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Grant: Engage Grants Program

Université de Moncton

$25,000.00

Optimization of a non-Agrobacterium mediated approach for transforming potato plants (Solanum tuberosum)

FY 2013-14

Summary
Solanum Genomics International Inc (Fredericton, NB, Canada) is a privately held bioscience company whosemission is to develop and adapt methods to improve potatoes for commercial markets. Due to all the patentsissued and licensing fees required to use Agrobacterium-mediated plant transformation, the company relies onthe use of a publicly available non-Agrobacterium mediated transformation system to insert variousgenes/alleles of interest into potato plants. This system, named TransBacter (Cambia, Canberra, Australia),involves the use of the vector pCAMBIA1105.1r, in which genes of interest are inserted and then transferredinto potato plants using the bacterium Sinorhizobium meliloti, which acts as a messenger by delivering thevector into potato cells. Unfortunately, the efficiency of this approach has so far been very low (transformationefficiencies below 1%) and limiting for transforming the potato plant. Also, one of the selection marker geneused in this system, hyg, which encodes resistance to the antibiotic hygromycin, is expensive, difficult to obtainand fairly toxic. For all these reasons, the company has requested my help to modify/optimize theirtransformation system. Similar work has been previosuly conducted in my laboratory and we have the expertiseto perform this project. Therefore, in this project, we propose three objectives:Objective 1: Validate the feasibility of using a novel Ensifer adhaerens OV14/pCAMBIA5105 system fortransforming the potato cultivars Bintje and Shepody.Objective 2: Test and optimize the transformation parameters for achieving high and constant potatotransformation efficiencies.Objective 3: Replace the hyg marker gene in pCAMBIA5105 by another selectable marker gene.Optimizing this novel transformation system will allow fast-tracking the development and commercializationof novel superior potato cultivars. This will provide a commercial competitive advantage to the companySolanum Genomics by improving its efficiency and reducing costs.
Program
Engage Grants Program
Location
New Brunswick, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
446561-2013
Name nom
Filion, Martin
Department département
Biologie
Organization id
73
Institution établissement
Université de Moncton
Province en
New Brunswick
Province fr
Nouveau-Brunswick
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2013
Competition year année de concours
2013
Award amount
25000
Program id
EGP
Program name en
Engage Grants Program
Program name fr
Programme de subventions d'engagement partenariat
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
1551
Committee name en
Atlantic Internal Decision Committee
Committee name fr
Comité de décision interne pour l'Atlantique
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
4900
Research subject group en
Plant and treebiology
Research subject group fr
Biologie végétale et des arbres
Research subject en
Plant and treebiology
Research subject fr
Biologie végétale et des arbres
Partie
1
Nb partie
1
Application title
Optimization of a non-Agrobacterium mediated approach for transforming potato plants (Solanum tuberosum)
Keyword
NSERC
Application summary
Solanum Genomics International Inc (Fredericton, NB, Canada) is a privately held bioscience company whosemission is to develop and adapt methods to improve potatoes for commercial markets. Due to all the patentsissued and licensing fees required to use Agrobacterium-mediated plant transformation, the company relies onthe use of a publicly available non-Agrobacterium mediated transformation system to insert variousgenes/alleles of interest into potato plants. This system, named TransBacter (Cambia, Canberra, Australia),involves the use of the vector pCAMBIA1105.1r, in which genes of interest are inserted and then transferredinto potato plants using the bacterium Sinorhizobium meliloti, which acts as a messenger by delivering thevector into potato cells. Unfortunately, the efficiency of this approach has so far been very low (transformationefficiencies below 1%) and limiting for transforming the potato plant. Also, one of the selection marker geneused in this system, hyg, which encodes resistance to the antibiotic hygromycin, is expensive, difficult to obtainand fairly toxic. For all these reasons, the company has requested my help to modify/optimize theirtransformation system. Similar work has been previosuly conducted in my laboratory and we have the expertiseto perform this project. Therefore, in this project, we propose three objectives:Objective 1: Validate the feasibility of using a novel Ensifer adhaerens OV14/pCAMBIA5105 system fortransforming the potato cultivars Bintje and Shepody.Objective 2: Test and optimize the transformation parameters for achieving high and constant potatotransformation efficiencies.Objective 3: Replace the hyg marker gene in pCAMBIA5105 by another selectable marker gene.Optimizing this novel transformation system will allow fast-tracking the development and commercializationof novel superior potato cultivars. This will provide a commercial competitive advantage to the companySolanum Genomics by improving its efficiency and reducing costs.