scispace - formally typeset
Journal ArticleDOI

An E. coli Cell-Free Expression Toolbox: Application to Synthetic Gene Circuits and Artificial Cells

Jonghyeon Shin, +1 more
- 06 Jan 2012 - 
- Vol. 1, Iss: 1, pp 29-41
Reads0
Chats0
TLDR
The construction and the phenomenological characterization of synthetic gene circuits engineered with a cell-free expression toolbox that works with the seven E. coli sigma factors are reported, revealing the importance of the global mRNA turnover rate and of passive competition-induced transcriptional regulation.
Abstract
Cell-free protein synthesis is becoming a powerful technique to construct and to study complex informational processes in vitro. Engineering synthetic gene circuits in a test tube, however, is seriously limited by the transcription repertoire of modern cell-free systems, composed of only a few bacteriophage regulatory elements. Here, we report the construction and the phenomenological characterization of synthetic gene circuits engineered with a cell-free expression toolbox that works with the seven E. coli sigma factors. The E. coli endogenous holoenzyme E70 is used as the primary transcription machinery. Elementary circuit motifs, such as multiple stage cascades, AND gate and negative feedback loops are constructed with the six other sigma factors, two bacteriophage RNA polymerases, and a set of repressors. The circuit dynamics reveal the importance of the global mRNA turnover rate and of passive competition-induced transcriptional regulation. Cell-free reactions can be carried out over long periods of ...

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Principles of genetic circuit design

TL;DR: In this article, a review describes new tools that aid the construction of genetic circuits and discusses the failure modes encountered when assembling circuits, quantify their impact on performance, and review mitigation efforts.

Principles of genetic circuit design

TL;DR: Better tools, well-characterized parts and a comprehensive understanding of how to compose circuits are leading to a breakthrough in the ability to program living cells for advanced applications, from living therapeutics to the atomic manufacturing of functional materials.
Journal ArticleDOI

Gene-Expressing Liposomes as Synthetic Cells for Molecular Communication Studies.

TL;DR: A review focused on the exchange of chemical signals between liposome-based synthetic cells (operating by gene expression) and biological cells, as well as between two populations of synthetic cells.
Journal ArticleDOI

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

Protocols for implementing an Escherichia coli based TX-TL cell-free expression system for synthetic biology.

TL;DR: The preparation and execution of an efficient endogenous E. coli based transcription-translation (TX-TL) cell-free expression system that can produce equivalent amounts of protein as T7-based systems at a 98% cost reduction to similar commercial systems is described.
References
More filters
Journal ArticleDOI

Folding DNA to create nanoscale shapes and patterns

TL;DR: This work describes a simple method for folding long, single-stranded DNA molecules into arbitrary two-dimensional shapes, which can be programmed to bear complex patterns such as words and images on their surfaces.
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.
Journal ArticleDOI

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.
Journal ArticleDOI

Cell-free translation reconstituted with purified components

TL;DR: A protein-synthesizing system reconstituted from recombinant tagged protein factors purified to homogeneity was developed, and omission of a release factor allowed efficient incorporation of an unnatural amino acid using suppressor transfer RNA (tRNA).
Journal ArticleDOI

Enzyme-Free Nucleic Acid Logic Circuits

TL;DR: The design and experimental implementation of DNA-based digital logic circuits using single-stranded nucleic acids as inputs and outputs are reported, suggesting applications in biotechnology and bioengineering.
Related Papers (5)