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Molecular approaches towards control of sulfur flux in plants through selective deregulation of cysteine synthase complexes

Fachliche Zuordnung Pflanzenphysiologie
Förderung Förderung von 2008 bis 2014
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 87777596
 
Erstellungsjahr 2013

Zusammenfassung der Projektergebnisse

The plant cysteine synthase complex generates cysteine from serine, acetyl-coenzyme A and sulfide in the cytosol, plastids and mitochondria. The reversible association and dissociation of the constituting enzymes serine acetyltransferase (SAT) and O-acetylserine (thiol) lyase (OAS-TL) and the concomitant changes in enzymatic activity control the rate of cysteine synthesis is response to sulfide and OAS availability. The regulatory function of the cysteine synthase complex was analyzed using a de-regulation approach. Originally based on the model-based design of peptides that interfere with SAT/OAS-TL interaction in vitro and in vivo, the Arabidopsis mitochondrial cysteine synthase complex underwent a detailed and combined experimental and in silico analysis. The quaternary composition, peptide scanning and three-dimensional structure using dynamic modeling revealed an unusual structure with likely only one interaction site on each protein. Sulfide was shown to stabilize the cysteine synthase complex and to be partially detoxified by mitochondrial OAS-TL activity. A combination of reverse genetics and targeted mutation achieved de-regulation the cysteine synthase complex and suggested an additional function of this protein-protein interaction system with respect to cellular sulfur sensing. The proposed functions of the cysteine synthase complex were thus confirmed and complemented by new findings of functions in sulfide scavenging and signaling.

Projektbezogene Publikationen (Auswahl)

 
 

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