Bradyrhizobium japonicum TlpA, a novel membrane-anchored thioredoxin-like protein involved in the biogenesis of cytochrome aa3 and development of symbiosis.

Abstract

We report the discovery of a bacterial gene, tlpA, that codes for a hitherto unknown type of thioredoxin‐like protein. The gene was found in the course of studying a Tn5 insertion mutant of the soybean root nodule symbiont Bradyrhizobium japonicum. The TlpA protein shared up to 31% amino acid sequence identity with various eukaryotic and prokaryotic thioredoxins and protein disulfide isomerases, and possessed a characteristic active‐site sequence, Trp‐Cys‐Val‐Pro‐Cys. In contrast to all members of the thioredoxin family known to date, TlpA was shown to be anchored to the cytoplasmic membrane by means of an N‐terminal transmembrane domain, while the active site‐containing part of the protein faced the periplasm. The tlpA mutant had a pleiotropic phenotype in that it was defective in the development of a nitrogen fixing endosymbiosis and exhibited a strongly decreased oxidase activity, as compared with the wild‐type. Holocytochrome aa3 was spectroscopically undetectable in the mutant, whereas the apoprotein of subunit one (CoxA) of this oxidase was still synthesized and incorporated into the cytoplasmic membrane. Since cytochrome aa3 is not a prerequisite for the development of symbiosis, the results suggest that TlpA is involved in at least two independent cellular processes, one of which is an essential periplasmic step in the maturation of cytochrome aa3.

Histidine 131, not histidine 43, of the Bradyrhizobium japonicum FixN protein is exposed towards the periplasm and essential for the function of the cbb3‐type cytochrome oxidase

“…13-Galactosidase and alkaline phosphatase activities were measured in duplicate from 100-ml samples of three independent cultures as described [22]. Tetramethyl-p-phenylenediamine (TMPD) oxidase activity, cytochrome c oxidase activity with reduced horse heart cytochrome c as an electron donor and the nitrogen fixation activity were measured as described before [5].…”

Bacillus subtilis ResA Is a Thiol-Disulfide Oxidoreductase involved in Cytochrome c Synthesis

“…E. coli DsbC, which functions in the redistribution of disulfide bonds among the cysteine residues of target proteins (2); and reduction reactions, e.g. Bradyrhizobium japonicum TlpA, which functions in the assembly of cytochrome aa 3 (3).…”

The Acidic Nature of the CcmG Redox-Active Center Is Important for CytochromecMaturation inEscherichia coli

“…Asp26 in TRX has been implicated in deprotonating the second cysteine in the Cys-X-X-Cys motif via a nearby water molecule (4,17). Interestingly, B. japonicum TlpA, a periplasmic TRX-like protein that is required for the maturation of aa 3 -type cytochromes (2,19), contains an acidic residue (Glu78) that aligns with the equivalent residue in CcmG. Therefore, Glu86 in CcmG and Glu78 in TlpA are in a prime position to fulfill a role in catalysis similar to that of Asp26 in TRX.…”