Literature DB >> 3384802

Lectin-enhanced accumulation of manganese-limited Rhizobium leguminosarum cells on pea root hair tips.

J W Kijne1, G Smit, C L Díaz, B J Lugtenberg.   

Abstract

The ability of Rhizobium leguminosarum 248 to attach to developing Pisum sativum root hairs was investigated during various phases of bacterial growth in yeast extract-mannitol medium. Direct cell counting revealed that growth of the rhizobia transiently stopped three successive times during batch culture in yeast extract-mannitol medium. These interruptions of growth, as well as the simultaneous autoagglutination of the bacteria, appeared to be caused by manganese limitation. Rhizobia harvested during the transient phases of growth inhibition appeared to have a better attachment ability than did exponentially growing rhizobia. The attachment characteristics of these manganese-limited rhizobia were compared with those of carbon-limited rhizobia (G. Smit, J. W. Kijne, and B. J. J. Lugtenberg, J. Bacteriol. 168:821-827, 1986, and J. Bacteriol. 169:4294-4301, 1987). In contrast to the attachment of carbon-limited cells, accumulation of manganese-limited rhizobia (cap formation) was already in full progress after 10 min of incubation; significantly delayed by 3-O-methyl-D-glucose, a pea lectin haptenic monosaccharide; partially resistant to sodium chloride; and partially resistant to pretreatment of the bacteria with cellulase. Binding of single bacteria to the root hair tips was not inhibited by 3-O-methyl-D-glucose. Whereas attachment of single R. leguminosarum cells to the surface of pea root hair tips seemed to be similar for both carbon- and manganese-limited cells, the subsequent accumulation of manganese-limited rhizobia at the root hair tips is apparently accelerated by pea lectin molecules. Moreover, spot inoculation tests with rhizobia grown under various culture conditions indicated that differences in attachment between manganese- and carbon-limited R. leguminosarum cells are correlated with a significant difference in infectivity in that manganese-limited rhizobia, in contrast to carbon-limited rhizobia, are infective. This growth-medium-dependent behavior offers and explanation for the seemingly conflicting data on the involvement of host plant lectins in attachment of rhizobia to root hairs of leguminous plants. Sym plasmid-borne genes do not play a role in manganese-limitation-induced attachment of R. leguminosarum.

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Year:  1988        PMID: 3384802      PMCID: PMC211240          DOI: 10.1128/jb.170.7.2994-3000.1988

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  21 in total

1.  Host-symbiont interactions. I. The lectins of legumes interact with the o-antigen-containing lipopolysaccharides of their symbiont Rhizobia.

Authors:  J S Wolpert; P Albersheim
Journal:  Biochem Biophys Res Commun       Date:  1976-06-07       Impact factor: 3.575

2.  A plant flavone, luteolin, induces expression of Rhizobium meliloti nodulation genes.

Authors:  N K Peters; J W Frost; S R Long
Journal:  Science       Date:  1986-08-29       Impact factor: 47.728

Review 3.  Signal exchange in plant-microbe interactions.

Authors:  L J Halverson; G Stacey
Journal:  Microbiol Rev       Date:  1986-06

4.  Binding of pea lectins to a glycan type polysaccharide in the cell walls of Rhizobium leguminosarum.

Authors:  K Planqué; J W Kijne
Journal:  FEBS Lett       Date:  1977-01-15       Impact factor: 4.124

5.  Involvement of both cellulose fibrils and a Ca2+-dependent adhesin in the attachment of Rhizobium leguminosarum to pea root hair tips.

