CN1778932A - Improvement for exogenous protein accumulation in transgene plant - Google Patents

Improvement for exogenous protein accumulation in transgene plant Download PDF

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CN1778932A
CN1778932A CN 200510030446 CN200510030446A CN1778932A CN 1778932 A CN1778932 A CN 1778932A CN 200510030446 CN200510030446 CN 200510030446 CN 200510030446 A CN200510030446 A CN 200510030446A CN 1778932 A CN1778932 A CN 1778932A
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protein
offspring
transgenic plant
antibody
plant
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CN1325652C (en
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王彪
武天龙
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Shanghai Jiaotong University
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Shanghai Jiaotong University
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Abstract

A method belongs to the field of biology technology that can improve the cumulation of portein in transgenic plant. The steps is: (1) using the restriction enzyme with pCAMBIA2300 and pCAMBIA3300 plasmid and human granulocyte macrophage colony stimulating factor hGM-CSF gene, flating, dephosphorylation,(2) constructing another expression vector as the same method, (3)taking feasible agrobacterium into YEP substrate with antibiotic, cultivating 36hr under 28 deg.c, 250rpm,(4)crossbreeding its offspring of the two transgenic plants, and get the offspring of the crossbreed;(5)analysis the albumen of the offspring and parents. This invention crossbreeds the offspring of the two transgenic plants, and the expression of the portein is higher 50% than its parents. Without changing the other sequence, it can improve the cumulation of protein in the plant only by adding the endoplasmic reticulum and indexing signal of vacuole on the end of target gene. It can improve the cumulation of portein in the transgenic plant, and reach the aim that to improve the cumulation of portein in the plant seeds.

