"Trialkylgermyl functionalization allows development of high-performance soluble small-molecule organic semiconductors with mobilities greater than 5 cm2 V−1 s−1. Spray-deposited organic thin-film transistors show a record mobility of 2.2 cm2 V−1 s−1 and demonstrate the potential for incorporation in large-area, low-cost electronic applications." http://bit.ly/ZnPBPH
comment: High performance semiconductor spray paint could be a game changer for organic electronics http://bit.ly/ZQ2nmu
"In 2010 there were more than 200 million cases of malaria, and at least 655,000 deaths1. The World Health Organization has recommended artemisinin-based combination therapies (ACTs) for the treatment of uncomplicated malaria caused by the parasite Plasmodium falciparum. Artemisinin is a sesquiterpene endoperoxide with potent antimalarial properties, produced by the plant Artemisia annua. However, the supply of plant-derived artemisinin is unstable, resulting in shortages and price fluctuations, complicating production planning by ACT manufacturers2. A stable source of affordable artemisinin is required. Here we use synthetic biology to develop strains of Saccharomyces cerevisiae (baker’s yeast) for high-yielding biological production of artemisinic acid, a precursor of artemisinin. Previous attempts to produce commercially relevant concentrations of artemisinic acid were unsuccessful, allowing production of only 1.6 grams per litre of artemisinic acid3. Here we demonstrate the complete biosynthetic pathway, including the discovery of a plant dehydrogenase and a second cytochrome that provide an efficient biosynthetic route to artemisinic acid, with fermentation titres of 25 grams per litre of artemisinic acid. Furthermore, we have developed a practical, efficient and scalable chemical process for the conversion of artemisinic acid to artemisinin using a chemical source of singlet oxygen, thus avoiding the need for specialized photochemical equipment. The strains and processes described here form the basis of a viable industrial process for the production of semi-synthetic artemisinin to stabilize the supply of artemisinin for derivatization into active pharmaceutical ingredients (for example, artesunate) for incorporation into ACTs. Because all intellectual property rights have been provided free of charge, this technology has the potential to increase provision of first-line antimalarial treatments to the developing world at a reduced average annual price."
"Synthetic biology is an emerging engineering field focused on designing artificial biological systems with novel func- tionalities for use in therapeutics, basic science, biotech- nology, and diagnostics [1,2]. Continuous advancements in DNA synthesis and sequencing technologies coupled with new techniques for genomic modification and assem- bly have opened the door for harnessing the power and diversity of biology for applications. For example, natural bacteriophage products, such as ListShield (Intralytix) and Agriphage (Omnilytics), are commercially available for reducing unwanted bacterial contamination. Natural bacteriophages can be genetically modified to deliver engineered payloads into bacteria, thus selectively func- tionalizing target bacterial populations to produce active biomolecules. This strategy can endow bacteriophages with the ability to efficiently destroy bacterial biofilms or increase the bactericidal efficacy of antibiotics used in combination with phages by many orders of magnitude [3]. In addition, bacteriophages can be engineered as near- real-time microbial diagnostics by using them to trans- form target bacteria into factories for detectable molecules...." http://bit.ly/XXyJ15
TechCrunch is a leading technology media property, dedicated to obsessively profiling startups, reviewing new Internet products, and breaking tech news.
"Synthetic biology is often understood in terms of the pursuit for well-characterized biological parts to create synthetic wholes. Accordingly, it has typically been conceived of as an engineering dominated and application oriented field. We argue that the relationship of synthetic biology to engineering is far more nuanced than that and involves a sophisticated epistemic dimension, as shown by the recent practice of synthetic modeling. Synthetic models are engineered genetic networks that are implanted in a natural cell environment. Their construction is typically combined with experiments on model organisms as well as mathematical modeling and simulation. What is especially interesting about this combinational modeling practice is that, apart from greater integration between these different epistemic activities, it has also led to the questioning of some central assumptions and notions on which synthetic biology is based. As a result synthetic biology is in the process of becoming more "biology inspired."
