TY - JOUR
T1 - Multistep signaling in nature
T2 - A close-up of geobacter chemotaxis sensing
AU - Silva, Marta A.
AU - Salgueiro, Carlos A.
N1 - Funding Information:
info:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FBIA-BQM%2F31981%2F2017/PT#
info:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FBIA-BQM%2F4967%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F04378%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04378%2F2020/PT#
Funding: This work was supported by Fundação para a Ciência e Tecnologia (FCT—Portugal) through the following grants: PTDC/BIA-BQM/31981/2017 (to CAS), PTDC/BIA-BQM/4967/2020 (to CAS). This work is also supported by national funds from FCT, I.P.,of the Research Unit on Applied Molecular Biosciences— UCIBIO and the project LA/P/0140/2020 of the Associate Laboratory Institute for Health and Bioe-conomy—i4HB.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/8/2
Y1 - 2021/8/2
N2 - Environmental changes trigger the continuous adaptation of bacteria to ensure their sur-vival. This is possible through a variety of signal transduction pathways involving chemoreceptors known as methyl-accepting chemotaxis proteins (MCP) that allow the microorganisms to redirect their mobility towards favorable environments. MCP are two-component regulatory (or signal transduction) systems (TCS) formed by a sensor and a response regulator domain. These domains synchronize transient protein phosphorylation and dephosphorylation events to convert the stimuli into an appropriate cellular response. In this review, the variability of TCS domains and the most common signaling mechanisms are highlighted. This is followed by the description of the overall cellular topology, classification and mechanisms of MCP. Finally, the structural and functional properties of a new family of MCP found in Geobacter sulfurreducens are revisited. This bacterium has a diverse repertoire of chemosensory systems, which represents a striking example of a survival mechanism in challenging environments. Two G. sulfurreducens MCP—GSU0582 and GSU0935— are members of a new family of chemotaxis sensor proteins containing a periplasmic PAS-like sensor domain with a c-type heme. Interestingly, the cellular location of this domain opens new routes to the understanding of the redox potential sensing signaling transduction pathways.
AB - Environmental changes trigger the continuous adaptation of bacteria to ensure their sur-vival. This is possible through a variety of signal transduction pathways involving chemoreceptors known as methyl-accepting chemotaxis proteins (MCP) that allow the microorganisms to redirect their mobility towards favorable environments. MCP are two-component regulatory (or signal transduction) systems (TCS) formed by a sensor and a response regulator domain. These domains synchronize transient protein phosphorylation and dephosphorylation events to convert the stimuli into an appropriate cellular response. In this review, the variability of TCS domains and the most common signaling mechanisms are highlighted. This is followed by the description of the overall cellular topology, classification and mechanisms of MCP. Finally, the structural and functional properties of a new family of MCP found in Geobacter sulfurreducens are revisited. This bacterium has a diverse repertoire of chemosensory systems, which represents a striking example of a survival mechanism in challenging environments. Two G. sulfurreducens MCP—GSU0582 and GSU0935— are members of a new family of chemotaxis sensor proteins containing a periplasmic PAS-like sensor domain with a c-type heme. Interestingly, the cellular location of this domain opens new routes to the understanding of the redox potential sensing signaling transduction pathways.
KW - C-type heme sensor domains
KW - Geobacter
KW - Methyl-accepting chemotaxis proteins
KW - Redox-sensing
KW - Signal transduction
KW - Two-component system
UR - http://www.scopus.com/inward/record.url?scp=85113212448&partnerID=8YFLogxK
U2 - 10.3390/ijms22169034
DO - 10.3390/ijms22169034
M3 - Review article
C2 - 34445739
AN - SCOPUS:85113212448
SN - 1661-6596
VL - 22
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 16
M1 - 9034
ER -