TY - JOUR
T1 - Positioning of the motility machinery in halophilic archaea
AU - Li, Zhengqun
AU - Kinosita, Yoshiaki
AU - Rodriguez-Franco, Marta
AU - Nußbaum, Phillip
AU - Braun, Frank
AU - Delpech, Floriane
AU - Quax, Tessa E. F.
AU - Albers, Sonja Verena
N1 - Funding Information:
This research was supported by a Margarete von Wrangell grant to T.E.F.Q. from the Ministerium für Wissenschaft, Forschung und Kunst of Baden-Württemberg and a fellowship to Z.L. from the Chinese Scholarship Council. P.N., F.B., and F.D. were supported by funding from the European Union’s Horizon 2020 research and innovation program under grant agreement no. 686647 (MARA [Molecular Analytical Robotics Assays]). Y.K. was supported by a postdoctoral Fellowship from the Japan Society for the Promotion of Science. Additionally, P.N. was supported by a grant from the German-Israeli Foundation (GIF 1290).
Funding Information:
The article processing charge was funded by the German Research Foundation (DFG) and the University of Freiburg in the funding programme Open Access Publishing.
Funding Information:
We thank Marleen van Wolferen for help with fluorescence microscopy, Iain Duggin for providing the GFP and mCherry sequences, and Thorsten Allers for advice on genetics. This research was supported by a Margarete von Wrangell grant to T.E.F.Q. from the Ministerium für Wissenschaft, Forschung und Kunst of Baden-Württemberg and a fellowship to Z.L. from the Chinese Scholarship Council. P.N., F.B., and F.D. were supported by funding from the European Union’s Horizon 2020 research and innovation program under grant agreement no. 686647 (MARA [Molecular Analytical Robotics Assays]). Y.K. was supported by a postdoctoral Fellowship from the Japan Society for the Promotion of Science. Additionally, P.N. was supported by a grant from the German-Israeli Foundation (GIF 1290). T.E.F.Q. and S.-V.A. designed research. Z.L., Y.K., M.R.-F., and T.E.F.Q. performed research and interpreted data. P.N., F.B., and F.D. supported experiments. Z.L., T.E.F.Q., and S.-V.A. wrote the paper. All of us read and contributed to the manuscript. The article processing charge was funded by the German Research Foundation (DFG) and the University of Freiburg in the funding programme Open Access Publishing.
Publisher Copyright:
© 2019 Li et al.
PY - 2019/5/1
Y1 - 2019/5/1
N2 - Bacteria and archaea exhibit tactical behavior and can move up and down chemical gradients. This tactical behavior relies on a motility structure, which is guided by a chemosensory system. Environmental signals are sensed by membrane-inserted chemosensory receptors that are organized in large ordered arrays. While the cellular positioning of the chemotaxis machinery and that of the flagellum have been studied in detail in bacteria, we have little knowledge about the localization of such macromolecular assemblies in archaea. Although the archaeal motility structure, the archaellum, is fundamentally different from the flagellum, archaea have received the chemosensory machinery from bacteria and have connected this system with the archaellum. Here, we applied a combination of time-lapse imaging and fluorescence and electron microscopy using the model euryar-chaeon Haloferax volcanii and found that archaella were specifically present at the cell poles of actively dividing rod-shaped cells. The chemosensory arrays also had a polar preference, but in addition, several smaller arrays moved freely in the lateral membranes. In the stationary phase, rod-shaped cells became round and chemosensory arrays were disassembled. The positioning of archaella and that of chemosensory arrays are not interdependent and likely require an independent form of positioning machinery. This work showed that, in the rod-shaped haloarchaeal cells, the positioning of the archaellum and of the chemosensory arrays is regulated in time and in space. These insights into the cellular organization of H. volcanii suggest the presence of an active mechanism responsible for the positioning of macromolecular protein complexes in archaea. IMPORTANCE Archaea are ubiquitous single cellular microorganisms that play important ecological roles in nature. The intracellular organization of archaeal cells is among the unresolved mysteries of archaeal biology. With this work, we show that cells of haloarchaea are polarized. The cellular positioning of proteins involved in chemotaxis and motility is spatially and temporally organized in these cells. This suggests the presence of a specific mechanism responsible for the positioning of macromolecular protein complexes in archaea.
AB - Bacteria and archaea exhibit tactical behavior and can move up and down chemical gradients. This tactical behavior relies on a motility structure, which is guided by a chemosensory system. Environmental signals are sensed by membrane-inserted chemosensory receptors that are organized in large ordered arrays. While the cellular positioning of the chemotaxis machinery and that of the flagellum have been studied in detail in bacteria, we have little knowledge about the localization of such macromolecular assemblies in archaea. Although the archaeal motility structure, the archaellum, is fundamentally different from the flagellum, archaea have received the chemosensory machinery from bacteria and have connected this system with the archaellum. Here, we applied a combination of time-lapse imaging and fluorescence and electron microscopy using the model euryar-chaeon Haloferax volcanii and found that archaella were specifically present at the cell poles of actively dividing rod-shaped cells. The chemosensory arrays also had a polar preference, but in addition, several smaller arrays moved freely in the lateral membranes. In the stationary phase, rod-shaped cells became round and chemosensory arrays were disassembled. The positioning of archaella and that of chemosensory arrays are not interdependent and likely require an independent form of positioning machinery. This work showed that, in the rod-shaped haloarchaeal cells, the positioning of the archaellum and of the chemosensory arrays is regulated in time and in space. These insights into the cellular organization of H. volcanii suggest the presence of an active mechanism responsible for the positioning of macromolecular protein complexes in archaea. IMPORTANCE Archaea are ubiquitous single cellular microorganisms that play important ecological roles in nature. The intracellular organization of archaeal cells is among the unresolved mysteries of archaeal biology. With this work, we show that cells of haloarchaea are polarized. The cellular positioning of proteins involved in chemotaxis and motility is spatially and temporally organized in these cells. This suggests the presence of a specific mechanism responsible for the positioning of macromolecular protein complexes in archaea.
KW - Archaea
KW - Archaellum
KW - Cell polarity
KW - Chemotaxis
KW - Motility
UR - http://www.scopus.com/inward/record.url?scp=85065781865&partnerID=8YFLogxK
U2 - 10.1128/mBio.00377-19
DO - 10.1128/mBio.00377-19
M3 - Article
C2 - 31064826
AN - SCOPUS:85065781865
SN - 2161-2129
VL - 10
JO - mBio
JF - mBio
IS - 3
M1 - e00377-19
ER -