"Synthetic biology is often referred to as “the field of the future,” the foundation of a fuels, materials, medicines, as well as the way we produce knowledge of biological systems. But while the self-consciously revolutionary language of synthetic biology declares a change of the industrial status quo, the metaphors we rely on are explicit references to the successful revolutions of past industrial technologies. The term synthetic biology echoes the successes of synthetic chemistry, while the guiding concept of standardization in genetic components is modeled on 19th century standardization of interchangeable parts. Industrial metaphors mix further as we climb the abstraction hierarchy; genetic parts are assembled to fit into a cellular chassis, creating logic gates and circuits that can compute biological information, leading to the control of cellular factories, rapidly designed, built, and commercialized on an “Ikea”-like scale.
These metaphors help us to understand how an industrial revolution might emerge from a biology lab, showing a possible path from ideas to industry. Like the “horseless carriage,” perhaps the analogies of living cells to computers give us a sense of familiarity with a technology whose potential we have not yet fully grasped. Industrial metaphors have long played a role in how we understand biology and the human body, from Fritz Kahn’s 1927 paintings of “Man as Industrial Palace to analogies between brains and computers. By referencing the products and methods of previous industrial revolutions, synthetic biology aims not only to aid understanding but also to demonstrate the future potential of the field. These metaphors draw the projected lines of Moore’s exponential increase as strands of DNA, imagining analogous and expanding industries based on carbon and sunlight rather than silicon and fossil fuels...."
bySaragliadis A, Krajewski SS, Rehm C, Narberhaus F, Hartig JS. "Synthetic biology approaches often combine natural building blocks to generate new cellular activities. Here, we make use of two RNA elements to design a regulatory device with novel functionality. The system is based on a hammerhead ribozyme (HHR) that cleaves itself to generate a liberated ribosome-binding site and, thus, permits expression of a downstream gene. We connected a temperature-responsive RNA hairpin to the HHR and, thus, generated a temperature-controlled ribozyme that we call thermozyme. Specifically, a Salmonella RNA thermometer (RNAT) known to modulate small heat shock gene expression by temperature-controlled base-pairing and melting was fused to the ribozyme. Following an in vivo screening approach, we isolated two functional thermozymes. In vivo expression studies and in vitro structure probing experiments support a mechanism in which rising temperatures melt the thermometer structure impairing the self-cleavage reaction of the ribozyme. Since RNA cleavage is necessary to liberate the RBS, these engineered thermozymes shut off gene expression in response to a temperature increase and, thus, act in a reverse manner as the natural RNAT. Our results clearly emphasize the highly modular nature and biotechnological potential of ribozyme-based RNA thermometers." http://bit.ly/11t4gWi
*Synthetic Biology: Tools and Applications* Book edited by Huimin Zhao
"...... from the content:
Protein Engineering as an Enabling Tool for Synthetic BiologyPC Cirino, S Qian - Synthetic Biology: Tools and Applications, 2013Proteins are essential ingredients in any natural or synthetic biological system, and the extent to which properties of one or more proteins can be modified in direct and desired ways often dictates success in synthetic biology and metabolically engineered systems. ... Synthetic Biology: Tools and ApplicationsH Zhao - 2013Synthetic Biology provides a framework to examine key enabling components in the emerging area of synthetic biology. Chapters contributed by leaders in the field address tools and methodologies developed for engineering biological systems at many levels, ... Design and Application of Synthetic Biology DevicesBC Heng, M Fussenegger - Synthetic Biology: Tools and Applications, 2013Synthetic biology is the rational and systematic design/construction of biological systems with desired functionalityl—4 This is achieved through applying engineering and computational principles within the field of molecular biology. 1_4 As such, synthetic ... Transforming Synthetic Biology with Cell-Free SystemsA Ranjil, JC Wu, BC Bundy, MC Jewett - Synthetic Biology: Tools and Applications, 2013Synthetic biology is a new approach for engineering biology by design. At its heart, this emerging discipline seeks to make biology easier to engineer and to harness biology to serve society. Already, this new paradigm for engineering biology is enabling a deeper ... Pathway Engineering as an Enabling Synthetic Biology ToolDT Eriksen, S Li, H Zhao - Synthetic Biology: Tools and Applications, 2013Pathway engineering has proven indispensable in the design of microbes for production of value-added products such as drugs, biofuels, and specialty chemicals. 1—4 Typically, a heterologous metabolic pathway producing the value-added compound is introduced into ..."
