Eukaryotes often form symbioses with microorganisms. Among these, associations between plants and nitrogen-fixing bacteria are responsible for the nitrogen input into various ecological niches. Plants of many different families have evolved the capacity to develop root or stem nodules with diverse genera of soil bacteria. Of these, symbioses between legumes and rhizobia (Azorhizobium, Bradyrhizobium, Mesorhizobium, and Rhizobium) are the most important from an agricultural perspective. Nitrogen-fixing nodules arise when symbiotic rhizobia penetrate their hosts in a strictly controlled and coordinated manner. Molecular codes are exchanged between the symbionts in the rhizosphere to select compatible rhizobia from pathogens. Entry into the plant is restricted to bacteria that have the “keys” to a succession of legume “doors”. Some symbionts intimately associate with many different partners (and are thus promiscuous), while others are more selective and have a narrow host range. For historical reasons, narrow host range has been more intensively investigated than promiscuity. In our view, this has given a false impression of specificity in legume-Rhizobium associations. Rather, we suggest that restricted host ranges are limited to specific niches and represent specialization of widespread and more ancestral promiscuous symbioses. Here we analyze the molecular mechanisms governing symbiotic promiscuity in rhizobia and show that it is controlled by a number of molecular keys.

Molecular Basis of Symbiotic Promiscuity

Plant growth promoting bacteria (PGPR) associations range in degree of bacterial proximity to the root and intimacy of association. In general, these can be separated into extracellular PGPR (ePGPR), existing in the rhizosphere, on the rhizoplane or in the spaces between cells of the root cortex, and intracellular PGPR (iPGPR), which exist inside root cells, generally in specialized nodular structures. The latter includes rhizobia and Frankia species, both of which fix nitrogen in symbiosis with higher plants. There has been considerable development in understanding signaling mechanisms of rhizobia (iPGPR) during the establishment of the rhizobia–legume symbiosis, and this may serve as a model of knowledge regarding cross-talk and plant growth promoting mechanisms. We provide a detailed review of this process, including plant-to-bacteria signal molecules, followed by bacterial perception and consequent production of bacteria-to-plant signals. A history of PGPR discovery is also provided, indicating progress in understanding each of the PGPR groups. Recent advances in understanding plant growth responses to microbial signals are reviewed, along with the research areas that require attention. Based on new understandings of signaling mechanisms in the iPGPR (rhizobia) and recent findings with ePGPR we are able to speculate regarding general patterns of signaling in the ePGPR.

Intracellular and extracellular PGPR: commonalities and distinctions in the plant–bacterium signaling processes

Anomeric-oxygen activation for glycoside synthesis: the trichloroacetimidate method.

Metabolites from symbiotic bacteria

Although glycosaminoglycans contribute to diverse physiological processes, an understanding of their molecular mechanisms has been hampered by the inability to access homogeneous glycosaminoglycan structures. Here, we assembled well-defined chondroitin sulfate oligosaccharides using a convergent, synthetic approach that permits installation of sulfate groups at precise positions along the carbohydrate backbone. Using these defined structures, we demonstrate that specific sulfation motifs function as molecular recognition elements for growth factors and modulate neuronal growth. These results provide both fundamental insights into the role of sulfation and direct evidence for a 'sulfation code' whereby glycosaminoglycans encode functional information in a sequence-specific manner analogous to that of DNA, RNA and proteins.

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Sulfation patterns of glycosaminoglycans encode molecular recognition and activity

The use of 2-deoxy-2-trichloroacetamido-d-glucopyranose derivatives in syntheses of oligosaccharides

Phosphorylation and Sulfation of Oligosaccharide Substrates Critically Influence the Activity of Human β1,4-Galactosyltransferase 7 (GalT-I) and β1,3-Glucuronosyltransferase I (GlcAT-I) Involved in the Biosynthesis of the Glycosaminoglycan-Protein Linkage Region of Proteoglycans

Syntheses of the methyl glycosides of the repeating units of chondroitin 4- and 6-sulfate

The use of 2-deoxy-2-trichloroacetamido-d-glucopyranose derivatives in syntheses of hyaluronic acid-related tetra-, hexa-, and octa-saccharides having a methyl β-d-glucopyranosiduronic acid at the reducing end

Jean-Claude Jacquinet

Papers

The use of 2-deoxy-2-trichloroacetamido-d-glucopyranose derivatives in syntheses of oligosaccharides

Phosphorylation and Sulfation of Oligosaccharide Substrates Critically Influence the Activity of Human β1,4-Galactosyltransferase 7 (GalT-I) and β1,3-Glucuronosyltransferase I (GlcAT-I) Involved in the Biosynthesis of the Glycosaminoglycan-Protein Linkage Region of Proteoglycans

Syntheses of the methyl glycosides of the repeating units of chondroitin 4- and 6-sulfate

The use of 2-deoxy-2-trichloroacetamido-d-glucopyranose derivatives in syntheses of hyaluronic acid-related tetra-, hexa-, and octa-saccharides having a methyl β-d-glucopyranosiduronic acid at the reducing end

Synthesis of glycopeptides from the carbohydrate-protein linkage region of proteoglycans.