Polyamines and Regulation of Ripening and Senescence - Postharvest Biology and Technology of Fruits, Vegetables, and Flowers - page 334

Alcazar, R., Garcıa-Martınez, J.L., Cuevas, J.C., Tiburcio, A.F., and Altabella, T. 2005. Overexpression of ADC2
in Arabidopsis induces dwarfism and late-flowering through GA deficiency. Plant J., 43: 425-436.
Apelbaum, A., Burgoon, A.C., Anderson, J.D., Lieberman, M., Ben-Arie, R., and Mattoo, A.K. 1981. Polyamines
inhibit biosynthesis of ethylene in higher plant tissue and protoplasts. Plant Physiol., 68: 453-456.
Apelbaum, A., Canellakis, Z.N., Applewhite, P.B., Kaur-Sawhney R., and Galston, A.W. 1988. Binding of sper-
midine to a unique protein in thin-layer tobacco tissue culture. Plant Physiol., 88: 996-998.
Armengaud, P., Breitling, R., and Amtmann, A. 2004. The potassium-dependent transcriptome of Arabidopsis
reveals a prominent role of jasmonic acid in nutrient signalling. Plant Physiol., 136: 2556-2576.
Aziz, A. 2003. Spermidine and related-metabolic inhibitors modulate sugar and amino acid levels in Vitisvinifera
L: possible relationship with initial fruitlet abscission. J. Exp. Bot., 54: 355-363.
Bagga, S., Rochford, J., Klaene, Z., Kuehn, G.D., and Phillips, G.C. 1997. Putrescine aminopropyltransferase is
responsible for biosynthesis of spermidine, spermine, and multiple uncommon polyamines in osmotic stress-
tolerant alfalfa. Plant Physiol., 114: 445-454.
Ben-Arie, R., Lurie, S., and Mattoo, A.K. 1982. Temperature-dependent inhibitory effects of calcium and spermine
on ethylene biosynthesis in apple discs correlate with changes in microsomal membrane microviscosity. Plant
Sci. Lett., 24: 239-247.
Besford, R.T., Richardson, C.M., Campos, J.L., and Tiburcio, A.F. 1993. Effect of polyamines on stabilization of
molecular complexes in thylakoid membranes of osmotically stressed oat leaves. Planta, 189: 201-206.
Bonghi, C., Ferrarese, L., Ruperti, B., Tonutti, P., and Ramina, A. 1998. Endo- -1,4-glucanases are involved in

peach fruit growth and ripening, and regulated by ethylene. Physiol. Plant., 102: 346-352.
Borrell, A., Carbonell, L., Farras, R., Puigparellada, P., and Tiburcio, A.F. 1997. Polyamines inhibit lipid peroxi-
dation in senescing oat leaves. Physiol. Plant., 99: 385-390.
Borrell, A., Culiaııez-Macia, F.A., Altabella, T., Besford, R.T., Flores, D., and Tiburcio, A.F. 1995. Arginine
decarboxylase is localized in chloroplasts. Plant Physiol., 109: 771-776.
Bouchereau, A., Aziz, A., Larher, F., and Martin-Tanguy, J. 1999. Polyamines and environmental challenges:
recent development. Plant Sci., 140: 103-125.
Bramley, P.M. 2002. Regulation of carotenoid formation during tomato fruit ripening and development. J. Exp.
Bot., 53: 2107-2113.
Bregoli, A.M., Scaramagli, S., Costa, G., Sabatini, E., Ziosi, V., Biondi, S., and Torrigiani, P. 2002. Peach ( Prunus
persica ) fruit ripening: aminoethoxyvinylglycine (AVG) and exogenous polyamines affect ethylene emission
and flesh firmness. Physiol. Plant., 114: 472-481.
Bregoli, A.M., Ziosi, V., Biondi, S., Claudio, B., Costa, G., and Torrigiani, P. 2006. A comparison between intact
fruit and fruit explants to study the effect of polyamines and aminoethoxyvinylglycine (AVG) on fruit ripening
in peach and nectarine ( Prunus persica L. Batch). Postharvest Biol. Technol., 42: 31-40.
Brune, B., Hartzell, P., Nicotera, P., and Orrenius, S. 1991. Spermine prevents endonuclease activation and apoptosis
in thymocytes. Exp. Cell Res., 195: 323-329.
Bryson, K. and Greenall, R.J. 2000. Binding sites of the polyamines putrescine, cadaverine, spermidine and
spermine on A- and B-DNA located by simulated annealing. J. Biomol. Struct. Dyn., 18: 393-412.
Capell, T., Bassie, L., and Christou, P. 2004. Modulation of the polyamine biosynthetic pathway in transgenic rice
confers tolerance to drought stress. Proc. Natl. Acad. Sci. U.S.A., 101: 9909-9914.
Capell, T., Escobar, C., Lui, H., Burtin, D., Lepri, O., and Christou, P. 1998. Over-expression of the oat arginine
decarboxylase cDNA in transgenic rice ( Oryza sativa L.) affects normal development patterns in vitro and
results in putrescine accumulation in transgenic plants. Theor. Appl. Genet., 97: 246-254.
Casero, R.A., Jr and Marton, L.J. 2007. Targeting polyamine metabolism and function in cancer and other hyper-
proliferative diseases. Nat. Rev. Drug Discov., 6: 373-390.
Cassol, T. and Mattoo, A.K. 2003. Do polyamines and ethylene interact to regulate plant growth, development
and senescence? In: Molecular Insights in Plant Biology (eds, P. Nath, A.K. Mattoo, S.R. Ranade, and J.H.
Weil), Science Publishers, Inc., Enfield, NH, pp. 121-132.
Childs, A.C., Mehta, D.J., and Gerner, E.W. 2003. Polyamine-dependent gene expression. Cell. Mol. Life Sci.,
60: 1394-1406.
Christ, M., Harr, J., and Felix, H. 1989. Transport of polyamines in sugar beet seedlings. Z. Naturforsch., 44c:
59-63.
Cohen, E., Heimer, Y.M., and Mizrahi, Y. 1982. Ornithine decarboxylase and arginine decarboxylase activities in
meristematic tissues of tomato and potato plants. Plant Physiol., 70: 544-546.
Cohen, S.S. 1998. A Guide to the Polyamines , Oxford University Press, New York, pp. 1-595.
Cohen, S.S., Balint, R., and Sindhu, R.K. 1981. The synthesis of polyamines from methionine in intact and
disrupted leafprotoplasts of virus-infected Chinese cabbage. Plant Physiol., 68: 1150-1155.

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