by Timothy R. Sampson,Sunil D. Saroj,Anna C. Llewellyn,Yih-Ling Tzeng& David S. Weiss
"CRISPR/Cas (clustered regularly interspaced palindromic repeats/CRISPR-associated) systems are a bacterial defence against invading foreign nucleic acids derived from bacteriophages or exogenous plasmids1, 2, 3, 4. These systems use an array of small CRISPR RNAs (crRNAs) consisting of repetitive sequences flanking unique spacers to recognize their targets, and conserved Cas proteins to mediate target degradation5, 6, 7, 8. Recent studies have suggested that these systems may have broader functions in bacterial physiology, and it is unknown if they regulate expression of endogenous genes9, 10. Here we demonstrate that the Cas protein Cas9 of Francisella novicida uses a unique, small, CRISPR/Cas-associated RNA (scaRNA) to repress an endogenous transcript encoding a bacterial lipoprotein. As bacterial lipoproteins trigger a proinflammatory innate immune response aimed at combating pathogens11, 12, CRISPR/Cas-mediated repression of bacterial lipoprotein expression is critical for F. novicida to dampen this host response and promote virulence. Because Cas9 proteins are highly enriched in pathogenic and commensal bacteria, our work indicates that CRISPR/Cas-mediated gene regulation may broadly contribute to the regulation of endogenous bacterial genes, particularly during the interaction of such bacteria with eukaryotic hosts."
"Accelerating the process of industrial bacterial host strain development, aimed at increasing productivity, generating new bio-products or utilizing alternative feedstocks, requires the integration of complementary approaches to manipulate cellular metabolism and regulatory networks. Systems metabolic engineering extends the concept of classical metabolic engineering to the systems level by incorporating the techniques used in systems biology and synthetic biology, and offers a framework for the development of the next generation of industrial strains. As one of the most useful tools of systems metabolic engineering, protein design allows us to design and optimize cellular metabolism at a molecular level. Here, we review the current strategies of protein design for engineering cellular synthetic pathways, metabolic control systems and signaling pathways, and highlight the challenges of this subfield within the context of systems metabolic engineering."
"Australian scientists made headlines last month when they revealed that they were close to cloning a frog, Rheobatrachus silus, last seen in the wild three decades ago. If they succeed, it may take another emerging technology to keep that frog alive.
Synthetic biology aims to endow organisms with new sets of genes and new abilities. Along with cloning, it has been portrayed in the press as a hubristic push to do fantastical things: bring back woolly mammoths or resurrect the passenger pigeons that darkened the skies of North America before they were eradicated by nineteenth-century settlers..."
An interview with the synthetic biologist Christina Agapakis
byALEXIS C. MADRIGAL
"As tools for engineering life’s building blocks have proliferated in recent years, our definition of human life has become more expansive. For example, we are learning that the vast ecosystems of microbes inside our bodies are as integral to our health as our own tissues, affecting everything from our immune systems to our brain chemistry. Meanwhile, the field of biology itself keeps expanding—see, for example, synthetic biology, the new subfield that uses the combined insights of molecular biology, engineering, and chemistry to construct biological parts and processes. The synthetic biologist Christina Agapakis, a postdoctoral researcher at UCLA, works at the intersection of these developments. She is also part of a cohort of scientists rethinking the role of biology in our culture. Alexis Madrigal: People have big expectations for biology in the 21st century. Many say that biotech will be as big as information technology was in recent decades. Is that true? Christina Agapakis: People want synthetic biology and biotechnology to be the next industrial revolution. Looking back, people have tended over time to imagine bodies functioning in ways that were analogous to the dominant technological paradigm of their day, whether that was steam engines or computers. I hope that soon biology will be the technology we judge things by. Maybe we’re going to see industry and computational stuff start to look more like biology, rather than biology looking more like industry and computation. AM: Some synthetic biologists have pushed to bring an engineering mind-set to biology. People talk about creating standard DNA “parts,” called BioBricks. What are those? CA: The idea behind BioBrick parts is that you can have a collection of pieces of DNA that have specific useful functions—off-the-shelf DNA parts. You are able to say, “Okay, I need a part that is fluorescent,” or “I need a part that will activate in response to this chemical.” Then you can mix and match: you put them both in a bacterium, and then you have fluorescence in response to some chemical—so we can have this kind of RadioShack. AM: You’ve looked at how communities of bacteria work together in the human body and elsewhere. To what extent could we actively engineer our own microbial ecosystem in the future? CA: We can influence it—we can change the diversity in our gut, and that can influence health. There’s the fecal-transplant example: Sometimes even antibiotics can’t clear up serious digestive infections, and you can’t repopulate the gut with enough good bacteria to get rid of the bad ones. But if you transplant the microbial community from a healthy gut into the person who has this infection, the healthy bacteria will push out the infectious bacteria. The challenge is, you can’t say “You need this many of this and this many of this, and it’s going to stay like that forever.” It’s more a matter of setting the right initial conditions...."
