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Method for changing nitrogen utilization efficiency in plants

a technology of nitrogen utilization efficiency and plant, which is applied in the direction of plant/algae/fungi/lichens ingredients, peptide sources, peptide sources, etc., can solve the problems of nitrogen fertilizer being one of the most expensive nutrients to supply, and achieve the effects of enhancing plant growth, high or low expression, and changing nitrogen utilization efficiency

Inactive Publication Date: 2011-01-13
ACAD SINIC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Benefits of technology

[0008]In another aspect, the present invention provides a new chimera nitrate transporter of a NRT1.1 and NRT1.2, providing a high nitrate transport efficiency, wherein the chimera nitrate transporter has the amino acid sequence of SEQ ID NO: 11. In one embodiment of the invention, a transgenic plant having enhanced nitrogen utilization efficiency by transforming a plant with the chimera nitrate transporter, whereby the transgenic plant has an enhanced growth.
[0009]According to the present invention, the nitrogen utilization efficiency in a plant is enhanced by overexpression of NRT1.7 or an enhanced expression of the NRT 1.7, whereby the nitrate remobilization from older leaves to young leaves in the plant is enhanced, and then the plant growth is improved.
[0010]The invention also provides an isolated DNA molecule encoding a chimera nitrate transporter having a amino acid sequence of SEQ ID NO:11, which was evidenced in Example 9 to provide high nitrate uptake so that it is believed that the nitrogen utilization efficiency can be enhanced. In one example of the invention, the nucleotide sequence encoding NRT 1.7 has a nucleotide sequence of SEQ ID NO: 10.
[0011]In a further yet aspect, the present invention provides a transgenic plant, which is transformed with an expression construct causing overexpression of NRT1.7 or enhancement of NRT1.7 function within the transgenic plant, whereby the transgenic plant enhances the nitrate remobilization from older leaves to young leaves in the plant, and the nitrogen utilization efficiency is improved. On the other hand, the present invention also provide a transgenic plant, which is transformed with an construct that has a defect in the gene of NRT1.7, wherein the defect results in inhibiting the expression of NRT1.7 or NRT1.7 mRNA to decrease quantity or availability of functional NRT1.7, whereby the nitrogen remobilization from older leaves to younger leaves in the transgenic plant is defective.

Problems solved by technology

Nitrogen fertilizer is one of the most expensive nutrients to supply.

Method used

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  • Method for changing nitrogen utilization efficiency in plants
  • Method for changing nitrogen utilization efficiency in plants
  • Method for changing nitrogen utilization efficiency in plants

Examples

Experimental program
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Effect test

example 1

NRT1.7 Encodes a Low Affinity Nitrate Transporter

[0084]In Arabidopsis, there are 53 NRT1 (PTR) genes, some of which are known to transport nitrate, while others transport dipeptides. To determine the substrate specificity of NRT1.7, in vitro-synthesized cRNA was injected into Xenopus oocytes for electrophysiological analysis. After 2-day incubation in ND96, oocytes were voltage clamped at −60 mV, and then subjected to 300 ms voltage pulses from 0˜160 mV in −20 mV increments. NRT1.7-injected oocytes responded to 10 mM nitrate at pH 5.5 with inward currents. And the inward currents were elicited by nitrate but not by the dipeptides tested (FIG. 1A). The current elicited by nitrate was pH-dependent, with little or no current detected when exposed to nitrate at pH7.4. The pH dependence of the nitrate elicited currents suggested that NRT1.7 is a proton-coupled nitrate transporter.

[0085]Most of the nitrate transporters in NRT1 (PTR1) family function as a low-affinity transporter with exce...

example 2

NRT1.7 is Expressed in Phloem Tissue of Old Leaves

[0086]Microarray data from the public resource A. thaliana Expression Database CSB.DB shows that little or no expression of NRT1.7 can be detected in root, and that transcription levels in leaves increased as leaves age (FIG. 2). The differential expression of NRT1.7 in old and young leaves was further confirmed here by Western Blot analysis (FIG. 3A). Using BiP as loading control, the NRT1.7 protein level in the oldest leaves was about 25 times higher than that in the youngest leaves. In addition, the leaves were separated into distal lamina, proximal lamina, and central part including midrib and petiole for quantitative RT-PCR analysis. The NRT1.7 mRNA level was higher in the distal lamina of older leaves (FIG. 3B).

[0087]To determine where NRT1.7 is expressed, 13 independent transgenic lines expressing GUS driven by NRT1.7 promoter were analyzed. Consistent with Western Blot result, GUS staining was stronger in the older leaves, wh...

example 3

NRT1.7 is Localized to the Plasma Membrane

[0089]To investigate the subcellular localization of NRT1.7, green fluorescent protein (GFP) fused either N-terminally or C-terminally to NRT 1.7 was transiently expressed in Arabidopsis protoplasts under the control of the cauliflower mosaic virus 35S promoter. Green fluorescence was seen in cytoplasm in the GFP control, while the green fluorescence of NRT1.7-GFP and GFP-NRT1.7 (FIG. 5) was detected as a fine ring at the cell periphery, external to the chloroplasts, indicating that NRT1.7 is localized in the plasma membrane.

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Abstract

The present invention provides a method for changing nitrogen utilization efficiency in a plant comprises regulating the expression of Arabidopsis NRT 1.7 or an orthologue thereof so that the nitrate remobilization from older leaves to young leaves in the plant is regulated, thereby the nitrogen utilization efficiency is changed. The present invention also provides a transgenic plant obtainable by transforming a plant with an expression construct with a high or low level of expression of NRT 1.7. On the other hand, the present invention yet provides a chimera nitrate transporter, a DNA molecule coding for this chimera transporter and an expression vector thereof.

Description

RELATED APPLICATIONS[0001]This application claims benefit of U.S. Provisional Application 61 / 223,744, filed on Jul. 8, 2009, which is incorporated by reference in its entirety herein.SUBMISSION OF SEQUENCE LISTING[0002]The Sequence Listing associated with this application is filed in electronic format via EFS-Web and hereby incorporated by reference into the specification in its entirety. The name of the text file containing the Sequence Listing is Sequence_List—16024—00012_US_ST25.txt. The size of the text file is 39 KB, and the text file was created on Jul. 8, 2010.FIELD OF THE INVENTION[0003]The present invention is related to a method for changing nitrogen utilization efficiency in a plant by regulating expression of a nitrate transporter.BACKGROUND OF THE INVENTION[0004]Nitrogen fertilizer is one of the most expensive nutrients to supply. 50-70% of the applied nitrogen is lost from the plant-soil system and causes water pollution (Peoples, 1995, in: P. E. Bacon, Editor, Nitroge...

Claims

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Application Information

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IPC IPC(8): A01H5/00C12N15/82C07K14/415C07H21/04
CPCC07K14/415C12N15/8243C12N15/8261Y02A40/146
Inventor TSAY, YI-FANGFAN, SHU-CHUNCHEN, HUI-YU
Owner ACAD SINIC
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