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Opposite Effects of Lysophosphatidylethanolamines on Conformation of OmpF-like Porin from Yersinia pseudotuberculosis
Ludmila A Davydova, Nina M Sanina1, Olga D Novikova
1Department of Biochemistry, Microbiology and Biotechnology, School of Natural Sciences, Far Eastern Federal University, 690950, Vladivostok, Russia. sanina.nm@dvfu.ru.
Abstract:
Lysophosphatidyletnolamine (LPE) is one of enigmatic lipids of bacteria. It is generated from major membrane lipid - phosphatidylethanolamine at severe changes of the bacterial growth conditions. Accumulation of this phospholipid in cells of Gram-negative enterobacterium Yersinia pseudotuberculosis results in the enhanced thermostability of OmpF-like porin (YOmpF) from the same bacteria. The respective integral conformational rearrangements may disturb the channel permeability of protein under stress conditions. However, role of fatty acid composition of LPE in this effect remained unclear. Present work demonstrated that the level of unsaturated LPE is 3.5 times higher than saturated one in total LPE of bacterial cells exposed to stress (phenol treatment). Unsaturated 1-oleoyl-2-hydroxy-sn-glycero-3-phosphoethanolamine (MOPE) and saturated LPE 1-palmitoyl-2- hydroxy-sn-glycero-3-phosphoethanolamine (MPPE) oppositely affect the conformation of YOmpF. MOPE increases the protein thermal stability due to more dense packing of monomers in porin and preserves its trimeric form at elevated temperature, while MPPE weakens the contact between monomers and promotes dissociation of the protein.
Insights
Bacterial stress induces lysophosphatidylethanolamine (LPE), a lipid that alters OmpF-like porin (YOmpF) stability. Unsaturated LPE enhances YOmpF thermostability, while saturated LPE destabilizes it.
Area of Science:
- Microbiology
- Biochemistry
- Structural Biology
Background:
- Lysophosphatidylethanolamine (LPE) is a bacterial lipid formed under stress conditions.
- LPE accumulation enhances the thermostability of Yersinia pseudotuberculosis OmpF-like porin (YOmpF).
- The influence of LPE's fatty acid composition on YOmpF conformation was previously unclear.
Purpose of the Study:
- To investigate the role of LPE fatty acid composition in YOmpF conformational changes.
- To determine how saturated and unsaturated LPE affect YOmpF stability and function.
Main Methods:
- Analysis of LPE composition in Yersinia pseudotuberculosis under phenol stress.
- Comparative studies using unsaturated MOPE and saturated MPPE on YOmpF conformation.
- Assessment of YOmpF thermal stability and oligomeric state.
Main Results:
- Under stress, unsaturated LPE levels were 3.5 times higher than saturated LPE.
- Unsaturated MOPE increased YOmpF thermal stability by promoting dense monomer packing and preserving trimeric form.
- Saturated MPPE weakened inter-monomer contacts, leading to YOmpF dissociation at elevated temperatures.
Conclusions:
- LPE's fatty acid composition critically influences YOmpF conformation and stability.
- Unsaturated LPE stabilizes YOmpF, potentially affecting channel permeability under stress.
- Saturated LPE destabilizes YOmpF, suggesting differential roles in bacterial stress response.
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