Authors:  G Smit; J W Kijne; B J Lugtenberg
Journal:  J Bacteriol       Date:  1987-09       Impact factor: 3.490

6.  Induction of the nodA promoter of Rhizobium leguminosarum Sym plasmid pRL1JI by plant flavanones and flavones.

Authors:  S A Zaat; C A Wijffelman; H P Spaink; A A van Brussel; R J Okker; B J Lugtenberg
Journal:  J Bacteriol       Date:  1987-01       Impact factor: 3.490

7.  Adsorption of bacteria to roots as related to host specificity in the Rhizobium-clover symbiosis.

Authors:  F B Dazzo; C A Napoli; D H Hubbell
Journal:  Appl Environ Microbiol       Date:  1976-07       Impact factor: 4.792

8.  Correlation between extracellular fibrils and attachment of Rhizobium leguminosarum to pea root hair tips.

Authors:  G Smit; J W Kijne; B J Lugtenberg
Journal:  J Bacteriol       Date:  1986-11       Impact factor: 3.490

9.  Application of two new methods for cleavage of polysaccharides into specific oligosaccharide fragments. Structure of the capsular and extracellular polysaccharides of Rhizobium japonicum that bind soybean lectin.

Authors:  A J Mort; W D Bauer
Journal:  J Biol Chem       Date:  1982-02-25       Impact factor: 5.157

10.  Stimulation of clover root hair infection by lectin-binding oligosaccharides from the capsular and extracellular polysaccharides of Rhizobium trifolii.

Authors:  M Abe; J E Sherwood; R I Hollingsworth; F B Dazzo
Journal:  J Bacteriol       Date:  1984-11       Impact factor: 3.490

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  19 in total

1.  Exocytosis and endocytosis

Authors: 
Journal:  Plant Cell       Date:  1999-04       Impact factor: 11.277

Review 2.  Cellulose biosynthesis and function in bacteria.

Authors:  P Ross; R Mayer; M Benziman
Journal:  Microbiol Rev       Date:  1991-03

3.  Distribution of glucose/mannose-specific isolectins in pea (Pisum sativum L.) seedlings.

Authors:  C L Díaz; M Hosselet; G J Logman; E van Driessche; B J Lugtenberg; J W Kijne
Journal:  Planta       Date:  1990-07       Impact factor: 4.116

4.  Genetic Structure of Rhizobium etli biovar phaseoli Associated with Wild and Cultivated Bean Plants (Phaseolus vulgaris and Phaseolus coccineus) in Morelos, Mexico.

Authors:  V Souza; L Eguiarte; G Avila; R Cappello; C Gallardo; J Montoya; D Piñero
Journal:  Appl Environ Microbiol       Date:  1994-04       Impact factor: 4.792

5.  Surface Properties and Motility of Rhizobium and Azospirillum in Relation to Plant Root Attachment

Authors: 
Journal:  Microb Ecol       Date:  1996-07       Impact factor: 4.552

6.  Insertion of pea lectin into a phospholipid monolayer.

Authors:  P Booij; R A Demel; B S de Pater; J W Kijne
Journal:  Plant Mol Biol       Date:  1996-04       Impact factor: 4.076

7.  Adaptation to nutrient starvation in Rhizobium leguminosarum bv. phaseoli: analysis of survival, stress resistance, and changes in macromolecular synthesis during entry to and exit from stationary phase.

Authors:  S H Thorne; H D Williams
Journal:  J Bacteriol       Date:  1997-11       Impact factor: 3.490

8.  Five Nodulation Mutants of White Sweetclover (Melilotus alba Desr.) Exhibit Distinct Phenotypes Blocked at Root Hair Curling, Infection Thread Development, and Nodule Organogenesis.

Authors:  L. J. Utrup; A. J. Cary; J. H. Norris
Journal:  Plant Physiol       Date:  1993-11       Impact factor: 8.340

9.  A Peanut Nodule Lectin in Infected Cells and in Vacuoles and the Extracellular Matrix of Nodule Parenchyma.

Authors:  K. A. VandenBosch; L. R. Rodgers; D. J. Sherrier; B. D. Kishinevsky
Journal:  Plant Physiol       Date:  1994-02       Impact factor: 8.340

10.  Early Interactions of Rhizobium leguminosarum bv. phaseoli and Bean Roots: Specificity in the Process of Adsorption and Its Requirement of Ca(sup2+) and Mg(sup2+) Ions.

Authors:  A R Lodeiro; A Lagares; E N Martinez; G Favelukes
Journal:  Appl Environ Microbiol       Date:  1995-04       Impact factor: 4.792

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