Literature DB >> 16661952

Soluble Cell Wall Polysaccharides Released from Pea Stems by Centrifugation : I. EFFECT OF AUXIN.

M E Terry1, R L Jones.   

Abstract

The metabolism of polysaccharides by pea stem segments treated with and without auxin was investigated using a centrifugation technique for removing solution from the free space of the cell wall. Glucose is the predominant sugar in both the ethanol-soluble and ethanol-insoluble fractions of the cell wall solution extracted with water. In the water-soluble, ethanol-insoluble polysaccharides, arabinose, xylose, galactose, and glucose make up 9.5, 23.8, 23.9, and 39.9%, respectively, of the neutral sugars, while rhamnose, fucose, and mannose are present at concentrations between 0.5 and 2.0%.Auxin treatment enhances the levels of xylose and glucose in ethanol-insoluble polysaccharides relative to controls, and this difference can be detected within 30 minutes of auxin treatment. Cellulose-binding experiments show that the enhanced levels of xylose and glucose are in a polymer having the cellulose-binding properties of xyloglucan. (3)H-glucose labeling experiments confirm the auxin-enhanced metabolism of the xyloglucan fraction; however, increased labeling of arabinose is also observed in auxin-treated sections. Auxin treatment also causes a marked increase in the level of uronic acids centrifuged from pea internode sections. Thus, after 3 hours of incubation in indoleacetic acid, the level of uronic acids in the ethanol-insoluble polysaccharides which can be recovered by centrifugation is increased 2- to 3-fold over sections incubated in water. These auxin-enhanced changes in xylose, glucose, and uronic acids are correlated with enhanced rates of section growth.Incubation of excised pea internode sections in acidic buffers also enhances the rate of xyloglucan and polyuronide metabolism. This acid-enhanced metabolism of xyloglucan and polyuronide is inhibited by low temperature, suggesting that it is enzyme-mediated.Extraction of the cell wall solution with CaCl(2) increases the yield of all neutral sugars. Arabinose and mannose are increased 4- and 3-fold, respectively, and xylose and glucose by about 20%, while galactose levels are 40% higher in cell wall solution extracted with CaCl(2) than in that extracted with water. Although calcium increases the amount of neutral sugars extracted, it does not affect the auxin-induced changes in neutral sugars. Extraction of the cell wall solution with ethyleneglycol-bis-(beta-aminoethyl ether)-N,N'tetraacetic acid enhances the yield of uronic acids and also increases the difference due to auxin treatment.

Entities:  

Year:  1981        PMID: 16661952      PMCID: PMC425934          DOI: 10.1104/pp.68.3.531

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  13 in total

1.  Promotion of Xyloglucan Metabolism by Acid pH.

Authors:  M Jacobs; P M Ray
Journal:  Plant Physiol       Date:  1975-09       Impact factor: 8.340

2.  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.

Authors:  K Keegstra; K W Talmadge; W D Bauer; P Albersheim
Journal:  Plant Physiol       Date:  1973-01       Impact factor: 8.340

3.  Enhancement of wall loosening and elongation by Acid solutions.

Authors:  D L Rayle; R Cleland
Journal:  Plant Physiol       Date:  1970-08       Impact factor: 8.340

4.  The structure of plant cell walls: v. On the binding of xyloglucan to cellulose fibers.

Authors:  B S Valent; P Albersheim
Journal:  Plant Physiol       Date:  1974-07       Impact factor: 8.340

5.  An Examination of Centrifugation as a Method of Extracting an Extracellular Solution from Peas, and Its Use for the Study of Indoleacetic Acid-induced Growth.

