Cited by 367Bacterial Genetics and BiotechnologyDrug Transport and Resistance MechanismsEscherichia coli research studies

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New substrates for TonB-dependent transport: do we only see the ‘tip of the iceberg’?

Schauer, Kristine, Rodionov, Dmitry A., de Reuse, Hilde·2008·Trends in Biochemical Sciences

DOI 10.1016/j.tibs.2008.04.012

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Abstract

TonB-dependent transport is a mechanism for active uptake across the outer membrane of Gram-negative bacteria. The system promotes transport of rare nutrients and was thought to be restricted to iron complexes and vitamin B12. Recent experimental evidence of TonB-energized transport of nickel and different carbohydrates, in addition to bioinformatic-based predictions, challenges this notion and reveals that the number and variety of TonB-dependent substrates is underestimated. It is becoming clear that the chemical nature of the substrates, the energetic requirements for transport and the subsequent translocation across the cytoplasmic membrane can differ from those of the well-studied systems for iron complexes and vitamin B12. These findings question the understanding of TonB-dependent uptake and provide insights into the adaptation of bacteria to their environments.

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References
(2010) · Calcium binding proteins · doi:10.1002/9780470872390.refs
Porins and TonB-like proteins in Anabaena sp. PCC 7120
Schätzle, H. (2022) · Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) · doi:10.21248/gups.66905
Applications of Site-directed Spin Labeling Electron Paramagnetic Resonance to Studying the Structure, Dynamics and Interactions of Membrane Proteins
Freed, D. M. (2012) · doi:10.18130/v3xp1z
Hemophore Has A
Izadi‐Pruneyre, N., Wolff, N., Delepierre, M., & Lecroisey, A. (2004) · Handbook of Metalloproteins · doi:10.1002/0470028637.met273
In vivo tests of the E. coli TonB system working model—interaction of ExbB with unknown proteins, identification of TonB-ExbD transmembrane heterodimers and PMF-dependent ExbD structuresPreprint
Postle, K., Kopp, D. R., & Jana, B. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.10.602958
Unusual Ecofunctional Traits of Endozoicomonas : A Pan-Genomic PerspectivePreprint
Lim, S. L., Chin, C., Chiou, Y., Hsu, M., Chiang, P., Chen, H., Tu, Y., & Tang, S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.06.641946
Plants, Microbes, and Carbon: The Interplay of Carbon Cycling and Sequestration
Kumar, D., Saraf, M. S., & Glick, B. R. (2025) · Microorganisms for sustainability · doi:10.1007/978-981-96-3425-5_8
Receptor-substrate competition for the TonB homologue FusB suggests a model for ferredoxin import in Pectobacterium sppPreprint
Wojnowska, M., Flores, V. M. Q., Yelland, T., Fisher, S. R., Bogucka, A., Stott, K. M., & Walker, D. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.16.682781
Nickel Pollution, Resistance and its Bioremediation Mechanisms – A Review
Zarka Babar, A. F. (2021) · International Journal of Biosciences (IJB) · doi:10.12692/ijb/18.3.74-88
Additional file 1 of Lipid membrane remodeling and metabolic response during isobutanol and ethanol exposure in Zymomonas mobilis
Vazquez, J. C. R., Trujillo, E. A., Williams, J., She, F., Getahun, F., Callaghan, M. M., Coon, J. J., & Amador‐Noguez, D. (2024) · Figshare · doi:10.6084/m9.figshare.26673711
Additional file 7 of Lipid membrane remodeling and metabolic response during isobutanol and ethanol exposure in Zymomonas mobilis
Vazquez, J. C. R., Trujillo, E. A., Williams, J., She, F., Getahun, F., Callaghan, M. M., Coon, J. J., & Amador‐Noguez, D. (2024) · Figshare · doi:10.6084/m9.figshare.26673741
Additional file 3 of The TonB system in Aeromonas hydrophila NJ-35 is essential for MacA2B2 efflux pump-mediated macrolide resistance
Dong, Y., Li, Q., Geng, J., Cao, Q., Zhao, D., Jiang, M., Li, S., Lu, C., & Liu, Y. (2021) · Figshare · doi:10.6084/m9.figshare.14516392
Additional file 3 of Lipid membrane remodeling and metabolic response during isobutanol and ethanol exposure in Zymomonas mobilis
Vazquez, J. C. R., Trujillo, E. A., Williams, J., She, F., Getahun, F., Callaghan, M. M., Coon, J. J., & Amador‐Noguez, D. (2024) · Figshare · doi:10.6084/m9.figshare.26673717
Additional file 1 of The TonB system in Aeromonas hydrophila NJ-35 is essential for MacA2B2 efflux pump-mediated macrolide resistance
Dong, Y., Li, Q., Geng, J., Cao, Q., Zhao, D., Jiang, M., Li, S., Lu, C., & Liu, Y. (2021) · Figshare · doi:10.6084/m9.figshare.14516386
Additional file 2 of The TonB system in Aeromonas hydrophila NJ-35 is essential for MacA2B2 efflux pump-mediated macrolide resistance
Dong, Y., Li, Q., Geng, J., Cao, Q., Zhao, D., Jiang, M., Li, S., Lu, C., & Liu, Y. (2021) · Figshare · doi:10.6084/m9.figshare.14516389
Additional file 6 of Lipid membrane remodeling and metabolic response during isobutanol and ethanol exposure in Zymomonas mobilis
