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Development and regulation of (1→3,1→4)-β-glucan endohydrolases in germinating wheat (Triticum aestivum)

Published online by Cambridge University Press:  19 September 2008

Doreen M. L. Lai
Affiliation:
Department of Biochemistry, La Trobe University, Bundoora, Victoria 3083, Australia
Amanda M. Slade
Affiliation:
Department of Biochemistry, La Trobe University, Bundoora, Victoria 3083, Australia
Geoffrey B. Fincher*
Affiliation:
Department of Biochemistry, La Trobe University, Bundoora, Victoria 3083, Australia
*
* Correspondence

Abstract

The development of (1→3,1→4)-β-glucan 4-glucanohydrolase (EC 3.2.1.73) has been examined in germinating wheat (Triticum aestivum cv. Millewa) grain, and in isolated aleurone layers and scutella. Activity is first detected in extracts of intact grain 2–3 days after the initiation of germination and thereafter increases until 6 days. In isolated aleurone layers, (1→3,1→4)-β-glucanase activity is secreted for up to 4 days. Treatment of aleurone layers with gibberellic acid (GA3) results in a 2-fold enhancement of secreted enzyme for the first 2 days, but activity decreases after 2 days. (1→3,1→4)-β-Glucanase secretion from GA3-treated aleurone layers clearly precedes the secretion of amylase and (1→4)-β-xylanase. Small but significant levels of cellulase are secreted from aleurone layers after GA3 treatment. Isolated scutella also secrete (1→3,1→4)-β-glucanase but GA3 has little apparent effect on secretion patterns from this tissue. Proteins secreted from excised aleurone layers and scutella, together with those in homogenates of intact, germinated grain, have been examined by Western blot analysis, using monoclonal antibodies against barley (1→3,1→4)-β-glucanases as probes. In each case the wheat (1→3,1→4)-β-glucanase is recognised only by the monoclonal antibody that is specific for barley isoenzyme El.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 1993

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Footnotes

1

Present address: School of Chemistry, University of Melbourne, Parkville, Victoria 3052, Australia

