A Genetic Engineering Toolbox for the Lignocellulolytic Anaerobic Gut Fungus Neocallimastix frontalis

Abstract
Anaerobic fungi are powerful platforms for biotechnology that remain unexploited due to a lack of genetic tools. These gut fungi encode the largest number of lignocellulolytic carbohydrate active enzymes (CAZymes) in the fungal kingdom, making them attractive for applications in renewable energy and sustainability. However, efforts to genetically modify anaerobic fungi have remained limited due to inefficient methods for DNA uptake and a lack of characterized genetic parts. We demonstrate that anaerobic fungi are naturally competent for DNA and leverage this to develop a nascent genetic toolbox informed by recently acquired genomes for transient transformation of anaerobic fungi. We validate multiple selectable markers (HygR and Neo), an anaerobic reporter protein (iRFP702), enolase and TEF1A promoters, TEF1A terminator, and a nuclear localization tag for protein compartmentalization. This work establishes novel methods to reliably transform the anaerobic fungus Neocallimastix frontalis, thereby paving the way for strain development and various synthetic biology applications.
Description
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Synthetic Biology, copyright © 2023 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acssynbio.2c00502. This article will be embargoed until 04/21/2024.
Keywords
anaerobic gut fungi, transformation, parts, protein localization, gene expression, anaerobic reporter
Citation
Hooker, Casey A., Radwa Hanafy, Ethan T. Hillman, Javier Muñoz Briones, and Kevin V. Solomon. “A Genetic Engineering Toolbox for the Lignocellulolytic Anaerobic Gut Fungus Neocallimastix Frontalis.” ACS Synthetic Biology 12, no. 4 (April 21, 2023): 1034–45. https://doi.org/10.1021/acssynbio.2c00502.