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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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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. |
format | Online Article Text |
id | pubmed-5534457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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