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- W1935417005 abstract "Chemoreceptors are at the beginning of chemosensory pathways that mediate chemotaxis. Pseudomonas putida KT2440 is predicted to have 27 chemoreceptors, most of which uncharacterized. We have previously identified McpS as chemoreceptor for Krebs cycle intermediates. Citrate is primarily present in the environment as metal complex, which, however, is not recognized by McpS. We show here that the McpS paralogue McpQ recognizes specifically citrate and citrate/metal2+ complexes. The McpQ ligand binding domain (McpQ-LBD) binds citrate/metal2+ complexes with higher affinity than citrate. McpQ-LBD is present in a monomer-dimer equilibrium and citrate and particularly citrate/Mg2+ binding stabilize the dimer. The bacterium showed much stronger responses to citrate/Mg2+ than to citrate and mcpQ inactivation caused a dramatic reduction in chemotaxis. Responses to Krebs cycle intermediates are thus mediated by the broad range McpS and McpQ that responds specifically to an intermediate not recognized by McpS. Interesting parallels exist to the paralogous amino acid chemoreceptors of Pseudomonas aeruginosa and Bacillus subtilis. Whereas one paralogue recognizes most amino acids, the remaining paralogue binds specifically one of the few acids not recognized by the broad range receptors. Therefore, chemotaxis to compound families by the concerted action of broad and narrow range receptors may represent a general mechanism." @default.
- W1935417005 created "2016-06-24" @default.
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- W1935417005 creator A5061404485 @default.
- W1935417005 date "2015-10-14" @default.
- W1935417005 modified "2023-10-17" @default.
- W1935417005 title "McpQ is a specific citrate chemoreceptor that responds preferentially to citrate/metal ion complexes" @default.
- W1935417005 cites W128133615 @default.
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- W1935417005 cites W1562607711 @default.
- W1935417005 cites W1564881569 @default.
- W1935417005 cites W1573831007 @default.
- W1935417005 cites W1579422048 @default.
- W1935417005 cites W1631101819 @default.
- W1935417005 cites W1749993378 @default.
- W1935417005 cites W1824614244 @default.
- W1935417005 cites W1841773228 @default.
- W1935417005 cites W1885931955 @default.
- W1935417005 cites W1899503782 @default.
- W1935417005 cites W1920238277 @default.
- W1935417005 cites W1965100720 @default.
- W1935417005 cites W1972918463 @default.
- W1935417005 cites W1974636817 @default.
- W1935417005 cites W1975317507 @default.
- W1935417005 cites W1975993749 @default.
- W1935417005 cites W1977125035 @default.
- W1935417005 cites W1980828843 @default.
- W1935417005 cites W1986874145 @default.
- W1935417005 cites W1989639494 @default.
- W1935417005 cites W1991174368 @default.
- W1935417005 cites W2012031105 @default.
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- W1935417005 cites W2029024880 @default.
- W1935417005 cites W2043488671 @default.
- W1935417005 cites W2050499271 @default.
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- W1935417005 doi "https://doi.org/10.1111/1462-2920.13030" @default.
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