# Two Optimized Methods for Efficient, Stable and Transient Transformation of Broccoli (Brassica oleracea Var. Italica)

**Authors:** Alberto Coronado-Martín, Alejandro Atarés, Rosa Porcel, Lynne Yenush, José M. Mulet

PMC · DOI: 10.3390/plants15060978 · Plants · 2026-03-22

## TL;DR

The paper introduces two optimized methods for transforming broccoli plants, improving genetic studies and genome editing.

## Contribution

The study provides genotype-specific protocols for stable and transient transformation in broccoli, enhancing functional genomics.

## Key findings

- Optimized organogenic medium supports efficient broccoli regeneration while maintaining diploidy.
- Stable transformation efficiency reached 10.4% in genotype 'S1' and 2.8% in 'Naxos'.
- A transient expression system using protoplasts and electroporation successfully expressed GFP in broccoli.

## Abstract

Broccoli (Brassica oleracea var. italica) is an important crop valued for its nutritional and health-promoting properties, yet its biotechnological improvement is limited by low effectivity and genotype-dependent transformation protocols. The absence of reliable transient expression systems further constrains functional genomics and genome-editing applications. Here, we optimized regeneration and transformation protocols for different broccoli genotypes. Endoreduplication patterns in young tissues were analyzed by flow cytometry to identify suitable explants, and combinations of plant growth regulators were tested to develop an efficient organogenic medium. Stable transformation was achieved via Agrobacterium tumefaciens using nptII and eGFP markers. Cotyledons and hypocotyls up to day 7 showed similar endoreduplication patterns, with abundant 2n cells, but hypocotyls exhibited higher regeneration capacity. The optimized medium supported efficient organogenesis while maintaining diploidy. Transformation efficiency reached 10.4% in ‘S1’ and 2.8% in ‘Naxos’, highlighting genotype dependence. In parallel, a transient expression system was established using cotyledon-derived protoplasts and electroporation-mediated DNA delivery. GFP expression was confirmed through fluorescence microscopy, confocal imaging, and Western blotting. These protocols provide a robust toolkit for broccoli genetic manipulation, facilitating molecular biology studies in the native plant, functional genomics and genome-editing strategies, including CRISPR-based approaches.

## Linked entities

- **Proteins:** NAL1 (Protein NARROW LEAF 1)
- **Species:** Brassica oleracea var. italica (taxon 36774)

## Full-text entities

- **Chemicals:** eGFP (-)
- **Species:** Brassica oleracea var. italica (asparagus broccoli, varietas) [taxon 36774], Agrobacterium tumefaciens (species) [taxon 358]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13030244/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC13030244/full.md

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Source: https://tomesphere.com/paper/PMC13030244