6533b7d8fe1ef96bd126ae3a

RESEARCH PRODUCT

Structural determination of the lipo-chitin oligosaccharide nodulation signals produced by Rhizobium giardinii bv. giardinii H152

Antonio M. Gil-serranoCarolina SousaJane Thomas-oatesManuel MegíasMiguel A. Rodríguez-carvajalM. Eugenia Soria-díazNoëlle AmargerPilar Tejero-mateoJosé L. EsparteroBelén Morón

subject

Lipopolysaccharides[CHIM.POLY] Chemical Sciences/PolymersMagnetic Resonance SpectroscopySTRUCTUREStereochemistrySubstituentRoot hairBiochemistryMass SpectrometryAnalytical ChemistryResidue (chemistry)chemistry.chemical_compoundSulfationGlucosamineCarbohydrate ConformationChromatographyMolecular StructurebiologyFatty AcidsMonosaccharidesOrganic ChemistryGeneral MedicineMethylationbiology.organism_classification[CHIM.POLY]Chemical Sciences/PolymersCarbohydrate SequencechemistryAcetylationPhaseolusRhizobium

description

Abstract Rhizobium giardinii bv. giardinii is a microsymbiont of plants of the genus Phaseolus and produces extracellular signal molecules that are able to induce deformation of root hairs and nodule organogenesis. We report here the structures of seven lipochitooligosaccharide (LCO) signal molecules secreted by R. giardinii bv. giardinii H152. Six of them are pentamers of GlcNAc carrying C 16:0 , C 18:0 , C 20:0 and C 18:1 fatty acyl chains on the non-reducing terminal residue. Four are sulfated at C-6 of the reducing terminal residue and one is acetylated in the same position. Six of them are N -methylated on the non-reducing GlcN residue and all the nodulation factors are carbamoylated on C-6 of the non-reducing terminal residue. The structures were determined using monosaccharide composition and methylation analyses, 1D- and 2D-NMR experiments and a range of mass spectrometric techniques. The position of the carbamoyl substituent on the non-reducing glucosamine residue was determined using a CID-MSMS experiment and an HMBC experiment.

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