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1.
Sci Rep ; 7(1): 4599, 2017 07 04.
Article in English | MEDLINE | ID: mdl-28676696

ABSTRACT

Riboswitches are structural genetic regulatory elements that directly couple the sensing of small molecules to gene expression. They have considerable potential for applications throughout synthetic biology and bio-manufacturing as they are able to sense a wide range of small molecules and regulate gene expression in response. Despite over a decade of research they have yet to reach this considerable potential as they cannot yet be treated as modular components. This is due to several limitations including sensitivity to changes in genetic context, low tunability, and variability in performance. To overcome the associated difficulties with riboswitches, we have designed and introduced a novel genetic element called a ribo-attenuator in Bacteria. This genetic element allows for predictable tuning, insulation from contextual changes, and a reduction in expression variation. Ribo-attenuators allow riboswitches to be treated as truly modular and tunable components, thus increasing their reliability for a wide range of applications.


Subject(s)
Escherichia coli/growth & development , Genetic Engineering/methods , Riboswitch , Bacterial Proteins/genetics , Cloning, Molecular , Escherichia coli/genetics , Synthetic Biology , Vibrio vulnificus/genetics , Vibrio vulnificus/metabolism
2.
ACS Synth Biol ; 6(9): 1663-1671, 2017 09 15.
Article in English | MEDLINE | ID: mdl-28602075

ABSTRACT

Accurate control of a biological process is essential for many critical functions in biology, from the cell cycle to proteome regulation. To achieve this, negative feedback is frequently employed to provide a highly robust and reliable output. Feedback is found throughout biology and technology, but due to challenges posed by its implementation, it is yet to be widely adopted in synthetic biology. In this paper we design a synthetic feedback network using a class of recombinase proteins called integrases, which can be re-engineered to flip the orientation of DNA segments in a digital manner. This system is highly orthogonal, and demonstrates a strong capability for regulating and reducing the expression variability of genes being transcribed under its control. An excisionase protein provides the negative feedback signal to close the loop in this system, by flipping DNA segments in the reverse direction. Our integrase/excisionase negative feedback system thus provides a modular architecture that can be tuned to suit applications throughout synthetic biology and biomanufacturing that require a highly robust and orthogonally controlled output.


Subject(s)
DNA/genetics , Feedback, Physiological/physiology , Gene Expression Regulation/genetics , Genes, Switch/genetics , Genes, Synthetic/genetics , Models, Genetic , Recombinases/genetics , Computer Simulation , Escherichia coli/genetics , Genetic Enhancement/methods , Protein Engineering/methods , Recombinant Proteins/biosynthesis , Recombinant Proteins/genetics , Synthetic Biology/methods
3.
Sci Rep ; 4: 5844, 2014 Jul 28.
Article in English | MEDLINE | ID: mdl-25068650

ABSTRACT

Effective application of whole-cell devices in synthetic biology and biocatalysis will always require consideration of the uptake of molecules of interest into the cell. Here we demonstrate that the AlkL protein from Pseudomonas putida GPo1 is an alkane import protein capable of industrially relevant rates of uptake of C7-C16 n-alkanes. Without alkL expression, native E.coli n-alkane uptake was the rate-limiting step in both the whole-cell bioconversion of C7-C16 n-alkanes and in the activation of a whole-cell alkane biosensor by C10 and C11 alkanes. By coexpression of alkL as a transporter plug-in, specific yields improved by up to 100-fold for bioxidation of >C12 alkanes to fatty alcohols and acids. The alkL protein was shown to be toxic to the host when overexpressed but when expressed from a vector capable of controlled induction, yields of alkane oxidation were improved a further 10-fold (8 g/L and 1.7 g/g of total oxidized products). Further testing of activity on n-octane with the controlled expression vector revealed the highest reported rates of 120 µmol/min/g and 1 g/L/h total oxidized products. This is the first time AlkL has been shown to directly facilitate enhanced uptake of C10-C16 alkanes and represents the highest reported gain in product yields resulting from its use.


Subject(s)
Alkanes/metabolism , Bacterial Proteins/metabolism , Biosensing Techniques , Carrier Proteins/metabolism , Escherichia coli/metabolism , Pseudomonas putida/chemistry , Bacterial Proteins/genetics , Biocatalysis , Biological Transport , Carrier Proteins/genetics , Escherichia coli/genetics , Fatty Acids/biosynthesis , Fatty Alcohols/metabolism , Gene Expression , Genetic Vectors/chemistry , Genetic Vectors/metabolism , Metabolic Engineering , Models, Molecular , Oxidation-Reduction , Pseudomonas putida/metabolism , Transgenes
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