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Projekt Druckansicht

Regulation der substratabhängigen Expression und Aktivität von dehalogenierenden Enzymen in Dehalococcoides mccartyi strain CBDB1

Fachliche Zuordnung Stoffwechselphysiologie, Biochemie und Genetik der Mikroorganismen
Förderung Förderung von 2011 bis 2018
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 171475307
 
Erstellungsjahr 2020

Zusammenfassung der Projektergebnisse

Wichtigste Ergebnisse: Thermal proteome profiling (TPP) was modified for analyzing bacterial oxygen-sensitive enzymes. Protein-trichloroethene interactions in organohalide-respiring Sulfurospirillum multivorans were identified. Interaction of the tetrachloroethene reductive dehalogenase with trichloroethene was confirmed. A first hint for the interaction of a response regulator and a chlorinated ethene was provided. - First integrated omics approach including proteomics and acetylomics of an Epsilonproteobacterium. Systematic comparison of protein production and regulatory mechanisms in organohalide respiration. Improved protein extraction allowed higher coverage of membrane proteins. Lysine acetylations within the two-component regulatory system might be involved in long-term downregulation. - First reference proteome of Dehalococcoides mccartyi strain CBDB1. Identification of 8491 distinct peptides which represent 1023 proteins that cover 70% of all annotated proteins in strain CBDB1. Spectra library was generated to allow fast and precise protein identifications for the scientific community. A proteogenomics workflow led to a refinement of gene annotation of CBDB1 and identified 4 new to date not annotated gene sequences. - An optimal quantification assay for proteins (namely selective reaction monitoring (SRM) and precursor reaction monitoring (PRM)) with the focus on those involved in housekeeping functions and putative reductive dehalogenase proteins from the strictly anaerobic bacterium Dehalococcoides mccartyi strain CBDB1 was established.

Projektbezogene Publikationen (Auswahl)

 
 

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