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Here, we present two protocols to transform potato plants. The Agrobacterium tumefaciens transformation leads to a complete transgenic plant while the Agrobacterium rhizogenes produces transgenic hairy roots in a wild type shoot that can be self-propagated. We then detect promoter activity by GUS staining in the transformed roots.
Agrobacterium sp. is one of the most widely used methods to obtain transgenic plants as it has the ability to transfer and integrate its own T-DNA into the plant's genome. Here, we present two transformation systems to genetically modify potato (Solanum tuberosum) plants. In A. tumefaciens transformation, leaves are infected, the transformed cells are selected and a new complete transformed plant is regenerated using phytohormones in 18 weeks. In A. rhizogenes transformation, stems are infected by injecting the bacteria with a needle, the new emerged transformed hairy roots are detected using a red fluorescent marker and the non-transformed roots are removed. In 5-6 weeks, the resulting plant is a composite of a wild type shoot with fully developed transformed hairy roots. To increase the biomass, the transformed hairy roots can be excised and self-propagated. We applied both Agrobacterium-mediated transformation methods to obtain roots expressing the GUS reporter gene driven by a suberin biosynthetic gene promoter. The GUS staining procedure is provided and allows the cell localization of the promoter induction. In both methods, the transformed potato roots showed GUS staining in the suberized endodermis and exodermis, and additionally, in A. rhizogenes transformed roots the GUS activity was also detected in the emergence of lateral roots. These results suggest that A. rhizogenes can be a fast alternative tool to study the genes that are expressed in roots.
Aside from economic interest, the generation of transgenic plants has its own relevance in research to demonstrate the ultimate function of genes and to better understand plant physiology and development. The most widely used method for plant DNA insertion is Agrobacterium-mediated transformation. Agrobacterium tumefaciens is able to generate crown galls in the infected tissue of many plant species by the action of its tumour-inducing (Ti) plasmid. The plasmid contains a T-DNA region with a set of genes that will be integrated in the plant genome and induce tissue dedifferentiation1,2. The ex....
The A. rhizogenes transformation protocol was adapted and modified from Horn et al.7 and the genotype tested was S. tuberosum ssp. tuberosum (cv. Désirée). The A. tumefaciens transformation protocol was adapted and modified from Banerjee et al.22 and the genotypes tested were S. tuberosum ssp. tuberosum (cv. Désirée) and S. tuberosum ssp. andigena. The main steps of both procedures a.......
Agrobacterium rhizogenes-mediated potato transformation
In this manuscript, the step-by-step procedure set up to obtain transformed root with A. rhizogenes is presented. Figure 1 presents an overview of the procedure, which altogether takes around 5-6 weeks (from injection of A. rhizogenes to obtaining fully developed hairy roots). Then, .......
In potato, the most common system to obtain stable complete transgenic plants uses the transformation by Agrobacterium tumefaciens strains that require organogenesis using exogenous phytohormones. Although the Agrobacterium based protocols has the potential to integrate non-T-DNA vector sequence25, this methodology is still the easiest and less expensive available to transform potato plants. During last years, the interest in A. rhizogenes-mediated transformation has got.......
This work was supported by the Ministerio de Innovación y Ciencia (AGL2009-13745, FPI grant to PB), the Ministerio de Economía y Competitividad and FEDER funding (AGL2012-36725, AGL2015-67495-C2-1-R), and the University of Girona (PhD grant to SF, and grant SING11/1). The authors are grateful to Dr. Inge Broer (Institute for Land Use, University of Rostock, Rostock, Germany) and Dr. Salomé Prat (Centro Nacional de Biotecnología, Madrid, Spain) for providing the A. rhizogenes and the A. tumefaciens strain, respectively, and Dr. Marçal Soler and Dr. Anna Plasencia for the help and support received in initiating the A. rhizo....
Name | Company | Catalog Number | Comments |
Acetone |
Panreac |
1.310.071.21 | |
Acetosyringone |
Acros |
115540050 | |
Aquarium pump |
Prodac |
MP350 | |
Autoclave |
Ragpa Strelimatic | ||
Bacteriological agar |
Lab Conda |
1800 | |
BAP |
Duchefa |
B0904 | |
Beef extract |
Lab Conda |
1700 | |
Plant growing cabinet |
Nuaire | ||
Carbenicillin |
Duchefa |
C0109 | |
Cefotaxime sodium |
Duchefa |
C0111 | |
DMSO |
Merck |
1029310161 | |
Ecotron infors |
HT |
29378 | |
Ethanol |
Merck |
1,009,831,011 | |
Falcon tube |
Control tecnica |
CFT011500 | |
Ferricyanate |
Sigma |
101001081 | |
Ferrocyanate |
Sigma |
100979088 | |
Flask (8.06 cm diameter and 11.3 cm height) and plastic lid for in vitro culture |
Apiglass |
ref16 | |
GA3 |
Sigma |
G7645 | |
Gamborg B5 media |
Duchefa |
G0210 | |
Gelrite |
Duchefa |
G1101 | |
Glucosa |
Sigma |
G5767 | |
Kanamycin |
Sigma |
K1377 | |
Leukopor tape |
BSN Leukopor |
BDF47467 | |
Lupe |
Wild-Heerbrugg |
M420 | |
Magnetic shaker |
Agimatic |
7000243 | |
MES hydrate |
Sigma |
M2933-25G | |
MgSO4 |
Panreac |
131404 | |
Microscope |
Olympus | ||
Minufugue centrifugue 5415R |
Eppendorf | ||
Murashige and Skoog media |
Duchefa |
M0254.0050 | |
Na2HPO4 |
Panreac |
131679 | |
NAA |
Duchefa |
N0903 | |
NaCl |
Panreac |
131659 | |
NaH2PO4 |
Sigma |
58282 | |
NightSea Stereo |
SFA Moonting Adapter | ||
Parafilm |
Anorsa |
PRFL-001-001 | |
Peptone |
Lab Conda |
1616 | |
Petri dishes (90 x 14) |
Anorsa |
200200 | |
pHmetre |
Crison | ||
Phytotron |
Inkoa |
RFTI-R5485 | |
Plant Agar |
Duchefa |
P1001 | |
Refrigeratot |
Liebherr Medline | ||
Rifampicin |
Duchefa |
R0146 | |
Spectinomycin |
Sigma |
59007 | |
Spectrophotometer |
Shimadzu | ||
Square plates (120 x 120) |
Deltalab |
200204 | |
Streptomycin |
Sigma |
S6501 | |
Sucrose |
Panreac |
131621 | |
Surgical blades |
Swann-Morton |
201 | |
Surgical needle |
NIPRO |
015/0204 | |
Triptone |
Lab Conda |
1612 | |
Triton |
Serva |
37240 | |
Unimax 1010 shaker |
Heidolph | ||
Vacuum |
Dinko | ||
x-GlcA (5-Bromo-4-chloro-3-indoxyl-beta-D-glucuronic acid, sodium salt anhydrous) |
Biosynth |
B-7398 | |
Yeast extract |
Lab Conda |
1702.00 | |
Zeatin riboside |
Sigma |
1001042850 |
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