Trans-kingdom conjugation is a phenomenon by which DNA is transferred into a eukaryotic cell by a bacterial conjugal transfer system. Improvement in this method to facilitate the rapid co-cultivation of donor bacterial and recipient eukaryotic cell cultures could make it the simplest transformation method, requiring neither isolation of vector DNA nor preparation of competent recipient cells. To evaluate this potential advantage of trans-kingdom conjugation, we examined this simple transformation method using vector combinations, helper plasmids, and recipient Saccharomyces cerevisiae strains. Mixing donor Escherichia coli and recipient S. cerevisiae overnight cultures (50 μL each) consistently yielded on the order of 101 transformants using the popular experimental strain BY4742 derived from S288c and a shuttle vector for trans-kingdom conjugation. Transformation efficiency increased to the order of 102 using a high receptivity trans-kingdom conjugation strain. In addition, either increasing the amount of donor cells or pretreating the recipient cells with thiols such as dithiothreitol improved the transformation efficiency by one order of magnitude. This simple trans-kingdom conjugation-mediated transformation method could be used as a practical yeast transformation method upon enrichment of available vectors and donor E. coli strains.
Citation: Moriguchi K, Yamamoto S, Ohmine Y, Suzuki K (2016) A Fast and Practical Yeast Transformation Method Mediated by Escherichia coli Based on a Trans-Kingdom Conjugal Transfer System: Just Mix Two Cultures and Wait One Hour. PLoS ONE 11(2): e0148989. doi:10.1371/journal.pone.0148989
Editor: Alvaro Galli, CNR, ITALY
Received: August 22, 2015; Accepted: January 26, 2016; Published: February 5, 2016
Copyright: © 2016 Moriguchi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported in part by JSPS KAKENHI (21510209 and 25660007). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Trans-kingdom conjugation (TKC) enables transfer of a vector DNA cloned and amplified in Escherichia coli into Saccharomyces cerevisiae directly using a bacterial conjugal transfer system based on the Type-4 Secretion System (T4SS). In a donor cell, the transfer starts from a site called the origin of transfer (oriT) located on a TKC vector. Mob proteins nick and disentangle one strand of the vector DNA. Genes for Mob proteins are encoded in either the vector or a helper plasmid. The disentangled liner ssDNA is transferred into a recipient cell via T4SS, which establishes physical contact with the recipient cell and secretes the DNA from the donor. Genes for T4SS are encoded in the helper plasmid [1, 2]. While the influence of TKC on eukaryotic evolution is still controversial , this system is attractive for potential applications to yeast transformation methodology. A recent study of this system showed that the transfer of vector plasmids occurs accurately and allows for the excision of unnecessary DNA vector regions during the transfer . While these characteristics are necessary conditions for developing TKC as a gene introduction method, the system is still insufficient for adoption as a preferred method among researchers.
In previous studies, the TKC reaction was performed on solid, non-selective medium for 5–12 h [3, 4]. Bates et al. later found that a 1-h reaction time is sufficient when combining a vector bearing the IncP1α-type oriT and a helper plasmid with the IncP1α-type conjugal transfer system . Recent studies have further shown that the IncQ-type plasmid vector also transfers quickly, and the reaction is applicable under liquid condition with middle pH buffers [1, 6]. These findings exhibit two potential advantages of TKC-mediated gene introduction: time-saving and simplicity.
When performing transformation reactions with multiple samples, if transformants are consistently obtained, a smaller reaction scale and fewer manipulation steps are generally preferred over high transformation efficiency. Using TKC, a recent study reported that 1 h was sufficient to obtain transformants consistently from a mixture of a minute lump of recipient yeast BY4742 cells and a donor cell suspension (25 μL) containing 3.8 × 106 cfu. However, the experiment used cells in the growing stage, requiring adjustment of the cell concentration, and included a step involving transfer of a donor suspension from its growth medium to a middle pH buffer . A simplified application of the TKC method has not yet been reported.
This study aims to develop a simplified method for the use of TKC. We mixed a small volume of E. coli stationary phase liquid overnight cultures directly with recipient yeast and evaluated transformation efficiency. We propose an improved TKC-mediated transformation method that shows higher transformation efficiency.
