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      Bottom-Up Construction of Complex Biomolecular Systems With Cell-Free Synthetic Biology

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          Abstract

          Cell-free systems offer a promising approach to engineer biology since their open nature allows for well-controlled and characterized reaction conditions. In this review, we discuss the history and recent developments in engineering recombinant and crude extract systems, as well as breakthroughs in enabling technologies, that have facilitated increased throughput, compartmentalization, and spatial control of cell-free protein synthesis reactions. Combined with a deeper understanding of the cell-free systems themselves, these advances improve our ability to address a range of scientific questions. By mastering control of the cell-free platform, we will be in a position to construct increasingly complex biomolecular systems, and approach natural biological complexity in a bottom-up manner.

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          Most cited references249

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          Foundations for engineering biology.

          Drew Endy (2005)
          Engineered biological systems have been used to manipulate information, construct materials, process chemicals, produce energy, provide food, and help maintain or enhance human health and our environment. Unfortunately, our ability to quickly and reliably engineer biological systems that behave as expected remains quite limited. Foundational technologies that make routine the engineering of biology are needed. Vibrant, open research communities and strategic leadership are necessary to ensure that the development and application of biological technologies remains overwhelmingly constructive.
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            Self-splicing RNA: autoexcision and autocyclization of the ribosomal RNA intervening sequence of Tetrahymena.

            In the macronuclear rRNA genes of Tetrahymena thermophila, a 413 bp intervening sequence (IVS) interrupts the 26S rRNA-coding region. A restriction fragment of the rDNA containing the IVS and portions of the adjacent rRNA sequences (exons) was inserted downstream from the lac UV5 promoter in a recombinant plasmid. Transcription of this template by purified Escherichia coli RNA polymerase in vitro produced a shortened version of the pre-rRNA, which was then deproteinized. When incubated with monovalent and divalent cations and a guanosine factor, this RNA underwent splicing. The reactions that were characterized included the precise excision of the IVS, attachment of guanosine to the 5' end of the IVS, covalent cyclization of the IVS and ligation of the exons. We conclude that splicing activity is intrinsic to the structure of the RNA, and that enzymes, small nuclear RNAs and folding of the pre-rRNA into an RNP are unnecessary for these reactions. We propose that the IVS portion of the RNA has several enzyme-like properties that enable it to break and reform phosphodiester bonds. The finding of autocatalytic rearrangements of RNA molecules has implications for the mechanism and the evolution of other reactions that involve RNA.
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              The second wave of synthetic biology: from modules to systems.

              Synthetic biology is a research field that combines the investigative nature of biology with the constructive nature of engineering. Efforts in synthetic biology have largely focused on the creation and perfection of genetic devices and small modules that are constructed from these devices. But to view cells as true 'programmable' entities, it is now essential to develop effective strategies for assembling devices and modules into intricate, customizable larger scale systems. The ability to create such systems will result in innovative approaches to a wide range of applications, such as bioremediation, sustainable energy production and biomedical therapies.
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                Author and article information

                Contributors
                Journal
                Front Bioeng Biotechnol
                Front Bioeng Biotechnol
                Front. Bioeng. Biotechnol.
                Frontiers in Bioengineering and Biotechnology
                Frontiers Media S.A.
                2296-4185
                24 March 2020
                2020
                : 8
                : 213
                Affiliations
                [1] 1School of Biological Sciences, Institute of Quantitative Biology, Biochemistry, and Biotechnology, University of Edinburgh , Edinburgh, United Kingdom
                [2] 2School of Engineering, Institute of Bioengineering, École Polytechnique Fédérale de Lausanne , Lausanne, Switzerland
                Author notes

                Edited by: Simon J. Moore, University of Kent, United Kingdom

                Reviewed by: Pasquale Stano, University of Salento, Italy; Guy-Bart Vincent Stan, Imperial College London, United Kingdom

                *Correspondence: Sebastian J. Maerkl sebastian.maerkl@ 123456epfl.ch

                This article was submitted to Synthetic Biology, a section of the journal Frontiers in Bioengineering and Biotechnology

                Article
                10.3389/fbioe.2020.00213
                7105575
                32266240
                7416ca20-60e1-4fe7-ad85-0249828516c9
                Copyright © 2020 Laohakunakorn, Grasemann, Lavickova, Michielin, Shahein, Swank and Maerkl.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 13 January 2020
                : 03 March 2020
                Page count
                Figures: 7, Tables: 0, Equations: 0, References: 272, Pages: 26, Words: 21458
                Funding
                Funded by: Human Frontier Science Program 10.13039/100004412
                Award ID: RGP0032/2015
                Funded by: H2020 European Research Council 10.13039/100010663
                Award ID: 723106
                Funded by: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 10.13039/501100001711
                Award ID: 182019
                Award ID: 323530_171144
                Categories
                Bioengineering and Biotechnology
                Review

                cell-free synthetic biology,cell-free protein synthesis,in vitro reconstitution,microfluidics,compartmentalization,artificial cell,in vitro replication

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