor in the biosynthesis of quinolizidine alkaloids, secondary metabolites that are involved in insect defense and also display therapeutic pharmacological properties. Cadaverine is also present in the environment; it can be produced by rhizosphere and phyllosphere microbes. Markedly, exogenous cadaverine application causes alterations in root-system architecture. Previous research suggests cadaverine has a role in stress response, with groups reporting an increase in content upon exposure to heat, drought, salt, and oxidative stress. However, data regarding the role of cadaverine in stress response remains conflicted, as some plant systems show enhanced tolerance to stresses in its presence, while others show increased sensitivity to the same stresses. In this review, we summarize recent findings on the role of cadaverine in plant growth, development, and stress response. We also address the possible roles rhizosphere and phyllosphere microbes may play in the delivery of exogenous cadaverine near plant organs, and discuss our current understanding of the molecular pathways that contribute to cadaverine homeostasis and response in plants.

Keywords: cadaverine; metabolism; phyllosphere; plant development; polyamine; rhizosphere; root architecture; stress response.

PubMed Disclaimer

Figures

FIGURE 1
FIGURE 1
Cadaverine metabolism. Lysine serves as a precursor for cadaverine, and is critical for fatty acid metabolism, the citric acid cycle, and amino acid synthesis. Cadaverine can be conjugated to phenolics, or used to construct higher-order polyamines. Cadaverine can also be oxidized, or converted to quinolizidine alkaloids. Bound cadaverine may affect cell-wall properties, membrane stability, gene expression and nucleic acid stability.

References

    1. Alcázar R., Altabella T., Marco F., Bortolotti C., Reymond M., Koncz C., et al. (2010). Polyamines: molecules with regulatory functions in plant abiotic stress tolerance. Planta 231 1237–1249. 10.1007/s00425-010-1130-0 - DOI - PubMed
    1. Andronis E. A., Moschou P. N., Toumi I., Roubelakis-Angelakis K. A. (2014). Peroxisomal polyamine oxidase and NADPH-oxidase cross-talk for ROS homeostasis which affects respiration rate in Arabidopsis thaliana. Front. Plant Sci. 5:132 10.3389/fpls.2014.00132 - DOI - PMC - PubMed
    1. Aziz A., Martin-Tanguy J., Larher F. (1998). Stress-induced changes in polyamine and tyramine levels can regulate proline accumulation in tomato leaf discs treated with sodium chloride. Physiol. Plant. 104 195–202. 10.1034/j.1399-3054.1998.1040207.x - DOI
    1. Bagni N., Tassoni A. (2001). Biosynthesis, oxidation and conjugation of aliphatic polyamines in higher plants. Amino Acids 20 301–317. 10.1007/s007260170046 - DOI - PubMed
    1. Bai D. L., Tang X. C., He X. C. (2000). Huperzine A, a potential therapeutic agent for treatment of Alzheimer’s disease. Curr. Med. Chem. 7 355–374. 10.2174/0929867003375281 - DOI - PubMed

LinkOut - more resources