With such ambitious goals as helping cure cancer and eradicating pervasive disease, some of the most talented scientists in the country from the emerging field of synthetic biology are breaking new ground at Northwestern University.
MIT biological and electrical engineers have combined E.coli cells with gold nanoparticles to make the bacteria conductive -- all using "sticky" biofilms
A study published on March 20, 2014 reports on the possibility of computers to accurately create virtual mugshots of an individual based solely on that person’s DNA. Several scientists from around ...
"Microbes have long been adapted for the biosynthetic production of useful compounds. There is increasing demand for the rapid and cheap microbial production of diverse molecules in an industrial setting. Microbes can now be designed and engineered for a particular biosynthetic purpose, thanks to recent developments in genome sequencing, metabolic engineering, and synthetic biology. Advanced tools exist for the genetic manipulation of microbes to create novel metabolic circuits, making new products accessible. Metabolic processes can be optimized to increase yield and balance pathway flux. Progress is being made towards the design and creation of fully synthetic microbes for biosynthetic purposes. Together, these emerging technologies will facilitate the production of designer microbes for biosynthesis."
Terry Johnson of UC Berkeley and Synberc provides a perspective on the unique features of synthetic biology that require special consideration above and beyo...
"Take Synthetic biology and turn it from where it is now the purview of big corporates and academia and turn it into a fertile field for entrepreneurship and particularly interested in an Open Sour...
CRISPR-Cas systems are adaptive immune systems present in bacteria and archaea.
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Cas9 in complex with guide RNAs can localize to specific DNA sequences.
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Cas9 variants can activate or repress transcription in bacteria and eukaryotes.
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Post-transcriptional control strategies using CRISPR-Cas systems are emerging."
"The clustered regularly interspaced short palindromic repeat (CRISPR) arrays and their CRISPR associated (Cas) proteins constitute adaptive immune systems in bacteria and archaea that provide protection from bacteriophages, plasmids and other mobile genetic elements (MGEs). Recently, the ability to direct these systems to DNA in a sequence-specific manner has led to the emergence of new technologies for engineered gene regulation in bacteria and eukaryotes. These systems have the potential to enable facile high-throughput functional genomics studies aimed at identifying gene function and will be a crucial tool for synthetic biology. Here, we review the recent engineering of these systems for controlling gene expression."
Cork County Hall hosted the Synthetic Biology Future event on 13 March, bringing in some of the leading authorities on the future technology from Ireland and the world.
by Jonathan W. Kotula, S. Jordan Kernsa, Lev A. Shaket, Layla Sirajb, James J. Collins, Jeffrey C. Way, and Pamela A. Silver
"Significance
The human microbiota represents the trillions of bacteria that live on the skin, in the oral, nasal, and aural cavities, and throughout the gastrointestinal tract. The species that live in the gastrointestinal tract, the gut microbiota, closely interact with host cells and have a profound impact on health. To develop tools to effectively monitor the gut microbiota and ultimately help in disease diagnosis, we have engineered Escherichia coli to sense and record environmental stimuli, and demonstrated that E. coli with such memory systems can survive and function in the mammalian gut. This work demonstrates that E. coli can be engineered into living diagnostics capable of nondestructively probing the mammalian gut.
Abstract
The mammalian gut is a dynamic community of symbiotic microbes that interact with the host to impact health, disease, and metabolism. We constructed engineered bacteria that survive in the mammalian gut and sense, remember, and report on their experiences. Based on previous genetic memory systems, we constructed a two-part system with a “trigger element” in which the lambda Cro gene is transcribed from a tetracycline-inducible promoter, and a “memory element” derived from the cI/Cro region of phage lambda. The memory element has an extremely stable cI state and a Cro state that is stable for many cell divisions. When Escherichia coli bearing the memory system are administered to mice treated with anhydrotetracycline, the recovered bacteria all have switched to the Cro state, whereas those administered to untreated mice remain in the cI state. The trigger and memory elements were transferred from E. coli K12 to a newly isolated murine E. coli strain; the stability and switching properties of the memory element were essentially identical in vitro and during passage through mice, but the engineered murine E. coli was more stably established in the mouse gut. This work lays a foundation for the use of synthetic genetic circuits as monitoring systems in complex, ill-defined environments, and may lead to the development of living diagnostics and therapeutics."
"The paradigm of synthetic biology has been evolving, along with relevant engineering, to achieve designed bio-systems. Synthetic biology has reached the point where it is possible to develop microbial strains to produce desired chemicals. Recent advances in this field have promoted metabolic engineering of C. glutamicum as an amino-acid producer for use in intelligent microbial-cell factories. Here, we review recent advances that address C. glutamicum as a potential model organism for synthetic biology, and evaluate their industrial applications. Finally, we highlight the perspective of developing C. glutamicum as a step towards advanced microbial-cell factories that could produce valuable chemicals from renewable resources."
