Professor Jason Micklefield at the Manchester Institute of Biotechnology
Born
Jason Micklefield
Education
Hull University (BSc)
University of Cambridge (PhD)
Knownfor
Discovery, characterisation and engineering of enzymes and biosynthetic pathways. Biocatalysis and integrated catalysis. Modified nucleic acids and orthogonal riboswitches.
Scientific career
Fields
Organic Chemistry, Biochemistry and Molecular Biology
Workplaces
University of Washington
Birkbeck College, University of London
University of Manchester
Jason Micklefield is a British Biochemist and a professor in the Department of Chemistry at Imperial College London. His research involves the discovery, characterisation and engineering of biosynthetic pathways to new bioactive natural products, particularly antibiotics. He is also interested in the discovery, structure, mechanism and engineering of enzymes for synthetic applications, including the integration of enzymes with chemocatalysis for telescoping routes to pharmaceuticals and other valuable products.
Education
Micklefield attended Royds Comprehensive School in Leeds. He received his BSc. Degree in Chemistry from Hull University in 1989 and earned a Ph.D. from the University of Cambridge in 1993 working with Professor Sir Alan Battersby to complete the first total synthesis of haem d1, a coenzyme in bacteria.
Micklefield's research focuses on natural product biosynthesis, pathway engineering and biocatalysis. His lab developed new methods for engineering complex NRPS enzymes that deliver new lipopeptide antibiotics. They have discovered and characterised hybrid NRPS-PKS assembly lines producing the structurally unique antibiotic K16. Micklefield's team also discovered and determined structures of novel ATP-dependent ligase enzymes, from PKS-NRPS pathways, which were engineered to produce agrochemicals and pharmaceuticals including drugs in clinical trials for COVID-19. New synthetic biology approaches were also used to create a de novo pathway to thaxtomin phytotoxin derivatives, with improved herbicidal properties for crop protection. In addition to biosynthesis, Micklefield is widely recognised for his research in biocatalysis. His lab employed structure-guided mutagenesis and directed evolution to improve activity, expand the substrate scope and switch the regioselectivities of halogenase enzymes. They showed how engineered halogenases can be integrated with Pd-catalysed cross-coupling chemistry, in one-pot reactions, to affect the direct regioselective arylation, alkenylation, cyanation and further functionalisation of C-H positions in diverse scaffolds. Micklefield's lab also characterised various methyltransferases, demonstrating how these can be used in the regioselective alkyl-diversification of tetrahydroisoquinolines, rapamycin immunosuppressive agents and other bioactive natural and non-natural products. His lab succeeded in engineering orthogonal methyltransferases creating alternative bioalkylation pathways and developed methods for selective derivatisation of tyrosine residues in peptides/proteins using methyltransferases and SAM analogues for labelling etc. His team also characterised, engineered and developed many other important biocatalysts. The Micklefield lab is also engaged in nucleic acids research, re-engineering the first orthogonal riboswitches (genetic tools and biosensors).