Literature DB >> 24500017

[Characterization of root initiation and root senescence in callus- and organ-cultures of Daucus carota through determination of the specific activity of the glutamate-dehydrogenase (NAD)].

D Werner1, D Gogolin.   

Abstract

In callus tissues of Daucus carota rhizogenesis was influenced by addition to the cultures of solutions with different kinetin concentrations (0-0.1-0.5-2 mg/l) and a constant auxin content (1 mg/l). In these cultures the specific activity of glutamate-dehydrogenase (E.C. 1.4.1.2.), aspartate-aminotransferase (E.C. 2.6.1.1.), isocitrate-dehydrogenase (E.C. 1.1.1.42) and of acid phosphatase (E.C. 3.1.3.2.) was determined. Before root initiation can be seen morphologically in tissues grown on low kinetin concentrations, the specific activity of glutamate-dehydrogenase increases to more than three times the level found in cultures with no subsequent root initiation, whereas the specific activity of the other three enzymes changes far less. Total soluble protein measured as percentage of fresh weight remains nearly the same in all callus cultures. The activity of the same enzymes was measured in liquid grown roots of Daucus carota during a period of ageing of 130 days. During this time, the specific activity of glutamate-dehydrogenase is reduced to 1/10 of the value found in growing roots, whereas the activity of the other three enzymes is reduced only to 1/2 or to 1/3 of this value. Therefore, the state of senescence and the capacity for further growth can be characterized by the specific activity of the glutamate-dehydrogenase in the roots. The changes in the specific activity of glutamate-dehydrogenase in callus tissue and in the roots do not depend on inhibitory substances in the cell-free extracts.

Entities:  

Year:  1970        PMID: 24500017     DOI: 10.1007/BF00386099

Source DB:  PubMed          Journal:  Planta        ISSN: 0032-0935            Impact factor:   4.116


  8 in total

1.  Chemical regulation of growth and organ formation in plant tissues cultured in vitro.

Authors:  F SKOOG; C O MILLER
Journal:  Symp Soc Exp Biol       Date:  1957

2.  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

3.  Some aspects of differentiation in cells of Picea glauca cultivated in vitro.

Authors:  P R White
Journal:  Am J Bot       Date:  1967-03       Impact factor: 3.844

4.  Further studies on the growth and differentiation of single, isolated cells of tobacco in vitro.

Authors:  V Vasil; A C Hildebrandt
Journal:  Planta       Date:  1967-06       Impact factor: 4.116

5.  Intracellular localization of nitrate reductase, nitrite reductase, and glutamic Acid dehydrogenase in green leaf tissue.

Authors:  G L Ritenour; K W Joy; J Bunning; R H Hageman
Journal:  Plant Physiol       Date:  1967-02       Impact factor: 8.340

6.  Isolation, Purification, and Characterization of an Endogenous Root-promoting Factor Obtained from Basal Sections of Pear Hardwood Cuttings.

Authors:  M S Fadl; H T Hartmann
Journal:  Plant Physiol       Date:  1967-04       Impact factor: 8.340

7.  Ontogeny of Adventive Embryos of Wild Carrot.

Authors:  W Halperin; D F Wetherell
Journal:  Science       Date:  1965-02-12       Impact factor: 47.728

8.  Growth and division of single cells of higher plants in vitro.

Authors:  L BERGMANN
Journal:  J Gen Physiol       Date:  1960-03       Impact factor: 4.086

  8 in total

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