Literature DB >> 16666048

Rapid wall relaxation in elongating tissues.

R Matyssek1, S Maruyama, J S Boyer.   

Abstract

Reported differences in the relaxation of cell walls in enlarging stem tissues of soybean (Glycine max [L.] Merr.) and pea (Pisum sativum L.) cause measurements of the yield threshold turgor, an important growth parameter, to be in doubt. Using the pressure probe and guillotine psychrometer, we investigated wall relaxation in these species by excising the elongating tissue in air to remove the water supply. We found that the rapid kinetics usually exhibited by soybean could be delayed and made similar to the slow kinetics previously reported for pea if slowly growing or mature tissue was left attached to the rapidly growing tissue when relaxation was initiated. The greater the amount of attached tissue, the slower the relaxation, suggesting that slowly growing tissue acted as a water source. Consistent with this concept was a lower water potential in the rapidly elongating tissue than in the slowly growing tissue. Previous reports of wall relaxation in pea included slowly growing tissue. If this tissue was removed from pea, relaxation became as rapid as usually exhibited by soybean. It is concluded that the true relaxation of cell walls to the yield threshold requires only a few minutes and that the yield threshold should be constant during so short a time, thus reflecting the yield threshold in the intact plant before excision. Under these conditions, the yield threshold was close to the turgor in the intact plant regardless of the species. The presence of slowly growing or mature tissue delays wall relaxation and should be avoided during such measurements. However, this delay can be used to advantage when turgor of intact growing tissues is being measured using excised tissues because turgor does not change for a considerable time after excision.

Entities:  

Year:  1988        PMID: 16666048      PMCID: PMC1054645          DOI: 10.1104/pp.86.4.1163

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


  12 in total

1.  Stress relaxation of cell walls and the yield threshold for growth: demonstration and measurement by micro-pressure probe and psychrometer techniques.

Authors:  D J Cosgrove; E Van Volkenburgh; R E Cleland
Journal:  Planta       Date:  1984       Impact factor: 4.116

2.  Metabolic and physical control of cell elongation rate: in vivo studies in nitella.

Authors:  P B Green; R O Erickson; J Buggy
Journal:  Plant Physiol       Date:  1971-03       Impact factor: 8.340

3.  Augmented growth equation for cell wall expansion.

Authors:  J K Ortega
Journal:  Plant Physiol       Date:  1985-09       Impact factor: 8.340

4.  Cell wall yield properties of growing tissue : evaluation by in vivo stress relaxation.

Authors:  D J Cosgrove
Journal:  Plant Physiol       Date:  1985-06       Impact factor: 8.340

5.  Dynamic Relation between Expansion and Cellular Turgor in Growing Grape (Vitis vinifera L.) Leaves.

Authors:  K A Shackel; M A Matthews; J C Morrison
Journal:  Plant Physiol       Date:  1987-08       Impact factor: 8.340

6.  Pressure probe and isopiestic psychrometer measure similar turgor.

Authors:  H Nonami; J S Boyer; E Steudle
Journal:  Plant Physiol       Date:  1987-03       Impact factor: 8.340

7.  Water potentials induced by growth in soybean hypocotyls.

Authors:  A J Cavalieri; J S Boyer
Journal:  Plant Physiol       Date:  1982-02       Impact factor: 8.340

8.  Transpiration- and growth-induced water potentials in maize.

Authors:  M E Westgate; J S Boyer
Journal:  Plant Physiol       Date:  1984-04       Impact factor: 8.340

9.  Growth-induced Water Potentials in Plant Cells and Tissues.

Authors:  F J Molz
Journal:  Plant Physiol       Date:  1978-09       Impact factor: 8.340

10.  Relationship of water potential to growth of leaves.

Authors:  J S Boyer
Journal:  Plant Physiol       Date:  1968-07       Impact factor: 8.340

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  10 in total

1.  Growth at reduced turgor: irreversible and reversible cell-wall extension of maize coleoptiles and its implications for the theory of cell growth.

Authors:  M Hohl; P Schöpfer
Journal:  Planta       Date:  1992-05       Impact factor: 4.116

2.  Primary events regulating stem growth at low water potentials.

Authors:  H Nonami; J S Boyer
Journal:  Plant Physiol       Date:  1990-08       Impact factor: 8.340

3.  Gradients of turgor, osmotic pressure, and water potential in the cortex of the hypocotyl of growing ricinus seedlings : effects of the supply of water from the xylem and of solutes from the Phloem.

Authors:  A Meshcheryakov; E Steudle; E Komor
Journal:  Plant Physiol       Date:  1992-03       Impact factor: 8.340

4.  Turgor and growth at low water potentials.

Authors:  H Nonami; J S Boyer
Journal:  Plant Physiol       Date:  1989-03       Impact factor: 8.340

5.  Wall extensibility and cell hydraulic conductivity decrease in enlarging stem tissues at low water potentials.

Authors:  H Nonami; J S Boyer
Journal:  Plant Physiol       Date:  1990-08       Impact factor: 8.340

6.  Temperature-dependent water and ion transport properties of barley and sorghum roots : I. Relationship to leaf growth.

Authors:  H Bassirirad; J W Radin; K Matsuda
Journal:  Plant Physiol       Date:  1991-09       Impact factor: 8.340

7.  Abscisic Acid accumulates at positive turgor potential in excised soybean seedling growing zones.

Authors:  R A Creelman; J E Mullet
Journal:  Plant Physiol       Date:  1991-04       Impact factor: 8.340

8.  Rapid Response of the Yield Threshold and Turgor Regulation during Adjustment of Root Growth to Water Stress in Zea mays.

Authors:  J. Frensch; T. C. Hsiao
Journal:  Plant Physiol       Date:  1995-05       Impact factor: 8.340

9.  Decreased Growth-Induced Water Potential (A Primary Cause of Growth Inhibition at Low Water Potentials).

Authors:  H. Nonami; Y. Wu; J. S. Boyer
Journal:  Plant Physiol       Date:  1997-06       Impact factor: 8.340

10.  Plant vigour at establishment and following defoliation are both associated with responses to drought in perennial ryegrass (Lolium perenne L.).

Authors:  Jean-Hugues B Hatier; Marty J Faville; Michael J Hickey; John P Koolaard; Jana Schmidt; Brandi-Lee Carey; Chris S Jones
Journal:  J Exp Bot       Date:  2014-08-06       Impact factor: 6.992

  10 in total

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