Location: Vegetable Crops Research Unit
2013 Annual Report
(2) Quantify asparagine and reducing sugars in cold-stored tubers of these lines.
(3) Measure acrylamide in potato chips made from these lines and relate to asparagine and reducing sugar content in raw tubers.
(4) Evaluate the growth of suppressed lines and identify potential agronomic problems.
Biochemical characterization of tubers: Tuber sucrose, glucose and fructose contents will be quantified by HPLC. Tuber asparagine content will be measured with the L-asparagine/L-glutamine assay kit (Megazyme). Acrylamide content of fried chips will be measured in the Department of Bacteriology, UW Madison.
Evaluation of plant growth: Transformed lines will be grown in greenhouses using standard procedures to produce tubers for biochemical analysis. Growth characteristics of plants and tuber number, weight and shape will be documented for each line and for Atlantic controls. Differences between controls and silenced lines may indicate potential limits on agronomic performance that will be investigated further in subsequent years.
Tissue culture plantlets in which the genes for asparagine synthetase and vacuolar acid invertase are suppressed were generated and planted in the greenhouse. Asparagine synthetase and vacuolar acid invertase are the enzymes primarily responsible for producing asparagine, glucose and fructose in potato tubers. Decreasing the expression of the genes needed to make these enzymes is hypothesized to produce tubers with less glucose, fructose and asparagine than that found in control tubers. Plants were evaluated for healthy appearance and for relative expression of the gene-silencing constructs. Tubers were harvested from pots after plants had senesced. Multiple lines that together covered a broad range of gene-silencing, from very effective to ineffective for each enzyme, were selected for further analysis. Tubers of gene-silencing lines derived from cultivar Russet Burbank were planted in research field plots in 2013 and plant emergence, canopy development, and overall health are being evaluated. Tubers based on cultivar Atlantic were planted in the greenhouse and are being evaluated for plant health and normal development. Tubers will be harvested from all lines in the fall and used for detailed molecular and biochemical analysis. The acrylamide-forming potential of each line will be evaluated. Targets for tuber asparagine, glucose, and fructose will be developed that can be used to guide future potato breeding efforts focused on acrylamide mitigation.
This research completes Objective 1), Develop lines of potato cultivar Atlantic in which the genes for asparagine synthetase (ASy) and vacuolar acid invertase (VInv) are suppressed. It also make substantial progress toward Objective 2), Quantify asparagine and reducing sugars in cold-stored tubers of these lines, and Objective 3), Measure acrylamide in potato chips made from these lines and relate to asparagine and reducing sugar content in raw tubers, in that tubers are currently being produced for post-harvest analysis. This research partially completes Objective 4), Evaluate the growth of suppressed lines and identify potential agronomic problems in that above ground growth of plants is being assessed. Completion of this objective will occur after harvest when tuber size and yield will be evaluated.