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      CRISPR Gene Perturbations Provide Insights for Improving Bacterial Biofuel Tolerance

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          Abstract

          Economically-viable biofuel production is often limited by low levels of microbial tolerance to high biofuel concentrations. Here we demonstrate the first application of deactivated CRISPR perturbations of gene expression to improve Escherichia coli biofuel tolerance. We construct a library of 31 unique CRISPR inhibitions and activations of gene expression in E. coli and explore their impacts on growth during 10 days of exposure to n-butanol and n-hexane. We show that perturbation of metabolism and membrane-related genes induces the greatest impacts on growth in n-butanol, as does perturbation of redox-related genes in n-hexanes. We identify uncharacterized genes yjjZ and yehS with strong potential for improving tolerance to both biofuels. Perturbations demonstrated significant temporal dependencies, suggesting that rationally designing time-sensitive gene circuits can optimize tolerance. We also introduce a sgRNA-specific hyper-mutator phenotype (~2,600-fold increase) into our perturbation strains using error-prone Pol1. We show that despite this change, strains exhibited similar growth phenotypes in n-butanol as before, demonstrating the robustness of CRISPR perturbations during prolonged use. Collectively, these results demonstrate the potential of CRISPR manipulation of gene expression for improving biofuel tolerance and provide constructive starting points for optimization of biofuel producing microorganisms.

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          Most cited references56

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          CRISPR interference (CRISPRi) for sequence-specific control of gene expression.

          Sequence-specific control of gene expression on a genome-wide scale is an important approach for understanding gene functions and for engineering genetic regulatory systems. We have recently described an RNA-based method, CRISPR interference (CRISPRi), for targeted silencing of transcription in bacteria and human cells. The CRISPRi system is derived from the Streptococcus pyogenes CRISPR (clustered regularly interspaced palindromic repeats) pathway, requiring only the coexpression of a catalytically inactive Cas9 protein and a customizable single guide RNA (sgRNA). The Cas9-sgRNA complex binds to DNA elements complementary to the sgRNA and causes a steric block that halts transcript elongation by RNA polymerase, resulting in the repression of the target gene. Here we provide a protocol for the design, construction and expression of customized sgRNAs for transcriptional repression of any gene of interest. We also provide details for testing the repression activity of CRISPRi using quantitative fluorescence assays and native elongating transcript sequencing. CRISPRi provides a simplified approach for rapid gene repression within 1-2 weeks. The method can also be adapted for high-throughput interrogation of genome-wide gene functions and genetic interactions, thus providing a complementary approach to RNA interference, which can be used in a wider variety of organisms.
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            Long-Term Experimental Evolution in Escherichia coli. I. Adaptation and Divergence During 2,000 Generations

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              Metabolic engineering of Escherichia coli for 1-butanol production.

              Compared to ethanol, butanol offers many advantages as a substitute for gasoline because of higher energy content and higher hydrophobicity. Typically, 1-butanol is produced by Clostridium in a mixed-product fermentation. To facilitate strain improvement for specificity and productivity, we engineered a synthetic pathway in Escherichia coli and demonstrated the production of 1-butanol from this non-native user-friendly host. Alternative genes and competing pathway deletions were evaluated for 1-butanol production. Results show promise for using E. coli for 1-butanol production.
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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
                04 September 2018
                2018
                : 6
                : 122
                Affiliations
                [1] 1Department of Chemical and Biological Engineering, University of Colorado at Boulder , Boulder, CO, United States
                [2] 2BioFrontiers Institute, University of Colorado at Boulder , Boulder, CO, United States
                Author notes

                Edited by: Zhanglin Lin, South China University of Technology, China

                Reviewed by: Syed Shams Yazdani, International Centre for Genetic Engineering and Biotechnology, India; Anne M. Ruffing, Sandia National Laboratories (SNL), United States

                *Correspondence: Anushree Chatterjee chatterjee@ 123456colorado.edu

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

                Article
                10.3389/fbioe.2018.00122
                6131188
                a548c045-ead9-4f0b-b29b-75f5fa18ecb6
                Copyright © 2018 Otoupal and Chatterjee.

                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
                : 27 April 2018
                : 14 August 2018
                Page count
                Figures: 7, Tables: 0, Equations: 0, References: 69, Pages: 15, Words: 12154
                Funding
                Funded by: National Science Foundation 10.13039/100000001
                Award ID: DGE1144083
                Award ID: MCB1714564
                Funded by: W. M. Keck Foundation 10.13039/100000888
                Funded by: Defense Advanced Research Projects Agency 10.13039/100000185
                Award ID: D17AP00024
                Funded by: University of Colorado 10.13039/100010174
                Categories
                Bioengineering and Biotechnology
                Original Research

                dcas9,gene expression,biofuels,tolerance,n-butanol,n-hexane,pol1
                dcas9, gene expression, biofuels, tolerance, n-butanol, n-hexane, pol1

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