# Engineering Industrial Strain of Acremonium chrysogenum for Deacetoxycephalosporin C Overproduction Using CRISPR/Cas9

**Authors:** Zhiping Hou, Mengliu Peng, Xiaozhi Ju, Yaqi Sun, Liping Du, Ye Liang, Shu-Shan Gao

PMC · DOI: 10.3390/antibiotics15020202 · Antibiotics · 2026-02-12

## TL;DR

Researchers used CRISPR/Cas9 to create a high-yield strain of Acremonium chrysogenum for making a key antibiotic precursor, DAOC, in a single step.

## Contribution

A single-step CRISPR/Cas9 method for simultaneous gene deletion and overexpression in industrial A. chrysogenum strains.

## Key findings

- The edited strain achieved a DAOC titer of 12.4 ± 0.2 g/L, suitable for industrial production.
- The method improved DAOC production compared to the initial strain (7.2 ± 0.22 g/L).
- CRISPR/Cas9 offers a strategy for enhancing other cephalosporin precursor production.

## Abstract

Background: The fungus Acremonium chrysogenum is crucial for producing cephalosporin antibiotics. While CRISPR/Cas9 has been developed for this species, it has not been applied to first-line industrial strains, to the best of our knowledge. For example, engineering industrial A. chrysogenum for overproducing deacetoxycephalosporin C (DAOC, an important precursor for clinically used cephalosporin antibiotics) is currently often a multi-step and inefficient process. Methods: Here, we applied CRISPR/Cas9 to create a DAOC overproducer in a single step. Our method uses a donor template to simultaneously delete and overexpress genes, offering a simple, efficient, and time-saving solution. Results: Furthermore, through methodological optimization, the final homozygous multigene-edited strain achieved an industrial-scale DAOC titer of 12.4 ± 0.2 g/L, representing a significant improvement over the initial edited strain (7.2 ± 0.22 g/L). Conclusions: This demonstrates that CRISPR/Cas9 can effectively edit industrial A. chrysogenum, providing a strategy to enhance the production of other cephalosporin precursors.

## Linked entities

- **Chemicals:** deacetoxycephalosporin C (PubChem CID 160139), cephalosporin antibiotics (PubChem CID 25058126)

## Full-text entities

- **Diseases:** DAOC (OMIM:211750), cytotoxicity (MESH:D064420), injury to (MESH:D014947)
- **Chemicals:** thiazolidine (MESH:D053778), sucrose (MESH:D013395), cefradine (MESH:D002515), isopenicillin N (MESH:C006414), PEG (MESH:C000595215), glucose (MESH:D005947), H (MESH:D006859), KCl (MESH:D011189), beta-lactam (MESH:D047090), penicillin (MESH:D010406), cephalexin (MESH:D002506), DAOC (MESH:C025578), K (MESH:D011188), soybean oil (MESH:D013024), maltose (MESH:D008320), DAOC-2, 3, 4 (-), avermectin (MESH:C019264), 7-ADCA (MESH:C014320), MgSO4 (MESH:D008278), glufosinate (MESH:C003121), cephalosporin (MESH:D002511), DCPC (MESH:C025071), water (MESH:D014867), CPC (MESH:C025163), NaOH (MESH:D012972), erythromycin (MESH:D004917), CaCl2 (MESH:D002122), formic acid (MESH:C030544), MgCl2 (MESH:D015636), CaCO3 (MESH:D002119), acetonitrile (MESH:C032159), hygromycin (MESH:C026273), agar (MESH:D000362), K2HPO4 (MESH:C013216), nitrogen (MESH:D009584)
- **Species:** Sphingomonas dokdonensis (species) [taxon 344880], Saccharopolyspora erythraea (species) [taxon 1836], Mycobacteroides abscessus (species) [taxon 36809], Homo sapiens (human, species) [taxon 9606], Streptomyces clavuligerus (species) [taxon 1901], Streptomyces avermitilis (species) [taxon 33903], Penicillium chrysogenum (species) [taxon 5076], Aspergillus nidulans (species) [taxon 162425], Arachis hypogaea (goober, species) [taxon 3818], Streptococcus pyogenes (species) [taxon 1314], Escherichia coli (E. coli, species) [taxon 562], Hapsidospora chrysogena (species) [taxon 5044], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]
- **Cell lines:** pDC-1 — Mus musculus (Mouse), Conditionally immortalized cell line (CVCL_RX86), DAOC — Mus musculus (Mouse), Finite cell line (CVCL_S361), -3 — Mus musculus (Mouse), Hybridoma (CVCL_C6V6), DH5alpha — Drosophila hydei (Fruit fly), Spontaneously immortalized cell line (CVCL_Z531), DAOC-4 — Mus musculus (Mouse), Hybridoma (CVCL_J640), -4 — Homo sapiens (Human), Ataxia telangiectasia syndrome, Finite cell line (CVCL_F083), Mc-1 — Mus musculus (Mouse), Hybridoma (CVCL_C7H9), DAOC-5 — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_M132), DAOC-1 — Pan troglodytes (Chimpanzee), Induced pluripotent stem cell (CVCL_1G30)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938259/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938259/full.md

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Source: https://tomesphere.com/paper/PMC12938259