Literature DB >> 16660840

Differential Ion Stimulation of Plasmalemma Adenosine Triphosphatase from Leaf Epidermis and Mesophyll of Nicotiana rustica L.

S Lurie1.   

Abstract

An ATPase preparation, presumed to be associated with plasma membrane due to the coincidence on isopycnic gradients of cellulase and beta-glucan synthetase at high substrate, has been isolated from the epidermal and mesophyll of tobacco leaf. The ATPase from both tissues was found to prefer ATP over other nucleotides. The pH optimum was 7.0 in the presence of 3 millimolar MgCl(2) and pH 6.5 in the presence of 3 millimolar MgCl(2) and 100 millimolar KCl. Monovalent ion stimulation patterns of the ATPases from these tissues were found to differ and ion accumulation patterns in these tissues reflect this difference: mesophyll accumulated roughly equal amounts of Na(+) and Rb(+) and its plasma membrane ATPase is also equally stimulated by these ions; on the other hand, epidermal ATPase preparations showed a stronger stimulation by Rb(+) than Na(+) and this tissue was found to accumulate Rb(+) in preference to Na(+). Abscisic acid and fusicoccin affected both ATPase activity and ion uptake, the former inhibiting and the latter stimulating these parameters. These data support the hypothesis that the epidermal plasmalemma ATPase is involved in stomatal opening.

Entities:  

Year:  1979        PMID: 16660840      PMCID: PMC542947          DOI: 10.1104/pp.63.5.936

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


  13 in total

1.  Membrane-bound Adenosine Triphosphatase Activities of Oat Roots.

Authors:  R T Leonard; D Hansen; T K Hodges
Journal:  Plant Physiol       Date:  1973-04       Impact factor: 8.340

2.  Malate Dehydrogenases of Pisum sativum: Tissue Distribution and Properties of the Particulate Forms.

Authors:  W C Zschoche; I P Ting
Journal:  Plant Physiol       Date:  1973-06       Impact factor: 8.340

3.  Light sensitivity of na, rb, and k absorption by different tissues of bean leaves.

Authors:  B Jacoby
Journal:  Plant Physiol       Date:  1975-06       Impact factor: 8.340

4.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

5.  Purification of a plasma membrane-bound adenosine triphosphatase from plant roots.

Authors:  T K Hodges; R T Leonard
Journal:  Methods Enzymol       Date:  1974       Impact factor: 1.600

6.  Plasma Membrane-associated Adenosine Triphosphatase Activity of Isolated Cortex and Stele from Corn Roots.

Authors:  R T Leonard; C W Hotchkiss
Journal:  Plant Physiol       Date:  1978-02       Impact factor: 8.340

7.  Adenosine triphosphatase from soybean callus and root cells.

Authors:  D L Hendrix; R M Kennedy
Journal:  Plant Physiol       Date:  1977-02       Impact factor: 8.340

8.  Association of latent cellulase activity with plasma membranes from kidney bean abscission zones.

Authors:  D E Koehler; R T Leonard; W J Vanderwoude; A E Linkins; L N Lewis
Journal:  Plant Physiol       Date:  1976-09       Impact factor: 8.340

9.  Specific requirement of potassium for light-activated opening of stomata in epidermal strips.

Authors:  G D Humble; T C Hsiao
Journal:  Plant Physiol       Date:  1969-02       Impact factor: 8.340

10.  beta-Glucan Synthetases of Plasma Membrane and Golgi Apparatus from Onion Stem.

Authors:  W J Van Der Woude; C A Lembi; D J Morré
Journal:  Plant Physiol       Date:  1974-09       Impact factor: 8.340

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  10 in total

1.  Labeling and isolation of plasma membranes from corn leaf protoplasts.

Authors:  D S Perlin; R M Spanswick
Journal:  Plant Physiol       Date:  1980-06       Impact factor: 8.340

2.  Utilization of enzyme markers to determine the location of plasma membrane from Pisum epicotyls on sucrose gradients.

Authors:  W S Pierce; D L Hendrix
Journal:  Planta       Date:  1979-01       Impact factor: 4.116

3.  Functional reconstitution of a proton-translocating system responsive to fusicoccin.

Authors:  P Aducci; A Ballio; J P Blein; M R Fullone; M Rossignol; R Scalla
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

4.  Stomatal responses to water stress and to abscisic Acid in phosphorus-deficient cotton plants.

Authors:  J W Radin
Journal:  Plant Physiol       Date:  1984-10       Impact factor: 8.340

5.  Synthesis of potato virus X RNAs by membrane-containing extracts.

Authors:  S V Doronin; C Hemenway
Journal:  J Virol       Date:  1996-07       Impact factor: 5.103

6.  The Effect of Abscisic Acid and Other Inhibitors on Photosynthetic Capacity and the Biochemistry of CO(2) Assimilation.

Authors:  J R Seemann; T D Sharkey
Journal:  Plant Physiol       Date:  1987-07       Impact factor: 8.340

7.  Characterization of ATPase activity associated with corn leaf plasma membranes.

Authors:  D S Perlin; R M Spanswick
Journal:  Plant Physiol       Date:  1981-09       Impact factor: 8.340

8.  Phospholipid requirement of the vanadate-sensitive ATPase from maize roots evaluated by two methods.

Authors:  D Brauer; S I Tu
Journal:  Plant Physiol       Date:  1989-03       Impact factor: 8.340

9.  Partial characterization of fusicoccin binding to receptor sites on oat root membranes.

Authors:  R G Stout; R E Cleland
Journal:  Plant Physiol       Date:  1980-09       Impact factor: 8.340

10.  Protein phosphorylation in intact cultured sycamore (Acer pseudoplatanus) cells and its response to fusicoccin.

Authors:  L Tognoli; R Colombo
Journal:  Biochem J       Date:  1986-04-01       Impact factor: 3.857

  10 in total

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