Literature DB >> 16658877

The Metabolism of Oat Leaves during Senescence: I. Respiration, Carbohydrate Metabolism, and the Action of Cytokinins.

R M Tetley1, K V Thimann.   

Abstract

When the detached first leaves of green or etiolated oat (Avena sativa cv. Victory) seedlings senesce in the dark, their oxygen consumption shows a large increase, beginning after 24 hours and reaching a peak of up to 2.5 times the initial rate by the 3rd day. This effect takes place while the chlorophyll of green leaves, or the carotenoid of etiolated leaves, is steadily decreasing. Kinetin, at a concentration which inhibits the decrease in pigment, completely prevents the respiratory rise; instead, the oxygen consumption drifts downwards. Lower kinetin concentrations have a proportional effect, 50% reduction of respiration being given by about 0.1 mg/l. About one-fifth of the respiratory rise may be attributed to the free amino acids which are liberated during senescence; several amino acids are shown to cause increases of almost 50% in the oxygen consumption when supplied at the concentrations of total amino acid present during senescence. A smaller part of the rise may also be due to soluble sugars liberated during senescence, largely coming from the hydrolysis of a presumptive fructosan. The remainder, and the largest part, of the increase is ascribed to a natural uncoupling of respiration from phosphorylation. This is deduced from the fact that dinitrophenol causes a similar large rise in the oxygen consumption of the fresh leaves or of leaf segments kept green with kinetin, but causes only a very small rise when the oxygen consumption is near its peak in senescent controls. The respiration of these leaves is resistant to cyanide, and 10 mm KCN even increases it by some 30%; in contrast, etiolated leaves of the same age, which undergo a similar rise in oxygen consumption over the same time period, show normal sensitivity to cyanide. The respiratory quotient during senescence goes down as low as 0.7, both with and without kinetin, though it is somewhat increased by supplying sugars or amino acids; glucose or alanine at 0.3 m bring it up to 1.0 and 0.87, respectively.N(6)-Benzylaminopurine and Delta-2-isopentenylaminopurine act similarly to kinetin in repressing the respiratory rise, the former being five times as active as kinetin, while the latter has only 1% of the activity of kinetin. Zeatin also powerfully prevents senescence. Because the repression of the respiratory rise is shown by each cytokinin at the concentration at which it inhibits senescence, the action is ascribed in both cases to the maintenance of a tight coupling between respiration and phosphorylation. It is pointed out that such an effect would explain many features of cytokinin action.A change in the methodology of the senescence experiments is described and compared with the method previously used, and the influence of temperature and age of the plants on the course of leaf senescence are presented in detail.

Entities:  

Year:  1974        PMID: 16658877      PMCID: PMC367400          DOI: 10.1104/pp.54.3.294

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


  11 in total

1.  Phosphorylation coupled with the oxidation of alpha-ketoglutarate by heart-muscle sarcosomes. 3. Experiments with ferricytochrome c as hydrogen acceptor.

Authors:  E C SLATER
Journal:  Biochem J       Date:  1955-03       Impact factor: 3.857

2.  Explanation of cocaine desensitization of blood pressure responses to ephedrine.

Authors:  C CANNON; F F COWAN; T KOPPANYI; G D MAENGWYN-DAVIES
Journal:  Science       Date:  1961-10-13       Impact factor: 47.728

3.  Terminal Respiration of Vegetative Cells and Zygospores in Chlamydomonas reinhardi.

Authors:  M H Hommersand; K V Thimann
Journal:  Plant Physiol       Date:  1965-11       Impact factor: 8.340

4.  Effect of N-Benzylaminopurine on Respiration & Storage Behavior of Broccoli (Brassica oleracea var. italica).

Authors:  R R Dedolph; S H Wittwer; V Tuli; D Gilbart
Journal:  Plant Physiol       Date:  1962-07       Impact factor: 8.340

