Abstract:Tobacco callus cultures grown on defined agar-solidified media produced ethylene in differing amounts, which were related to cultural treatment and age of the callus. There was a close correlation between the rate of etbylene production and growth. In darkness, maximal rates occurred in the third week of growth with ethylene production in the range of 750 ni (calius piece)^^ d^' (fr, wt, = 1,5 g),, and in the light, maximal rates occurred in the first week of growth, 200 nl (callus piece)"' d"' (fr, wt, = 200 … Show more
“…Whether AtEBP expression in callus is due to elevated ethylene levels or other factors is not clear. There are conflicting reports on ethylene production in callus cultures and the amount of ethylene produced appears to be dependent on the culturing conditions (41). Chitinases have been shown to be inducible by ethylene in yam callus (42), suggesting that ethylene levels are not saturating in this tissue type.…”
Ocs elements are a group of promoter sequences required for the expression of both pathogen genes in infected plants and plant defense genes. Genes for ocs element binding factors (OBFs), belonging to a specific class of basic-region leucine zipper (
“…Whether AtEBP expression in callus is due to elevated ethylene levels or other factors is not clear. There are conflicting reports on ethylene production in callus cultures and the amount of ethylene produced appears to be dependent on the culturing conditions (41). Chitinases have been shown to be inducible by ethylene in yam callus (42), suggesting that ethylene levels are not saturating in this tissue type.…”
Ocs elements are a group of promoter sequences required for the expression of both pathogen genes in infected plants and plant defense genes. Genes for ocs element binding factors (OBFs), belonging to a specific class of basic-region leucine zipper (
“…Studies on lavandin callus cultures showed that callus growth was not affected by ethylene production (Mensuali-Sodi et al, 1989), but the regeneration of lavandin callus was associated with a low rate of ethylene production (Panizza et al, 1997). Conversely, a close positive correlation between ethylene production and callus growth was found in tobacco (Huxter et al, 1979) as well as in carob callus cultures (Martins-Loucao and Rodriguez-Barrueco, 1983) . From these results, a clear conclusion has not been drawn on the interaction between ethylene production and the growth in tissue culture.…”
Section: Discussionmentioning
confidence: 95%
“…In plant tissue and cell cultures, the cells are fairly uniform and undiffe~entiated and it is possible to study the studies also gave different results about the correlation between ethylene production and growth even in the same species (Huxter et al, 1979;Koves and Szab6, 1987). It is also known that dicot plants produce a larger amount of ethylene and are more sensitive to· exogenous ethylene than monocot plants (Tittle et al, 1990;Grossmann and Kwiatkowski, 1993).…”
“…The influence on ethylene, 1-aminocyclopropanecarboxylic acid (ACC), and N-malonyl-ACC (MACC) Undifferentiated plant cell suspensions are able to produce ethylene depending on the kind of plant from which the cell originated but also on their physiological state (2-4, 15, 17, 21, 24). With respect to its physiological significance, data suggested no functional relationship between growth and ethylene synthesis (10,15,24). Ethylene was assumed to be a by-product of actively dividing cells.…”
mentioning
confidence: 99%
“…With respect to its physiological significance, data suggested no functional relationship between growth and ethylene synthesis (10,15,24). Ethylene was assumed to be a by-product of actively dividing cells.…”
From a variety of undifferentiated plant cell suspensions, 2,4-dichlorophenoxyacetic acid-dependent cells of sunflower (Helianthus annuus L. Spanners Allzweck) produced large quantities of ethylene. The maximum rate was about 1 nanomole x gram fresh weight-' x hour-' during the exponential growth phase. The action of various compounds known to interfere with ethylene formation in plant tissue was studied in sunflower cell suspensions. The influence on ethylene, 1-aminocyclopropanecarboxylic acid (ACC), and N-malonyl-ACC (MACC) Undifferentiated plant cell suspensions are able to produce ethylene depending on the kind of plant from which the cell originated but also on their physiological state (2-4, 15, 17, 21, 24). With respect to its physiological significance, data suggested no functional relationship between growth and ethylene synthesis (10,15,24). Ethylene was assumed to be a by-product of actively dividing cells. Nevertheless, undifferentiated cell suspensions should be an appropriate tool for analyzing in detail the effects of biologically active compounds on cellular ethylene biosynthesis.In particular, plant growth retardants of the norbornenodiazetine (e.g. tetcyclacis) and triazole (e.g. LAB 150 978) type inhibited both the formation of ethylene and shoot growth of sunflower seedlings (25). Likewise, preliminary results indicated that both compounds decreased the ethylene production and cell division rate in cell suspensions of sunflower (24). Although their mode of action in regulating growth processes is seen in an interaction with gibberellin and to some extent sterol biosynthesis (5,7,12,22), the question arises as to whether there is a direct effect on ethylene biosynthesis, too.In the work reported we have analyzed the levels of ethylene and ACC2 produced in undifferentiated sunflower suspension cells under the influence of the growth retardants tetcyclacis and LAB 150 978. In addition to ACC, the direct precursor of eth-' Dedicated to Professor Dr. Helmut Doerfel on the occasion of his 60th birthday. The cells, grown in culture for several years, were subcultured at intervals of 7 d in the exponential growth phase under the following conditions: 250 ml Erlenmeyer flasks containing 80 ml of cell suspension were shaken on a rotary shaker at 110 rpm in the dark at 25°C. Solutions of chemical compounds used were prepared in acetone or in water (sterile-filtered) and were added to the medium shortly before inoculation. The final acetone concentration in the medium (1%) had no adverse effects on the growth of the culture.
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