The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Bacterial membrane lipids: diversity in structures and pathways
Open accessAbstract
For many decades, Escherichia coli was the main model organism for the study of bacterial membrane lipids. The results obtained served as a blueprint for membrane lipid biochemistry, but it is clear now that there is no such thing as a typical bacterial membrane lipid composition. Different bacterial species display different membrane compositions and even the membrane composition of cells belonging to a single species is not constant, but depends on the environmental conditions to which the cells are exposed. Bacterial membranes present a large diversity of amphiphilic lipids, including the common phospholipids phosphatidylglycerol, phosphatidylethanolamine and cardiolipin, the less frequent phospholipids phosphatidylcholine, and phosphatidylinositol and a variety of other membrane lipids, such as for example ornithine lipids, glycolipids, sphingolipids or hopanoids among others. In this review, we give an overview about the membrane lipid structures known in bacteria, the different metabolic pathways involved in their formation, and the distribution of membrane lipids and metabolic pathways across taxonomical groups.
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Cites
Molecular Basis of Bacterial Outer Membrane Permeability Revisited
Nikaido, H. (2003) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.67.4.593-656.2003 · Cited by 4,316
Functional convergence of hopanoids and sterols in membrane ordering
Sáenz, J. P., Sezgin, E., Schwille, P., & Simons, K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1212141109 · Cited by 181 · cited 3×
“Due to their structural similarities, HOPs have been consideredmolecular surrogates of eukaryotic sterols (Saenz et al. 2012a).”
BackgroundWELANDER, P. V., DOUGHTY, D. M., WU, C. ‐., MEHAY, S., SUMMONS, R. E., & NEWMAN, D. K. (2012) · Geobiology · doi:10.1111/j.1472-4669.2011.00314.x · Cited by 101
Cited by
Akkermansia muciniphila phospholipid induces homeostatic immune responses
Bae, M., Cassilly, C. D., Liu, X., Park, S.-M., Tusi, B. K., Chen, X., Kwon, J., Filipčík, P., Bolze, A. S., Liu, Z., et al. (2022) · Nature · doi:10.1038/s41586-022-04985-7 · Cited by 413
Recent progress in fluorescent probes for bacteria
Huang, Y., Chen, W., Chung, J., Yin, J., & Yoon, J. (2021) · Chemical Society Reviews · doi:10.1039/d0cs01340d · Cited by 299
Direct protein-lipid interactions shape the conformational landscape of secondary transporters
Martens, C., Shekhar, M., Borysik, A. J., Lau, A. M., Reading, E., Tajkhorshid, E., Booth, P. J., & Politis, A. (2018) · Nature Communications · doi:10.1038/s41467-018-06704-1 · Cited by 134
Biotin, a universal and essential cofactor: synthesis, ligation and regulation
Sirithanakorn, C., & Cronan, J. E. (2021) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuab003 · Cited by 106
Zhang, Q., Linke, V., Overmyer, K. A., Traeger, L. L., Kasahara, K., Miller, I. J., Manson, D. E., Polaske, T. J., Kerby, R. L., Kemis, J. H., et al. (2023) · Nature Microbiology · doi:10.1038/s41564-023-01326-w · Cited by 43
Metadata
- Authors
- Sohlenkamp, C., & Geiger, O.
- Venue
- FEMS Microbiology Reviews
- Publisher
- Oxford University Press (OUP)
- Published
- 2015-04-09
- Volume
- 40
- Issue
- 1
- Pages
- 133-159
- ISSN
- 0168-6445 (ISSN-L)
- 1574-6976
- OpenAlex
- W2117349454
- Cited by
- 1,185
- References
- 3
- FWCI
- 20.39
- Type
- journal article
- Language
- en
- Open access
- bronze
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