28,904 research outputs found
Chemical communication between synthetic and natural cells: a possible experimental design
The bottom-up construction of synthetic cells is one of the most intriguing
and interesting research arenas in synthetic biology. Synthetic cells are built
by encapsulating biomolecules inside lipid vesicles (liposomes), allowing the
synthesis of one or more functional proteins. Thanks to the in situ synthesized
proteins, synthetic cells become able to perform several biomolecular
functions, which can be exploited for a large variety of applications. This
paves the way to several advanced uses of synthetic cells in basic science and
biotechnology, thanks to their versatility, modularity, biocompatibility, and
programmability. In the previous WIVACE (2012) we presented the
state-of-the-art of semi-synthetic minimal cell (SSMC) technology and
introduced, for the first time, the idea of chemical communication between
synthetic cells and natural cells. The development of a proper synthetic
communication protocol should be seen as a tool for the nascent field of
bio/chemical-based Information and Communication Technologies (bio-chem-ICTs)
and ultimately aimed at building soft-wet-micro-robots. In this contribution
(WIVACE, 2013) we present a blueprint for realizing this project, and show some
preliminary experimental results. We firstly discuss how our research goal
(based on the natural capabilities of biological systems to manipulate chemical
signals) finds a proper place in the current scientific and technological
contexts. Then, we shortly comment on the experimental approaches from the
viewpoints of (i) synthetic cell construction, and (ii) bioengineering of
microorganisms, providing up-to-date results from our laboratory. Finally, we
shortly discuss how autopoiesis can be used as a theoretical framework for
defining synthetic minimal life, minimal cognition, and as bridge between
synthetic biology and artificial intelligence.Comment: In Proceedings Wivace 2013, arXiv:1309.712
Steps in Metagenomics: Letâs Avoid Garbage in and Garbage Out
Is metagenomics a revolution or a new fad? Metagenomics is tightly associated with the availability of next-generation sequencing in all its implementations. The key feature of these new technologies, moving beyond the Sanger-based DNA sequencing approach, is the depth of nucleotide sequencing per sample.1 Knowing much more about a sample changes the traditional paradigms of âWhat is the most abundant?â or âWhat is the most significant?â to âWhat is present and potentially sigÂnificant that might influence the situation and outcome?â Letâs take the case of identifying proper biomarkers of disease state in the context of chronic disease prevention. Prevention has been deemed as a viable option to avert human chronic diseases and to curb healthÂcare management costs.2 The actual implementation of any effective preventive measures has proven to be rather difficult. In addition to the typically poor compliance of the general public, the vagueness of the successful validation of habit modification on the long-term risk, points to the need of defining new biomarkers of disease state. Scientists and the public are accepting the fact that humans are super-organisms, harboring both a human genome and a microbial genome, the latter being much bigger in size and diversity, and key for the health of individuals.3,4 It is time to investigate the intricate relationship between humans and their associated microbiota and how this relationship modÂulates or affects both partners.5 These remarks can be expanded to the animal and plant kingdoms, and holistically to the Earthâs biome. By its nature, the evolution and function of all the Earthâs biomes are influenced by a myriad of interactions between and among microbes (planktonic, in biofilms or host associated) and the surrounding physical environment.
The general definition of metagenomics is the cultivation-indepenÂdent analysis of the genetic information of the collective genomes of the microbes within a given environment based on its sampling. It focuses on the collection of genetic information through sequencing that can target DNA, RNA, or both. The subsequent analyses can be solely foÂcused on sequence conservation, phylogenetic, phylogenomic, function, or genetic diversity representation including yet-to-be annotated genes. The diversity of hypotheses, questions, and goals to be accomplished is endless. The primary design is based on the nature of the material to be analyzed and its primary function
The Scientist, Spring 2007
https://scholarworks.sjsu.edu/scientist/1000/thumbnail.jp
Joint assembly and genetic mapping of the Atlantic horseshoe crab genome reveals ancient whole genome duplication
Horseshoe crabs are marine arthropods with a fossil record extending back
approximately 450 million years. They exhibit remarkable morphological
stability over their long evolutionary history, retaining a number of ancestral
arthropod traits, and are often cited as examples of "living fossils." As
arthropods, they belong to the Ecdysozoa}, an ancient super-phylum whose
sequenced genomes (including insects and nematodes) have thus far shown more
divergence from the ancestral pattern of eumetazoan genome organization than
cnidarians, deuterostomes, and lophotrochozoans. However, much of ecdysozoan
diversity remains unrepresented in comparative genomic analyses. Here we use a
new strategy of combined de novo assembly and genetic mapping to examine the
chromosome-scale genome organization of the Atlantic horseshoe crab Limulus
polyphemus. We constructed a genetic linkage map of this 2.7 Gbp genome by
sequencing the nuclear DNA of 34 wild-collected, full-sibling embryos and their
parents at a mean redundancy of 1.1x per sample. The map includes 84,307
sequence markers and 5,775 candidate conserved protein coding genes. Comparison
to other metazoan genomes shows that the L. polyphemus genome preserves
ancestral bilaterian linkage groups, and that a common ancestor of modern
