Kylie Vincent's Group
Department of Chemistry,
University of Oxford,
Inorganic Chemistry Laboratory,
South Parks Road, OX1 3QR
kylie.vincent@chem.ox.ac.uk
Opportunities and Vacancies
Enquiries are always welcome from qualified students or postdoctoral scientists with scholarships or fellowships to support their research.
Our research is in the area of catalysis, and is split into two broad themes; fundamental mechanisms of catalysis and applications of immobilised enzyme cascades for selective chemical synthesis:
Spectroelectrochemistry Designed by former Part II students in the Group:
Sophie Kendall-Price and Kathy Page
Redox biocatalysis Designed by former Part II students in the Group:
Kathy Page and Rachael Ng

Our research is mainly in the areas of bioinorganic chemistry and chemical biology or industrial biotechnology. We are driven by the excitement of discovering fundamental mechanisms of catalysis in biology, and the possibilities for exploiting biocatalysis in new ways for chemical synthesis.

The activation of small molecules in biology is a key research theme in the Vincent group. Chemists have a lot to learn from catalytic processes which occur in microorganisms. For example, nature has tuned hydrogenase enzymes to oxidise and produce H2 efficiently at earth-abundant iron or nickel-iron catalytic sites. Nitrogenase catalyses the fixation of N2 to ammonia under mild conditions. Carbon monoxide reducing enzymes fix CO2 selectively into CO or formate. These chemical reactions represent some of the greatest chemical challenges for solving the world's energy problems, and we hope that what we learn from studying the biocatalytic reactions will inspire development of new catalysts for energy technologies. The Vincent group has developed a suite of spectroscopic techniques that bridge gaps between measurements of enzyme activity, spectroscopy and structure. With significant funding from the BBSRC and the European Research Council (ERC) we are employing these to great effect in probing the mechanisms of metalloenzymes involved biological hydrogen, carbon and nitrogen cycles.

In parallel we are excited by the interface between academic discovery and technology innovation. We have developed and patented a H2-driven approach to biocatalysis, known as the HydRegen system. This bridges the advantages of clean, metal-driven hydrogenations and selective biocatalysis under mild conditions. By immobilising all the enzymes for a desired C=X bond reduction on a carbon support, we enable heterogeneous biocatalytic hydrogenations which can be readily translated into continuous flow processes. We have extended this to biocatalytic deuterium insertion, and to chemo-bio catalytic cascades. With significant funding from Innovate UK, EPSRC and BBSRC, and close industrial collaborations, we are taking these areas forward towards commercialisation on a project led by Dr Holly Reeve.

Get in touch if you are interested in joining us in these research initiatives, or have your own ideas for research that could feed into these areas.