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Biotechnol Bioeng. 2017 Sep;114(9):2137-2141. doi: 10.1002/bit.26333. Epub 2017 May 23.

Short DNA containing χ sites enhances DNA stability and gene expression in E. coli cell-free transcription-translation systems.

Author information

1
School of Physics and Astronomy, University of Minnesota, Minneapolis, Minnesota 55455.
2
Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina.

Abstract

Escherichia coli cell-free transcription-translation (TXTL) systems offer versatile platforms for advanced biomanufacturing and for prototyping synthetic biological parts and devices. Production and testing could be accelerated with the use of linear DNA, which can be rapidly and cheaply synthesized. However, linear DNA is efficiently degraded in TXTL preparations from E. coli. Here, we show that double-stranded DNA encoding χ sites-eight base-pair sequences preferentially bound by the RecBCD recombination machinery-stabilizes linear DNA and greatly enhances the TXTL-based expression and activity of a fluorescent reporter gene, simple regulatory cascades, and T7 bacteriophage particles. The χ-site DNA and the DNA-binding λ protein Gam yielded similar enhancements, and DNA with as few as four χ sites was sufficient to ensure robust gene expression in TXTL. Given the affordability and scalability of producing the short χ-site DNA, this generalized strategy is expected to advance the broad use of TXTL systems across its many applications. Biotechnol. Bioeng. 2017;114: 2137-2141.

KEYWORDS:

Escherichia coli; RecBCD; TXTL; gene circuits; prototyping; synthetic biology

PMID:
28475211
PMCID:
PMC5522353
DOI:
10.1002/bit.26333
[Indexed for MEDLINE]
Free PMC Article

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