Investigating MerR's Selectivity: The Crosstalk Between Cadmium and Copper Under Elevated Stress Conditions
Bacteria respond to metal pollution through sensors that control the uptake and the detoxification machineries. Specificity in metal recognition is therefore a prerequisite for triggering the appropriate response, particularly when facing a mixture of metals. In response to Cu , the purple bacterium...
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Veröffentlicht in: | Biomolecules (Basel, Switzerland) Switzerland), 2024-11, Vol.14 (11), p.1429 |
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Sprache: | eng |
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Zusammenfassung: | Bacteria respond to metal pollution through sensors that control the uptake and the detoxification machineries. Specificity in metal recognition is therefore a prerequisite for triggering the appropriate response, particularly when facing a mixture of metals. In response to Cu
, the purple bacterium
induces the efflux Cu
-ATPase CopA by the Cu
regulator CopR. However, genetic analyses have suggested the presence of additional regulators. Here, we show that CadR, the Cd
sensor, is involved in Cd
and Cu
tolerance and demonstrate that CopR and CadR share common target genes. Interestingly, expression of the Cu
detoxification and efflux (CopI/CopA) system was induced by Cd
and downregulated in the double mutant
. This double mutant was more sensitive to low Cu
concentration than the single
mutant, and accumulation of coproporphyrin III pointed to a significantly decreased expression of CopA. Furthermore, analyses of Cd
toxicity in the
mutant suggested that although CopR is Cu
selective, CopR is involved in Cd
response since the addition of Cu
alleviates Cd
toxicity. Based on our current knowledge of metal transport across the inner membrane, Cd
and Cu
do not share common efflux routes nor do they share common regulators. Nevertheless, the crosstalk between Cd
and Cu
tolerance systems is demonstrated in the present study. The modulation of Cu
detoxification by a Cd
regulator in vivo places emphasis on the relaxed selectivity, under elevated metal concentration, in MerR regulators. |
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ISSN: | 2218-273X 2218-273X |
DOI: | 10.3390/biom14111429 |