Identification of the Arabidopsis Calmodulin-Dependent NAD+ Kinase That Sustains the Elicitor-Induced Oxidative Burst. Issue 4 (25th September 2019)
- Record Type:
- Journal Article
- Title:
- Identification of the Arabidopsis Calmodulin-Dependent NAD+ Kinase That Sustains the Elicitor-Induced Oxidative Burst. Issue 4 (25th September 2019)
- Main Title:
- Identification of the Arabidopsis Calmodulin-Dependent NAD+ Kinase That Sustains the Elicitor-Induced Oxidative Burst
- Authors:
- Dell'Aglio, Elisa
Giustini, Cécile
Kraut, Alexandra
Couté, Yohann
Costa, Alex
Decros, Guillaume
Gibon, Yves
Mazars, Christian
Matringe, Michel
Finazzi, Giovanni
Curien, Gilles - Abstract:
- Abstract : A long-sought calmodulin- and Ca 2+ -dependent NAD kinase that is conserved in the plant lineage is the missing link between Ca 2+ signaling, metabolism, and the oxidative burst. Abstract: NADP(H) is an essential cofactor of multiple metabolic processes in all living organisms, and in plants, NADP(H) is required as the substrate of Ca 2+ -dependent NADPH oxidases, which catalyze a reactive oxygen species burst in response to various stimuli. While NADP + production in plants has long been known to involve a calmodulin (CaM)/Ca 2+ -dependent NAD + kinase, the nature of the enzyme catalyzing this activity has remained enigmatic, as has its role in plant physiology. Here, we used proteomic, biochemical, molecular, and in vivo analyses to identify an Arabidopsis ( Arabidopsis thaliana ) protein that catalyzes NADP + production exclusively in the presence of CaM/Ca 2+ . This enzyme, which we named NAD kinase-CaM dependent (NADKc), has a CaM-binding peptide located in its N-terminal region and displays peculiar biochemical properties as well as different domain organization compared with known plant NAD + kinases. In response to a pathogen elicitor, the activity of NADKc, which is associated with the mitochondrial periphery, contributes to an increase in the cellular NADP + concentration and to the amplification of the elicitor-induced oxidative burst. Based on a phylogenetic analysis and enzymatic assays, we propose that the CaM/Ca 2+ -dependent NAD + kinase activityAbstract : A long-sought calmodulin- and Ca 2+ -dependent NAD kinase that is conserved in the plant lineage is the missing link between Ca 2+ signaling, metabolism, and the oxidative burst. Abstract: NADP(H) is an essential cofactor of multiple metabolic processes in all living organisms, and in plants, NADP(H) is required as the substrate of Ca 2+ -dependent NADPH oxidases, which catalyze a reactive oxygen species burst in response to various stimuli. While NADP + production in plants has long been known to involve a calmodulin (CaM)/Ca 2+ -dependent NAD + kinase, the nature of the enzyme catalyzing this activity has remained enigmatic, as has its role in plant physiology. Here, we used proteomic, biochemical, molecular, and in vivo analyses to identify an Arabidopsis ( Arabidopsis thaliana ) protein that catalyzes NADP + production exclusively in the presence of CaM/Ca 2+ . This enzyme, which we named NAD kinase-CaM dependent (NADKc), has a CaM-binding peptide located in its N-terminal region and displays peculiar biochemical properties as well as different domain organization compared with known plant NAD + kinases. In response to a pathogen elicitor, the activity of NADKc, which is associated with the mitochondrial periphery, contributes to an increase in the cellular NADP + concentration and to the amplification of the elicitor-induced oxidative burst. Based on a phylogenetic analysis and enzymatic assays, we propose that the CaM/Ca 2+ -dependent NAD + kinase activity found in photosynthetic organisms is carried out by NADKc-related proteins. Thus, NADKc represents the missing link between Ca 2+ signaling, metabolism, and the oxidative burst. … (more)
- Is Part Of:
- Plant physiology. Volume 181:Issue 4(2019)
- Journal:
- Plant physiology
- Issue:
- Volume 181:Issue 4(2019)
- Issue Display:
- Volume 181, Issue 4 (2019)
- Year:
- 2019
- Volume:
- 181
- Issue:
- 4
- Issue Sort Value:
- 2019-0181-0004-0000
- Page Start:
- 1449
- Page End:
- 1458
- Publication Date:
- 2019-09-25
- Subjects:
- Plant physiology -- Periodicals
Botany -- Periodicals
Periodicals
Electronic journals
571.2 - Journal URLs:
- https://academic.oup.com/plphys/issue ↗
http://www.plantphysiol.org/ ↗
http://www.jstor.org/journals/00320889.html ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=69 ↗
http://www-us.ebsco.com/online/direct.asp?JournalID=101725 ↗
http://www.oxfordjournals.org/ ↗ - DOI:
- 10.1104/pp.19.00912 ↗
- Languages:
- English
- ISSNs:
- 0032-0889
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 22701.xml