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Abstract

KHS3 is a marine bacterium whose genome codes for two different chemosensory pathways. Chemosensory gene cluster 1 is very similar to the canonical Che cluster from . Chemosensory cluster 2 includes a gene coding for a diguanylate cyclase with receiver domains, suggesting that it belongs to the functional group that regulates alternative cellular functions other than chemotaxis. In this work we assess the functional roles of both chemosensory pathways through approaches that include the heterologous expression of proteins in strains and phenotypic analyses of mutants. Our results confirm that chemosensory cluster 1 is indeed involved in chemotaxis behaviour, and only proteins from this cluster complement defects. We present evidence suggesting that chemosensory cluster 2 resembles the Wsp pathway from , since the corresponding methylesterase mutant shows an increased methylation level of the cognate receptor and develops a wrinkly colony morphology correlated with an increased ability to form biofilm. Consistently, mutational interruption of this gene cluster correlates with low levels of biofilm. Our results suggest that the proteins from each pathway assemble and function independently. However, the phenotypic characteristics of the mutants show functional connections between the pathways controlled by each chemosensory system.

Funding
This study was supported by the:
  • Fondo para la Investigación Científica y Tecnológica (Award PICT2016-1629)
    • Principle Award Recipient: ClaudiaA. Studdert
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/content/journal/micro/10.1099/mic.0.001251
2022-10-10
2024-05-20
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