Plant Physiology 89:69-73 (1989)
© 1989 American Society of Plant Biologists
Development and Growth Regulation
Diamine Oxidase Activity in Different Physiological Stages of Helianthus tuberosus Tuber 1
Patrizia Torrigiani,
Donatella Serafini-Fracassini and
Angela Fara
Dipartimento di Biologia Evoluzionistica Sperimentale, Università di Bologna, 40126 Bologna, Italy
Diamine oxidase (DAO, EC 1.4.3.6) activity was examined in relation to polyamine content in Helianthus tuberosus L. during the first synchronous cell cycle induced in vitro by 2,4,-dichloro-phenoxyacetic acid in tuber slices and during the in vivo formation of the tuber. The optimal pH, buffer and dithiothreitol concentrations for the enzyme extraction and assay were determined. When added in the assay mixture, catalase enhanced DAO activity, while polyvinylpyrrolidone had no effect; both aminoguanidine and hydrazine inhibited enzyme activity. The time course of the reaction, based on the recovery of 1-pyrroline from labeled putrescine in lipophilic solvents, showed that it was linear up to 30 minutes; the Km of the enzyme for putrescine was of the order of 104 molar. During the first cell cycle, DAO activity exhibited a peak at 15 hours of activation while putrescine content gave a peak at 12 hours. During tuber formation (from August till October) DAO activity was relatively high during the first phase of growth (cell division), decreased until flowering (end of September-early October), and then newly increased during the cell enlargement phase preceding the entry into dormancy (November). Maximum putrescine content was observed at the end of October. The increase in DAO activity paralleled the accumulation of putrescine. This indicates a direct correlation between the biosynthesis and oxidation of putrescine which, as already demonstrated in animal systems, occur simultaneously in physiological stages of intense metabolism such as cell division or organ formation.
1 Supported by funds for scientific research from Ministero della Pubblica Istruzione, Italy.
This article has been cited by other articles:

|
 |

|
 |
 
K. A. Paschalidis and K. A. Roubelakis-Angelakis
Sites and Regulation of Polyamine Catabolism in the Tobacco Plant. Correlations with Cell Division/Expansion, Cell Cycle Progression, and Vascular Development
Plant Physiology,
August 1, 2005;
138(4):
2174 - 2184.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Asthir, C. M. Duffus, R. C. Smith, and W. Spoor
Diamine oxidase is involved in H2O2 production in the chalazal cells during barley grain filling
J. Exp. Bot.,
April 1, 2002;
53(369):
677 - 682.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Biondi, S. Scaramagli, F. Capitani, M. Maddalena Altamura, and P. Torrigiani
Methyl jasmonate upregulates biosynthetic gene expression, oxidation and conjugation of polyamines, and inhibits shoot formation in tobacco thin layers
J. Exp. Bot.,
February 1, 2001;
52(355):
231 - 242.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. Bhatnagar, R. Minocha, and S. C. Minocha
Genetic Manipulation of the Metabolism of Polyamines in Poplar Cells. The Regulation of Putrescine Catabolism
Plant Physiology,
April 1, 2002;
128(4):
1455 - 1469.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|