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Electronic Journal of Biotechnology

versión On-line ISSN 0717-3458

Electron. J. Biotechnol. v.11 n.1 Valparaíso ene. 2008


Molecular Biology and Genetics

Plant Biotechnology

Electronic Journal of Biotechnology ISSN: 0717-3458 Vol. 11 No. 1, Issue of January 15, 2008
© 2007 by Pontificia Universidad Católica de Valparaíso -- Chile Received January 26, 2007 / Accepted May 4, 2007
DOI: 10.2225/vol11-issue1-fulltext-1 How to reference this article

Multiple pulses improve electroporation efficiency in Agrobacterium tumefaciens

Tariq Mahmood#
Department of Plant Sciences
Quaid-i-Azam University
Islamabad, Pakistan
Tel: 92 51 4845 623
Fax: 92 51 9290 160

Tamkina Zar
Department of Plant Sciences
Quaid-i-Azam University
Islamabad, Pakistan
Tel: 92 51 4845 623
Fax: 92 51 9290 160

S.M. Saqlan Naqvi*
Department of Biochemistry
University of Arid Agriculture Rawalpindi
Murree Road, Rawalpindi, 46300, Pakistan
Tel: 92 51 4845 623
Fax: 92 51 9290 160

*Corresponding author

Financial support: This study was supported by a grant No. 01-03-01-19 from Agricultural Linkages Program of the Pakistan Agricultural Research Council.

Present address: #Department of Plant Sciences, Quaid-i-Azam University, Islamabad, Pakistan.

Keywords: Agrobacterium, electroporation, pulse number, transformation efficiency.


Kb: Kilo base pair
LB: Luria Bertani
PCR: polymerase chain reaction

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Electroporation entails brief, high intensity pulse to create transient pores in the cell membrane to facilitate the entry of exogenous macromolecules, which may otherwise be excluded. Removal of the external field leads to the resealing of the membrane electropores permitting the survival of the electrically stimulated recipient cells. Using this technique foreign deoxyribonucleic acid (DNA) has been successfully introduced into many cell types both from prokaryotes and eukaryotes. Increase in pulse voltage and length beyond a critical limit has been reported to decrease transformation efficiency, hence in this study we have investigated another strategy i.e. increase in the number of pulses at constant high voltage and pulse duration. Commonly used Agrobacterium strains LBA4404 and EHA101 and binary vector pCAMBIA1301 were used. Transformants were selected on a combination of hygromycin and kanamycin, and confirmed by polymerase chain reaction (PCR) and restriction analysis. Increase in the number of pulses was found to show a significant and linear increase in transformation efficiency.

Materials and Methods

  • Competent cell preparation
  • Viability testing
  • Transformation of EHA101 and LBA4404
  • Confirmation of transformation
    Results and Discussion
  • Confirmation of transformation by PCR and restriction digestion
  • Comparison of cell viability
  • Comparison of transformation efficiencies
    Figure 1
    Figure 2
  • Application of deoxyribonucleic acid (DNA) technology to genetically manipulate cellular functions requires a suitable high efficiency transformation system. There are many approaches available for introducing foreign DNA into eukaryotic and prokaryotic cells, however electroporation is the most commonly used technique and currently of more practical interest. It is a gene transfection technique, which entails brief, high intensity pulse to facilitate the entry of exogenous molecules like DNA, ribonucleic acid (RNA), and protein. Removal of the external field leads to the resealing of the membrane electropores.

