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Title: CRISPR/Cas9 mediated targeted mutagenesis of the fast growing cyanobacterium Synechococcus elongatus UTEX 2973

Abstract

As autotrophic prokaryotes, cyanobacteria are ideal chassis organisms for sustainable production of various useful compounds. The newly characterized cyanobacterium Synechococcus elongatus UTEX 2973 is a promising candidate for serving as a microbial cell factory because of its unusually rapid growth rate. Here, we seek to develop a genetic toolkit that enables extensive genomic engineering of Synechococcus 2973 by implementing a CRISPR/Cas9 editing system. We targeted the nblA gene because of its important role in biological response to nitrogen deprivation conditions. First, we determined that the Streptococcus pyogenes Cas9 enzyme is toxic in cyanobacteria, and conjugational transfer of stable, replicating constructs containing the cas9 gene resulted in lethality. However, after switching to a vector that permitted transient expression of the cas9 gene, we achieved markerless editing in 100 % of cyanobacterial exconjugants after the first patch. Moreover, we could readily cure the organisms of antibiotic resistance, resulting in a markerless deletion strain. In conclusion, high expression levels of the Cas9 protein in Synechococcus 2973 appear to be toxic and result in cell death. However, introduction of a CRISPR/Cas9 genome editing system on a plasmid backbone that leads to transient cas9 expression allowed for efficient markerless genome editing in a wild typemore » genetic background.« less

Authors:
; ; ; ; ORCiD logo
Publication Date:
Research Org.:
Washington Univ., St. Louis, MO (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Biological and Environmental Research (BER)
OSTI Identifier:
1618804
Alternate Identifier(s):
OSTI ID: 1375815
Resource Type:
Journal Article: Published Article
Journal Name:
Microbial Cell Factories
Additional Journal Information:
Journal Name: Microbial Cell Factories Journal Volume: 15 Journal Issue: 1; Journal ID: ISSN 1475-2859
Publisher:
Springer Science + Business Media
Country of Publication:
United Kingdom
Language:
English
Subject:
59 BASIC BIOLOGICAL SCIENCES; Cyanobacteria; Synechococcus; CRISPR; Cas9; Genome modification

Citation Formats

Wendt, Kristen E., Ungerer, Justin, Cobb, Ryan E., Zhao, Huimin, and Pakrasi, Himadri B. CRISPR/Cas9 mediated targeted mutagenesis of the fast growing cyanobacterium Synechococcus elongatus UTEX 2973. United Kingdom: N. p., 2016. Web. doi:10.1186/s12934-016-0514-7.
Wendt, Kristen E., Ungerer, Justin, Cobb, Ryan E., Zhao, Huimin, & Pakrasi, Himadri B. CRISPR/Cas9 mediated targeted mutagenesis of the fast growing cyanobacterium Synechococcus elongatus UTEX 2973. United Kingdom. https://doi.org/10.1186/s12934-016-0514-7
Wendt, Kristen E., Ungerer, Justin, Cobb, Ryan E., Zhao, Huimin, and Pakrasi, Himadri B. 2016. "CRISPR/Cas9 mediated targeted mutagenesis of the fast growing cyanobacterium Synechococcus elongatus UTEX 2973". United Kingdom. https://doi.org/10.1186/s12934-016-0514-7.
@article{osti_1618804,
title = {CRISPR/Cas9 mediated targeted mutagenesis of the fast growing cyanobacterium Synechococcus elongatus UTEX 2973},
author = {Wendt, Kristen E. and Ungerer, Justin and Cobb, Ryan E. and Zhao, Huimin and Pakrasi, Himadri B.},
abstractNote = {As autotrophic prokaryotes, cyanobacteria are ideal chassis organisms for sustainable production of various useful compounds. The newly characterized cyanobacterium Synechococcus elongatus UTEX 2973 is a promising candidate for serving as a microbial cell factory because of its unusually rapid growth rate. Here, we seek to develop a genetic toolkit that enables extensive genomic engineering of Synechococcus 2973 by implementing a CRISPR/Cas9 editing system. We targeted the nblA gene because of its important role in biological response to nitrogen deprivation conditions. First, we determined that the Streptococcus pyogenes Cas9 enzyme is toxic in cyanobacteria, and conjugational transfer of stable, replicating constructs containing the cas9 gene resulted in lethality. However, after switching to a vector that permitted transient expression of the cas9 gene, we achieved markerless editing in 100 % of cyanobacterial exconjugants after the first patch. Moreover, we could readily cure the organisms of antibiotic resistance, resulting in a markerless deletion strain. In conclusion, high expression levels of the Cas9 protein in Synechococcus 2973 appear to be toxic and result in cell death. However, introduction of a CRISPR/Cas9 genome editing system on a plasmid backbone that leads to transient cas9 expression allowed for efficient markerless genome editing in a wild type genetic background.},
doi = {10.1186/s12934-016-0514-7},
url = {https://www.osti.gov/biblio/1618804}, journal = {Microbial Cell Factories},
issn = {1475-2859},
number = 1,
volume = 15,
place = {United Kingdom},
year = {Thu Jun 23 00:00:00 EDT 2016},
month = {Thu Jun 23 00:00:00 EDT 2016}
}

Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record at https://doi.org/10.1186/s12934-016-0514-7

Citation Metrics:
Cited by: 133 works
Citation information provided by
Web of Science

Figures / Tables:

Fig. 1 Fig. 1: Plasmids were generated using pCRISPomyces-2 backbone to engineer the ∆nblA line. a The nblA deletion plasmid including cas9 and b the nblA editing plasmid excluding cas9 are depicted

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Works referenced in this record:

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Works referencing / citing this record:

Identifying the Metabolic Differences of a Fast-Growth Phenotype in Synechococcus UTEX 2973
journal, January 2017


Progress and challenges in engineering cyanobacteria as chassis for light‐driven biotechnology
journal, August 2019


Current status and perspectives of genome editing technology for microalgae
journal, November 2017


The primary transcriptome of the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973
journal, August 2018


Dual-function chromogenic screening-based CRISPR/Cas9 genome editing system for actinomycetes
journal, December 2019


On the use of oxygenic photosynthesis for the sustainable production of commodity chemicals
journal, March 2019


Metabolic Engineering of Oleaginous Yeasts for Production of Fuels and Chemicals
journal, November 2017


Engineering Halomonas species TD01 for enhanced polyhydroxyalkanoates synthesis via CRISPRi
journal, April 2017


Emerging Species and Genome Editing Tools: Future Prospects in Cyanobacterial Synthetic Biology
journal, September 2019


Cpf1 Is A Versatile Tool for CRISPR Genome Editing Across Diverse Species of Cyanobacteria
journal, December 2016


Editing streptomycete genomes in the CRISPR/Cas9 age
journal, January 2019


Engineering cyanobacteria for production of terpenoids
journal, November 2018


New Applications of Synthetic Biology Tools for Cyanobacterial Metabolic Engineering
journal, February 2019


Recent Developments on Genetic Engineering of Microalgae for Biofuels and Bio‐Based Chemicals
journal, September 2017


CRISPR/Cas-based genome engineering in natural product discovery
journal, January 2019


A Cloning-Free Method for CRISPR/Cas9-Mediated Genome Editing in Fission Yeast
journal, April 2018


Efficient Cas9-based genome editing of Rhodobacter sphaeroides for metabolic engineering
journal, November 2019


Characterization of Cas proteins for CRISPR‐Cas editing in streptomycetes
journal, May 2019


Optimizing Systems for Cas9 Expression in Toxoplasma gondii
journal, June 2019


Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum
journal, November 2017


Advances and challenges in genetic engineering of microalgae
journal, January 2019


A single plasmid based CRISPR interference in Synechocystis 6803 – A proof of concept
journal, November 2019


Recent advances in synthetic biology of cyanobacteria
journal, May 2018


Cryopreservation of Synechococcus elongatus UTEX 2973
journal, January 2019


Synthetic Biology Toolkits for Metabolic Engineering of Cyanobacteria
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Cyanobacteria as Chassis for Industrial Biotechnology: Progress and Prospects
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journal, August 2018


Comparative Genomics of DNA Recombination and Repair in Cyanobacteria: Biotechnological Implications
journal, November 2016


Figures/Tables have been extracted from DOE-funded journal article accepted manuscripts.