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Engineering the Bacterial Microcompartment Domain for Molecular Scaffolding Applications

As synthetic biology advances the intricacy of engineered biological systems, the importance of spatial organization within the cellular environment must not be marginalized. Increasingly, biological engineers are investigating means to control spatial organization within the cell, mimicking strateg...

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Autores principales: Young, Eric J., Burton, Rodney, Mahalik, Jyoti P., Sumpter, Bobby G., Fuentes-Cabrera, Miguel, Kerfeld, Cheryl A., Ducat, Daniel C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534457/
https://www.ncbi.nlm.nih.gov/pubmed/28824573
http://dx.doi.org/10.3389/fmicb.2017.01441
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author Young, Eric J.
Burton, Rodney
Mahalik, Jyoti P.
Sumpter, Bobby G.
Fuentes-Cabrera, Miguel
Kerfeld, Cheryl A.
Ducat, Daniel C.
author_facet Young, Eric J.
Burton, Rodney
Mahalik, Jyoti P.
Sumpter, Bobby G.
Fuentes-Cabrera, Miguel
Kerfeld, Cheryl A.
Ducat, Daniel C.
author_sort Young, Eric J.
collection PubMed
description As synthetic biology advances the intricacy of engineered biological systems, the importance of spatial organization within the cellular environment must not be marginalized. Increasingly, biological engineers are investigating means to control spatial organization within the cell, mimicking strategies used by natural pathways to increase flux and reduce cross-talk. A modular platform for constructing a diverse set of defined, programmable architectures would greatly assist in improving yields from introduced metabolic pathways and increasing insulation of other heterologous systems. Here, we review recent research on the shell proteins of bacterial microcompartments and discuss their potential application as “building blocks” for a range of customized intracellular scaffolds. We summarize the state of knowledge on the self-assembly of BMC shell proteins and discuss future avenues of research that will be important to realize the potential of BMC shell proteins as predictively assembling and programmable biological materials for bioengineering.
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spelling pubmed-55344572017-08-18 Engineering the Bacterial Microcompartment Domain for Molecular Scaffolding Applications Young, Eric J. Burton, Rodney Mahalik, Jyoti P. Sumpter, Bobby G. Fuentes-Cabrera, Miguel Kerfeld, Cheryl A. Ducat, Daniel C. Front Microbiol Microbiology As synthetic biology advances the intricacy of engineered biological systems, the importance of spatial organization within the cellular environment must not be marginalized. Increasingly, biological engineers are investigating means to control spatial organization within the cell, mimicking strategies used by natural pathways to increase flux and reduce cross-talk. A modular platform for constructing a diverse set of defined, programmable architectures would greatly assist in improving yields from introduced metabolic pathways and increasing insulation of other heterologous systems. Here, we review recent research on the shell proteins of bacterial microcompartments and discuss their potential application as “building blocks” for a range of customized intracellular scaffolds. We summarize the state of knowledge on the self-assembly of BMC shell proteins and discuss future avenues of research that will be important to realize the potential of BMC shell proteins as predictively assembling and programmable biological materials for bioengineering. Frontiers Media S.A. 2017-07-31 /pmc/articles/PMC5534457/ /pubmed/28824573 http://dx.doi.org/10.3389/fmicb.2017.01441 Text en Copyright © 2017 Young, Burton, Mahalik, Sumpter, Fuentes-Cabrera, Kerfeld and Ducat. http://creativecommons.org/licenses/by/4.0/ 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) or licensor 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.
spellingShingle Microbiology
Young, Eric J.
Burton, Rodney
Mahalik, Jyoti P.
Sumpter, Bobby G.
Fuentes-Cabrera, Miguel
Kerfeld, Cheryl A.
Ducat, Daniel C.
Engineering the Bacterial Microcompartment Domain for Molecular Scaffolding Applications
title Engineering the Bacterial Microcompartment Domain for Molecular Scaffolding Applications
title_full Engineering the Bacterial Microcompartment Domain for Molecular Scaffolding Applications
title_fullStr Engineering the Bacterial Microcompartment Domain for Molecular Scaffolding Applications
title_full_unstemmed Engineering the Bacterial Microcompartment Domain for Molecular Scaffolding Applications
title_short Engineering the Bacterial Microcompartment Domain for Molecular Scaffolding Applications
title_sort engineering the bacterial microcompartment domain for molecular scaffolding applications
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534457/
https://www.ncbi.nlm.nih.gov/pubmed/28824573
http://dx.doi.org/10.3389/fmicb.2017.01441
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