PLANT PHYSIOLOGY · 1997 · 48 citations · 15 references
Life SciencesBiochemistryEnzyme MechanismEnzymologyMetabolismEnzyme InhibitionPlant Natural Product BiosynthesisEnzymatic Reaction MechanismsEnzyme ActivityEnzyme Reaction MechanismsInhibitor SpecificityPolyamine Biosynthesis
The biosynthesis of polyamines from the diamine putrescine is not fully understood in higher plants. A putrescine aminopropyltransferase (PAPT) enzyme activity was characterized in alfalfa (Medicago sativa L.). This enzyme activity was highly specific for putrescine as the initial substrate and did not recognize another common diamine, 1,3-diaminopropane, or higher-molecular-weight polyamines such as spermidine and spermine as alternative initial substrates. The enzyme activity was inhibited by a general inhibitor of aminopropyltransferases, 5[prime]-methylthioadenosine, and by a specific inhibitor of PAPTs, cyclohexylammonium sulfate. The initial substrate specificity and inhibition characteristics of the enzyme activity suggested that it is a classical example of a PAPT. However, this enzyme activity yielded multiple polyamine products, which is uncharacteristic of PAPTs. The major reaction product of PAPT activity in alfalfa was spermidine. The next most abundant products of the enzyme reaction using putrescine as the initial substrate included the tetramines spermine and thermospermine. These two tetramines were distinguished by thin-layer chromatography to be distinct reaction products exhibiting differential rates of formation. In addition, the uncommon polyamines homocaldopentamine and homocaldohexamine were tentatively identified as minor enzymatic reaction products but only in extracts prepared from osmotic stresstolerant alfalfa cultivars. PAPT activity from alfalfa was highest in meristematic shoot tip and floral bud tissues and was not detected in older, nonmeristematic tissues. Product inhibition of the enzyme activity was observed after spermidine was added into the in vitro assay for alfalfa PAPT activity. A biosynthetic pathway is proposed that accounts for the characteristics of this PAPT activity and accommodates a novel scheme by which certain uncommon polyamines are produced in plants.
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Studies of inhibition of rat spermidine synthase and spermine synthase
Hiroshige Hibasami, Ronald T. Borchardt, Shiang Yuan Chen et al. · Biochemical Journal · 1980 · 113 citations · Full text
Dicyclohexylamine, a potent inhibitor of spermidine synthase in mammalian cells
Hiroshige Hibasami, Minoru Tanaka, Jun Nagai et al. · FEBS Letters · 1980 · 92 citations · Full text
Stephen A. Margosiak, Abdi Dharma, Megan Carver et al. · PLANT PHYSIOLOGY · 1990 · 74 citations · Full text