Materials and Methods
E. coli and S. cerevisiae strains and plasmids
Donor E. coli strains, recipient S. cerevisiae strains, and the plasmids used in this study are detailed in Table 1. The primary donor strain used was HB101 bearing the vector pAY205, which carries the IncQ-type plasmid RSF1010 backbone, and the helper plasmid pRH210, which carries an IncP1α-type plasmid RK2 (RP4) conjugal transfer system. YNN281α is isogenic with YNN281 except at the mating type locus. The strain is a MATα segregant arising from the diploid strain YNN281a/α, in which diploidy was induced by the homotalism gene HO as described by Suzuki and Yanagishima .
E. coli and S. cerevisiae culture conditions
Donor E. coli strains were cultured in 3 mL of liquid Luria Bertani (LB) broth with appropriate antibiotics overnight (12–15 h) at 37°C. LB+1.5% agar was used alternatively when the donor was inoculated on solid medium. Recipient S. cerevisiae strains were cultured in 3 mL of liquid yeast-extract/peptone/dextrose (YPD) broth for one day (18–22 h) at 28°C. Yeast extract-peptone/adenine/dextrose (YPAD) broth was used alternatively if a recipient strain was auxotrophic for adenine. For cultures used in the adjusted trans-kingdom conjugation reaction, donor E. coli overnight culture (100–150 μL) was inoculated into 3 mL of fresh medium and cultured for 3–4 h to recover cell growth. In parallel, recipient yeast cells were streaked onto fresh YPD+2% agar medium and cultured for 1 day.
Simple trans-kingdom conjugation
Schematic flow of the method is shown on Fig 1. Each 50 μL of donor E. coli and recipient yeast liquid saturated cultures were mixed and incubated for 1 h at 28°C.
For method 1, donor E. coli bearing a vector and recipient S. cerevisiae stationary phase cultures (50 μL each) were mixed. In method 2, the donor E. coli was changed to a solid culture. The donor was picked up with a toothpick and mixed with 50 μL of recipient S. cerevisiae stationary phase culture.
In case of using concentrated donor cells, 500 μL of the donor culture was centrifuged, and then 450 μL of supernatant was removed. The remaining culture of 50 μL was resuspended and was served for TKC reaction. The reaction mix was then gently resuspended, and 25 μL of it was then streaked on a plate with synthetic complete (SC) medium without uracil and incubated at 28°C for three to five days. In parallel, to calculate the recipient cell number included in the reaction, 10 μL of 1000-fold to 4000-fold diluted reaction mix was streaked on a YPD (or YPAD) plate. Appropriate antibiotics were added in each plate.
When donor cells grown on solid LB medium were directly used for TKC, cells were picked by toothpick and suspended in 50 μL of recipient culture. After the TKC reaction, 50 μL of TNB was added to the reaction mixture, and 25 μL of the mixed suspension were streaked on a solid selection plate.
As for dithiothreitol (DTT) treatment, 1 M DTT solution was added into 50 μL of yeast recipient culture at a final concentration of 100 mM and incubated for 30 min at 28°C. After collecting cells by centrifugation, cells were re-suspended in 50 μL of YPD and served for the TKC reaction.
Adjusted trans-kingdom conjugation
The reaction was performed as previously described . Briefly, cells in the growing stage collected from liquid LB and solid YPD (or YPAD if necessary) cultures were used for the donor and recipient, respectively.
Furthermore, 25 μL of TNB buffer (80 mM Tris-HCl [pH 7.5] and 0.05% NaCl) containing 3.8 × 106 cfu of donor and 1.0×106 cfu of recipient were incubated at 28°C for 1 h and plated on selection medium. In case of pretreatment by chemical reagents, recipient cells collected from solid medium were incubated in 50 μL of TNB including each thiol for 1 h at 28°C. The mixture was re-suspended three times during the incubation. After the treatment, cells were collected and suspended with fresh TNB without thiol, and the concentration was adjusted to 1.0 × 106 cfu/12.5 μL by measuring turbidity. Then, 12.5 μL of the thiol treated recipient suspension was mixed with the same volume of the donor suspension containing 3.8 × 106 cfu and TKC reaction was performed. Thiols used in this study were DTT, 2-aminoethanethiol (AET), and 3-mercapto-1, 2-propanediol (MPD) at 100 mM. All chemicals were obtained from Wako Pure Chemical Ind., Ltd. (Osaka, Japan).
