Sk. Nandi et Lms. Palni, METABOLISM OF ADENINE AND HYPOXANTHINE IN A HORMONE AUTONOMOUS GENETIC TUMOR LINE OF TOBACCO, Biologia plantarum, 40(4), 1998, pp. 555-563
Genetic tumour tissues of Nicotiana glauca (Grah.) x N. langsdorffii (
Weinm.), which grow on auxin and cytokinin-free medium, were incubated
with [C-14]-/[H-3]-adenine or [H-3]-hypoxanthine to investigate cytok
inin biosynthesis. Adenine was supplied to tissues of two different ag
es (2- and 3.5-week-old) for 8, 24 or 30 h, The uptake was over 91.0 %
(of ''supplied radioactivity'') by 2-week-old tissues as compared to
around 50.0 % uptake by 3.5-week-old tissues. Incorporation into cytok
inins could not be detected. While unmetabolized adenine accounted for
only about 24.0 and 13.4 % of ''extracted radioactivity'' (following
8 and 30 h incubation, respectively) in 2-week-old tissues, relatively
higher levels, i.e. 36.0 and 34.5 % (following 8 and 24 h incubation,
respectively) were present in 3.5-week-old tissues. The metabolites f
ormed were adenosine and its nucleotides (4.5 - 16.5 % and 37.4 - 60.2
% of the extracted radioactivity, respectively). Hypoxanthine was sup
plied to 3.5-week-old tissues for 8 and 24 h, While the uptake was low
(< 28.0 % of supplied radioactivity), the major proportion of extract
ed radioactivity was due to unmetabolized hypoxanthine (79.8 % and 85.
9 % after 8 and 24 h incubation periods, respectively); the minor meta
bolites were inosine and adenosine (both < 0.5 %) and their nucleotide
s (< 3.5 %). Radioactivity incorporation into cytokinins from hypoxant
hine was not detected. Thus in the present investigations precursor in
corporation from either adenine or hypoxanthine into cytokinins could
not be demonstrated. It is possible that this may be due to slow rate
of cytokinin turnover in these tissues.