5.  Role of Protein Synthesis in the Senescence of Leaves: II. The Influence of Amino Acids on Senescence.

Authors:  C Martin; K V Thimann
Journal:  Plant Physiol       Date:  1972-10       Impact factor: 8.340

6.  The role of protein synthesis in the senescence of leaves: I. The formation of protease.

Authors:  C Martin; K V Thimann
Journal:  Plant Physiol       Date:  1972-01       Impact factor: 8.340

7.  Effects of cytokinins on the respiration of soybean callus tissue.

Authors:  T S Moore; C O Miller
Journal:  Plant Physiol       Date:  1972-11       Impact factor: 8.340

8.  Senescence inhibition and respiration induced by growth retardants and N-benzyladenine.

Authors:  A H Halevy; D R Dilley; S H Wittwer
Journal:  Plant Physiol       Date:  1966-09       Impact factor: 8.340

9.  KINETIN-LIKE GROWTH-PROMOTING ACTIVITY OF 1-SUBSTITUTED ADENINES (1-BENZYL-6-AMINOPURINE AND 1-(GAMMA, GAMMA-DIMETHYLALLYL)-6-AMINOPURINE.

Authors:  H Q HAMZI; F SKOOG
Journal:  Proc Natl Acad Sci U S A       Date:  1964-01       Impact factor: 11.205

10.  Sarcocystis sp. in the red-legged partridge, Alectoris rufa, and the pheasant, Phasianus colchicus.

Authors:  P A CLAPHAM
Journal:  Nature       Date:  1957-12-07       Impact factor: 49.962

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  47 in total

1.  Chromium-induced biochemical changes in Eichhornia crassipes (Mart) solms and Pistia stratiotes L.

Authors:  G Satyakala; K Jamil
Journal:  Bull Environ Contam Toxicol       Date:  1992-06       Impact factor: 2.151

2.  The Metabolism of Oat Leaves during Senescence: III. The Senescence of Isolated Chloroplasts.

Authors:  H T Choe; K V Thimann
Journal:  Plant Physiol       Date:  1975-05       Impact factor: 8.340

3.  The Metabolism of Oat Leaves during Senescence: II. Senescence in Leaves Attached to the Plant.

Authors:  K V Thimann; R R Tetley; T Van Thanh
Journal:  Plant Physiol       Date:  1974-12       Impact factor: 8.340

4.  The Metabolism of Oat Leaves during Senescence: IV. The Effects of alphaalpha'-Dipyridyl and other Metal Chelators on Senescence.

Authors:  R M Tetley; K V Thimann
Journal:  Plant Physiol       Date:  1975-07       Impact factor: 8.340

5.  Relation between leaf senescence and stomatal closure: Senescence in light.

Authors:  K V Thimann; S O Satler
Journal:  Proc Natl Acad Sci U S A       Date:  1979-05       Impact factor: 11.205

6.  Catalase, Peroxidase, and Polyphenoloxidase Activities during Rice Leaf Senescence.

Authors:  M Kar; D Mishra
Journal:  Plant Physiol       Date:  1976-02       Impact factor: 8.340

7.  Effect of benzyladenine on some enzymes of mitochondria and microbodies in excised sunflower cotyledons.

Authors:  O Servettaz; F Cortesi; C P Longo
Journal:  Plant Physiol       Date:  1976-10       Impact factor: 8.340

8.  Metabolism of Oat Leaves during Senescence: V. Senescence in Light.

Authors:  K V Thimann; R M Tetley; B M Krivak
Journal:  Plant Physiol       Date:  1977-03       Impact factor: 8.340

9.  Induced senescence of intact wheat seedlings and its reversibility.

Authors:  V A Wittenbach
Journal:  Plant Physiol       Date:  1977-06       Impact factor: 8.340

10.  Kinetin action on the development of microbody enzymes in sunflower cotyledons in the dark.

Authors:  R R Theimer; G Anding; P Matzner
Journal:  Planta       Date:  1976-01       Impact factor: 4.116

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