Excess copper catalyzes protein disulfide bond formation in the bacterial periplasm but not in the cytoplasm.

ABSTRACT: Copper avidly binds thiols and is redox active, and it follows that one element of copper toxicity may be the generation of undesirable disulfide bonds in proteins. In the present study, copper oxidized the model thiol N-acetylcysteine in vitro. Alkaline phosphatase (AP) requires disulfide bonds for activity, and copper activated reduced AP both in vitro and when it was expressed in the periplasm of mutants lacking their native disulfide-generating system. However, AP was not activated when it was expressed in the cytoplasm of copper-overloaded cells. Similarly, this copper stress failed to activate OxyR, a transcription factor that responds to the creation of a disulfide bond. The elimination of cellular disulfide-reducing systems did not change these results. Nevertheless, in these cells

SUBMITTER: Eben SS 

PROVIDER: S-EPMC10155707 | biostudies-literature | 2023 Apr

REPOSITORIES: biostudies-literature