"designer Alexandra Daisy Ginsberg discusses synthetic biology - a new field of science that could see designers creating artificial lifeforms. For example, bacteria could one day be developed to excrete brightly coloured pigments when they detect disease inside your body, alerting you via vividly coloured poo. Synthetic biology is a development of the age-old practice of selective breeding, Ginsberg explains: "We've been designing biology for 10,000 years or more," she says. "Every crop, or your pet dog - it has all been designed in a way. It's been iterated and iterated by human decisions into the thing that we want. The idea behind synthetic biology is that you can get much more control and start moving things across living kingdoms that haven't interacted at a genetic level before." Ginsberg gives the example of E.chromi, a project she worked on with fellow designer James King and undergraduate students at Cambridge University, which won the International Genetically Engineered Machine competition in 2009. "It's a competition where thousands of students from around the world get together to design a bacteria that does something cool," she explains. "We were working with students at Cambridge who were designing bacteria that produce different coloured pigments." As part of the project, Ginsberg and her team considered the possible future applications and implications of their work. "We imagined that in about 2039 it would become culturally acceptable to drink a Yakult-type yoghurt laced with E.chromi bacteria that would start to detect diseases in your gut," she says. "If you had a disease they'd start producing a corresponding coloured pigment. So coloured poo is the thing that everyone has taken from this project, as a new kind of interface for biological computing." Not content to simply present the project as a series of diagrams, Ginsberg and King created a mock-up of what the imagined excrement might look like. "We wanted to challenge the scientists and engineers who are actually inventing the technology with what we thought was an interesting aesthetic response," She explains. "They're representing it as cogs and machines, but this is biology. We shouldn't be shy or coy about talking about what's unique about this technology."
"In many ways, the fast-paced evolution of the internet parallels the move toward “big data” in science. In less than a decade, online tools have exploded in popularity and witnessed rapid expansion (Figure 1), with an increasing number of scientists now looking to take advantage of these web-based resources (see Box 1 and Table 1 for an overview and comparison of existing tools). Social media portals in particular undergo regular reinvention and transformation, with different tools becoming popular for different populations [1]. Although a number of guides exist online, many researchers still feel overwhelmed and hesitant toward the virtual world, lacking sufficient information and guidance through formal scientific channels such as peer-reviewed journals. To better familiarize researchers with existing internet resources, here we discuss prospective benefits that can stem from online science conversations, explain how scientists can efficiently and effectively harness online resources, and provide an overview of popular online tools."
