Avena nuda farnesyl diphosphate synthase gene YFPS and detection method for separation and clone, site-specific mutagenesis and enzyme functions

A technology of farnesyl pyrophosphate and enzyme gene, which is applied in the technical field of enzyme function detection

Active Publication Date: 2013-03-27
CROP RES INST SHANDONG ACAD OF AGRI SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

So far, farnesyl pyrophosphate synthase genes have been isolated and cloned from 40 plant species including Arabidopsis thaliana, rice (Oryza sativa), corn (Zea mays), sorghum (Sorghum bicolor), and rubber (Heveabrasiliensis). Before the application of the present invention, there has not been disclosed or published about the isolation and cloning of the farnesyl pyrophosphate synthase gene from the whea...

Method used

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  • Avena nuda farnesyl diphosphate synthase gene YFPS and detection method for separation and clone, site-specific mutagenesis and enzyme functions
  • Avena nuda farnesyl diphosphate synthase gene YFPS and detection method for separation and clone, site-specific mutagenesis and enzyme functions
  • Avena nuda farnesyl diphosphate synthase gene YFPS and detection method for separation and clone, site-specific mutagenesis and enzyme functions

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0058] Example 1 (Wheat leaf RNA extraction)

[0059] (1) Use vermiculite in a constant temperature incubator (28°C) to cultivate jade wheat until the three-leaf stage.

[0060] (2) Grind the leaves into powder in liquid nitrogen, and transfer them to DEPC-treated EP tubes.

[0061] (3) Add appropriate amount of RNAiso Plus.

[0062] (4) Let stand at room temperature for 5 minutes.

[0063] (5) Add 1 / 5 volume of RNAiso Plus in chloroform. Shake until creamy.

[0064] (6) Let stand at room temperature for 5 minutes.

[0065] (7) Centrifuge at 12000g for 15 minutes at 4°C.

[0066] (8) Transfer the supernatant to a new DEPC-treated EP tube, add an equal volume of isopropanol to the supernatant, and mix well. Stand at room temperature for 10 minutes.

[0067] (9) Centrifuge at 12000g for 10min at 4°C.

[0068] (10) Add 1 mL of 75% ethanol prepared with DEPC water to the precipitate. Centrifuge at 12000g for 5min at 4°C.

[0069] (11) Keep the precipitate and dry it in...

Embodiment 2

[0071] Example 2 (synthesis of the first strand of cDNA)

[0072] Follow the instructions of the Takara reverse transcription kit.

[0073] (1) Prepare the following mixture in a microtube

[0074]

[0075] (2) Carry out denaturation and annealing reactions under the following conditions on a PCR instrument: 5 minutes at 65°C—quick cooling on ice.

[0076] (3) Prepare the following reverse transcription reaction solution in the above-mentioned Microtube tube.

[0077]

[0078] (4) Carry out the reverse transcription reaction on the PCR instrument according to the following conditions: 42°C, 60min; 70°C, 15min; 4°C cooling.

Embodiment 3

[0079] Embodiment 3 (intermediate sequence amplification)

[0080] 1 Primer design for intermediate sequences

[0081]Using Primer5.0 primer design software and DNAMAN software, primers were designed according to the highly conserved region of the amino acid sequence of FPS in plants. The upstream primer is YRF:5'TCAACGCCACTTCAGAGGAAAACCG3', whose gene sequence is shown in Seq ID No:4; the downstream primer is: YRR:5'TCCCGCTCATACTTGTGAAATGCCGT3', whose gene sequence is shown in Seq ID No:5.

[0082] The PCR system is: cDNA 2ul, buffer 1.5μL, Taq enzyme 0.3μL, dNTP 0.7μL, YRF 0.6μL, YRR 0.6μL, 10%DMSO, ddH2O 9.8μL.

[0083] The PCR program is: 94°C for 3min, 94°C for 45s, 62°C for 45s, 72°C for 1min, 72°C for 6min, 32cycles.

[0084] 2 PCR result detection of intermediate sequence

[0085] Mix 8 μL of PCR amplification product with 1 μL of bromophenol blue, point it into 1.5% agarose gel, electrophoresis at 120V for 45 min, observe and take pictures with an ultraviolet gel i...

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Abstract

The invention belongs to the field of molecular biology and relates to a detection technology for separation and clone, site-specific mutagenesis, zymoprotein prokaryotic expression, zymoprotein separation and purification and enzyme functions of a branch-point key enzyme gene participating in synthesis of an isoprenoid matter in a wheat mevalonic acid metabolic pathway. The method can provide important technical storage for further performing the gene improvement and modification, constructing an eucaryon gene expression carrier of a farnesyl diphosphate synthase gene, and converting corresponding crops; secondly can be used for obtaining plants with important commercial values in virtue of secondary metabolism, and discussing a relationship of the overexpression of the farnesyl diphosphate synthase gene in a receiver plant and important agronomic traits such as secondary metabolites, crop grain sizes and crop grain weights; and improving the yield of the crops, analyzing structures of introns, exons and promoters, studying functions of the promoters, developing related molecular markers.

Description

technical field [0001] The invention belongs to the field of molecular biology, and relates to the isolation and cloning of a key enzyme gene involved in the branch point of the synthesis of isoprenoid substances in the metabolic pathway of wheat mevalonate, the site-directed mutation of the gene, the prokaryotic expression of the enzyme protein, and the enzyme protein Separation and purification and enzyme function detection technology. Background technique [0002] Isoprenoid substances are important substances necessary for maintaining plant growth and development, photosynthesis, electron transfer, and coping with environmental stress. Such substances can be used as photosynthetic pigments (such as chlorophyll, carotenoids), growth substances and plant hormones (such as cytokinins, abscisic acid, gibberellins and brassinosteroids), part of membrane structures such as sitosterol, electron transport Receptors such as plastoquinone, receptors for glucose in glucosylation r...

Claims

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Application Information

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IPC IPC(8): C12N15/54C12N15/10C12N15/70C12N9/10C12Q1/48
Inventor 楚秀生李永波李玉莲樊庆琦黄承彦隋新霞郭栋高洁李根英
Owner CROP RES INST SHANDONG ACAD OF AGRI SCI
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