Golden EGG, a simplified Golden Gate cloning system to assemble multiple fragments

The Golden Gate method is an efficient tool for seamless assembly of multiple DNA fragments, which uses Type IIS restriction endonucleases, cleaving the DNA outside of their recognition site to release DNA parts from PCR fragments or entry clones, thus allowing the design of overhangs for ligation at will. However, the construction of the entry clones requires the use of other restriction enzyme(s) or cloning techniques and different entry vectors for the individual overhangs. Here, we present a simplified Golden Gate cloning approach termed Golden EGG. It features (1) a single entry vector with a specific cloning site to host the DNA parts; (2) a unique primer design to create the restriction enzyme recognition site to release the fragments with the overhangs at will; (3) the use of a single Type IIS enzyme for the construction of both the entry and destination clones; (4) a specific temperature profile during the digestion-ligation reaction. Our user-friendly, streamlined method retains the key attributes of the Golden Gate technique, while offering the potential to generate compatible parts with any existing Golden Gate toolkit and to be accessible to a wide user base without the need for extensive acquisition of new vectors or expensive enzymes.

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Publication Details

Journal
Scientific Reports
Published
2024-10-25
DOI
https://doi.org/10.1038/s41598-024-77327-4
Citations
4
Primary Topic
Microbial Metabolic Engineering and Bioproduction
Type
article
Field-Weighted Citation Impact
0.94

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article

Golden EGG, a simplified Golden Gate cloning system to assemble multiple fragments

Zita Szegletes, Attila Kereszt, János Barnabás Biró, Berivan Güngör et al.
4 citations
Scientific Reports
Microbial Metabolic Engineering and Bioproduction
0.94
article

Golden EGG, a simplified Golden Gate cloning system to assemble multiple fragments

Zita Szegletes, Attila Kereszt, János Barnabás Biró, Berivan Güngör, Ting Wang, Péter Kaló, Kristóf Kecskés
article en
4 citations

Abstract

The Golden Gate method is an efficient tool for seamless assembly of multiple DNA fragments, which uses Type IIS restriction endonucleases, cleaving the DNA outside of their recognition site to release DNA parts from PCR fragments or entry clones, thus allowing the design of overhangs for ligation at will. However, the construction of the entry clones requires the use of other restriction enzyme(s) or cloning techniques and different entry vectors for the individual overhangs. Here, we present a simplified Golden Gate cloning approach termed Golden EGG. It features (1) a single entry vector with a specific cloning site to host the DNA parts; (2) a unique primer design to create the restriction enzyme recognition site to release the fragments with the overhangs at will; (3) the use of a single Type IIS enzyme for the construction of both the entry and destination clones; (4) a specific temperature profile during the digestion-ligation reaction. Our user-friendly, streamlined method retains the key attributes of the Golden Gate technique, while offering the potential to generate compatible parts with any existing Golden Gate toolkit and to be accessible to a wide user base without the need for extensive acquisition of new vectors or expensive enzymes.

Scientific ReportsVol. 14(1)
Magyar Agrár- és Élettudományi Egyetem (HU), University of Szeged (HU), HUN-REN Szegedi Biológiai Kutatóközpont (HU), Institute of Genetics (HU), Northwest A&F University (CN)
National Research, Development and Innovation Office
Openalex Percentile: Top 25%
Microbial Metabolic Engineering and Bioproduction
0.94
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Golden EGG, a simplified Golden Gate cloning system to assemble multiple fragments — Zita Szegletes, Attila Kereszt, et al. · Scientific Reports (2024) | TGRS Research Map | TGRS