"Synthetic biology is a rapidly emerging discipline with long-term ramifications that range from single-molecule detection within cells to the creation of synthetic genomes and novel life forms. Truly phenomenal results have been obtained by pioneering groups - for instance, the combinatorial synthesis of genetic networks, genome synthesis using BioBricks, and hybridization chain reaction (HCR), in which stable DNA monomers assemble only upon exposure to a target DNA fragment, biomolecular self-assembly pathways, etc. Such work strongly suggests that nanotechnology and synthetic biology together seem poised to constitute the most transformative development of the 21st century. In this paper, we present a Constraint Programming (CP) approach to solve the RNA inverse folding problem. Given a target RNA secondary structure, we determine an RNA sequence which folds into the target structure; i.e. whose minimum free energy structure is the target structure. Our approach represents a step forward in RNA design - we produce the first complete RNA inverse folding approach which allows for the specification of a wide range of design constraints. We also introduce a Large Neighborhood Search approach which allows us to tackle larger instances at the cost of losing completeness, while retaining the advantages of meeting design constraints (motif, GC-content, etc.). Results demonstrate that our software, RNAiFold, performs as well or better than all state-of-the-art approaches; nevertheless, our approach is unique in terms of completeness, flexibility, and the support of various design constraints. The algorithms presented in this paper are publicly available via the interactive webserver http://bioinformatics.bc.edu/clotelab/RNAiFold ; additionally, the source code can be downloaded from that site." http://bit.ly/17VdVv*
"For over the last two decades, positively selected amino acid sites have been inferred almost exclusively by showing that the number of nonsynonymous substitutions per nonsynonymous site (dn) is greater than that of synonymous substitutions per synonymous site (ds). However, virtually none of these statistical results have been experimentally tested and remain as hypotheses. To perform such experimental tests, we must connect genotype and phenotype and relate the phenotypic changes to the environmental and behavioral changes of the organism. The genotype-phenotype relationship can be established only by synthesizing and manipulating “proper” ancestral phenotypes, while the actual functions of adaptive mutations can be learned by studying their chemical roles in phenotypic changes."
"Startups on the menuBoston University’s (BU) Jim Collins presented work from hislab on a network biology approach to antibiotic discovery at the Boston SciCafé, Nature Biotechnology’s and Nature Medicine’s tri-annual gather- ing of academic researchers and business people. He’s now a cofounder of EnBiotix, a startup focused around this technology, todevelop new classes of antibiotics and antibiotic poten-tiators to tackle multidrug-resistant microbes. Nature Biotechnology talked to him about the company Jim Collins: Jeff Wager and I met in the fall of 2011, via BU’s Office of Technology Development. Jeff was lookingfor new commercialization opportunities in biotech, and I was looking to partner with a serial entrepreneur to commercialize our antibiotics platforms. We met extensively over several months, and by the time we headed into 2012, we had already decided to form EnBiotix. Jeff reached out to NAEJA Pharmaceutical and Great Lakes DrugDevelopment and brought them on as cofounders, in addition to Apeiron Partners and BU, and officially named the company and issued shares to co-founders in July 2012. NBT: What programs are you prioritizing within the company?JC: Our top priority within the company is our reactive oxygen species (ROS) program—we are working to find small molecules that enhance the endogenous microbial production of ROS and can be used to potentiate the bacte- ricidal activity of existing antibiotics against Gram-negative bacteria.NBT: What do you most enjoy about starting a company?JC: I am most intrigued and excited by the challenges of transforminga project into a product...."
"Drew Endy wants to build a programming language for the body.
Endy is the co-director of the International Open Facility Advancing Biotechnology — BIOFAB, for short — where he’s part of a team that’s developing a language that will use genetic data to actually program biological cells. That may seem like the stuff of science fiction, but the project is already underway, and the team intends to open source the language, so that other scientists can use it and modify it and perfect it.
The effort is part of a sweeping movement to grab hold of our genetic data and directly improve the way our bodies behave — a process known as bioengineering. With the Supreme Court exploring whether genes can be patented, the bioengineering world is at crossroads, but scientists like Endy continue to push this technology forward.
Genes contain information that defines the way our cells function, and some parts of the genome express themselves in much the same way across different types of cells and organisms. This would allow Endy and his team to build a language scientists could use to carefully engineer gene expression – what they call “the layer between the genome and all the dynamic processes of life.”...."
"Caffeine has a significant role in human culture, but it has become a pollutant where caffeine-containing products are processed. Pseudomonas putida CBB5 can degrade caffeine to xanthine, a triply demethylated analog that can be further transformed into guanine. To transfer this pathway to Escherichia coli, Quandt et al. developed a screen for functional pathways by knocking out IMP dehydrogenase—an enzyme involved in guanine metabolism—without which cells require an alternate source of xanthine for growth. This…"
by Shiksha Mantri,K. Tanuj Sapra,Stephen Cheley,Thomas H. Sharp& Hagan Bayley
"The bottom-up construction of artificial tissues is an underexplored area of synthetic biology. An important challenge is communication between constituent compartments of the engineered tissue, and between the engineered tissue and additional compartments, including extracellular fluids, further engineered tissue and living cells. Here we present a dimeric transmembrane pore that can span two adjacent lipid bilayers, and thereby allow aqueous compartments to communicate. Two heptameric staphylococcal α-hemolysin pores were covalently linked in an aligned cap-to-cap orientation. The structure of the dimer, (α7)2, was confirmed by biochemical analysis, transmission electron microscopy and single-channel electrical recording. We show that one of two β-barrels of (α7)2 can insert into the lipid bilayer of a small unilamellar vesicle, while the other spans a planar lipid bilayer. The (α7)2 pores spanning two bilayers were also observed by transmission electron microscopy."