Statistical comparison of the transformation efficiency of vector and helper plasmid combinations or strains was performed based on the log10-converted value of each TKC efficiency. This method was used due to the wide range of TKC efficiency observed in trials (S1 Fig). All statistical analyses were performed using either Microsoft Excel or the public domain R program (http://www.r-project.org/). The statistical tests used for data analysis and the number of experimental replicates are shown in figure legends and S1 Table.
Applicability of simple TKC method in various helper, vector, donor, and recipient combinations
Using the vector/helper plasmid combination of pAY205 and pRH210, transformants were consistently obtained from BY4742, a derivative of the widely used experimental strain S288c (Fig 2A). Transformants were produced on the order of 101 per reaction. The range of transformants per reaction was 4–272 over 16 experiments using this vector and helper combination (S1 Table).
(A) Evaluation of the transformation method with various donors. pAY205 and pRS316oriT (represents pRS316::oriTP) are TKC vectors. pRH210, pDPT51, and pRH220 are helper plasmids. Host E. coli strains are shown at the bottom. (B) Evaluation of the transformation method with various recipients. Recipient S. cerevisiae strains are shown under the value bars, and the vector and helper combination is shown at the bottom. HB101 served as the host. The far left lane, shown as “BY4742,” is from the same data set used in Fig 2A. (C) Evaluation of the transformation method between liquid- and solid-cultured donors. Lanes labeled “liquid” represent results obtained by “Method 1” in Fig 1; data set is the same as that used in Fig 2A. Lanes labeled as “solid” represent results obtained by “Method 2” in Fig 1. The vector and helper combination is shown at the bottom. HB101 served as the host. White bars represent Log10 converted value of transformants/reaction, and the scale is shown on the left side of each graph as “Log (transformants)”. Gray bars represent the Log10 converted value of transformation efficiency (transformants/recipient cells), and the scale is shown on the right side of each graph as “Log (TKC effi)”. Data are represented as the mean ± SD. Number of trials of each experiment are shown in S1 Table. Asterisks indicate statistically significant differences in two-tailed t-test: *p < 0.05, **p < 0.01, and ***p < 0.001.
This method was also successful using pDPT51, which carries the IncP1β-type plasmid R751 conjugal transfer system, in place of the helper plasmid and using the vector pRS316::oriTP carrying the IncP1α-type origin of transfer (oriTP) and another IncP1α helper plasmid pRH220 derived from the RK2 plasmid, demonstrating the broad applicability of this method (Fig 2A). While there was no statistically significant difference between the IncP1α (pRH210) and IncP1β (pDPT51) helper plasmids, the pRS316::oriTP (IncP1α) vector demonstrated a higher transformation efficiency than the pAY205 (IncQ) vector. This tendency was also observed using another recipient strain, YNN281α (S1 Table).
To know the preference of donor strain, two E. coli strains were examined in addition to HB101. DH10B is a commercial strain and is widely used as well as HB101. S17-1 λpir has been used as a donor strain for bacterial conjugation experiments  and is available from several bioresource banks. In this strain, conjugal transfer system genes of the RK2 plasmid are integrated into the host chromosome. Thus, if this strain shows constant TKC activity, use of a helper plasmid is not required.
As shown in Fig 2A and S1 Table, pRS316::oriTP was successfully introduced into BY4742 from these two strains, although the transformation efficiency was lower than that of HB101 by one order of magnitude. pAY205 was also successfully introduced from the S17-1 λpir donor, but the transfer was below the detection threshold in a trial (S1 Table).
Of several yeast strains transformed using this simple TKC method, YNN281α possessing a defective allele (ssd1-d) in TKC blocking  had the highest transformation efficiency, regardless of the vector/helper combination (Fig 2B, S1 Table). This strain consistently yielded on the order of 102 transformants per reaction (100 μL), and the maximum number of transformants per reaction was 3692 using pAY205 and pDPT51. This simple method was also applicable to other strains of S. cerevisiae, which were derivatives of wild and industrial strains. NCYC3623 (Fig 2B), NCYC3625, and NCYC3630 yielded TKC transformants on the order of 101 to 102. NCYC3627 and NCYC3631 also yielded transformants, although they did not yield consistently at this 100 μL reaction scale (S1 Table).
