AI Article Synopsis

  • The development of recombinant DNA technology over 40 years ago revolutionized both society and the scientific community, primarily through the creation and adaptation of plasmid vectors for genetic engineering.
  • This evolution has led to significant advancements in studying microorganisms, particularly through synthetic biology, enabling deeper insights into bacteri and fungi, as well as metagenomics.
  • Future goals include creating modular vectors with standardized components and overcoming challenges in vector design to foster further innovation in genetic engineering.

Article Abstract

When recombinant DNA technology was developed more than 40 years ago, no one could have imagined the impact it would have on both society and the scientific community. In the field of genetic engineering, the most important tool developed was the plasmid vector. This technology has been continuously expanding and undergoing adaptations. Here, we provide a detailed view following the evolution of vectors built throughout the years destined to study microorganisms and their peculiarities, including those whose genomes can only be revealed through metagenomics. We remark how synthetic biology became a turning point in designing these genetic tools to create meaningful innovations. We have placed special focus on the tools for engineering bacteria and fungi (both yeast and filamentous fungi) and those available to construct metagenomic libraries. Based on this overview, future goals would include the development of modular vectors bearing standardized parts and orthogonally designed circuits, a task not fully addressed thus far. Finally, we present some challenges that should be overcome to enable the next generation of vector design and ways to address it.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302727PMC
http://dx.doi.org/10.1111/1751-7915.13318DOI Listing

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