A membrane-free spot-plating protocol for Agrobacterium-mediated transformation of diverse yeasts

Agrobacterium -mediated transformation (AMT) is a critical method for genetic manipulation of non-model fungi, yet it remains a laborious and inefficient technique. When co-cultured in acetosyringone-supplemented induction medium, Agrobacterium transfers DNA directly into yeast cells using its virulence machinery. Membrane filters are commonly used to support the co-culture of yeast and Agrobacterium on agar plates, however some reports demonstrate that these filters are unnecessary for specific yeast species. Here we confirm across diverse budding yeasts that membrane filters are not necessary for effective AMT. Concentrating the cells via centrifugation and “spotting” the cell pellet directly onto the induction medium proved effective. This reduces hands-on time to 15 minutes and eliminates filter cost. In the oleaginous basidiomycete yeast, Rhodotorula toruloides , this simplified method increases transformation efficiency by 66% to 2,500 transformants per 10 6 recipient cells. We further optimized the Agrobacterium : Rhodotorula cell ratio and culture resuspension volume to achieve more than 200,000 CFU per transformation representing a 2–3 fold improvement over previously implemented protocols. This spot-plating method was successfully applied to seven yeast species of a distantly related phylum, Ascomycota, including one for which genetic transformation has not previously been reported, Botryozyma nematodophila. This approach highlights the broad applicability of the spot-plating method across diverse yeast systems. Furthermore, this method could facilitate high-throughput transformation workflows that are critical for genome-scale functional studies.

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Publication Details

Journal
PLoS ONE
Published
2026-10-08
DOI
https://doi.org/10.1371/journal.pone.0359072
Primary Topic
Fungal and yeast genetics research
Type
article
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article

A membrane-free spot-plating protocol for Agrobacterium-mediated transformation of diverse yeasts

Matthew R. Incha, Amy Lanctot, John M. Gladden, Valentina Elizabeth Garcia et al.
PLoS ONE
Fungal and yeast genetics research
article

A membrane-free spot-plating protocol for Agrobacterium-mediated transformation of diverse yeasts

Matthew R. Incha, Amy Lanctot, John M. Gladden, Valentina Elizabeth Garcia, Patrick M. Shih, Paul Adamczyk, Robin A. Herbert, Matthew J. Szarzanowicz, Gina M. Geiselman, Di Liu, Mitchell G. Thompson
article en

Abstract

Agrobacterium -mediated transformation (AMT) is a critical method for genetic manipulation of non-model fungi, yet it remains a laborious and inefficient technique. When co-cultured in acetosyringone-supplemented induction medium, Agrobacterium transfers DNA directly into yeast cells using its virulence machinery. Membrane filters are commonly used to support the co-culture of yeast and Agrobacterium on agar plates, however some reports demonstrate that these filters are unnecessary for specific yeast species. Here we confirm across diverse budding yeasts that membrane filters are not necessary for effective AMT. Concentrating the cells via centrifugation and “spotting” the cell pellet directly onto the induction medium proved effective. This reduces hands-on time to 15 minutes and eliminates filter cost. In the oleaginous basidiomycete yeast, Rhodotorula toruloides , this simplified method increases transformation efficiency by 66% to 2,500 transformants per 10 6 recipient cells. We further optimized the Agrobacterium : Rhodotorula cell ratio and culture resuspension volume to achieve more than 200,000 CFU per transformation representing a 2–3 fold improvement over previously implemented protocols. This spot-plating method was successfully applied to seven yeast species of a distantly related phylum, Ascomycota, including one for which genetic transformation has not previously been reported, Botryozyma nematodophila. This approach highlights the broad applicability of the spot-plating method across diverse yeast systems. Furthermore, this method could facilitate high-throughput transformation workflows that are critical for genome-scale functional studies.

PLoS ONEVol. 21(10)
Lawrence Berkeley National Laboratory (US), Sandia National Laboratories California (US), Sandia National Laboratories (US), Innovative Genomics Institute (US), CSIRO BioFoundry, Joint BioEnergy Institute (US)
Openalex Percentile: Top 22%
Fungal and yeast genetics research
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