    Applying high intensity electric fields to reversibly permeablize biomembranes to create structural distortions, allowing the uptake of DNA was first demonstrated by Neuman in mouse myeloma cells (Neuman et al. 1982). Since then it has been used as a routine transformation technique. Rhee et al. (2007) have reported that in Bacillus coagulans transformation, electroporation is a better option than using chemical transformation protocols mediated by high Ca2+/Mg2+. There are different reports about the manipulations of electroporation conditions for increasing the transformation efficiency. Turgeon et al. (2006) evaluated the influence of modulating growth cycle, electric field and amino acid composition (glycine and threonine) to elaborate an electro-transformation procedure for Bacillus cereus to yield 2 x 109 cfu/μg/ml. Increase in transformation efficiency in response to electric field strength, pulse length, DNA quality and cell density has been documented (Myers and Tisa, 2003; Chen et al. 2006; Rodríguez et al. 2007). In another study, a method has been investigated to temporarily inactivate the host cell restriction machinery by heat treatment of the cells prior to electroporation to enable efficient transformation of Staphylococcus carnosus (Löfblom et al. 2007). Earlier, Gowrishankar et al. (1999) have characterized the effects of high voltage electric fields on the barrier properties of human skin resulting in structural changes by using high voltage pulses through exponential pulser (Electroporation System 600, BTX Industries, San Diego, CA).

    With the advancement of plant biotechnology, Agrobacterium-mediated transformation has gained enough momentum, as it is relatively inexpensive, well-studied, simple technique manipulated from a natural process. However, in few studies (Shen and Forde, 1989; Mersereau et al. 1990) very limited work has been reported for improving electroporation efficiency of A. tumefaciens. The fact that electroporation efficiency is still much lower in Agrobacterium than E. coli indicates the need for further studies. Mersereau et al. (1990)  reported the effect of voltage and Shen and Forde (1989) investigated both pulse voltage and length, while in this study we have analyzed the effect of multiple electric pulses on electroporation efficiency in Agrobacterium. The results of this study indicate that increase in number of electric pulses can improve the electroporation efficiency in A. tumefaciens.

    Materials and Methods

    Competent cell preparation

    A single colony of either EHA101, LBA4404 was picked up and cultured overnight in 5 ml Luria Bertani (LB) broth (Tryptone 10 g/L, Yeast extract 5 g/L, NaCl 10 g/L, pH 7.0) at 28ºC with 250 rpm shaking. Three ml of this culture was shifted to 1L LB medium, and incubated at 28ºC with 250 rpm until the A600 was about 0.5. The culture was centrifuged at 3500 x g for 15 min at 4ºC. The pellet was resuspended/washed with 15% glycerol in Nanopure water. After washing the bacteria were again pelleted. All the steps were performed on ice. This process of washing was repeated thrice. After final washing the pellet was divided into 50-100 μl aliquots and stored at -80ºC.

    Viability testing

    For the analysis of cell viability suitable dilutions of competent cells were spread on LB plate (Tryptone 10 g/L, Yeast extract 5 g/L, NaCl 10 g/L, Agar 10 g/L, pH 7.0) for counting number of cells. Similar procedure was adopted for counting cell viability after every electric pulse. Colony forming units were recorded for later comparisons.

    Transformation of EHA101 and LBA4404

    For electroporation 25 µl competent cells of the Agrobacterium strains (EHA101 or LBA4404) were suspended between two electrodes spaced by 0.15 cm. Electroporation was carried out with an electric pulse of 20.0 kV/cm and pulse length of ~10 ms (Cell-Porator® by Life Technologies). Number of high voltage pulses ranged from 1 to 5 for each strain, with ~15 seconds inter-pulse duration. After each transformation the bacterial cells were resuscitated by suspending in 1 ml of liquid LB media and subsequent incubation at 28ºC with 250 rpm shaking, before spreading on the LB plates. In all transformation experiments pCAMBIA1301 was used for electroporation. Screening of different transformants was performed on LB medium containing 50 µg/ml kanamycin and 50 µg/ml hygromycin.

    Confirmation of transformation

    Plasmid was isolated from positive clones. Polymerase chain reaction (PCR) was carried out to confirm the transformation using plasmid DNA as template and a pair of primers designed in sequence of hygromycin gene present on pCAMBIA1301. The PCR conditions used for the amplification of 700 bp fragment included, a PAD (Pre Amplification Denaturation) at 94ºC for 5 min followed by 35 cycles at 94ºC for 45 sec, 52ºC for 45 sec and 72ºC for 50 sec, with a final extension at 72ºC for 20 min.



    PCR results were further confirmed by restriction digestion using XhoI. Data were analyzed by one way ANOVA.