Authors:  M E Terry; B A Bonner
Journal:  Plant Physiol       Date:  1980-08       Impact factor: 8.340

6.  The Structure of Plant Cell Walls: VII. Barley Aleurone Cells.

Authors:  M McNeil; P Albersheim
Journal:  Plant Physiol       Date:  1975-01       Impact factor: 8.340

7.  Turnover of cell wall polysaccharides in elongating pea stem segments.

Authors:  J M Labavitch; P M Ray
Journal:  Plant Physiol       Date:  1974-05       Impact factor: 8.340

8.  The Structure of Plant Cell Walls: II. The Hemicellulose of the Walls of Suspension-cultured Sycamore Cells.

Authors:  W D Bauer; K W Talmadge; K Keegstra; P Albersheim
Journal:  Plant Physiol       Date:  1973-01       Impact factor: 8.340

9.  The Structure of Plant Cell Walls: I. The Macromolecular Components of the Walls of Suspension-cultured Sycamore Cells with a Detailed Analysis of the Pectic Polysaccharides.

Authors:  K W Talmadge; K Keegstra; W D Bauer; P Albersheim
Journal:  Plant Physiol       Date:  1973-01       Impact factor: 8.340

10.  Relationship between Promotion of Xyloglucan Metabolism and Induction of Elongation by Indoleacetic Acid.

Authors:  J M Labavitch; P M Ray
Journal:  Plant Physiol       Date:  1974-10       Impact factor: 8.340

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  24 in total

1.  Polar Calcium Flux in Sunflower Hypocotyl Segments : II. The Effect of Segment Orientation, Growth, and Respiration.

Authors:  C C de Guzman; R K Dela Fuente
Journal:  Plant Physiol       Date:  1986-06       Impact factor: 8.340

2.  Xyloglucan antibodies inhibit auxin-induced elongation and cell wall loosening of azuki bean epicotyls but not of oat coleoptiles.

Authors:  T Hoson; Y Masuda; Y Sone; A Misaki
Journal:  Plant Physiol       Date:  1991-06       Impact factor: 8.340

3.  Effect of IAA on Growth and Soluble Cell Wall Polysaccharides Centrifuged from Pine Hypocotyl Sections.

Authors:  M E Terry; D McGraw; R L Jones
Journal:  Plant Physiol       Date:  1982-02       Impact factor: 8.340

4.  Chemical structure of the cell walls of dwarf maize and changes mediated by gibberellin.

Authors:  N C Carpita; J Kanabus
Journal:  Plant Physiol       Date:  1988-11       Impact factor: 8.340

5.  Extracellular polysaccharides and proteins of tobacco cell cultures and changes in composition associated with growth-limiting adaptation to water and saline stress.

Authors:  N M Iraki; R A Bressan; N C Carpita
Journal:  Plant Physiol       Date:  1989-09       Impact factor: 8.340

6.  Xyloglucan Endotransglycosylase Activity in Carrot Cell Suspensions during cell Elongation and Somatic Embryogenesis.

Authors:  P. R. Hetherington; S. C. Fry
Journal:  Plant Physiol       Date:  1993-11       Impact factor: 8.340

7.  Effect of Xyloglucan Oligosaccharides on Growth, Viscoelastic Properties, and Long-Term Extension of Pea Shoots.

Authors:  A. Cutillas-Iturralde; E. P. Lorences
Journal:  Plant Physiol       Date:  1997-01       Impact factor: 8.340

8.  A Xyloglucan-Specific Endo-1,4-[beta]-Glucanase Isolated from Auxin-Treated Pea Stems.

Authors:  T. Matsumoto; F. Sakai; T. Hayashi
Journal:  Plant Physiol       Date:  1997-06       Impact factor: 8.340

9.  In-vivo formation of xyloglucan nonasaccharide: A possible biologically active cell-wall fragment.

Authors:  S C Fry
Journal:  Planta       Date:  1986-11       Impact factor: 4.116

10.  Inducible expression of Pisum sativum xyloglucan fucosyltransferase in the pea root cap meristem, and effects of antisense mRNA expression on root cap cell wall structural integrity.

Authors:  Fushi Wen; Rhodesia M Celoy; Trang Nguyen; Weiqing Zeng; Kenneth Keegstra; Peter Immerzeel; Markus Pauly; Martha C Hawes
Journal:  Plant Cell Rep       Date:  2008-03-18       Impact factor: 4.570

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