EVENTS | VIEW CALENDAR
Evonetix gains £1.3M for gene synthesis project
CAMBRIDGE, U.K.—Evonetix Ltd., a company pioneering an approach to enable scalable and high-fidelity gene synthesis, announced recently that it had been awarded substantial funding to support the development of a novel enzymatic approach to DNA synthesis. Innovate UK, the United Kingdom’s innovation agency, will co-fund the £1.3 million project, which will be undertaken in collaboration with Durham University.
Evonetix is aiming to revolutionize gene synthesis by producing DNA at scale to facilitate many applications in the rapidly growing field of synthetic biology, from the development of novel pharmaceuticals to industrial biotech, as well as renewable fuels and agriculture. Evonetix’s novel silicon array, combined with its unique synergistic thermal control chemistry and process of error detection throughout assembly, is said to permit “massive parallelism” in de-novo DNA synthesis, enabling high-throughput on-chip assembly of high-fidelity gene-length DNA at scale.
As part of the Innovate UK co-funded project, Evonetix will develop a novel enzymatic approach to gene synthesis and integrate it into its proprietary, thermally addressable silicon array.
The research will be directed by Dr. Raquel Sanches-Kuiper, director of biology at Evonetix, whose group will develop engineered enzymes that are able to efficiently incorporate modified nucleotides. The research group of Dr. David Hodgson, associate professor of chemistry at Durham University, will develop the modified nucleotides for enzymatic synthesis in Evonetix’s silicon array.
“The funding from Innovate UK will enable us to expand our approach to include enzymatic gene synthesis and will be vital in bringing this project to a successful outcome,” said Dr. Tim Brears, CEO at Evonetix. “The extension of our platform’s capabilities will be of great value as we seek to address the needs of the rapidly growing synthetic biology market, which is estimated to reach $40 billion by the mid-2020s.”
Sanches-Kuipe added: “We believe the use of enzymatic oligonucleotide synthesis, which operates under milder aqueous conditions compared to phosphoramidite chemistry, will provide a significant commercial advantage and offer a highly valuable tool for de-novo gene synthesis with our platform. It will achieve this by being more environmentally friendly and by further streamlining the industrialization of high-fidelity DNA synthesis. The team at Durham’s Department of Chemistry has many years of experience in nucleotide chemistry and will complement our expertise in protein engineering, DNA synthesis and assembly.”