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Madelon, although some completely normal cells were also present. We do not have any explanation for this phenomenon. An increase in leakage of electrolytes has been measured two days after flower harvest in the control petals of cv. Mercedes. This increase in leakage has been completely prevented for 10 days by GA3 treatment. On the other hand, the leakage of electrolytes from cv. Madelon petals was not affected by GA3 and remained stable during the experimental period (Fig. 1). 49 I. A. ), Phytohormones in Plant Biotechnology and Agriculture, 49-56 © 2003 Kluwer Academic Publishers.

Yephremov, A. and Palme, K. (1998) Regulation of polar auxin transport by AtPIN1 in Arabidopsis vascular tissue, Science 282, 22262230. , Juergens, G. and Palme, K. (2001) Auxin transport inhibitors block PIN1 cycling and vesicle trafficking, Nature 413, 425-428. Hagen, G. J. ), Plant Hormones: Physiology, Biochemistry and Molecular Biology, Kluwer Academic Publishers, Dordrecht, The Netherlands, Pp. 228-245. Hwang, I. and Sheen, J. (2001) Two-component circuitry in Arabidopsis cytokinin signal transduction, Nature London 413, 383-389.

The work of Jacobsen and Olszewski (1991) associated a special role for gibberellin (GA) in tomato by studying early flower and anther development in the GA deficient gib-1 mutant. The GA effects obtained with this mutant could not be achieved with other plant hormones. The role of the plant hormone gibberellin (GA) during early flower development has been studied by the use of the GA biosynthesis gib-1 mutant of tomato (Van den Heuvel, 2000). This gib-1 mutant is a monogenic recessive mutant in which GAbiosynthesis is blocked at the first step prior to ent-kaurene formation, an essential step in the GA-biosynthetic pathway.

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