-
Something wrong with this record ?
The antenna-like domain of the cyanobacterial ferrochelatase can bind chlorophyll and carotenoids in an energy-dissipative configuration
M. Pazderník, J. Mareš, J. Pilný, R. Sobotka,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 2008 to 1 year ago
Freely Accessible Science Journals
from 1905 to 1 year ago
PubMed Central
from 2005
Europe PubMed Central
from 2005 to 1 year ago
Open Access Digital Library
from 1905-10-01
Open Access Digital Library
from 1905-10-01
ROAD: Directory of Open Access Scholarly Resources
from 1905
- MeSH
- Chlorophyll A metabolism MeSH
- Chlorophyll metabolism MeSH
- Dimerization MeSH
- Ferrochelatase chemistry metabolism MeSH
- Phylogeny MeSH
- Carotenoids metabolism MeSH
- Protein Conformation MeSH
- Light-Harvesting Protein Complexes metabolism MeSH
- Synechocystis enzymology MeSH
- Binding Sites MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Ferrochelatase (FeCh) is an essential enzyme catalyzing the synthesis of heme. Interestingly, in cyanobacteria, algae, and plants, FeCh possesses a conserved transmembrane chlorophyll a/b binding (CAB) domain that resembles the first and the third helix of light-harvesting complexes, including a chlorophyll-binding motif. Whether the FeCh CAB domain also binds chlorophyll is unknown. Here, using biochemical and radiolabeled precursor experiments, we found that partially inhibited activity of FeCh in the cyanobacterium Synechocystis PCC 6803 leads to overproduction of chlorophyll molecules that accumulate in the thylakoid membrane and, together with carotenoids, bind to FeCh. We observed that pigments bound to purified FeCh are organized in an energy-dissipative conformation and further show that FeCh can exist in vivo as a monomer or a dimer depending on its own activity. However, pigmented FeCh was purified exclusively as a dimer. Separately expressed and purified FeCH CAB domain contained a pigment composition similar to that of full-length FeCh and retained its quenching properties. Phylogenetic analysis suggested that the CAB domain was acquired by a fusion between FeCh and a single-helix, high light-inducible protein early in the evolution of cyanobacteria. Following this fusion, the FeCh CAB domain with a functional chlorophyll-binding motif was retained in all currently known cyanobacterial genomes except for a single lineage of endosymbiotic cyanobacteria. Our findings indicate that FeCh from Synechocystis exists mostly as a pigment-free monomer in cells but can dimerize, in which case its CAB domain creates a functional pigment-binding segment organized in an energy-dissipating configuration.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20023817
- 003
- CZ-PrNML
- 005
- 20201214131316.0
- 007
- ta
- 008
- 201125s2019 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1074/jbc.RA119.008434 $2 doi
- 035 __
- $a (PubMed)31167780
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Pazderník, Marek $u Institute of Microbiology, Czech Academy of Sciences, Centre Algatech, Třeboň, 379 81, Czech Republic. Faculty of Science, University of South Bohemia, České Budějovice 370 05, Czech Republic.
- 245 14
- $a The antenna-like domain of the cyanobacterial ferrochelatase can bind chlorophyll and carotenoids in an energy-dissipative configuration / $c M. Pazderník, J. Mareš, J. Pilný, R. Sobotka,
- 520 9_
- $a Ferrochelatase (FeCh) is an essential enzyme catalyzing the synthesis of heme. Interestingly, in cyanobacteria, algae, and plants, FeCh possesses a conserved transmembrane chlorophyll a/b binding (CAB) domain that resembles the first and the third helix of light-harvesting complexes, including a chlorophyll-binding motif. Whether the FeCh CAB domain also binds chlorophyll is unknown. Here, using biochemical and radiolabeled precursor experiments, we found that partially inhibited activity of FeCh in the cyanobacterium Synechocystis PCC 6803 leads to overproduction of chlorophyll molecules that accumulate in the thylakoid membrane and, together with carotenoids, bind to FeCh. We observed that pigments bound to purified FeCh are organized in an energy-dissipative conformation and further show that FeCh can exist in vivo as a monomer or a dimer depending on its own activity. However, pigmented FeCh was purified exclusively as a dimer. Separately expressed and purified FeCH CAB domain contained a pigment composition similar to that of full-length FeCh and retained its quenching properties. Phylogenetic analysis suggested that the CAB domain was acquired by a fusion between FeCh and a single-helix, high light-inducible protein early in the evolution of cyanobacteria. Following this fusion, the FeCh CAB domain with a functional chlorophyll-binding motif was retained in all currently known cyanobacterial genomes except for a single lineage of endosymbiotic cyanobacteria. Our findings indicate that FeCh from Synechocystis exists mostly as a pigment-free monomer in cells but can dimerize, in which case its CAB domain creates a functional pigment-binding segment organized in an energy-dissipating configuration.
- 650 _2
- $a vazebná místa $7 D001665
- 650 _2
- $a karotenoidy $x metabolismus $7 D002338
- 650 _2
- $a chlorofyl $x metabolismus $7 D002734
- 650 _2
- $a chlorofyl a $x metabolismus $7 D000077194
- 650 _2
- $a dimerizace $7 D019281
- 650 _2
- $a ferrochelatasa $x chemie $x metabolismus $7 D005294
- 650 _2
- $a světlosběrné proteinové komplexy $x metabolismus $7 D045342
- 650 _2
- $a fylogeneze $7 D010802
- 650 _2
- $a konformace proteinů $7 D011487
- 650 _2
- $a Synechocystis $x enzymologie $7 D046939
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Mareš, Jan $u Institute of Microbiology, Czech Academy of Sciences, Centre Algatech, Třeboň, 379 81, Czech Republic. Faculty of Science, University of South Bohemia, České Budějovice 370 05, Czech Republic. Institute of Hydrobiology, Biology Centre of the Czech Academy of Sciences, České Budějovice 370 05, Czech Republic.
- 700 1_
- $a Pilný, Jan $u Institute of Microbiology, Czech Academy of Sciences, Centre Algatech, Třeboň, 379 81, Czech Republic.
- 700 1_
- $a Sobotka, Roman $u Institute of Microbiology, Czech Academy of Sciences, Centre Algatech, Třeboň, 379 81, Czech Republic sobotka@alga.cz. Faculty of Science, University of South Bohemia, České Budějovice 370 05, Czech Republic.
- 773 0_
- $w MED00002546 $t The Journal of biological chemistry $x 1083-351X $g Roč. 294, č. 29 (2019), s. 11131-11143
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31167780 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20201125 $b ABA008
- 991 __
- $a 20201214131315 $b ABA008
- 999 __
- $a ok $b bmc $g 1596136 $s 1114493
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 294 $c 29 $d 11131-11143 $e 20190605 $i 1083-351X $m The Journal of biological chemistry $n J Biol Chem $x MED00002546
- LZP __
- $a Pubmed-20201125