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PMID: 26347750 Published · epublish English Journal Article Review

Connecting proline metabolism and signaling pathways in plant senescence.

Frontiers in plant science ·Vol. 6 ·2015-00-00 ·Pages 552

Zhang L, Becker DF

Abstract

The amino acid proline has a unique biological role in stress adaptation. Proline metabolism is manipulated under stress by multiple and complex regulatory pathways and can profoundly influence cell death and survival in microorganisms, plants, and animals. Though the effects of proline are mediated by diverse signaling pathways, a common theme appears to be the generation of reactive oxygen species (ROS) due to proline oxidation being coupled to the respiratory electron transport chain. Considerable research has been devoted to understand how plants exploit proline metabolism in response to abiotic and biotic stress. Here, we review potential mechanisms by which proline metabolism influences plant senescence, namely in the petal and leaf. Recent studies of petal senescence suggest proline content is manipulated to meet energy demands of senescing cells. In the flower and leaf, proline metabolism may influence ROS signaling pathways that delay senescence progression. Future studies focusing on the mechanisms by which proline metabolic shifts occur during senescence may lead to novel methods to rescue crops under stress and to preserve post-harvest agricultural products.

Keywords
1Δ-pyrroline-5-carboxylate synthetase plant senescence proline proline dehydrogenase reactive oxygen species
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Zhang Lu
Redox Biology Center, Department of Biochemistry, University of Nebraska-Lincoln , Lincoln, NE, USA.
Becker Donald F
Redox Biology Center, Department of Biochemistry, University of Nebraska-Lincoln , Lincoln, NE, USA.
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Article Info
Journal
Frontiers in plant science
Abbr.
Front Plant Sci
ISSN
1664-462X
Published
2015-00-00
Epub
2015-00-22
Pages
552
Language
English
Region
Switzerland
NLM ID
101568200
PMCID
PMC4544304
Grants
NIGMS NIH HHS · P30 GM103335 · United States
NIGMS NIH HHS · R01 GM079393 · United States
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