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The dual role of MamB in magnetosome membrane assembly and magnetite biomineralization

URN zum Zitieren der Version auf EPub Bayreuth: urn:nbn:de:bvb:703-epub-4319-8

Titelangaben

Uebe, René ; Keren-Khadmy, Noa ; Zeytuni, Natalie ; Katzmann, Emanuel ; Navon, Yotam ; Davidov, Geula ; Bitton, Ronit ; Plitzko, Jürgen M. ; Schüler, Dirk ; Zarivach, Raz:
The dual role of MamB in magnetosome membrane assembly and magnetite biomineralization.
Bayreuth, Germany , 2017

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Angaben zu Projekten

Projekttitel:
Offizieller Projekttitel
Projekt-ID
European Union’s Horizon 2020 research and innovation programme
692637

Projektfinanzierung: European Research Council (ERC)
Israel Ministry of Science, Technology and Space (R.Z.)
Israel Science Foundation (grant No. 167/16; R.Z.)
European Molecular Biology Organization and CMST COST Action CM1306 (R.Z.)

Abstract

Magnetospirillum gryphiswaldense MSR-1 synthesizes membrane-enclosed magnetite (Fe3O4) nanoparticles, magnetosomes, for magnetotaxis. Formation of these organelles involves a complex process comprising key steps which are governed by specific magnetosome-associated proteins. MamB, a cation diffusion facilitator (CDF) family member has been implicated in magnetosome-directed iron transport. However, deletion mutagenesis studies revealed that MamB is essential for the formation of magnetosome membrane vesicles, but its precise role remains elusive. In this study, we employed a multi-disciplinary approach to define the role of MamB during magnetosome formation. Using site-directed mutagenesis complemented by structural analyses, fluorescence microscopy and cryo-electron tomography, we show that MamB is most likely an active magnetosome-directed transporter serving two distinct, yet essential functions. First, MamB initiates magnetosome vesicle formation in a transport-independent process, probably by serving as a landmark protein. Second, MamB transport activity is required for magnetite nucleation. Furthermore, by determining the crystal structure of the MamB cytosolic C-terminal domain, we also provide mechanistic insight into transport regulation. Additionally, we present evidence that magnetosome vesicle growth and chain formation are independent of magnetite nucleation and magnetic interactions, respectively. Together, our data provide novel insight into the role of the key bifunctional magnetosome protein MamB, and the early steps of magnetosome formation.

Weitere Angaben

Publikationsform: Preprint, Postprint
Zusätzliche Informationen (öffentlich sichtbar): erschienen in:
Molecular Microbiology. Bd. 107 (2018) Heft 4 . - S. 542-557.
DOI: https://doi.org/10.1111/mmi.13899

This project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (grant agreement No 692637, D.S.) and the Israel Ministry of Science, Technology and Space (R.Z.), the Israel Science Foundation (grant No. 167/16; R.Z.), the European Molecular Biology Organization and CMST COST Action CM1306 (R.Z.).
Keywords: Bacterial organelle; biomineralization; cation diffusion facilitators; iron transport; magnetosome biogenesis; magnetotactic bacteria; membrane invagination; structure-function analysis
Themengebiete aus DDC: 500 Naturwissenschaften und Mathematik > 570 Biowissenschaften; Biologie
Institutionen der Universität: Fakultäten > Fakultät für Biologie, Chemie und Geowissenschaften > Fachgruppe Biologie > Lehrstuhl Mikrobiologie > Lehrstuhl Mikrobiologie - Univ.-Prof. Dr. Dirk Schüler
Fakultäten
Fakultäten > Fakultät für Biologie, Chemie und Geowissenschaften
Fakultäten > Fakultät für Biologie, Chemie und Geowissenschaften > Fachgruppe Biologie
Fakultäten > Fakultät für Biologie, Chemie und Geowissenschaften > Fachgruppe Biologie > Lehrstuhl Mikrobiologie
Sprache: Englisch
Titel an der UBT entstanden: Ja
URN: urn:nbn:de:bvb:703-epub-4319-8
Eingestellt am: 25 Apr 2019 10:57
Letzte Änderung: 26 Mai 2021 10:31
URI: https://epub.uni-bayreuth.de/id/eprint/4319

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