Autologous DNA mobilization and multiplication expedite natural products discovery from bacteria
The transmission of antibiotic-resistance genes, comprising mobilization and relocation events, orchestrates the dissemination of antimicrobial resistance. Inspired by this evolutionarily successful paradigm, we developed ACTIMOT, a CRISPR-Cas9-based approach to unlock the vast chemical diversity concealed within bacterial genomes. ACTIMOT enables the efficient mobilization and relocation of large DNA fragments from the chromosome to replicative plasmids within the same bacterial cell. ACTIMOT circumvents the limitations of traditional molecular cloning methods involving handling and replicating large pieces of genomic DNA. Using ACTIMOT, we mobilized and activated four cryptic biosynthetic gene clusters from <i>Streptomyces</i>, leading to the discovery of 39 compounds across four distinct classes. This work highlights the potential of ACTIMOT for accelerating the exploration of biosynthetic pathways and the discovery of natural products.
Authors
- Chengzhang Fu (ORCID: https://orcid.org/0000-0002-3513-4768)
- Xiaoyi Wei (ORCID: https://orcid.org/0000-0002-4053-6999)
- Haowen Zhao (ORCID: https://orcid.org/0009-0006-4479-9581)
- Markus Neuber
- Jiaqi Liu (ORCID: https://orcid.org/0009-0007-6402-6428)
- Rolf Müller (ORCID: https://orcid.org/0000-0002-1042-5665)
- Jennifer E. Herrmann (ORCID: https://orcid.org/0000-0003-3398-9938)
- Xiao-Li Yang (ORCID: https://orcid.org/0009-0001-6695-7636)
- Amninder Kaur (ORCID: https://orcid.org/0009-0007-4369-5892)
- Olga V. Kalinina (ORCID: https://orcid.org/0000-0002-9445-477X)
- Feng Xie
- Amay Ajaykumar Agrawal
Institutions
- Chinese Academy of Sciences (CN)
- German Center for Infection Research (DE)
- Institut für Sozialforschung und Sozialwirtschaft (DE)
- South China Botanical Garden (CN)
- Helmholtz Centre for Infection Research (DE)
- Helmholtz Institute for Pharmaceutical Research Saarland (DE)
- Saarland University (DE)
Publication Details
- Journal
- Science
- Published
- 2024-12-12
- DOI
- https://doi.org/10.1126/science.abq7333
- Citations
- 24
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 5.61