Regulation of Methylbenzoate Emission after Pollination in Snapdragon and Petunia Flowers

Florence Negre(Purdue University West Lafayette), Christine M. Kish(Purdue University West Lafayette), Jennifer L. Boatright(Purdue University West Lafayette), Beverly A. Underwood(University of Florida), Kenichi Shibuya(University of Florida), Conrad Wagner(Vanderbilt University), David G. Clark(University of Florida), Natalia Dudareva(Purdue University West Lafayette)
The Plant Cell
November 20, 2003
Cited by 238Open Access
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Abstract

The molecular mechanisms responsible for postpollination changes in floral scent emission were investigated in snapdragon cv Maryland True Pink and petunia cv Mitchell flowers using a volatile ester, methylbenzoate, one of the major scent compounds emitted by these flowers, as an example. In both species, a 70 to 75% pollination-induced decrease in methylbenzoate emission begins only after pollen tubes reach the ovary, a process that takes between 35 and 40 h in snapdragon and 32 h in petunia. This postpollination decrease in emission is not triggered by pollen deposition on the stigma. Petunia and snapdragon both synthesize methylbenzoate from benzoic acid and S -adenosyl-L -methionine (SAM); however, they use different mechanisms to downregulate its production after pollination. In petunia, expression of the gene responsible for methylbenzoate synthesis is suppressed by ethylene. In snapdragon, the decrease in methylbenzoate emission is the result of a decrease in both S -adenosyl-L -methionine:benzoic acid carboxyl methyltransferase (BAMT) activity and the ratio of SAM to S -adenosyl-L -homocysteine ("methylation index") after pollination, although the BAMT gene also is sensitive to ethylene.


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