It takes two to tango: two TatA paralogues and two redox enzyme-specific chaperones are involved in the localization of twin-arginine translocase substrates in Campylobacter jejuni

• Published in: Microbiology (Society for General Microbiology) 2014-09, Vol.160 (Pt 9), p.2053-2066
• Main Authors: Liu, Yang-Wei, Hitchcock, Andrew, Salmon, Robert C, Kelly, David J
• Format: Article
• Language: English
• Subjects: Campylobacter jejuni - enzymology; Campylobacter jejuni - genetics; Campylobacter jejuni - growth & development; Campylobacter jejuni - metabolism; Enzymes - metabolism; Gene Deletion; Membrane Transport Proteins - genetics; Membrane Transport Proteins - metabolism; Molecular Chaperones - genetics; Molecular Chaperones - metabolism; Periplasmic Proteins - metabolism; Physiology and Biochemistry; Protein Transport
• ISSN: 1350-0872; 1465-2080
• DOI: 10.1099/mic.0.080713-0

The food-borne zoonotic pathogen Campylobacter jejuni has complex electron transport chains required for growth in the host, many of which contain cofactored periplasmic enzymes localized by the twin-arginine translocase (TAT). We report here the identification of two paralogues of the TatA translocase component in C. jejuni strain NCTC 11168, encoded by cj1176c (tatA1) and cj0786 (tatA2). Deletion mutants constructed in either or both of the tatA1 and tatA2 genes displayed distinct growth and enzyme activity phenotypes. For sulphite oxidase (SorAB), the multi-copper oxidase (CueO) and alkaline phosphatase (PhoX), complete dependency on TatA1 for correct periplasmic activity was observed. However, the activities of nitrate reductase (NapA), formate dehydrogenase (FdhA) and trimethylamine N-oxide reductase (TorA) were significantly reduced in the tatA2 mutant. In contrast, the specific rate of fumarate reduction catalysed by the flavoprotein subunit of the methyl menaquinone fumarate reductase (MfrA) was similar in periplasmic fractions of both the tatA1 and the tatA2 mutants and only the deletion of both genes abolished activity. Nevertheless, unprocessed MfrA accumulated in the periplasm of the tatA1 (but not tatA2) mutant, indicating aberrant signal peptide cleavage. Surprisingly, TatA2 lacks two conserved residues (Gln8 and Phe39) known to be essential in Escherichia coli TatA and we suggest it is unable to function correctly in the absence of TatA1. Finally, only two TAT chaperones (FdhM and NapD) are encoded in strain NCTC 11168, which mutant studies confirmed are highly specific for formate dehydrogenase and nitrate reductase assembly, respectively. Thus, other TAT substrates must use general chaperones in their biogenesis.