References

Bacic, A. and Stone, B.A. (1980) A (1→3)- and (1→4)-linked β-D-glucan in the endosperm cell walls of wheat. Carbohydrate Research 82, 372377.Google Scholar
Baulcombe, D.C. and Buffard, D. (1983) Gibberellic-acidregulated expression of α-amylase and six other genes in wheat aleurone layers. Planta 157, 493501.Google Scholar
Benjavongkulchai, E. and Spencer, M.S. (1986) Purification and characterization of barley-aleurone xylanase. Planta 169, 415419.Google Scholar
Carpita, N., Sabularse, D., Montezinos, D. and Delmer, D.P. (1979) Determination of the pore size of cell walls of living plant cells. Science 205, 1117.CrossRefGoogle ScholarPubMed
Chrispeels, M.J. and Varner, J.E. (1967) Gibberellic acidenhanced synthesis and release of α-amylase and ribonuclease by isolated barley aleurone layers. Plant Physiology 42, 398406.CrossRefGoogle Scholar
Dashek, W.V. and Chrispeels, M.J. (1977) Gibberellic-acidinduced synthesis and release of cell wall degrading endoxylanase by isolated aleurone layers of barley. Planta 134, 251256.Google Scholar
Fincher, G.B. (1975) Morphology and chemical composition of barley endosperm cell walls. Journal of the Institute of Brewing 81, 116122.CrossRefGoogle Scholar
Fincher, G.B. (1989) Molecular and cellular biology associated with endosperm mobilization in germinating cerealgrains. Annual Review of Plant Physiology and Plant Molecular Biology 40, 305346.CrossRefGoogle Scholar
Fincher, G.B. (1992) Cell wall metabolism in barley. pp 413437 in Shewry, P.R. (Ed.) Barley: genetics, biochemistry, molecular biology and biotechnology, Wallingford, UK CAB International.Google Scholar
Fincher, G.B. and Stone, B.A. (1974) Some chemical and morphological changes induced by gibberellic acid in embyro-free wheat grain. Australian Journal of Plant Physiology 1, 297311.Google Scholar
Gibbons, G.C. (1981) On the relative role of the scutellum and aleurone in the production of hydrolases during germination of barley. Carlsberg Research Communications 46, 215225.Google Scholar
Høj, P.B., Hoogenraad, N., Hartman, D.J., Yannakena, H. and Fincher, G.B. (1990) Identification of individual (1→3, 1→4)-β-D-glucanase isoenzymes in extracts of germinated barley using specific monoclonal antibodies. Journal of Cereal Science 11, 261268.Google Scholar
Hough, L., Jones, J.K.N. and Wadman, W.H. (1950) Quantitative analysis of mixtures of sugars by the method of partition chromatography. Part 5. Improved methods for the separation and detection of sugars and their methylated derivatives on the paper chromatogram. Journal of the Chemical Society 2, 17021706.CrossRefGoogle Scholar
Hoy, J.L., Macauley, B.J. and Fincher, G.B. (1981) Cellulases of plant and microbial origin in germinating barley. Journal of the Institute of Brewing 87, 7780.Google Scholar
Laemmli, U.K. (1970) Cleavage of structural proteins during the assembly of the head of the bacteriophage T4. Nature (London) 227, 680685.CrossRefGoogle ScholarPubMed
Loi, L., Ahluwalia, B. and Fincher, G.B. (1988) Chromosomal location of genes encoding barley (1→3,1→4)-β-glucan 4-glucanohydrolases. Plant Physiology 87, 300302.Google Scholar
Mares, D.J. and Stone, B.A. (1973) Studies on wheat endosperm. I. Chemical composition and ultrastructure of the cell walls. Australian Journal of Biological Science 26, 793812.Google Scholar
McFadden, G.I., Ahluwalia, B., Clarke, A.E. and Fincher, G.B. (1988) Expression sites and developmental regulation of genes encoding (1→3, 1→4)-β-glucanases in germinated barley. Planta 173, 500508.Google Scholar
Okamoto, K., Kitano, H. and Akazawa, T. (1980) Biosynthesis and excretion of hydrolases in germinating cereal seeds. Plant Cell Physiology 21, 201204.Google Scholar
Palmer, G.H. and Duffus, J.H. (1986) Aleurone or scutellar hydrolytic enzymes in malting. Journal of the Institute of Brewing 92, 512513.Google Scholar
Schmitz, J.F., McDonald, C.E., Gilles, K.A. and Medcalf, D.G. (1974) Arabinoxylanases and cellulases of wheat. Cereal Chemistry 51, 809821.Google Scholar
Slade, A.M., Høj, P.B., Morrice, N.A. and Fincher, G.B. (1989) Purification and characterization of three (1→4)-β-D-xylan endohydrolases from germinated barley. European Journal of Biochemistry 185, 533539.CrossRefGoogle Scholar
Slakeski, N., Baulcombe, D.C., Devos, K.M., Ahluwalia, B., Doan, D.N.P. and Fincher, G.B. (1990) Structure and tissue-specific regulation of genes encoding barley (1→3, 1→4)-β-glucan endohydrolases. Molecular and General Genetics 224, 437449.CrossRefGoogle Scholar
Slakeski, N. and Fincher, G.B. (1992) Developmental regulation of (1→3,1→4)-β-glucanase gene expression in barley. Tissue-specific expression of individual isoenzymes. Plant Physiology 99, 12261232.CrossRefGoogle Scholar
Stuart, I.M. and Fincher, G.B. (1983) Immunological determination of (1→3),(1→4)-β-D-glucan endohydrolase development in germinating barley (Hordeum vulgare). FEBS Letters 155, 201204.CrossRefGoogle Scholar
Stuart, I.M., Loi, L. and Fincher, G.B. (1986) Development of (1→3,1→4)-β-d-glucan endohydrolase isoenzymes in scutella and aleurone layers of barley (Hordeum vulgare). Plant Physiology 80, 310314.Google Scholar
Stuart, I.M., Loi, L. and Fincher, G.B. (1987) Immunological comparison of (1→3, 1→4)-β-glucan endohydrolases in germinating cereals. Journal of Cereal Science 6, 4552.Google Scholar
Taiz, L. and Honigman, W.A. (1976) Production of cell wall hydrolyzing enzymes by barley aleurone layers in response to gibberellic acid. Plant Physiology 58, 380386.Google Scholar
Viëtor, R.J., Voragen, A.G.J., Angelino, S.A.G.F. and Pilnik, W. (1991) Non-starch polysaccharides in barley and malt: a mass balance of flour fractionation. Journal of Cereal Science 14, 7383.Google Scholar
Woodward, J.R. and Fincher, G.B. (1982a) Purification and chemical properties of two 1,3; 1,4-β-glucan endohydrolases from germinating barley. European Journal of Biochemistry 121, 663669.Google Scholar
Woodward, J.R. and Fincher, G.B. (1982b) Substrate specificities and kinetic properties of two (1→3),(1→4)-β-d-glucan endo-hydrolases from germinating barley (Hordeum vulgare). Carbohydrate Research 106, 111122.CrossRefGoogle Scholar