Encoded by the atpB gene (locus tag: CFF8240_0771), this subunit is part of the F0 sector of the ATP synthase complex, which drives ATP synthesis via proton translocation .
The recombinant protein spans 226 amino acids (UniProt ID: A0RP13) and includes an N-terminal His tag for purification .
Essential for oxidative phosphorylation: Facilitates proton transport across the membrane, enabling ATP synthesis .
Structural analyses reveal conserved transmembrane helices critical for interactions with other F0 subunits (e.g., subunit c) .
Produced in Escherichia coli using plasmid vectors optimized for Campylobacter-specific codon usage .
Purification involves immobilized metal affinity chromatography (IMAC) via the His tag, yielding >90% purity .
Used in ELISA to detect C. fetus-specific antibodies in clinical samples .
Immunogenicity studies suggest potential as a diagnostic marker for bovine and human infections .
Proteomic analyses (e.g., LFQ-MS) reveal altered expression in C. fetus glycosylation mutants, linking ATP synthase activity to hydrogenase regulation and nickel homeostasis .
Comparative genomics identifies atpB as a stable genetic marker for subspecies differentiation (e.g., C. fetus subsp. fetus vs. venerealis) .
atpB is conserved across C. fetus subspecies but exhibits transcriptional differences in niche-adapted strains .
In C. fetus subsp. venerealis, ATP synthase activity correlates with enhanced virulence gene expression via a type IV secretion system (T4SS) .
No direct AMR linkage reported, but C. fetus subsp. fetus harbors plasmid-borne resistance genes (e.g., tet(O), aph(3')-III) .
Recombinant atpB serves as a control in studies assessing AMR-related metabolic shifts .
KEGG: cff:CFF8240_0771