Welcome, We are the MEC research group, a part of the research center Centro de Biologia Molecular e Ambiental (CBMA). We are located in the Department of Biology, University of Minho in the ancient city of Braga, Portugal.
Our interest is metabolic engineering of baker’s yeast Saccharomyces cerevisiae for consumption of new types of substrates and production of new biotechnologically interesting molecules. You can see this yeast growing under a microscope in the animated image above.
This process is important in nature, since fatty acids make up significant parts of fundamental structures such as cell membranes, but also serve as efficient energy storage for many cells and organisms.
The process could potentially be used for the green production of fuels and other chemicals in a future green economy.
As the field of metabolic engineering grow more complex, there is a need for new tools to solve different aspects of the overall process to increase throughput and maintain precision.
Yeast Pathway Kit
We have developed a metabolic pathway assembly method we call the Yeast Pathway Kit, that produces short metabolic pathways for a given number of genes compared to other methods. It relies on one library of promoters and another for terminators. Pathways are joined together by first making a set of single gene expression vectors by homologous recombination. The promoter-gene-terminator fragments (or transcriptional units) can then be stitched together by a second round of homologous recombination (see the figure below):
pydna (or Why Is So Much Cloning Documentation Wrong?)
We have developed a bioinformatics tool called
pydna that allow vector construction
experiments to be expressed in
This allows for “programming with DNA”, expressing cloning strategies as a computer
program. This produces a verifiable, complete description of a cloning strategy.
This is especially powerful in combination with
Jupyter notebooks to provide
both code and a readable document. See our Anaconda Maker
Series blog post.