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Münster (upm/kk).
For their research, the biologists used the model plant Arabidopsis thaliana (thale cress).<address>© Adobe Stock</address>
For their research, the biologists used the model plant Arabidopsis thaliana (thale cress).
© Adobe Stock

Thousands of protein switches enable plants to make the transition from dark to light

Biologists investigate molecular processes responsible for reprogramming at the protein level

We already learn in school that plants carry out photosynthesis in their chloroplasts when exposed to light. In the dark, this process comes to a halt. Instead, green plant tissue – for example the leaves – then activate cellular respiration, during which they consume carbohydrates and oxygen in the mitochondria, similarly to what humans are constantly doing. These two processes – photosynthesis and cellular respiration – take place separately in plant cells, both spatially and temporally. The fundamental switch which occurs in their metabolism is a tour de force which plants perform almost unnoticed – and in a very short time span – in the daily transition from light to dark.

What actually happens in the plant at the molecular level is something that has kept researchers busy for decades now. However, most studies so far focused on the regulation of individual proteins. Now a research team headed by Prof. Iris Finkemeier from the Institute of Biology and the Biotechnology of Plants at the University of Münster has published a study which analyses the central reprogramming at the protein level in an unprecedented sharpness of detail: the researchers analysed leaf tissue from plants during the transition from darkness to light and were able to confirm that the photosynthesis process was fully active within just 15 minutes after the onset of light. In doing so, the plant does not produce its entire stock of proteins anew, but rather undertakes targeted biochemical changes on the proteins which already exist – so-called post-translational modifications (PTMs for short). These PTMs can then, in turn, control the activity of enzymes and ultimately lead to a rapid, fundamental switchover in the cell’s function. The results of the study have now been published in “The Plant Journal”.

Background and methods used

The metabolism of plants is redirected during the transition from darkness to light by the changes in chemical modifications to proteins and enzymes. The chemical structures of the modified amino acids are shown on the left. After 30 minutes in the light, important metabolic pathways and signal transduction processes in the plant (Arabidopsis thaliana) are redirected by these chemical modifications to the proteins (schematic network of the modified proteins with functions, right).<address>© AG Finkemeier</address>
The metabolism of plants is redirected during the transition from darkness to light by the changes in chemical modifications to proteins and enzymes. The chemical structures of the modified amino acids are shown on the left. After 30 minutes in the light, important metabolic pathways and signal transduction processes in the plant (Arabidopsis thaliana) are redirected by these chemical modifications to the proteins (schematic network of the modified proteins with functions, right).
© AG Finkemeier
So far, many studies have only examined individual PTMs, such as phosphorylation, frequently investigating only selected proteins. “We looked at these processes for the entire stock of proteins,” says Iris Finkemeier, “and, for the first time, examined three of the most important modifications which control proteins’ functions: phosphorylation, lysine acetylation and cysteine-based redox switches. Our results represent an atlas of the protein modifications in the changeovers between light and dark in Arabidopsis thaliana, our model plant – better known as thale cress. Other researchers can look for a certain protein in our dataset and check to see whether it is changed chemically in the transition from dark to light – with possible consequences for its function.” Of the more than 24,000 detected post-translational protein modifications, over 1,700 underwent a change in the transition from dark to light.

In addition to applying physiological methods to measure the level of photosynthesis and the metabolite composition, the team used high-resolution protein mass spectrometry in order to be able to observe several thousand of proteins simultaneously. Using mass spectrometry, scientists determine the exact mass of complex molecules. If the molecule has a chemical modification, it has a different mass from a molecule without such a modification. “We can determine, to an accuracy of one ppm, the exact mass of more than ten thousand peptide molecules in a sample,” says Dr. Jürgen Eirich, a co-author of the study. “This corresponds to a deviation of just one milligram per kilogram. We can compare this to weighing all the residents of a small town to an accuracy of a tenth of a gram.” The first changes could already be seen after five minutes’ exposure to light – although at this point most of the changes to the proteins were still taking place in the chloroplasts, i.e. where the start of the photosynthesis process leads primarily to changes in the cell’s function. These changes are not, however, restricted to the chloroplast. After 30 minutes, the entire cell is affected by a variety of changes to its proteins.

The results of the study are freely available for public use. They offer biologists and biotechnologists, as well as plant breeders, a rich basis for modifying plants’ metabolism at decisive points or for switching metabolic pathways on or off in order to improve the growth, yields or resilience of plants.

Other researchers from the University of Bonn and the Max Planck Institute of Molecular Plant Physiology in Golm were involved in the study. The work received financial support from the German Research Foundation.

Original publication

Giese, J. et al (2023). The interplay of posttranslational protein modifications in Arabidopsis leaves during photosynthesis induction. The Plant Journal. DOI: 10.1111/tpj.16406

Further information