Azorhizobium caulinodans ORS571 synthesizes mainly pentameric Nod factors with a household fatty acid, an N-methyl, and a 6-O-carbamoyl group at the nonreducing-terminal residue and with a D-arabinosyl, an L-fucosyl group, or both at the reducing-terminal residue. Nodulation on Sesbania rostrata was carried out with a set of bacterial mutants that produce well characterized Nod factor populations. Purified Nod factors were tested for their capacity to induce root hair formation and for their stability in an in vitro degradation assay with extracts of uninfected adventitious rootlets. The glycosylations increased synergistically the nodulation efficiency and the capacity to induce root hairs, and they protected the Nod factor against degradation. The D-arabinosyl group was more important than the L-fucosyl group for nodulation efficiency. Replacement of the 6-O-L-fucosyl group by a 6-O-sulfate ester did not affect Nod factor stability, but reduced nodulation efficiency, indicating that the L-fucosyl group may play a role in recognition. The 6-O-carbamoyl group contributes to nodulation efficiency, biological activity, and protection, but could be replaced by a 6-O-acetyl group for root nodulation. The results demonstrate that none of the studied substitutions is strictly required for triggering normal nodule formation. However, the nodulation efficiency was greatly determined by the synergistic presence of substitutions. Within the range tested, fluctuations of Nod factor amounts had little impact on the symbiotic phenotype.
nodulation, Azorhizobium caulinodans, nod factors, Sesbania rostrata
NCBI PubMed ID: 10821846Publication DOI: 10.1074/jbc.275.21.15676Journal NLM ID: 2985121RPublisher: Baltimore, MD: American Society for Biochemistry and Molecular Biology
Correspondence: Holsters M
Institutions: Vakgroep Moleculaire Genetica en Departement Plantengenetica, Vlaams Interuniversitair Instituut voor Biotechnologie, Universiteit Gent, Gent, Belgium, Laboratoire de Spectromґetrie de Masse et Signaux Biologiques, Interactions Moléculaires et Réactivité Chimique et Photochimique-Unité Mixte de Recherche 5623 CNRS, Université Paul Sabatier, Toulouse, France
Methods: DNA techniques, biological assays, radiolabeling, radioactivity measurement, LSI-MS, extraction, cell growth, gene expression, RP-TLC
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