Nitrogen (N) is a key essential nutrient for plants. Crop yield depends critically on massive nitrogen fertilizer input. The annual production of 15 million tons of N-fertilizer needed currently consumes ~1% of the world's annual energy production. However, plants absorb only a fraction of the applied fertilizer and the rest leaches into the groundwater, pollutes the environment and damages drinking water supplies. Therefore, increased efficiency of nitrogen uptake and use by crop plants is desirable on a variety of levels. To promote this increase in efficiency, we need a better understanding of the cellular basis of N acquisition and distribution from roots to the rest of the plant. However, we do not understand exactly where, when and how roots acquire N or how they control uptake and distribution in the plant. A key impediment to this understanding is the lack of suitable technologies, with sufficient spatial and temporal resolution, for monitoring N acquisition and its regulation. Dr. Frommer's lab at the Carnegie Institution for Science recently pioneered the engineering of novel tools that monitor the activity of key proteins responsible for moving nitrogen from the soil into the roots. This project will improve these new tools, implement them in plants, and use them to directly monitor N acquisition. The project will also integrate knowledge from this and other publicly available plant biology resources to generate a spatio-temporal map of N-acquisition in roots under different N regimes. This project will also train the next generation of scientists. Specifically, postdoctoral scholars and graduate students will be trained in engineering and implementation of activity probes with the goal of improving the ability of plant roots to acquire fertilizers, thus reducing fertilizer use. Undergraduate and high school students will work with experienced scientists to develop a series of databases providing information on fertilizers, nutrition, as well as molecular detail on how plants acquire N. These resources will be available to scientists and the public.

The Frommer lab recently succeeded in engineering the key transporters for N-acquisition from the reference plant Arabidopsis as fluorescent biosensors that have the potential to report transporter activity and thus regulation of N uptake and distribution with high temporal and spatial resolution. Major aims of this project are to: (1) Engineer and optimize the fluorescent activity sensors for ammonium, nitrate and oligopeptide transporters, gain insights into their mechanism and use them for structure-function analyses; (2) Deploy the fluorescent sensors to characterize regulatory proteins that interact with N transporters to gain insights into their regulation by making use of candidates identified in a novel resource, the MIND membrane protein interactome database; (3) Implement the sensors in wild type and mutant plants and measure transport activity in individual cells of intact roots using quantitative fluorescence imaging technology; (4) Engineer fluorescent sensors for nitrogen forms, i.e. nitrate, ammonium, glutamate, glutamine and dipeptides and deploy them in plants to monitor the dynamics of the different nitrogen forms in vivo; (5) Integrate novel information gained in this project with that from public resources to create a cellular resolution root map of nitrogen uptake and its regulation (to be built by students). The project makes use of cutting edge technologies (fluorescent sensors, quantitative imaging, microfluidic devices, cell specific expression resources) to obtain an integrated quantitative view of the mechanisms of N acquisition in roots.

This project is funded jointly by the Cellular Dynamics and Function Cluster in the MCB Division and the Physiological and Structural Systems Cluster in the IOS Division.

Agency
National Science Foundation (NSF)
Institute
Division of Molecular and Cellular Biosciences (MCB)
Application #
1413254
Program Officer
Steve Clouse
Project Start
Project End
Budget Start
2014-09-01
Budget End
2021-08-31
Support Year
Fiscal Year
2014
Total Cost
$1,446,347
Indirect Cost
Name
Carnegie Institution of Washington
Department
Type
DUNS #
City
Washington
State
DC
Country
United States
Zip Code
20005