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PMID: 24196924 Published · ppublish English Journal Article

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

Planta ·Vol. 181 ·No. 4 ·1990-07-00 ·Pages 451-61

Díaz CL, Hosselet M, Logman GJ, van Driessche E, Lugtenberg BJ, Kijne JW

Abstract

We report on the distribution and initial characterization of glucose/mannose-specific isolectins of 4- and 7-d-old pea (Pisum sativum L.) seedlings grown with or without nitrate supply. Particular attention was payed to root lectin, which probably functions as a determinant of host-plant specificity during the infection of pea roots by Rhizobium leguminosarum bv. viciae. A pair of seedling cotyledons yielded 545±49 μg of affinity-purified lectin, approx. 25% more lectin than did dry seeds. Shoots and roots of 4-d-old seedlings contained 100-fold less lectin than cotyledons, whereas only traces of lectin could be found in shoots and roots from 7-d-old seedlings. Polypeptides with a subunit structure similar to the precursor of the pea seed lectin could be demonstrated in cotyledons, shoots and roots. Chromatofocusing and isoelectric focusing showed that seed and non-seed isolectin differ in composition. An isolectin with an isoelectric point at pH 7.2 appeared to be a typical pea seed isolectin, whereas an isolectin focusing at pH 6.1 was the major non-seed lectin. The latter isolectin was also found in root cell-wall extracts, detached root hairs and root-surface washings. All non-seed isolectins were cross-reactive with rabbit antiserum raised against the seed isolectin with an isolectric point at pH 6.1. A protein similar to this acidic glucose/mannose-specific seed isolectin possibly represents the major lectin to be encountered by Rhizobium leguminosarum bv. viciae in the pea rhizosphere and at the root surface. Growth of pea seedlings in a nitrate-rich medium neither affected the distribution of isolectins nor their hemagglutination activity; however, the yield of affinity-purified root lectin was significantly reduced whereas shoot lectin yield slightly increased. Agglutination-inhibition tests demonstrated an overall similar sugar-binding specificity for pea seed and non-seed lectin. However root lectin from seedlings grown with or without nitrate supplement, and shoot lectin from nitrate-supplied seedlings showed a slightly different spectrum of sugar binding. The absorption spectra obtained by circular dichroism of seed and root lectin in the presence of a hapten also differed. These data indicate that nutritional conditions may affect the sugar-binding activity of non-seed isolectin, and that despite their similarities, seed and non-seed isolectins have different properties that may reflect tissue-specialization.

Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Díaz C L
Center for Phytotechnology, Wassenaarseweg 64, NL-2333, AL Leiden, The Netherlands.
Hosselet M
Logman G J
van Driessche E
Lugtenberg B J
Kijne J W
References (33)
33 references, click to expand
  1. Host recognition in the Rhizobium-soybean symbiosis : evidence for the involvement of lectin in nodulation.
    Plant Physiol. 1985 Mar;77(3):621-5 PMID: 16664109
  2. Determination of pea (Pisum sativum L.) root lectin using an enzyme-linked immunoassay.
    Planta. 1984 Jun;161(4):302-7 PMID: 24253718
  3. Lectin-enhanced accumulation of manganese-limited Rhizobium leguminosarum cells on pea root hair tips.
    J Bacteriol. 1988 Jul;170(7):2994-3000 PMID: 3384802
  4. Trifolin: a Rhizobium recognition protein from white clover.
    Biochim Biophys Acta. 1978 Mar 20;539(3):276-86 PMID: 630002
  5. The pea lectin gene family contains only one functional gene.
    Plant Mol Biol. 1987 Sep;9(5):497-507 PMID: 24277136
  6. Examination of Le and lele Genotypes of Glycine max (L.) Merr. for Membrane-Bound and Buffer-Soluble Soybean Lectin.
    Plant Physiol. 1981 Oct;68(4):905-9 PMID: 16662023
  7. The immuno-histochemical localization of lectin in pea seeds (Pisum sativum L.).
    Planta. 1981 Dec;153(4):287-96 PMID: 24276930
  8. A developmentally regulated bud specific transcript in pea has sequence similarity to seed lectins.
    Plant Physiol. 1989 Mar;89(3):833-8 PMID: 16666629
  9. A comparison of silver staining methods for detecting proteins in ultrathin polyacrylamide gels on support film after isoelectric focusing.
    Anal Biochem. 1985 Aug 1;148(2):384-8 PMID: 2415020
  10. Lectins: a possible basis for specificity in the Rhizobium--legume root nodule symbiosis.
    Science. 1974 Jul 19;185(4147):269-71 PMID: 17812054
  11. Cross-reactive antigens and lectin as determinants of symbiotic specificity in the Rhizobium-clover association.
    Appl Microbiol. 1975 Dec;30(6):1017-33 PMID: 55100
  12. Tissue sulfhydryl groups.
    Arch Biochem Biophys. 1959 May;82(1):70-7 PMID: 13650640
  13. Detection and characterization of a lectin from non-seed tissue ofPhaseolus vulgaris.
    Planta. 1984 May;161(3):223-8 PMID: 24253647
  14. Subcellular Localizations of Two Dolichos biflorus Lectins.
    Plant Physiol. 1984 Dec;76(4):871-8 PMID: 16663962
  15. Isolation and chemical characterization of a mitogenic lectin from Pisum sativum.
    J Biol Chem. 1974 Sep 25;249(18):6004-12 PMID: 4414003
  16. Increased sensitivity in peroxidase immunocytochemistry. A comparative study of a number of peroxidase visualization methods employing a model system.
    Histochemistry. 1986;84(3):221-30 PMID: 3519544
  17. Evaluation of isoelectric focusing running conditions during two-dimensional isoelectric focusing/sodium dodecyl sulfate-polyacrylamide gel electrophoresis: variation of gel patterns with changing conditions and optimized isoelectric focusing conditions.
    Anal Biochem. 1984 Apr;138(1):144-55 PMID: 6731839
  18. Studies on phytohemagglutinins. XXIV. Isoelectric point and hybridization of the pea (Pisum sativum L.) isophytohemagglutinins.
    Biochim Biophys Acta. 1975 May 30;393(1):165-9 PMID: 237565
  19. Direct spectrophotometric measurement of the rate of reduction of disulfide bonds. The reactivity of the disulfide bonds of bovine -lactalbumin.
    J Biol Chem. 1973 Jan 25;248(2):707-10 PMID: 4734333
  20. The biosynthesis and primary structure of pea seed lectin.
    J Biol Chem. 1983 Aug 10;258(15):9544-9 PMID: 6688253
  21. Transcriptional and posttranscriptional regulation of seed storage-protein gene expression in pea (Pisum sativum L.).
    Planta. 1989 Oct;179(3):279-87 PMID: 24201656
  22. Lectin-gene expression in pea (Pisum sativum L.) roots.
    Planta. 1988 Mar;173(3):367-72 PMID: 24226543
  23. Isolation and characterization of a lectin from the roots of Dolichos biflorus.
    Arch Biochem Biophys. 1987 Nov 1;258(2):535-44 PMID: 3118811
  24. Effect of lectin on nodulation by wild-type Bradyrhizobium japonicum and a nodulation-defective mutant.
    Appl Environ Microbiol. 1986 Apr;51(4):753-60 PMID: 3707122
  25. Soybean lectin and related proteins in seeds and roots of le and le soybean varieties.
    Plant Physiol. 1986 Jun;81(2):558-65 PMID: 16664856
  26. Ultraviolet absorption spectra of proteins and amino acids.
    Adv Protein Chem. 1952;7:319-86 PMID: 14933256
  27. Protein transfer from isoelectric focusing Gels: the native blot.
    Anal Biochem. 1982 Jul 1;123(2):229-35 PMID: 6181706
  28. The isolation and characterization of a root lectin from soybean (Glycine max (L), cultivar Chippewa).
    J Biol Chem. 1981 Dec 25;256(24):12905-10 PMID: 7198118
  29. Effect of nitrate supply on the in-vivo synthesis and distribution of trifollin A, a Rhizobium trifolii-binding lectin, in Trifolium repens seedlings.
    Planta. 1984 Dec;162(6):540-7 PMID: 24253271
  30. Intracellular sites of synthesis and processing of lectin in developing pea cotyledons.
    J Biol Chem. 1983 Aug 10;258(15):9550-2 PMID: 6874702
  31. Correlation between infection by Rhizobium leguminosarum and lectin on the surface of Pisum sativum L. roots.
    Planta. 1986 Sep;168(3):350-9 PMID: 24232144
  32. Electrophoretic resolution of the "major outer membrane protein" of Escherichia coli K12 into four bands.
    FEBS Lett. 1975 Oct 15;58(1):254-8 PMID: 773686
  33. Properties of Lectins in the Root and Seed of Lotononis bainesii.
    Plant Physiol. 1984 Apr;74(4):773-8 PMID: 16663508
Article Info
Journal
Planta
Abbr.
Planta
ISSN
0032-0935
Published
1990-07-00
Pages
451-61
Language
English
Region
Germany
NLM ID
1250576
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