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Biotechnology, DNA and RNA synthesis and sequencing
The redesign of DNA, RNA, and proteins helps us understand the molecular science that stands behind biology, evolution, and natural history. It also is the foundation for biotechnology that supports research in molecular biology, as well as medical diagnostics and therapeutics.
For example, in 1984, the Benner laboratory was the first to synthesize a DNA molecule to encode an enzyme. This work introduced tactics now standard in synthetic biology, including optimized codons, restriction sites to facilitate downstream engineering, and watermarks to allow the provenance of a synthetic DNA genetic construct to be determined.
Our group also introduced the "aminoxy" reversible terminating group to support sequencing and enzymatic synthesis of DNA. This has been licensed for enzyme-based DNA synthesis at DNA Script. The same aminoxy moiety is licensed for DNA sequencing, including personal sequencing, and single molecule sequencing. FfAME researchers are using this group to develop tools for the enzymic synthesis of RNA, in work now supported by the National Human Genome Research Institute.
To make ultra-large constructs of DNA, our group invented architectures that exploit AEGIS and various enzyme systems that manipulate them. This ongoing research also seeks to prepare DNA having extremely high purity and fidelity, to allow one pot autonomous self-assembly of complete plasmids and genes. These projects are now supported by the Department of Energy through its bioeconomy synthetic biology program.