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Converting Escherichia coli into an archaebacterium with a hybrid heterochiral membrane
- Source :
- Proceedings of the National Academy of Sciences of the United States of America, 115(14), 3704-3709, Proceedings of the National Academy of Sciences of the United States of America 115 (2018) 14
- Publication Year :
- 2018
- Publisher :
- Proceedings of the National Academy of Sciences, 2018.
-
Abstract
- One of the main differences between bacteria and archaea concerns their membrane composition. Whereas bacterial membranes are made up of glycerol-3-phosphate ester lipids, archaeal membranes are composed of glycerol-1-phosphate ether lipids. Here, we report the construction of a stable hybrid heterochiral membrane through lipid engineering of the bacterium Escherichia coli. By boosting isoprenoid biosynthesis and heterologous expression of archaeal ether lipid biosynthesis genes, we obtained a viable E. coli strain of which the membranes contain archaeal lipids with the expected stereochemistry. It has been found that the archaeal lipid biosynthesis enzymes are relatively promiscuous with respect to their glycerol phosphate backbone and that E. coli has the unexpected potential to generate glycerol-1-phosphate. The unprecedented level of 20–30% archaeal lipids in a bacterial cell has allowed for analyzing the effect on the mixed-membrane cell’s phenotype. Interestingly, growth rates are unchanged, whereas the robustness of cells with a hybrid heterochiral membrane appeared slightly increased. The implications of these findings for evolutionary scenarios are discussed.
- Subjects :
- 0301 basic medicine
Lipid biosynthesis
030106 microbiology
medicine.disease_cause
Microbiology
Bacterial cell structure
03 medical and health sciences
Microbiologie
medicine
Escherichia coli
VLAG
chemistry.chemical_classification
Multidisciplinary
Bacteria
biology
Chemistry
Hybrid membranes
biology.organism_classification
Archaea
030104 developmental biology
Enzyme
Membrane
Biochemistry
Ether lipids
lipids (amino acids, peptides, and proteins)
Heterologous expression
Subjects
Details
- ISSN :
- 10916490 and 00278424
- Volume :
- 115
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences
- Accession number :
- edsair.doi.dedup.....4ad1b0052aa28f881fb7138fcdf4e42e
- Full Text :
- https://doi.org/10.1073/pnas.1721604115