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The All E. coli TX-TL Toolbox 2.0: A Platform for Cell-Free Synthetic Biology.

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TLDR
The performance and properties of a recently developed, all Escherichia coli, cell-free transcription and translation system, which is entirely based on the endogenous translation components and transcription machinery provided by an E. coli cytoplasmic extract, are reported on.
Abstract
We report on and provide a detailed characterization of the performance and properties of a recently developed, all Escherichia coli, cell-free transcription and translation system. Gene expression is entirely based on the endogenous translation components and transcription machinery provided by an E. coli cytoplasmic extract, thus expanding the repertoire of regulatory parts to hundreds of elements. We use a powerful metabolism for ATP regeneration to achieve more than 2 mg/mL of protein synthesis in batch mode reactions, and more than 6 mg/mL in semicontinuous mode. While the strength of cell-free expression is increased by a factor of 3 on average, the output signal of simple gene circuits and the synthesis of entire bacteriophages are increased by orders of magnitude compared to previous results. Messenger RNAs and protein degradation, respectively tuned using E. coli MazF interferase and ClpXP AAA+ proteases, are characterized over a much wider range of rates than the first version of the cell-free t...

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Artificial cells: synthetic compartments with life-like functionality and adaptivity

TL;DR: The ultimate goal here is to assemble a fully man-made cell that displays functionality and adaptivity as advanced as that found in nature, which will not only provide insight into the fundamental processes in natural cells but also pave the way for new applications of such artificial cells.
Journal ArticleDOI

Cell-free gene expression: an expanded repertoire of applications.

TL;DR: Advances provide exciting opportunities to profoundly transform synthetic biology by enabling new approaches to the model-driven design of synthetic gene networks, the fast and portable sensing of compounds, on-demand biomanufacturing, building cells from the bottom up, and next-generation educational kits.
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Portable, On-Demand Biomolecular Manufacturing

TL;DR: This paper presents a portable platform that provides the means for on-site, on-demand manufacturing of therapeutics and biomolecules and demonstrates the manufacture and functional validation of antimicrobial peptides and vaccines and presents combinatorial methods for the production of antibody conjugates and small molecules.
Journal ArticleDOI

Engineering genetic circuit interactions within and between synthetic minimal cells

TL;DR: It is demonstrated that it is possible to engineer genetic circuit-containing synthetic minimal cells (synells) to contain multiple-part genetic cascades, and that these cascades can be controlled by external signals as well as inter-liposomal communication without cross-talk.
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Enzyme-free nucleic acid dynamical systems.

TL;DR: The creation of a biochemical oscillator that requires no enzymes or evolved components, but rather is implemented through DNA molecules designed to function in strand displacement cascades is described.
References
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Journal ArticleDOI

Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoter.

TL;DR: The tight regulation of the PBAD promoter is exploited to study the phenotypes of null mutations of essential genes and the use of pBAD vectors as an expression system is explored.
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Network motifs: theory and experimental approaches

TL;DR: Network motifs are reviewed, suggesting that they serve as basic building blocks of transcription networks, including signalling and neuronal networks, in diverse organisms from bacteria to humans.
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Independent and Tight Regulation of Transcriptional Units in Escherichia Coli Via the LacR/O, the TetR/O and AraC/I1-I2 Regulatory Elements

TL;DR: Controlling the expression of the genes encoding luciferase, the low abundance E.coli protein DnaJ and restriction endonuclease Cfr9I not only demonstrates that high levels of expression can be achieved but also suggests that under conditions of optimal repression only around one mRNA every 3rd generation is produced.
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Macromolecular Crowding: Biochemical, Biophysical, and Physiological Consequences

TL;DR: This paper presents a meta-analyses of the macromolecular determinants of reaction rates and volume in a solution and describes the mechanisms leading to these rates and volumes.
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In vitro selection and evolution of functional proteins by using ribosome display.

TL;DR: Libraries of native folded proteins can now be screened and made to evolve in a cell-free system without any transformation or constraints imposed by the host cell.
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