Modification of the TKC method for further simplification or higher transformation efficiency
We reasoned that if donor E. coli samples grown on solid medium from frozen stocks could be used directly in recipient yeast suspensions for the TKC reaction, this method would be more practical for multi-sample use. To test the feasibility of this method, donor E. coli samples were picked up from solid medium with a toothpick and mixed with 50 μL of recipient suspension (in Fig 1, Method 2). The donor successfully transformed the recipients on the order of 101 (Fig 2C). pRS316::oriTP yielded a higher transformation efficiency than pAY205, as was observed in liquid donors, although this difference was not statistically significant. The donor cells from solid medium showed lower transformation efficiency by one order of magnitude.
We next tried to increase the transformation efficiency of this system by modifying the preparation method used for either donor or recipient cells.
In our previous studies, the basal level of TKC efficiency was adjusted via the number of donor cells to screen recipient mutants with high and low TKC efficiencies [1, 6]. In the course of these studies, we checked that the transformation efficiency increased with an increasing number of donor cells, at least up to the donor:recipient ratio of 50:1. In the simple TKC method, the ratio was approximately 10:1 to 15:1. Thus, we increased the number of donor cells ten times by concentrating the donor cell cultures. The transformation efficiency increased about 30-fold in the low TKC efficiency donor strains (DH10B and S17-1 λpir), and the efficiency was higher than that of HB101 donor transformation using the standard TKC method (Fig 3A). This result shows that these strains are sufficient for practical use if cultures are concentrated before the TKC reaction.
(A) Effect of increasing the number of donor E.coli on TKC-mediated transformation. Lanes labeled “1×” represent results obtained using standard number of donor cells (same data sets as Fig 2A); and lanes labeled “10×” represent results obtained using 10 times the number of donor cells. Host strains are indicated at the bottom. pRS316::oriTP was used as the TKC vector, and pRH220 was used as the helper plasmid in DH10B. White bars, log10 converted value of transformants/reaction; Gray bars, log10 converted value of transformation efficiency (transformants/recipient cells). Data are presented as mean ± SD. Number of trials of each experiment is shown in S1 Table. (B) Effect of thiol treatment of recipient yeast on TKC-mediated transformation. Lanes labeled as “DTT,” “AET” and “MPD” indicate recipient yeast samples pretreated with dithiothreitol, 2-Aminoethanethiol, and 3-Mercapto-1,2-propanediol, respectively. Lanes labeled as “Control” indicate non-treated controls. Control 1 is the same data set used in Fig 2A (dark gray bar). Control 2 (light gray bar), Control 3 and Control 4 (white bars) are control data sets treated in parallel with DTT 1 (light gray bar), DTT 2 through MPD (white bars) and DTT 3 (white bar), respectively. Methods and donor cells are shown at the bottom of the figure. Data are presented as the mean ± SD (Control 1, n = 16; Control 2 and DTT 1, n = 4; Control 3 through DTT 3, n = 3). Control 2 vs. DTT 1 and Control 3 vs. DTT 2, AET, and MPD showed a statistically significant difference at p < 0.05 (two-tailed t-test). The combination of host strain, vector, and helper is shown at the bottom. Asterisks indicate statistically significant differences: *p < 0.05 and **p < 0.01 (two-tailed t-test).
According to previous studies, pretreatment of recipient cells with thiols can increase the transformation efficiency in both chemical and electroporation methods [11, 12]. Although the precise mechanism of the influence of thiols on yeast cells is not clear, an increase in cell permeability in the presence of thiols has been reported . If T4SS of RK2 plasmid does not penetrate the plasma membrane of recipient yeast cells, thiol treatment is expected to positively affect TKC efficiency. Examining this possibility, we observed that using a 30-min treatment with dithiothreitol (DTT) added directly into the recipient cultures increased the transformation efficiency 3-fold over that of non-treated controls (Fig 3B, lanes Control 2 vs. DTT 1). However, compared to another non-treated control data set including results from other independent experiments, the transformation efficiency of this method was two-fold higher without statistical significance (lanes Control 1 vs. DTT 1). To further examine the effect of thiols, we used three different thiols (DTT, 2-Aminoethanethiol [AET] and 3-Mercapto-1,2-propanediol [MPD]) using the adjusted TKC method. As shown on Fig 3B, all thiols examined increased the transformation efficiency by one order of magnitude, a statistically significant difference over that of non-treated controls (lanes Control 1, 2, and 3 vs. DTT 2 to MPD). There was no statistically significant difference in this effect between thiols. DTT treatment of the recipient cells provided sufficient transformation efficiency using S17-1 λpir to warrant the use of this strain (lanes Control 4 vs. DTT 3).
