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. 1984 Sep 1;222(2):427–435. doi: 10.1042/bj2220427

Differential patterns of arabinosylation by membranes of suspension-cultured cells of Phaseolus vulgaris (French bean) after subculture or elicitation.

G P Bolwell
PMCID: PMC1144196  PMID: 6477524

Abstract

Suspension-cultured cells of Phaseolus vulgaris (French bean) incorporated [1-3H] arabinose in vivo into high-Mr polymers that could be separated into glycoprotein and polysaccharide. Microsomal membranes from suspension-cultured cells of beans incorporated arabinose from UDP-beta-L-arabinose in vitro into both polysaccharide and glycoprotein. The enzyme involved in arabinan synthesis, arabinan synthase, appeared to be immunologically distinct from the protein:arabinosyltransferase system. Both these activities are inducible, but behave differently with either plant-growth-regulator or fungal-elicitor treatments. After subculture of cells entering the stationary growth phase the arabinan synthase activity reaches much higher values than does that of the protein transferase system during the initial period of cell division and growth, whereas after elicitation at the same growth stage, all the increased incorporation of arabinose occurs into glycoprotein of Mr higher than 200 000 and to a greater extent into a specific glycoprotein of Mr 42 500. Preliminary characterization of these glycoproteins prepared under non-reducing conditions and after acid and alkaline hydrolysis suggests that the high-Mr glycoprotein material is similar to arabinogalactan protein, whereas the lower-Mr material may be a hydroxyproline-rich protein existing as a dimer and that specifically increases during the hypersensitive response of the cells to the fungal elicitor from Colletotrichum lindemuthianum.