Vazquez, J. C. R., Trujillo, E. A., Williams, J., She, F., Getahun, F., Callaghan, M. M., Coon, J. J., & Amador‐Noguez, D. (2024) · Figshare · doi:10.6084/m9.figshare.26673732
Additional file 2 of Lipid membrane remodeling and metabolic response during isobutanol and ethanol exposure in Zymomonas mobilis
Vazquez, J. C. R., Trujillo, E. A., Williams, J., She, F., Getahun, F., Callaghan, M. M., Coon, J. J., & Amador‐Noguez, D. (2024) · Figshare · doi:10.6084/m9.figshare.26673714
Additional file 5 of Lipid membrane remodeling and metabolic response during isobutanol and ethanol exposure in Zymomonas mobilis
Vazquez, J. C. R., Trujillo, E. A., Williams, J., She, F., Getahun, F., Callaghan, M. M., Coon, J. J., & Amador‐Noguez, D. (2024) · Figshare · doi:10.6084/m9.figshare.26673723
Additional file 4 of Lipid membrane remodeling and metabolic response during isobutanol and ethanol exposure in Zymomonas mobilis
Vazquez, J. C. R., Trujillo, E. A., Williams, J., She, F., Getahun, F., Callaghan, M. M., Coon, J. J., & Amador‐Noguez, D. (2024) · Figshare · doi:10.6084/m9.figshare.26673720
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Park, S.-N., Lim, Y. K., Ji, S., & Kook, J. (2025) · Microbiology and Biotechnology Letters · doi:10.48022/mbl.2510.10003
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Liu, T., Kong, L., Hong, H., & Shi, D. (2026) · Chinese Science Bulletin (Chinese Version) · doi:10.1360/csb-2025-5610
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Lebrette, H. (2013) · doi:10.70675/db633d2cz4ae0z4700zafc5z11106d16c2fc
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Golanowska, M. (2015) · theses.fr (ABES) · doi:10.70675/ba5a448azf019z4647zb78ez39cbffcfc3b5 · Cited by 3
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Boudehen, Y. (2020) · theses.fr (ABES) · doi:10.70675/4aae412fz4269z4058zb0e9zbf70d71e9d7a
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Jaho, S. (2021) · doi:10.70675/16504145z5ba6z43a1z9fb0zb86ddcc74218
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Roy, G. (2022) · theses.fr (ABES) · doi:10.70675/2eb0443bzd3a9z44e0zab2cz9c342bb4ae43
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Wojnowska, M., Flores, V., Yelland, T., Fisher, S. R., Bogucka, A., Stott, K., & Walker, D. (2026) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2026.113121 · Cited by 1
Genome-wide analysis and growth-promoting potential of Burkholderia gladioli YNK-FB0053
Wu, D.-X., Chen, Y., Pu, T., Shi, Z.-F., Pei, W., Tang, J., Hu, J., Chen, Q., & Yang, P.-W. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1858481
Cellular basis of B 12 uptake and remodelling in microalgae revealed using a novel bioassayPreprint
Harrison, E. L., Bunbury, F., Stadelmann, T., Sayer, A., Pasquina, M. L., Papadopoulos, K. P., Geisler, K., Mehrshahi, P., Davey, M. P., & Smith, A. G. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.07.738727
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Wojciechowska, M., Tsylents, U., & Trylska, J. (2026) · Methods in molecular biology · doi:10.1007/978-1-0716-5368-5_14
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Connolly, A. N., Moushtaq, L., Pu, Q., Brindley, A. A., Scanlan, D. J., van den Berg, B., Hitchcock, A., & Lidbury, I. D. E. A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.03.749221
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Hitch, T. C. A., & Clavel, T. (2026) · Springer eBooks · doi:10.1007/978-3-032-26410-7_2
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Authors: Schauer, K., Rodionov, D. A., & de Reuse, H.
Affiliations: Centre National de la Recherche Scientifique (FR)
Russian Academy of Sciences (RU)
ORCID: Schauer, Kristine
Rodionov, Dmitry A.
Venue: Trends in Biochemical Sciences
Publisher: Elsevier BV
Published: 2008-07
Volume: 33
Issue: 7
Pages: 330-338
ISSN: 0968-0004 (ISSN-L)
DOI: 10.1016/j.tibs.2008.04.012
OpenAlex: W2130630244
Cited by: 360
References: 70
Citations by year: 2026: 12 · 2025: 20 · 2024: 11 · 2023: 5 · 2022: 25 · 2021: 19 · 2020: 28 · 2019: 20 · 2018: 17 · 2017: 29 · 2016: 28 · 2015: 11 · 2014: 23 · 2013: 30 · 2012: 23
FWCI: 1.78
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Trends in Biochemical Sciences (publishedVersion)
PubMed (publishedVersion)
Funders: Deutscher Akademischer Austauschdienst
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
Life Sciences › Immunology and Microbiology › Microbiology › Escherichia coli research studies
Keywords: TonB-dependent transport, Gram-negative bacteria, iron complexes, vitamin B12, nickel uptake, carbohydrate transport, substrate specificity, bacterial adaptation
MeSH terms: Bacterial Proteins, Biological Transport, Membrane Proteins, Models, Biological, Phylogeny, Vitamin B 12

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New substrates for TonB-dependent transport: do we only see the ‘tip of the iceberg’?

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