Influence of ionic composition of the culture medium on de novo flower formation in tobacco thin cell layers

1993 ◽  
Vol 71 (3) ◽  
pp. 506-511 ◽  
Author(s):  
Alain Cousson ◽  
Kiem Tran Thanh Van

Floral and vegetative organogenesis in thin cell layers of Nicotiana tabacum cv. Samsun was studied in relation to the ionic composition of the medium. The control liquid medium was buffered to pH 5.5. NH4+, NO3−, K+, and Ca2+ were separately varied between 0 or 0.1 times and 2, 3 or 4 times their initial control concentration. Increasing the concentrations of NO3−, and Ca2+ above their control concentration promoted the formation of vegetative buds instead of flowers. When K+ at 80.0 mM, Na+ at 78.9 mM, and NH4+ as the sole nitrogen source used, neither flower formation nor morphogenesis were observed in 70, 100, and 100% of the explants, respectively. NH4+ as the sole nitrogen source acidified the medium to pH 4.2, whereas the other ionic conditions did not change the external pH. NO3− at 7.9 mM prevented this acidification and allowed flower formation in 75% of the explants. This acidification could increase the K+ and Na+ influxes via a possible lowering of the intracellular pH. This hypothesis corroborates the morphogenic effect of K+ and Na+. Key words: absence of morphogenesis, acidification of medium, floral and vegetative organogenesis, ionic composition of the medium, thin cell layers, Nicotiana tabacum cv. Samsun.

1987 ◽  
Vol 70 (3) ◽  
pp. 453-460 ◽  
Author(s):  
Patrizia Torrigiani ◽  
Maria Maddalena Altamura ◽  
Gabriella Pasqua ◽  
Barbara Monacelli ◽  
Donatella Serafini-Fracassini ◽  
...  

1990 ◽  
Vol 68 (11) ◽  
pp. 2501-2508 ◽  
Author(s):  
G. Mersch ◽  
C. Nassogne ◽  
A. Havelange

Our aim was to analyse comparatively the spatial and temporal changes in mitotic activity in tobacco thin cell layers cultured in vitro during the expression of two organogenetic programs, namely the flower bud and root programs. These biological materials were found to be so complex and heterogeneous that we had to rely on sophisticated statistical models for the planned study. Using these models we could detect differences not only between the two programs, but also within each program between different time intervals and, in the flower bud program, between different longitudinal segments of the thin cell layers. Key words: Nicotiana tabacum, flower bud, root, statistical analysis, mitotic activity.


Genetics ◽  
2001 ◽  
Vol 158 (3) ◽  
pp. 999-1011
Author(s):  
Zoran Gojković ◽  
Michael P B Sandrini ◽  
Jure Piškur

Abstract β-Alanine synthase (EC 3.5.1.6), which catalyzes the final step of pyrimidine catabolism, has only been characterized in mammals. A Saccharomyces kluyveri pyd3 mutant that is unable to grow on N-carbamyl-β-alanine as the sole nitrogen source and exhibits diminished β-alanine synthase activity was used to clone analogous genes from different eukaryotes. Putative PYD3 sequences from the yeast S. kluyveri, the slime mold Dictyostelium discoideum, and the fruit fly Drosophila melanogaster complemented the pyd3 defect. When the S. kluyveri PYD3 gene was expressed in S. cerevisiae, which has no pyrimidine catabolic pathway, it enabled growth on N-carbamyl-β-alanine as the sole nitrogen source. The D. discoideum and D. melanogaster PYD3 gene products are similar to mammalian β-alanine synthases. In contrast, the S. kluyveri protein is quite different from these and more similar to bacterial N-carbamyl amidohydrolases. All three β-alanine synthases are to some degree related to various aspartate transcarbamylases, which catalyze the second step of the de novo pyrimidine biosynthetic pathway. PYD3 expression in yeast seems to be inducible by dihydrouracil and N-carbamyl-β-alanine, but not by uracil. This work establishes S. kluyveri as a model organism for studying pyrimidine degradation and β-alanine production in eukaryotes.


1989 ◽  
Vol 77 (3) ◽  
pp. 294-301 ◽  
Author(s):  
Patrizia Torrigiani ◽  
Maria Maddalena Altamura ◽  
Francesca Capitani ◽  
Donatella Serafini-Fracassini ◽  
Nello Bagni

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