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Inspired by the chemistry of the eye: Münster University chemists have succeeded in turning to their advantage a chemical reaction which takes place in the eye and enables us to see light and dark. It can be used to create important carbon compounds which need a lot of energy to be produced by other means.
Nature can do it, and chemists in the lab often dream of doing it: producing substances simply and ecologically – as far as possible without any undesirable side-products. A team of researchers from Münster University has now succeeded in turning to its advantage a chemical reaction which takes place in the eye and enables us to see light and dark. This process, say the researchers, is of great interest for the chemical industry because it could be used to create special variants (isomers) of important carbon compounds which need a lot of energy to be produced by other means.
In the eye, the light-absorbing pigment rhodopsin plays an elementary role as a light sensor. When light enters the eye, rhodopsin triggers a chemical signal chain, thereby activating the photoreceptor cells. “We were inspired by this process,” says Jan Metternich, a doctoral student of chemistry who carried out the study together with Dr. Ryan Gilmour, Professor of Chemical Biology in the “Cells in Motion” Cluster of Excellence at Münster University.
One of the central components of the light-absorbing pigment rhodopsin is retinal (“Vitamin A”). To activate the photoreceptor cells, however, a very special variant of the retinal molecule is needed. As a result of light entering the eye, it is converted into a second, very similar form, thereby starting off the chemical signal chain. “Isomers” are what chemists call the different forms of a molecule.
“The selective formation of isomers is important not only for our ability to see, but also, for example, for the production of medicines, and agrochemicals,” says Ryan Gilmour. “Our innovative method has provided us with a simple way of selectively producing these valuable isomers that are needed for both academic and industrial chemistry.” The reaction is triggered by light – just as in the eye. The so-called catalyst which the reactions require – which increases the speed of the reaction – is a cheap and ecological molecule: riboflavin, a B vitamin which is also used, for example, as a food colour additive.
Original literature:
Jan B. Metternich and Ryan Gilmour (2015): A Bio-Inspired, Catalytic E → Z Isomerization of Activated Olefin. J. Am. Chem. Soc.; DOI: 10.1021/jacs.5b07136
http://pubs.acs.org/doi/full/10.1021/jacs.5b07136 Original publication
http://www.uni-muenster.de/Cells-in-Motion/de/people/all/gilmour-r.php CiM Professor Ryan Gilmour
Prof. Ryan Gilmour (l.) and Jan Metternich
Photo: private
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Inspiration to the chemists: the eye
Photo: Colourbox.de/A. Tiplyashin (Permission for photo use only in connection with this press release and with indication of photo credit)
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Criteria of this press release:
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Chemistry
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Prof. Ryan Gilmour (l.) and Jan Metternich
Photo: private
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Inspiration to the chemists: the eye
Photo: Colourbox.de/A. Tiplyashin (Permission for photo use only in connection with this press release and with indication of photo credit)
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