horseshoe crabs underwent one or more ancient whole genome duplications (WGDs)
~ 300 MYA, followed by extensive chromosome fusion
Construction of membrane-bound artificial cells using microfluidics: a new frontier in bottom-up synthetic biology
The quest to construct artificial cells from the bottom-up using simple building blocks has received much attention over recent decades and is one of the grand challenges in synthetic biology. Cell mimics that are encapsulated by lipid membranes are a particularly powerful class of artificial cells due to their biocompatibility and the ability to reconstitute biological machinery within them. One of the key obstacles in the field centres on the following: how can membrane-based artificial cells be generated in a controlled way and in high-throughput? In particular, how can they be constructed to have precisely defined parameters including size, biomolecular composition and spatial organization? Microfluidic generation strategies have proved instrumental in addressing these questions. This article will outline some of the major principles underpinning membrane-based artificial cells and their construction using microfluidics, and will detail some recent landmarks that have been achieved
From cheek swabs to consensus sequences : an A to Z protocol for high-throughput DNA sequencing of complete human mitochondrial genomes
Background: Next-generation DNA sequencing (NGS) technologies have made huge impacts in many fields of biological research, but especially in evolutionary biology. One area where NGS has shown potential is for high-throughput sequencing of complete mtDNA genomes (of humans and other animals). Despite the increasing use of NGS technologies and a better appreciation of their importance in answering biological questions, there remain significant obstacles to the successful implementation of NGS-based projects, especially for new users.
Results: Here we present an âA to Zâ protocol for obtaining complete human mitochondrial (mtDNA) genomes â from DNA extraction to consensus sequence. Although designed for use on humans, this protocol could also be used to sequence small, organellar genomes from other species, and also nuclear loci. This protocol includes DNA extraction, PCR amplification, fragmentation of PCR products, barcoding of fragments, sequencing using the 454 GS FLX platform, and a complete bioinformatics pipeline (primer removal, reference-based mapping, output of coverage plots and SNP calling).
Conclusions: All steps in this protocol are designed to be straightforward to implement, especially for researchers who are undertaking next-generation sequencing for the first time. The molecular steps are scalable to large numbers (hundreds) of individuals and all steps post-DNA extraction can be carried out in 96-well plate format. Also, the protocol has been assembled so that individual âmodulesâ can be swapped out to suit available resources
Incorporating molecular data in fungal systematics: a guide for aspiring researchers
The last twenty years have witnessed molecular data emerge as a primary
research instrument in most branches of mycology. Fungal systematics, taxonomy,
and ecology have all seen tremendous progress and have undergone rapid,
far-reaching changes as disciplines in the wake of continual improvement in DNA
sequencing technology. A taxonomic study that draws from molecular data
involves a long series of steps, ranging from taxon sampling through the
various laboratory procedures and data analysis to the publication process. All
steps are important and influence the results and the way they are perceived by
the scientific community. The present paper provides a reflective overview of
all major steps in such a project with the purpose to assist research students
about to begin their first study using DNA-based methods. We also take the
opportunity to discuss the role of taxonomy in biology and the life sciences in
general in the light of molecular data. While the best way to learn molecular
methods is to work side by side with someone experienced, we hope that the
present paper will serve to lower the learning threshold for the reader.Comment: Submitted to Current Research in Environmental and Applied Mycology -
comments most welcom
CRISPR as a Driving Force: The Model T of Biotechnology
The CRISPR system for gene editing can break, repair, and replace targeted sections of DNA. Although CRISPR gene editing has important therapeutic potential, it raises several ethical concerns. Some bioethicists worry CRISPR is a prelude to a dystopian future, while others maintain it should not be feared because it is analogous to past biotechnologies. In the scientific literature, CRISPR is often discussed as a revolutionary technology. In this paper we unpack the framing of CRISPR as a revolutionary technology and contrast it with framing it as a value-threatening biotechnology or business-as-usual. By drawing on a comparison between CRISPR and the Ford Model T, we argue CRISPR is revolutionary as a product, process, and as a force for social change. This characterization of CRISPR offers important conceptual clarity to the existing debates surrounding CRISPR. In particular, conceptualizing CRISPR as a revolutionary technology structures regulatory goals with respect to this new technology. Revolutionary technologies have characteristic patterns of implementation, entrenchment, and social impact. As such, early identification of technologies as revolutionary may help construct more nuanced and effective ethical frameworks for public policy
Nonterrestrial utilization of materials: Automated space manufacturing facility
Four areas related to the nonterrestrial use of materials are included: (1) material resources needed for feedstock in an orbital manufacturing facility, (2) required initial components of a nonterrestrial manufacturing facility, (3) growth and productive capability of such a facility, and (4) automation and robotics requirements of the facility
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