Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024:2791:1-14.
doi: 10.1007/978-1-0716-3794-4_1.

Callus Induction Followed by Regeneration and Hairy Root Induction in Common Buckwheat

Affiliations

Callus Induction Followed by Regeneration and Hairy Root Induction in Common Buckwheat

Denis O Omelchenko et al. Methods Mol Biol. 2024.

Abstract

This section describes a set of methods for callus induction followed by the successful regeneration of whole plants and obtaining a culture of transgenic hairy roots from buckwheat plants (Fagopyrum esculentum Moench.). Callus induction and regeneration are key steps for many biotechnological, genetic, and breeding approaches, such as genetic modification, production of biologically active compounds, and propagation of valuable germplasm. Induction of hairy roots using Agrobacterium rhizogenes is also an important tool for functional gene research and plant genome modification. While many efforts were invested into the development of the corresponding protocols, they are not equally efficient for different cultivars. Here, we have tested and optimized the protocols of callus induction, regeneration, and transformation using A. rhizogenes for a set of cultivars of F. esculentum, including wild ancestor of cultivated buckwheat F. esculentum ssp. ancestrale and a self-pollinated accession KK8. The optimal medium for callus induction is Murashige-Skoog basal medium with 3% sucrose which includes hormones 2,4-dichlorophenoxyacetic acid 2 mg/L and kinetin 2 mg/L; for shoot initiation 6-benzylaminopurine 2 mg/L, kinetin 0.2 mg/L, and indole-3-acetic acid 0.2 mg/L; for shoot multiplication 6-benzylaminopurine 3 mg/L and indole-3-acetic acid 0.2 mg/L; and for root initiation half-strength Murashige-Skoog medium with 1.5% sucrose and indole-3-butyric acid 1 mg/L. A. rhizogenes R1000 strain proved to be the most efficient in inducing hairy roots in buckwheat and T-DNA transfer from binary vectors. Seedling explants cut at the root area and immersed in agrobacterium suspension, as well as prickling the cotyledonary area with agrobacteria dipped syringe needle, are the most labor-effective methods of infection, allowing to initiate hairy root growth in 100% of explants.

Keywords: Agrobacterium-mediated transformation; Callus; Fagopyrum esculentum; Hairy roots; Plant regeneration.

PubMed Disclaimer

Similar articles

References

    1. Tomasiak A, Zhou M, Betekhtin A (2022) Buckwheat in tissue culture research: current status and future perspectives. Int J Mol Sci 23:2298 - DOI - PubMed - PMC
    1. Srejović V, Nešković M (1981) Regeneration of plants from cotyledon fragments of buckwheat (Fagopyrum esculentum Moench). Zeitschrift für Pflanzenphysiologie 104:37–42 - DOI
    1. Gumerova EA, Galeeva EI, Chuyenkova SA et al (2003) Somatic embryogenesis and bud formation on cultured Fagopyrum esculentum hypocotyls. Russ J Plant Physiol 50:640–645 - DOI
    1. Woo SH, Nair A, Adachi T et al (2000) Plant regeneration from cotyledon tissues of common buckwheat (Fagopyrum esculentum Moench). In Vitro Cell Dev Biol Plant 36:358–361 - DOI
    1. Kojima M, Arai Y, Iwase N et al (2000) Development of a simple and efficient method for transformation of buckwheat plants (Fagopyrum esculentum) using Agrobacterium tumefaciens. Biosci Biotechnol Biochem 64:845–847 - DOI - PubMed

LinkOut - more resources