Activation potassium efflux from <i>Escherichia coli</i> by glutathione metabolites

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Abstract

<jats:title>Summary</jats:title><jats:p>The mechanism by which <jats:italic>N</jats:italic>‐ethylmaleimide (NEM) elicits potassium efflux from <jats:italic>Escherichia coli</jats:italic> has been investigated. The critical factor is the formation of specific glutathione metabolites that activate transport systems encoded by the <jats:italic>kefB</jats:italic> and <jats:italic>kefC</jats:italic> gene products. Formation of <jats:italic>N</jats:italic>‐ethyl‐succinimido‐<jats:italic>S</jats:italic>‐glutathione (ESG) leads to the activation of potassium efflux via these transport systems. The addition of dithiothreitol and other reducing agents to cells reverses this process by causing the breakdown of ESG and thus removing the activator of the systems. Chlorodinitrobenzene, <jats:italic>p</jats:italic>‐chloromercuribenzoate and phenylmaleimide provoke similar effects to NEM. Iodoacetate, which leads to the formation of <jats:italic>S</jats:italic>‐carboxymethyl‐glutathione, does not activate the systems but does prevent the action of NEM. It is concluded that the KefB and KefC systems are gated by glutathione metabolites and that the degree to which they are activated is dependent upon the nature of the substituent on the sulphydryl group.</jats:p>

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