Our results demonstrate that TKC shuttle vectors can be easily introduced into yeast by simply mixing E. coli and S. cerevisiae cultures at stationary phase, providing a simple, timesaving method. From another perspective, this result also indicates that trans-kingdom horizontal DNA transfer may have occurred more frequently in the natural environment than predicted, as we suggested previously .
In eukaryotic genetics, changing a recipient phenotype by gene introduction is generally called as “transformation,” and “conjugation” means the act of pairing a male and female for reproductive purposes. For these reasons, the term “transformation” is used in this report. Based on bacterial genetics, however, it might be better to use “conjugation” because TKC is driven by a bacterial conjugal transfer system, and because the gene transfer machinery is more strictly classified into three groups, transformation, conjugation, and transduction.
Transformation of S. cerevisiae using lithium acetate (LiAc) has been the most commonly used method since it was first reported by Ito et al. , and various modified methods have been established, including a simple method . The LiAc method can transform intact cells without preparing protoplasts. However, it still requires several steps and reagents for both preparation of vector DNA and the transformation itself. The TKC-mediated transformation method reported here is simpler, requiring only the mixing of a small volume of donor and recipient cultures directly. This method would be particularly advantageous for screening a large number of samples, as with interactome analysis using a yeast two-hybrid (Y2H) system. High receptivity strains may be preferred for this purpose, although the TKC method is applicable to a variety of yeast strains (Fig 2B; S1 Table). The introduction of an SSD1 gene knock out mutation in the EGY48 strain, which is often used for Y2H, successfully converted this strain into a high receptivity strain .
The simplified TKC method could also be used for yeast strains that are sensitive to heat shock and/or chemical reagents such as polyethylene glycol. This TKC method is a recipient-friendly method because it does not lead to cell death . Mutants for decreased transformation efficiency induced by TKC are not the same as those induced by chemical transformation methods [6, 16]. These methods may thus compensate for each other’s defects. The TKC method requires dedicated vectors that include an oriT (or oriT/mob) region and donor bacterial strains with T4SSs to mobilize the vectors. Most importantly, this method is never applicable when a DNA fragment is intended to be introduced directly into recipient cells.
Improving transformation efficiency is desirable for any transformation method. To make the best use of TKC-mediated yeast transformation, methods for increasing transformation efficiency should not increase the complexity of the procedure. We successfully achieved an increase in the transformation efficiency either by increasing the amount of donor cells or by treating recipient cells with thiols (Fig 3). The former will be more preferentially applied in practical use because it adds only one step on the simplest method and is easily applicable to large sample number experiments. The use of thiols also keeps the procedure simpler than that of other transformation methods. In our previous study, we observed that the addition of mitochondrial function inhibitors to a solid medium increased the competence of recipient yeast . Accordingly, we added erythromycin along with DTT to liquid yeast medium to determine the effects on transformation efficiency. No clear synergistic effect was observed in our preliminary data (data not shown). Clues as to the improvement of transformation efficiency may be obtained from functional analysis of low and high TKC receptivity mutants isolated previously [1, 6].
Another remaining plan to improve this method is to enrich the vector content and make it available non-commercially. Our TKC vectors, with several prototrophic markers, for Y2H have been deposited in a public bioresource bank (NBRP-Yeast, http://yeast.lab.nig.ac.jp/nig/index_en.html, ID: BYP7570-7577). We hope that these vectors will be used, further improved, and deposited by participants.
The trans-kingdom conjugation-mediated transformation method described here may be the simplest, most practical yeast transformation method. This method is also low-cost and timesaving. To be accepted as a general method, enrichment of TKC vectors and donor E. coli strains is critically important.
S1 Fig. Distribution of transformation efficiency in chemical and TKC transformation experiments.
S1 Table. Summary of results of a simple TKC-mediated transformation method.
We thank National Bio-Resource Project (NBRP) of the Ministry of Education, Culture, Sports, Science and Technology in Japan for providing E. coli strain S17-1 λpir. The helper plasmid pDPT51 was kindly provided by Dr. Y. Fujita (Graduate School of Bioagricultural Science, Nagoya University). This work was supported in part by JSPS KAKENHI (21510209 and 25660007). We also thank Satoko Kagei for the excellent technical assistance.
Conceived and designed the experiments: KM SY KS. Performed the experiments: KM. Analyzed the data: KM. Contributed reagents/materials/analysis tools: KM KS YO. Wrote the paper: KM YO.
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