Expanding Knowledge of Methylotrophic Capacity: Structure and Properties of the Rough-Type Lipopolysaccharide from Methylobacterium extorquens and Its Role on Membrane Resistance to Methanol.
Flaviana Di LorenzoSimone NicolardiRoberta MarchettiAdele VanacoreNoemi GallucciKatarzyna DudaFerran Nieto FabregatHa Ngoc Anh NguyenDjamel GullyJames SaenzEric GiraudLuigi PaduanoAntonio MolinaroGerardino D'ErricoAlba SilipoPublished in: JACS Au (2023)
The ability of Methylobacterium extorquens to grow on methanol as the sole carbon and energy source has been the object of intense research activity. Unquestionably, the bacterial cell envelope serves as a defensive barrier against such an environmental stressor, with a decisive role played by the membrane lipidome, which is crucial for stress resistance. However, the chemistry and the function of the main constituent of the M. extorquens outer membrane, the lipopolysaccharide (LPS), is still undefined. Here, we show that M. extorquens produces a rough-type LPS with an uncommon, non-phosphorylated, and extensively O -methylated core oligosaccharide, densely substituted with negatively charged residues in the inner region, including novel monosaccharide derivatives such as O -methylated Kdo/Ko units. Lipid A is composed of a non-phosphorylated trisaccharide backbone with a distinctive, low acylation pattern; indeed, the sugar skeleton was decorated with three acyl moieties and a secondary very long chain fatty acid, in turn substituted by a 3- O -acetyl-butyrate residue. Spectroscopic, conformational, and biophysical analyses on M. extorquens LPS highlighted how structural and tridimensional features impact the molecular organization of the outer membrane. Furthermore, these chemical features also impacted and improved membrane resistance in the presence of methanol, thus regulating membrane ordering and dynamics.
Keyphrases
- inflammatory response
- fatty acid
- molecular docking
- anti inflammatory
- toll like receptor
- healthcare
- carbon dioxide
- lps induced
- single cell
- molecular dynamics
- multidrug resistant
- single molecule
- stem cells
- molecular dynamics simulations
- quantum dots
- cell therapy
- risk assessment
- sensitive detection
- amino acid
- reduced graphene oxide
- human health