With such ambitious goals as helping cure cancer and eradicating pervasive disease, scientists from the emerging field of synthetic biology are breaking new ground at Northwestern University in Evanston.
Inspired by natural materials such as bone -- a matrix of minerals and other substances, including living cells -- engineers have coaxed bacterial cells to produce biofilms that can incorporate nonliving materials, such as gold nanoparticles and quantum dots. These "living materials" combine the advantages of live cells, which respond to their environment, produce complex biological molecules, and span multiple length scales, with the benefits of nonliving materials, which add functions such as conducting electricity or emitting light.
Arizona State University Synthetic biologist to discuss creating life in the lab at ASU lecture Arizona State University Benner is a Distinguished Fellow at the Foundation for Applied Molecular Evolution and a pioneer in the burgeoning field of...
(Phys.org) —Dreaming up nanostructures that have desirable optical, electronic, or magnetic properties is one thing. Figuring out how to make them is another. A new strategy uses the binding properties of complementary strands of DNA to attach nanoparticles to each other and builds up a layered thin-film ...
"We explore the possibilities of synthetic biology in Streptomyces bacteria, targetting their most important ability: producing a large variety of secondary metabolites, diverse in both chemical structure and bioactivity. The biosynthesis gene clusters are modular, thus an ideal system to apply synthetic biology and engineer new and diverse bioactive molecules (1, 2). As a first step towards re-engineering antibiotic biosynthesis, we studied the regulatory circuitry controlling antibiotic production in Streptomyces coelicolor A3(2), using experimentation and computational modelling. In this species, antibiotic production is regulated by γ-butyrolactones. We could show that the two major players of the butyrolactone signalling system, γ-butyrolactone synthase and the γ- butyrolactone receptor, exert a concerted regulation (3) set up to create a bistable switch. We also show how antibiotic biosynthesis is additionally regulated at the translational level by small non-coding RNAs. Now that we have a detailed understanding of the circuitry regulating antibiotic biosynthesis, we can start to re-engineer bacterial genomes to awaken cryptic antibiotic clusters, 20–50 of which are typically found in each newly sequenced genome (4). For this purpose, we are exploiting computational constraint-based modelling of bacterial metabolism to automatically identify suitable overproduction hosts and pinpoint biosynthetic bottlenecks that will be target for further cellular engineering (Figure) (5). We have also developed a high-throughput, in vivo reporter system to aid in creating a library of orthogonal promoters."
(PRWEB) March 19, 2014 -- Learn how to use GenoCAD, a Computer-Assited Design application for synthetic biology, Thursday, March 27th, at 18:00 p.m. UTC/2:00 p.m. ET/11:00 a.m. PT.
Trying to draw boundaries for a field of knowledge is a hopeless effort. The old joke about the undergrad that was very confused when he found out that Biology is Chemistry, Chemistry is Physics an...
"Think of them as tiny environmental health officers. Bacteria have been engineered to monitor the state of a live animal's gut. The work is a first step towards developing genetically modified bacteria that non-invasively diagnose problems such as gut infections or inflammation.
Synthetic biologists have made similar systems before in the lab, but never one designed to stand up to the harsh conditions in the gut of living mammals, says Jeffrey Way at Harvard Medical School. "No one else has really quite had the courage to try," he says. "There are a few examples, but for the most part people don't quite have the confidence to put their engineered systems out into the real world".
Way was part of a team led by Pamela Silver, also at Harvard Medical School, that inserted genes from a virus into E. coli bacteria. Normally these genes make a protein called cI, but when the bacteria are exposed to a substance called anhydrotetracycline, they instead produce a protein called Cro.
The team fed the bacteria to mice and collected faecal samples. Sure enough, only cI was detected unless the mice were given the chemical, in which case their faeces contained Cro proteins. The addition of the viral genetic switch meant the bacteria was effectively sensing and recording the chemical's presence.
"This is a really exciting advance," say Chris Voigt of MIT's Synthetic Biology Center, who was not involved with the study. "This is the first use of a genetic circuit in a real environment. It is remarkable that they were able to engineer the cells to perform a computational operation - albeit a simple one - in this environment."
Silver says it should be easy to engineer other genetic switches – ones that respond to telltale signs of inflammation, cancer, parasites or toxins in the gut, for example.
Programmable biobots
It might even be possible to engineer bacteria that deliver drugs if they detect disease. "You could think of them as little programmable robots that sense their environment and enact a therapeutic action when they discover a problem," says Voigt. Silver's team are already thinking about ways to do this, and not just in the gut. "You could engineer skin bacteria to sense inflammation and have a very early form of a diagnostic and a therapeutic reaction," she says.
"We always want to figure out what's going on in the dark recesses of our bowels," says Vincent Young, a microbiologist at the University of Michigan in Ann Arbor. "It's something people have been trying to do for a while."
"If [the modified bacteria] can tell that it's right next to the evil bug, then crank out a specific antibiotic, that would be cool."
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