| Eriko Takano (Manchester Centre for Synthetic Biology of Fine and Speciality Chemicals (SYNBIOCHEM), Manchester Institute of Biotechnology, University of Manchester) |
| Thu 08 Oct 2015, 12:00 - 13:00 |
| C.H Waddington Building, Seminar room 1.08, King's Building's |
If you have a question about this talk, please contact: Julie Fyffe (jfyffe)
Our ability to readily sequence complete genomes and to manipulate/re-design them on a large scale enables the design and construction of organisms with new functionalities of unprecedented scope (“synthetic biology”). We explore these possibilities in the context of high-value chemical production. Many microorganisms already have the machinery to produce diverse bioactive molecules that can be used in health, agriculture and food (Cimermancic et al., 2014). As a first step towards re-engineering these high-value chemical biosynthesis pathways for enhanced productivity and diversity, we aim to understand the interchangeability of biosynthetic parts and to create orthogonal transcription and translation mechanisms (based on promoter libraries, signalling molecule circuits and ncRNA). In addition, we are expanding our collection of computational tools for the detection and analysis of secondary metabolite biosynthesis gene clusters, to enrich our library of parts and building blocks for pathway engineering (Blin et al., 2013). We combine this analysis with high-resolution mass spectrometry analysis, which we also employ for the debugging of the engineered systems (Jankevics et al., 2012). Furthermore, we are using computational modelling (constraint-based descriptions of bacterial metabolism) to identify suitable overproduction hosts and pinpoint biosynthetic bottlenecks to target for further cellular engineering in a synthetic biology strategy (Breitling et al., 2013).
References:
Breitling R, Achcar F, Takano E Modeling challenges in the synthetic biology of secondary metabolism. ACS Synth. Biol. (2013) 19:373-378.
Blin K, Medema M, Kazempour D, Fischbach M, Breitling R, Takano E, Weber T. antiSMASH 2.0 – a versatile platform for genome mining of secondary metabolite producers. Nucl. Acids Res. (2013) 19:373-378.
Cimermancic P, Medema MH, Claesen J, Kurita K, Wieland Brown LC, Mavrommatis K, Pati A, Godfrey PA, Koehrsen M, Clardy J, Birren BW, Takano E, Sali A, Linington RG, Fischbach MA. Insights into secondary metabolism from a global analysis of bacterial biosynthetic gene clusters. Cell (2014) 158:412-21. highlighted in Nature Chemical Biology, 10 798-800 (2014)
Jankevics A, Merlo ME, de Vries M, Vonk RJ, Takano E, and Breitling R. Separating the wheat from the chaff: a prioritisation pipeline for the analysis of metabolomics datasets. Metabolomics (2012) 8:29-36.