Endogenous CRISPR/Cas systems for genome engineering in the acetogens Acetobacterium woodii and Clostridium autoethanogenum

Poulalier-Delavelle, Margaux; Baker, Jonathan P.; Millard, James; Winzer, Klaus; Minton, Nigel P.

doi:10.3389/fbioe.2023.1213236

Endogenous CRISPR/Cas systems for genome engineering in the acetogens Acetobacterium woodii and Clostridium autoethanogenum

Poulalier-Delavelle, Margaux; Baker, Jonathan P.; Millard, James; Winzer, Klaus; Minton, Nigel P.

Authors

Margaux Poulalier-Delavelle

Jonathan P. Baker

JAMES MILLARD James.Millard@nottingham.ac.uk
Research Fellow

KLAUS WINZER klaus.winzer@nottingham.ac.uk
Associate Professor

Professor NIGEL MINTON NIGEL.MINTON@NOTTINGHAM.AC.UK
Professor of Applied Molecular Microbiology

Abstract

Acetogenic bacteria can play a major role in achieving Net Zero through their ability to convert CO2 into industrially relevant chemicals and fuels. Full exploitation of this potential will be reliant on effective metabolic engineering tools, such as those based on the Streptococcus pyogenes CRISPR/Cas9 system. However, attempts to introduce cas9-containing vectors into Acetobacterium woodii were unsuccessful, most likely as a consequence of Cas9 nuclease toxicity and the presence of a recognition site for an endogenous A. woodii restriction–modification (R-M) system in the cas9 gene. As an alternative, this study aims to facilitate the exploitation of CRISPR/Cas endogenous systems as genome engineering tools. Accordingly, a Python script was developed to automate the prediction of protospacer adjacent motif (PAM) sequences and used to identify PAM candidates of the A. woodii Type I-B CRISPR/Cas system. The identified PAMs and the native leader sequence were characterized in vivo by interference assay and RT-qPCR, respectively. Expression of synthetic CRISPR arrays, consisting of the native leader sequence, direct repeats, and adequate spacer, along with an editing template for homologous recombination, successfully led to the creation of 300 bp and 354 bp in-frame deletions of pyrE and pheA, respectively. To further validate the method, a 3.2 kb deletion of hsdR1 was also generated, as well as the knock-in of the fluorescence-activating and absorption-shifting tag (FAST) reporter gene at the pheA locus. Homology arm length, cell density, and the amount of DNA used for transformation were found to significantly impact editing efficiencies. The devised workflow was subsequently applied to the Type I-B CRISPR/Cas system of Clostridium autoethanogenum, enabling the generation of a 561 bp in-frame deletion of pyrE with 100% editing efficiency. This is the first report of genome engineering of both A. woodii and C. autoethanogenum using their endogenous CRISPR/Cas systems.

Citation

Poulalier-Delavelle, M., Baker, J. P., Millard, J., Winzer, K., & Minton, N. P. (2023). Endogenous CRISPR/Cas systems for genome engineering in the acetogens Acetobacterium woodii and Clostridium autoethanogenum. Frontiers in Bioengineering and Biotechnology, 11, Article 1213236. https://doi.org/10.3389/fbioe.2023.1213236

Journal Article Type	Article
Acceptance Date	Jun 6, 2023
Online Publication Date	Jun 23, 2023
Publication Date	Jun 23, 2023
Deposit Date	Aug 30, 2023
Publicly Available Date	Sep 5, 2023
Journal	Frontiers in Bioengineering and Biotechnology
Electronic ISSN	2296-4185
Publisher	Frontiers Media
Peer Reviewed	Peer Reviewed
Volume	11
Article Number	1213236
DOI	https://doi.org/10.3389/fbioe.2023.1213236
Keywords	protospacer adjacent motif (PAM), Clostridium autoethanogenum, endogenous CRISPR/Cas, acetogen, in-frame deletion, Acetobacterium woodii
Public URL	https://nottingham-repository.worktribe.com/output/22990064
Publisher URL	https://www.frontiersin.org/articles/10.3389/fbioe.2023.1213236/full