BACKGROUND AND AIMS: Plants use a diverse range of visual and olfactory cues to advertize to pollinators. Australian Chiloglottis orchids employ one to three related chemical variants, all 2,5-dialkylcyclohexane-1,3-diones or 'chiloglottones' to sexually attract their specific male pollinators. Here an investigation was made of the physiological aspects of chiloglottone synthesis and storage that have not previously been examined. METHODS: The location of chiloglottone production was determined and developmental and diurnal changes by GC-MS analysis of floral tissue extracts was monitored in two distantly related Chiloglottis species. Light treatment experiments were also performed using depleted flowers to evaluate if sunlight is required for chiloglottone production; which specific wavelengths of light are required was also determined. KEY RESULTS: Chiloglottone production only occurs in specific floral tissues (the labellum calli and sepals) of open flowers. Upon flower opening chiloglottone production is rapid and levels remain more or less stable both day and night, and over the 2- to 3-week lifetime of the flower. Furthermore, it was determined that chiloglottone production requires continuous sunlight, and determined the optimal wavelengths of sunlight in the UV-B range (with peak of 300 nm). CONCLUSIONS: UV-B light is required for the synthesis of chiloglottones - the semiochemicals used by Chiloglottis orchids to sexually lure their male pollinators. This discovery appears to be the first case to our knowledge where plant floral odour production depends on UV-B radiation at normal levels of sunlight. In the future, identification of the genes and enzymes involved, will allow us to understand better the role of UV-B light in the biosynthesis of chiloglottones.
BACKGROUND AND AIMS: Plants use a diverse range of visual and olfactory cues to advertize to pollinators. Australian Chiloglottis orchids employ one to three related chemical variants, all 2,5-dialkylcyclohexane-1,3-diones or 'chiloglottones' to sexually attract their specific male pollinators. Here an investigation was made of the physiological aspects of chiloglottone synthesis and storage that have not previously been examined. METHODS: The location of chiloglottone production was determined and developmental and diurnal changes by GC-MS analysis of floral tissue extracts was monitored in two distantly related Chiloglottis species. Light treatment experiments were also performed using depleted flowers to evaluate if sunlight is required for chiloglottone production; which specific wavelengths of light are required was also determined. KEY RESULTS:Chiloglottone production only occurs in specific floral tissues (the labellum calli and sepals) of open flowers. Upon flower opening chiloglottone production is rapid and levels remain more or less stable both day and night, and over the 2- to 3-week lifetime of the flower. Furthermore, it was determined that chiloglottone production requires continuous sunlight, and determined the optimal wavelengths of sunlight in the UV-B range (with peak of 300 nm). CONCLUSIONS: UV-B light is required for the synthesis of chiloglottones - the semiochemicals used by Chiloglottis orchids to sexually lure their male pollinators. This discovery appears to be the first case to our knowledge where plant floral odour production depends on UV-B radiation at normal levels of sunlight. In the future, identification of the genes and enzymes involved, will allow us to understand better the role of UV-B light in the biosynthesis of chiloglottones.
Authors: Rod Peakall; Daniel Ebert; Jacqueline Poldy; Russell A Barrow; Wittko Francke; Colin C Bower; Florian P Schiestl Journal: New Phytol Date: 2010-06-07 Impact factor: 10.151
Authors: Björn Bohman; Lynne Jeffares; Gavin Flematti; Ryan D Phillips; Kingsley W Dixon; Rod Peakall; Russell A Barrow Journal: Org Lett Date: 2012-05-03 Impact factor: 6.005
Authors: Bobby A Brown; Catherine Cloix; Guang Huai Jiang; Eirini Kaiserli; Pawel Herzyk; Daniel J Kliebenstein; Gareth I Jenkins Journal: Proc Natl Acad Sci U S A Date: 2005-12-05 Impact factor: 11.205
Authors: Lucas Vanhaelewyn; András Viczián; Els Prinsen; Péter Bernula; Alejandro Miguel Serrano; Maria Veronica Arana; Carlos L Ballaré; Ferenc Nagy; Dominique Van Der Straeten; Filip Vandenbussche Journal: Plant Cell Date: 2019-07-09 Impact factor: 11.277
Authors: Ranamalie Amarasinghe; Jacqueline Poldy; Yuki Matsuba; Russell A Barrow; Jan M Hemmi; Eran Pichersky; Rod Peakall Journal: Ann Bot Date: 2015-02-02 Impact factor: 4.357
Authors: Darren C J Wong; Ranamalie Amarasinghe; Claudia Rodriguez-Delgado; Rodney Eyles; Eran Pichersky; Rod Peakall Journal: Front Plant Sci Date: 2017-07-19 Impact factor: 5.753