Axel Schwekendiek
Asst. Professor at University of Northern Iowa
IA United StatesWhat I Do:
Expertise:
Experience:
University of Northern Iowa
Asst. Professor
Publications:
A Temporary Immersion System for the Effective Shoot Regeneration of Hop.
Acta Hort. (ISHS)accepted.
2009Functional Characterization of Genes Controlling the Production of Bioactive Prenylflavonoids in Hop (Humulus lupulus L.).
Acta Hort. (ISHS)accepted.
2009Constitutive Expression of a Grapevine Stilbene Synthase Gene in Transgenic Hop (Humulus lupulus L.) Yields Reseveratrol and its Derivatives in Substantial Quantities.
J. Agric. Food Chem.55: 7002-7009
2007Transformation with Stilbene Synthase for Increasing Resistance Against Fungal Pathogens.
Acta Hort. (ISHS)668: 101-108
2005AFLP Fingerprinting in hop: analysis of the genetic variability of the Tettnang variety.
Genetic Resources and Crop Evolution51(2):211-220
2004
Pine stilbene synthase cDNA, a tool for probing environmental stress.
Characterization of a pine multigene family containing elicitor-responsive stilbene synthase genes.
Regeneration and Agrobacterium-mediated transformation of hop (Humulus lupulus L.).
Speaking Engagements:
2nd ISHS Hop Symposium, Melle, Belgium
A Temporary Immersion System for the Effective Micropropagation of Hop
The largest bottleneck for the genetic transformation of hop is the inefficiency of existing regeneration protocols. Successful hop transformation therefore requires large numbers of explants, is time consuming and labor intensive. We developed a fast and efficient shoot regeneration procedure for the ?US Tettnanger? cultivar, starting from green organogenic nodule clusters (GONCs). We induced GONCs under the sole influence of the hormone TDZ on internodal explants. Even though only 56% internodes produced GONCs, all of them were highly regenerative. In combination with a temporary immersion system (TIS), we produced on average 35 shoots per GONC in a single round of regeneration. Our overall regeneration efficiency therefore was 20-fold (35 shoots regenerating from a single GONC, 0.56 GONCs per explant), and compared to our previous report increased 30-fold. This increase could help overcome current limitations in biotechnological applications for hop. The use of a TIS further eliminated bi-weekly tissue transfers and thereby reduced labor and contamination problems. Our procedure, which works through de novo shoot induction via the callus route, seems to have high potential for the generation of virus-free hop material. It will also be useful for the production of large numbers of genetically transformed plants, for example in the arena of pathogen resistance, for improving flavor, or for the development of medicinal hops. Based on our improved regeneration procedure, we expect being able to increase Agrobacterium-based transformation efficiencies from currently 0.4% to 20%. Experiments to test this prediction are currently under way in our laboratory.