    Results and Discussion

    The term electroporation is used to describe the phenomenon that accompanies exposure of cells to transmembrane electrical pulses. Electroporation yields reversible and irreversible permiabilization of the cell membrane as a function of electrical pulse voltage parameters i.e. amplitude, length, shape of the pulse, and cell type and developmental stage. Since the first report on gene transfer by electroporation (Neuman et al. 1982), it has become a standard method for transfection of cells (Hapala, 1997). Electroporation has several advantages. It is technically simple, can be used to treat whole population of cells, has broad application for transfer of any macromolecule, provides greater efficiency of transfection for many cell lines, and can be applied equally successfully to prokaryotic and eukaryotic cells (Lurquin, 1997). Nevertheless, it needs to empirically determine through extensive studies, the conditions for efficient transfection for each cell type (Andreason, 1993). There are few reports about electroporation mediated transformation of Agrobacterium, despite the fact that it has gained tremendous importance for being a natural genetic engineer of plants and is being used very effectively for plant transformation for the nearly three decades. Keeping in view the importance and efficiency of this simple plant transformation system, this study was designed to improve electroporation mediated DNA uptake in Agrobacterium.

    Confirmation of transformation by PCR and restriction digestion

    In this study the commonly used strains of Agrobacterium tumefaciens (LBA4404 and EHA101) were used. Competent cells of these strains were transformed by pCAMBIA 1301 (11.8 kb) in cell porator. Plasmid uptake was confirmed by PCR and restriction digestion of the isolated plasmid. PCR generated a 700 bp fragment from hygromycin resistance gene from positives clones, while restriction digestion with XhoI generated a 1 kb fragment from pCAMBIA 1301 as seen on 1% agarose gel in TAE buffer.

    Comparison of cell viability

    Irreversible permiabilization of cells results in leakage of cell content and ultimate death. It was therefore important to determine the viability in response to increase in number of pulses. In this study major decline in cell survival was observed after first high voltage pulse, similar effect has been observed by many investigators in other bacterial species (Garg et al. 1999). Further but slight decrease was observed after second pulse. However the viability remained almost unchanged in response to further shocks (Figure 1) in both strains.

    As the viability curves under variable pulse regime remained somewhat similar, this parameter is not expected to influence the relative kinetics differences of plasmid uptake in different strains. Moreover, increasing number of pulses should have no contribution whatsoever, in the DNA uptake after second pulse.

    These results indicated that different cell types vary in their responses to electric pulse which may be due to differences in membrane makeup and cell wall thickness, structure, and density. There are reports about the effect of varying pulse length duration for electroporation resulting in differences in efficiency which were correlated to the cell viability (Liang and Lee, 1998). It was also noted that an increase in the pulse duration beyond 10 ms resulted in a 20 fold reduction in transformants competence in R. leguminosarum (Garg et al. 1999). Keeping in view these reports, rather than further increase in these parameters, multiple electric pulses were employed at 20 kV/cm at 10 ms. This procedure resulted in a pronounced decrease in cell viability after first pulse, however, it remained nearly constant after second pulse. Thus the strategy of multiple pulses appeared to have a distinct advantage over increase either in pulse voltage or duration.

    Comparison of transformation efficiencies

    The highest transformation efficiency observed in LBA4404 after five electric pulses was taken as reference while transformation efficiency for EHA101 was calculated accordingly. It was observed that with increase in the number of electric pulses, transformation efficiency increased gradually in both the strains. When compared with single pulse, efficiency increased to about 2.5 times in LBA4404 and five times in EHA101 after five electric pulses. In both these strains the increase was nearly linear (Figure 2).

    Electric field strength (amplitude) and pulse length (duration) of discharge waveform are important effectors of electroporation. Increase in electric field strength (12.5 to 20 kV) for maximizing the transformation in Pediococcus acidilactici was reported by Rodríguez et al. (2007). Transformation in Agrobacterium has already been investigated using variable voltage and pulse duration (Mersereau et al. 1990). However we reported another aspect i.e. increase in number of pulses, which results in considerable increase in DNA transformation efficiency at peak pulse voltage and duration used for single pulse.


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