The diamine putrescine, the triamine spermidine and
the tetramine spermine occur as free cations and as conjugates with phenolic
acids and macromolecules in plants. Their levels of concentration increase
greatly when the environment suffers changes; specially when there is potassium
deficiency, water deficits, salinity stress, anaerobiosis and acid stress.
Because polyamines are synthesized by amino acid decarboxylation reactions,
where H+ is consumed, polyamine accumulation may function as a way for plants to
keep their pH at a constant value. Polyamines also serve as precursors of
various alkaloids that play important roles in plants defense.
Polyamine
Structure
Occurrence
Putrescine
NH2(CH2)3NH2
Widespread
Cadaverine
NH2(CH2)5NH2
Restricted
Spermidine
NH2(CH2)3NH(CH2)4NH2
Widespread
Spermine
NH2(CH2)3NH(CH2)4NH(CH2)3NH
Widespread
The first polyamine formed is putrescine. This may
happen by decarboxylation of ornithine or arginine. These reactions are
catalyzed by the enzymes ornithine decarboxylase (ODC) or arginine decarboxylase
(ADC), respectively. The polyamines spermidine and spermine are formed by adding
an aminopropyl moeity to putrescine and spermidine, respectively.
Polyamines can occur as free molecular bases in plant cells, but they also occur
as conjugates, associated with small molecules like phenolic acids and
macromolecules such as proteins. Polyamines are usually conjugated to
cinnamic acids, very often to p-coumaric, ferulic and caffeic acids.
Adequate levels of polyamines are necessary for optimal growth and replication
of plants, bacteria and fungi.
End of
Characterization
1: Slocum, Robert D. Flores, Hector E. "Biochemistry and Physiology of Polyamines in Plants." CRC PRESS. 1991