*Computational Protein Design for Synthetic Biology*
byF Richter, D Baker
"The objective of (computational) protein design and engineering is to create proteins with functions that are not available in natural proteomes. In many synthetic biology applications, just like in natural organisms, proteins are the workhorses that carry out the actual desired ..."
by Alexander M. Jones, Guido Grossmann, Jonas ÅH Danielson, Davide Sosso, Li-Qing Chen, Cheng-Hsun Ho, Wolf B Frommer
"Revolutionary new technologies, namely in the areas of DNA sequencing and molecular imaging, continue to impact new discoveries in plant science and beyond. For decades we have been able to determine properties of enzymes, receptors and transporters in vitro or in heterologous systems, and more recently been able to analyze their regulation at the transcriptional level, to use GFP reporters for obtaining insights into cellular and subcellular localization, and tp measure ion and metabolite levels with unprecedented precision using mass spectrometry. However, we lack key information on the location and dynamics of the substrates of enzymes, receptors and transporters, and on the regulation of these proteins in their cellular environment. Such information can now be obtained by transitioning from in vitro to in vivo biochemistry using biosensors. Genetically encoded fluorescent protein-based sensors for ion and metabolite dynamics provide highly resolved spatial and temporal information, and are complemented by sensors for pH, redox, voltage, and tension. They serve as powerful tools for identifying missing processes (e.g., glucose transport across ER membranes), components (e.g., SWEET sugar transporters for cellular sugar efflux), and signaling networks (e.g., from systematic screening of mutants that affect sugar transport or cytosolic and vacuolar pH). Combined with the knowledge of properties of enzymes and transporters and their interactions with the regulatory machinery, biosensors promise to be key diagnostic tools for systems and synthetic biology."
Arizona State University is beginning to establish its place on the map in the burgeoning field of synthetic biology. Notable strides in research are being made by faculty members and students in t...
"Arizona State University is beginning to establish its place on the map in the burgeoning field of synthetic biology.
Notable strides in research are being made by faculty members and students in the School of Biological and Health Systems Engineering, one of ASU’s Ira A. Fulton Schools of Engineering. Assistant professor Karmella Haynes was recently the featured speaker on the subject of advances in synthetic biology for the Arizona Science Center’s New Frontiers in Medical Science lecture series. Some of the data Haynes presented in her talk was derived from research being conducted by bioengineering senior Caroline Hom. The research involving identification and production of reagents that activate genes in different types of cancer cells earned Hom an opportunity to give a talk about her work at the recent annual conference of the Institute of Biological Engineering (IBE) – a rare achievement for an undergraduate...."
Foto: ioengineering doctoral student Behzad Damadzedah (left) works in the lab with assistant professor +Karmella Haynes . They and others at ASU are seeking ways that synthetic biology research can contribute to new or better treatments for various diseases. Damazedah recently reported on his research at the annual Synthetic Biology Engineering Research Center retreat.
To get content containing either thought or leadership enter:
To get content containing both thought and leadership enter:
To get content containing the expression thought leadership enter:
You can enter several keywords and you can refine them whenever you want. Our suggestion engine uses more signals but entering a few keywords here will rapidly give you great content to curate.
by
Yaochuan Mei et al
"Trialkylgermyl functionalization allows development of high-performance soluble small-molecule organic semiconductors with mobilities greater than 5 cm2 V−1 s−1. Spray-deposited organic thin-film transistors show a record mobility of 2.2 cm2 V−1 s−1 and demonstrate the potential for incorporation in large-area, low-cost electronic applications."
http://bit.ly/ZnPBPH
comment:
High performance semiconductor spray paint could be a game changer for organic electronics http://bit.ly/ZQ2nmu