Respiratory and C4-photosynthetic NAD-malic enzyme coexist in bundle sheath cell mitochondria and evolved via association of differentially adapted subunits. Issue 1 (4th November 2021)
- Record Type:
- Journal Article
- Title:
- Respiratory and C4-photosynthetic NAD-malic enzyme coexist in bundle sheath cell mitochondria and evolved via association of differentially adapted subunits. Issue 1 (4th November 2021)
- Main Title:
- Respiratory and C4-photosynthetic NAD-malic enzyme coexist in bundle sheath cell mitochondria and evolved via association of differentially adapted subunits
- Authors:
- Hüdig, Meike
Tronconi, Marcos A
Zubimendi, Juan P
Sage, Tammy L
Poschmann, Gereon
Bickel, David
Gohlke, Holger
Maurino, Veronica G - Abstract:
- Abstract: In plant mitochondria, nicotinamide adenine dinucleotide-malic enzyme (NAD-ME) has a housekeeping function in malate respiration. In different plant lineages, NAD-ME was independently co-opted in C4 photosynthesis. In the C4 Cleome species, Gynandropsis gynandra and Cleome angustifolia, all NAD-ME genes ( NAD-MEα, NAD-MEβ1, and NAD-MEβ2 ) were affected by C4 evolution and are expressed at higher levels than their orthologs in the C3 species Tarenaya hassleriana . In T. hassleriana, the NAD-ME housekeeping function is performed by two heteromers, NAD-MEα/β1 and NAD-MEα/β2, with similar biochemical properties. In both C4 species, this role is restricted to NAD-MEα/β2. In the C4 species, NAD-MEα/β1 is exclusively present in the leaves, where it accounts for most of the enzymatic activity. Gynandropsis gynandra NAD-MEα/β1 (GgNAD-MEα/β1) exhibits high catalytic efficiency and is differentially activated by the C4 intermediate aspartate, confirming its role as the C4 -decarboxylase. During C4 evolution, NAD-MEβ1 lost its catalytic activity; its contribution to the enzymatic activity results from a stabilizing effect on the associated α-subunit and the acquisition of regulatory properties. We conclude that in bundle sheath cell mitochondria of C4 species, the functions of NAD-ME as C4 photosynthetic decarboxylase and as a housekeeping enzyme coexist and are performed by isoforms that combine the same α-subunit with differentially adapted β-subunits. Abstract : In C4Abstract: In plant mitochondria, nicotinamide adenine dinucleotide-malic enzyme (NAD-ME) has a housekeeping function in malate respiration. In different plant lineages, NAD-ME was independently co-opted in C4 photosynthesis. In the C4 Cleome species, Gynandropsis gynandra and Cleome angustifolia, all NAD-ME genes ( NAD-MEα, NAD-MEβ1, and NAD-MEβ2 ) were affected by C4 evolution and are expressed at higher levels than their orthologs in the C3 species Tarenaya hassleriana . In T. hassleriana, the NAD-ME housekeeping function is performed by two heteromers, NAD-MEα/β1 and NAD-MEα/β2, with similar biochemical properties. In both C4 species, this role is restricted to NAD-MEα/β2. In the C4 species, NAD-MEα/β1 is exclusively present in the leaves, where it accounts for most of the enzymatic activity. Gynandropsis gynandra NAD-MEα/β1 (GgNAD-MEα/β1) exhibits high catalytic efficiency and is differentially activated by the C4 intermediate aspartate, confirming its role as the C4 -decarboxylase. During C4 evolution, NAD-MEβ1 lost its catalytic activity; its contribution to the enzymatic activity results from a stabilizing effect on the associated α-subunit and the acquisition of regulatory properties. We conclude that in bundle sheath cell mitochondria of C4 species, the functions of NAD-ME as C4 photosynthetic decarboxylase and as a housekeeping enzyme coexist and are performed by isoforms that combine the same α-subunit with differentially adapted β-subunits. Abstract : In C4 bundle sheath cell mitochondria, the housekeeping and C4 -decarboxylase functions of NAD-ME are performed by isoforms that combine the same α subunit with differentially adapted β subunits. … (more)
- Is Part Of:
- The Plant Cell. Volume 34:Issue 1(2022)
- Journal:
- The Plant Cell
- Issue:
- Volume 34:Issue 1(2022)
- Issue Display:
- Volume 34, Issue 1 (2022)
- Year:
- 2022
- Volume:
- 34
- Issue:
- 1
- Issue Sort Value:
- 2022-0034-0001-0000
- Page Start:
- 597
- Page End:
- 615
- Publication Date:
- 2021-11-04
- Journal URLs:
- http://www.oxfordjournals.org/ ↗
- DOI:
- 10.1093/plcell/koab265 ↗
- Languages:
- English
- ISSNs:
- 1040-4651
- 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:
- 25231.xml