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Selected References

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  1. Allen A. K., Desai N. N., Neuberger A., Creeth J. M. Properties of potato lectin and the nature of its glycoprotein linkages. Biochem J. 1978 Jun 1;171(3):665–674. doi: 10.1042/bj1710665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Anderson-Prouty A. J., Albersheim P. Host-Pathogen Interactions: VIII. Isolation of a Pathogen-synthesized Fraction Rich in Glucan That Elicits a Defense Response in the Pathogen's Host. Plant Physiol. 1975 Aug;56(2):286–291. doi: 10.1104/pp.56.2.286. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ashford D., Desai N. N., Allen A. K., Neuberger A., O'Neill M. A., Selvendran R. R. Structural studies of the carbohydrate moieties of lectins from potato (Solanum tuberosum) tubers and thorn-apple (Datura stramonium) seeds. Biochem J. 1982 Jan 1;201(1):199–208. doi: 10.1042/bj2010199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bolwell G. P., Northcote D. H. Arabinan synthase and xylan synthase activities of Phaseolus vulgaris. Subcellular localization and possible mechanism of action. Biochem J. 1983 Feb 15;210(2):497–507. doi: 10.1042/bj2100497. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bolwell G. P., Northcote D. H. Induction by growth factors of polysaccharide synthases in bean cell suspension cultures. Biochem J. 1983 Feb 15;210(2):509–515. doi: 10.1042/bj2100509. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chrispeels M. J. Synthesis and secretion of hydroxyproline containing macromolecules in carrots. I. Kinetic analysis. Plant Physiol. 1969 Aug;44(8):1187–1193. doi: 10.1104/pp.44.8.1187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cooper J. B., Varner J. E. Insolubilization of hydroxyproline-rich cell wall glycoprotein in aerated carrot root slices. Biochem Biophys Res Commun. 1983 Apr 15;112(1):161–167. doi: 10.1016/0006-291x(83)91811-9. [DOI] [PubMed] [Google Scholar]
  8. Dalessandro G., Northcote D. H. Changes in enzymic activities of nucleoside diphosphate sugar interconversions during differentiation of cambium to xylem in pine and fir. Biochem J. 1977 Feb 15;162(2):281–288. doi: 10.1042/bj1620281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dalessandro G., Northcote D. H. Changes in enzymic activities of nucleoside diphosphate sugar interconversions during differentiation of cambium to xylem in sycamore and poplar. Biochem J. 1977 Feb 15;162(2):267–279. doi: 10.1042/bj1620267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dixon R. A., Lamb C. J. Stimulation of de novo synthesis of L-phenylalanine ammonia-lyase in relation to phytoalexin accumulation in Colletotrichum lindemuthianum elicitor-treated cell suspension cultures of french bean (Phaseolus vulgaris). Biochim Biophys Acta. 1979 Sep 3;586(3):453–463. doi: 10.1016/0304-4165(79)90035-7. [DOI] [PubMed] [Google Scholar]
  11. Ecklund P. R., Moore T. C. Correlations of Growth Rate and De-etiolation with Rate of Ent-Kaurene Biosynthesis in Pea (Pisum sativum L.). Plant Physiol. 1974 Jan;53(1):5–10. doi: 10.1104/pp.53.1.5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Esquerré-Tugayé M. T. Cell Surfaces in Plant-Microorganism Interactions: I. A Structural Investigation of Cell Wall Hydroxyproline-rich Glycoproteins Which Accumulate in Fungus-infected Plants. Plant Physiol. 1979 Aug;64(2):314–319. doi: 10.1104/pp.64.2.314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Esquerré-Tugayé M. T., Lafitte C., Mazau D., Toppan A., Touzé A. Cell Surfaces in Plant-Microorganism Interactions: II. Evidence for the Accumulation of Hydroxyproline-rich Glycoproteins in the Cell Wall of Diseased Plants as a Defense Mechanism. Plant Physiol. 1979 Aug;64(2):320–326. doi: 10.1104/pp.64.2.320. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Fry S. C. Isodityrosine, a new cross-linking amino acid from plant cell-wall glycoprotein. Biochem J. 1982 May 15;204(2):449–455. doi: 10.1042/bj2040449. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Gamborg O. L., Miller R. A., Ojima K. Nutrient requirements of suspension cultures of soybean root cells. Exp Cell Res. 1968 Apr;50(1):151–158. doi: 10.1016/0014-4827(68)90403-5. [DOI] [PubMed] [Google Scholar]
  16. Gardiner M., Chrispeels M. J. Involvement of the Golgi Apparatus in the Synthesis and Secretion of Hydroxyproline-rich Cell Wall Glycoproteins. Plant Physiol. 1975 Mar;55(3):536–541. doi: 10.1104/pp.55.3.536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Green J. R., Northcote D. H. The structure and function of glycoproteins synthesized during slime-polysaccharide production by membranes of the root-cap cells of maize (Zea mays). Biochem J. 1978 Mar 15;170(3):599–608. doi: 10.1042/bj1700599. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Harris P. J., Northcote D. H. Patterns of polysaccharide biosynthesis in differentiating cells of maize root-tips. Biochem J. 1970 Dec;120(3):479–491. doi: 10.1042/bj1200479. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Hayashi T., Maclachlan G. Biosynthesis of pentosyl lipids by pea membranes. Biochem J. 1984 Feb 1;217(3):791–803. doi: 10.1042/bj2170791. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Heath M. F., Northcote D. H. Glycoprotein of the wall of sycamore tissue-culture cells. Biochem J. 1971 Dec;125(4):953–961. doi: 10.1042/bj1250953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. KIVIRIKKO K. E. HYDROXYPROLINE-CONTAINING FRACTIONS IN NORMAL AND CORTISONE-TREATED CHICK EMBRYOS. Acta Physiol Scand Suppl. 1963:SUPPL 219–22092. [PubMed] [Google Scholar]
  22. KOLOR M. G., ROBERTS H. R. A new reagent for the detection of hydroxyproline on paper chromatograms. Arch Biochem Biophys. 1957 Aug;70(2):620–622. doi: 10.1016/0003-9861(57)90151-0. [DOI] [PubMed] [Google Scholar]
  23. Karr A. L. Isolation of an enzyme system which will catalyze the glycosylation of extensin. Plant Physiol. 1972 Aug;50(2):275–282. doi: 10.1104/pp.50.2.275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Keegstra K., Talmadge K. W., Bauer W. D., Albersheim P. The Structure of Plant Cell Walls: III. A Model of the Walls of Suspension-cultured Sycamore Cells Based on the Interconnections of the Macromolecular Components. Plant Physiol. 1973 Jan;51(1):188–197. doi: 10.1104/pp.51.1.188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  26. Laskey R. A., Mills A. D. Quantitative film detection of 3H and 14C in polyacrylamide gels by fluorography. Eur J Biochem. 1975 Aug 15;56(2):335–341. doi: 10.1111/j.1432-1033.1975.tb02238.x. [DOI] [PubMed] [Google Scholar]
  27. Lawton M. A., Dixon R. A., Hahlbrock K., Lamb C. J. Elicitor induction of mRNA activity. Rapid effects of elicitor on phenylalanine ammonia-lyase and chalcone synthase mRNA activities in bean cells. Eur J Biochem. 1983 Jan 17;130(1):131–139. [PubMed] [Google Scholar]
  28. Lawton M. A., Dixon R. A., Hahlbrock K., Lamb C. Rapid induction of the synthesis of phenylalanine ammonia-lyase and of chalcone synthase in elicitor-treated plant cells. Eur J Biochem. 1983 Jan 1;129(3):593–601. doi: 10.1111/j.1432-1033.1983.tb07090.x. [DOI] [PubMed] [Google Scholar]
  29. Leach J. E., Cantrell M. A., Sequeira L. Hydroxyproline-rich bacterial agglutinin from potato : extraction, purification, and characterization. Plant Physiol. 1982 Nov;70(5):1353–1358. doi: 10.1104/pp.70.5.1353. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Matsumoto I., Jimbo A., Mizuno Y., Seno N., Jeanloz R. W. Purification and characterization of potato lectin. J Biol Chem. 1983 Mar 10;258(5):2886–2891. [PubMed] [Google Scholar]
  31. Owens R. J., Northcote D. H. The location of arabinosyl:hydroxyproline transferase in the membrane system of potato tissue culture cells. Biochem J. 1981 Jun 1;195(3):661–667. doi: 10.1042/bj1950661. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Pope D. G. Relationships between Hydroxyproline-containing Proteins Secreted into the Cell Wall and Medium by Suspension-cultured Acer pseudoplatanus Cells. Plant Physiol. 1977 May;59(5):894–900. doi: 10.1104/pp.59.5.894. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Read S. M., Northcote D. H. Minimization of variation in the response to different proteins of the Coomassie blue G dye-binding assay for protein. Anal Biochem. 1981 Sep 1;116(1):53–64. doi: 10.1016/0003-2697(81)90321-3. [DOI] [PubMed] [Google Scholar]
  34. Stuart D. A., Varner J. E. Purification and Characterization of a Salt-extractable Hydroxyproline-rich Glycoprotein from Aerated Carrot Discs. Plant Physiol. 1980 Nov;66(5):787–792. doi: 10.1104/pp.66.5.787. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. van Holst G. J., Klis F. M., de Wildt P. J., Hazenberg C. A., Buijs J., Stegwee D. Arabinogalactan Protein from a Crude Cell Organelle Fraction of Phaseolus vulgaris L. Plant Physiol. 1981 Oct;68(4):910–913. doi: 10.1104/pp.68.4.910. [DOI] [PMC free article] [PubMed] [Google Scholar]

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