Periodic Reporting for period 1 - ConvergentDODA (Resolving the molecular basis underlying convergent evolution of DODA enzymes in the betalain synthesis pathway)
Período documentado: 2021-06-01 hasta 2023-05-31
The betalain biosynthesis pathway is led by 4,5-L-DOPA dioxygenase (DODA), the enzyme that catalyzes the ring cleavage of L-DOPA to yield betalamic acid, the chromophoric and structural unit of betalains. The distribution of betalain-producing families across Caryophyllales has been linked to the convergent evolution of DODA. Thus, there is evidence that betalain-producing plants do not share a common ancestor able to produce betalains but they have evolved independently 3-4 times.
This project aims to understand the molecular modifications that DODA enzymes have experienced through their evolution and how they are related to the betalain-producing capacity detected in Caryophyllales plants. Studying DODA as a symbol of convergent evolution allows us to understand the molecular bases underlying the different approaches that organisms pursue to address similar evolutionary problems.
The overall objectives are:
- Biochemical characterisation of high-activity DODA enzymes
- Characterisation of the ancestral biochemical function of the DODA enzymes
- Identification of candidate residues for high DODA activity using ancestral sequence reconstruction
- Validation of candidate residues using a high-throughput yeast heterologous expression system
- Reconstruction of the evolutionary history of essential residues to understand evolutionary mechanisms for each origin of DODA
An extensive collection of DODAa coding sequences across Caryophyllales species are used in this project to reconstruct the ancestral trait of betalain-producing Caryophyllales plants. It has allowed us to perform an ancestral reconstruction in the system model Saccharomyces cerevisiae. The expression of DODA genes in yeast has confirmed their independent evolution within Caryophyllales showing that the production of betalains is an acquired ability through the evolution of these enzymes. Thus, the betalain-producing capacities are related to neofunctionalization processes associated with independent duplications among the three lineages detected. The comparison of sequences throughout the different DODA lineages has also allowed the detection of candidate residues responsible for the gain of function. Those residues were individually mutated and the expression of these new sequences in yeast has shown their implication in the production of betalains.
The satisfactory results have been disseminated in the following activities:
a. Results shared with the scientific community:
- International congresses
- Peer-reviewed research articles
- Presentation of results in the lunchtime seminar of the Department of Plant Sciences at the University of Cambridge (United Kingdom)
b. Results communicated to different target public audiences:
- Science on Sundays of the Cambridge University Botanic Garden (Cambridge, United Kingdom)
- Festival of plants of the Cambridge University Botanic Garden
The expected results of this project will have remarkable importance in the study of convergent evolution at the molecular level. Additionally, the results obtained from the kinetic characterisation of DODA enzymes have helped to find enzymes with extraordinary capacities in the obtention of betalains in biofactories. Thus, these betalains will be applicable in food, cosmetic or pharmaceutical industries due to their health-promoting properties.