Electrophoresis method for removing Rubisco enzyme interference of watermelon leaves and separating residual low-abundance proteins

A protein and watermelon technology, applied in the biological field, can solve the problems that need to be further investigated and verified, different, complicated and complicated to operate.

Inactive Publication Date: 2012-07-18
NANJING AGRICULTURAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

This method is tedious and complicated to operate, and its removal operation needs to be carried out at high temperature (37°C or 42°C), which may lead to the degradation and loss of other proteins, especially some regulatory factors and signaling factors (Krishnan and Natarajan, 2009; Li Hongbing and Kang Zhensheng , 2011)
3) High-concentration dithiothreitol (DTT) precipitation method (Cho et al., 2008), its principle and effectiveness need further investigation and verification
However, due to the molecular weight and isoelectric point of proteins associated with the use of PEG to precipit

Method used

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  • Electrophoresis method for removing Rubisco enzyme interference of watermelon leaves and separating residual low-abundance proteins
  • Electrophoresis method for removing Rubisco enzyme interference of watermelon leaves and separating residual low-abundance proteins
  • Electrophoresis method for removing Rubisco enzyme interference of watermelon leaves and separating residual low-abundance proteins

Examples

Experimental program
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Effect test

Embodiment 1

[0028] The optimal PEG concentration screening of embodiment 1 precipitation watermelon leaf Rubisco

[0029] A. Take 2g of mature leaves of watermelon (Citrullus Ianatus Mansfeld) seedlings, place them in liquid nitrogen and quickly grind them to a fine powder (particle size is about 0.01mm), quickly transfer the powder to a 10ml centrifuge tube with a small medicine spoon, add 7ml pre- Chill the homogenization buffer, then shake to mix on a vortex, and incubate horizontally on ice for 10 minutes.

[0030] B. Centrifuge at 1500g for 3 minutes at 4°C, discard the precipitate, and keep the supernatant; then centrifuge at 1,5000g for 20 minutes at 4°C, discard the precipitate, and keep the supernatant.

[0031] C. Add different concentrations of PEG-4000 to the supernatant, incubate horizontally on ice for 20 minutes, centrifuge at 1,5000g at 4°C for 25 minutes, discard the precipitate, and keep the supernatant.

[0032] D. Quantify the protein in the supernatant obtained in step...

Embodiment 2

[0035] 1) Preparation of remaining protein samples after precipitation of watermelon leaf Rubisco

[0036] A. Repeat steps A-B of Example 1 to obtain the whole protein supernatant, add 60% PEG-4000 to the supernatant, so that the final concentration of PEG-4000 in the solution reaches 18%, vibrate and mix on a vortex instrument, and level Incubate on ice for 20 minutes, centrifuge at 1,5000g for 25 minutes at 4°C, discard the precipitate, and keep the supernatant.

[0037] B. Add 8 times the volume of 10% trichloroacetic acid-acetone solution (w / v, containing 0.07% β-mercaptoethanol) to the supernatant, and place it overnight at -20°C. Centrifuge at 2,5000 g for 25 minutes at 4°C, discard the supernatant and keep the precipitate.

[0038] C. Add 8ml of acetone (containing 0.07% β-mercaptoethanol) to the precipitate to wash the precipitate, place it at -20°C for 1 hour, centrifuge under the same conditions as step B, discard the supernatant, and keep the precipitate.

[0039]...

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Abstract

The invention belongs to the technical field of biology, and discloses an electrophoresis method for removing Rubisco from plant leaves and enriching and separating residual proteins. The method comprises the following steps of: removing Rubisco from watermelon leaves by using 18 percent PEG-4000; leaching residual proteins through a TCA-acetone precipitation method; and performing two-dimensional electrophoresis to separate residual proteins from watermelon leaves. Compared with a holoprotein two-dimensional electrophoretogram, the method has the advantages that: after Rubisco in watermelon leaves is precipitated by adopting the 18 percent PEG, most large and small subunits of Rubisco disappear, the expression levels of most residual proteins are raised, the quantity of proteins obtained by separating is increased by 48.4 percent, and a large quantity of new protein spots (65+/-15) appear in a region of which the molecular weight is smaller than 25.0kDa. As proved by repeated experiments, the electrophoresis method has the advantages of high repeatability, clear spectra and reliable result.

Description

technical field [0001] The invention belongs to the field of biotechnology, and relates to an electrophoresis method for removing Rubisco enzyme interference from plant leaves, enriching and separating remaining low-abundance proteins, and more particularly relates to an electrophoresis method for removing Rubisco enzyme interference from watermelon leaves, enriching and separating remaining low-abundance proteins. Electrophoretic Methods for Abundant Proteins. Background technique [0002] Watermelon is one of the important economic crops in my country, and it is also an important fruit-type vegetable in the world. It is especially important to study its stress resistance mechanism and nutritional quality functional factors for the cultivation and production of watermelon. Watermelon leaf proteomics research can provide important functional information for watermelon stress resistance cultivation and nutritional quality analysis. Protein two-dimensional electrophoresis is ...

Claims

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Application Information

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IPC IPC(8): C07K14/415C07K1/28C07K1/26
Inventor 郭世荣阳燕娟孙锦严蓓何立中李斌
Owner NANJING AGRICULTURAL UNIVERSITY
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