Description

Improve foreign protein cumulative method in transgenic plant
Technical field
What the present invention relates to is a kind of method of biological technical field, particularly a kind of raising foreign protein cumulative method in transgenic plant.
Background technology
Improve foreign protein cumulative method in transgenic plant, normally seek the promotor of high expression level and regulate sequence.Existing great mass of data shows, AFVY (Ala-Phe-Val-Tyr) the vacuole targeting signal of phaseollin C end is connected in the end of green fluorescent protein, can realize the accumulation of green fluorescent protein in vacuole.The end of green fluorescent protein is added KDEL (Lys-Asp-Glu-Leu) small peptide, and green fluorescent protein can accumulate in cytoplasmic endoplasmic reticulum.
Warp is to existing literature search, do not find as yet do not changing promotor and regulating under the prerequisite of sequence, only add the transportation signal of guiding endoplasmic reticulum and storage vacuole respectively at the gene end, utilize the approach of conventional hybridization breeding again, improve foreign protein cumulative method in plant, also do not find report with the constructed theme of the present invention.
Summary of the invention
The objective of the invention is to overcome deficiency of the prior art, a kind of raising foreign protein cumulative method in transgenic plant seed is provided.Make it improve the accumulation of foreign protein in transgenic plant.Make up two kinds of tissue specific expression carriers that contain endoplasmic reticulum and vacuole targeting signal, transformed plant obtains transgenic progeny, again with two kinds of transgenic plant advanced generation crosses respectively.The advantage of two kinds of systems is incorporated into together, improves the target that foreign protein accumulates in plant seed thereby reach.
The present invention is achieved by the following technical solutions, the present invention includes following steps:
1. use digestion with restriction enzyme pCAMBIA2300 and pCAMBIA3300 plasmid and human granulocyte macrophage colony stimulating factor (hGM-CSF) gene, mend and put down, use the alkaline phosphatase dephosphorylation.The carrier that hGM-CSF gene and enzyme were cut is connected with the T4 ligase enzyme, spends the night.The end of gene has KDEL endoplasmic reticulum targeting signal, and this small peptide can correctly be excised in mature peptide.
2. make up the expression vector of another kind of series with above-mentioned same method, be characterized in that the end of hGM-CSF gene has AFVY storage vacuole targeting signal, this small peptide can correctly be excised in mature peptide.
3. these two kinds of expression vectors are imported respectively among Agrobacterium GV3101 and the LBA4404, draw an amount of Agrobacterium add contain antibiotic YEP (every liter contains the 10g Tryptones, the 10g yeast extract, 5gNaCl) in the substratum, 28 ℃, 250rpm cultivates 36hr.When the OD value reaches about 0.8, begin to be used for arabidopsis thaliana transformation and soybean.Arabidopis thaliana transforms with reference to Clough and Bent document (Clough S J and Bent A F, 1998.Floral dip:a simplified method for Agrobacterium-mediatedtransformation of Arabidopsis thaliana.Plant J 16:735-743).The soybean that the conversion of soybean adopts this laboratory to set up transforms and the cultivation program, and its patent publication No. is ZL 02150782.1 (soybean transgene plant original position grow thickly shoot regeneration cultural method) and ZL 0250777.5 (vacuum infiltration assist soybean original position grow thickly bud method for transformation).
4. the offspring of these two kinds of transfer-gen plants is hybridized the offspring who obtains hybridizing.
5. offspring and parent are carried out the protein quantification analysis.
A) quantitative with reference to Bradford method (Bradford, 1976) to total soluble protein.Get 2 μ l protein samples, add 1mlBradford reagent, behind the mixing, spectrophotometric instrumentation OD 595
B) Protein Detection reference " molecular cloning " (Sambrook etc., 1989) on SDS-PAGE protein isolate and the film.Albumen electrophoresis in SDS-PAGE glue reaches the bottom of gel up to the indicator forward position.
C) protein shifts on nitrocellulose filter at room temperature and shifts 1h with the half dry type electroporation, and 3 layers of Whatman filter paper are respectively filled up in the gel both sides.
D) Protein Detection on the film: add first antibody (antibody of anti-human granulocyte macrophage colony stimulating factor), 37 ℃ of incubations 30 minutes; Wash three times; Adding second antibody (avidin-alkaline phosphatase enzyme complex), 37 ℃ of incubations 30 minutes, washed twice; Add the substrate colour developing and observe protein band.
The present invention makes up the plant expression vector that contains endoplasmic reticulum and vacuole targeting signal respectively, and transformed plant obtains transgenic progeny, and with these two kinds of transgenic plant advanced generation crosses, the expression amount of foreign protein improves more than 50% than the parent again.The present invention does not change other sequence, and only endoplasmic reticulum and the vacuole targeting signal that adds at the end of goal gene hybridized transgenic line again, utilizes the difference of targeting signal, realizes improving the accumulation of foreign protein in plant.Improve the accumulation of foreign protein in transgenic plant.Make up two kinds of tissue specific expression carriers that contain endoplasmic reticulum and vacuole targeting signal, transformed plant obtains transgenic progeny, again with two kinds of transgenic plant advanced generation crosses respectively.The advantage of two kinds of systems is incorporated into together, improves the target that foreign protein accumulates in plant seed thereby reach.
Embodiment:
Below in conjunction with specific embodiment technical scheme of the present invention is further described.
The expression of embodiment 1 human granulocyte macrophage colony stimulating factor in the Arabidopis thaliana seed
1. with XhoI digestion with restriction enzyme pCAMBIA2300 plasmid and human granulocyte macrophage colony stimulating factor (hGM-CSF) gene, flat with T4DNA polysaccharase benefit, with Shrimp alkaline phosphatase dephosphorylation.The hGM-CSF gene is connected with the T4 ligase enzyme with the pCAMBIA2300 carrier, spends the night.The gene end adds aaggatgagctt oligonucleotide targeting signal.
2. with XhoI digestion with restriction enzyme pCAMBIA2300 plasmid and human granulocyte macrophage colony stimulating factor (hGM-CSF) gene, flat with T4 archaeal dna polymerase benefit, with Shrimp alkaline phosphatase dephosphorylation.The hGM-CSF gene is connected with the T4 ligase enzyme with the pCAMBIA2300 carrier, spends the night.The gene end adds gctttcgtttac oligonucleotide targeting signal.
3. will contain in steps 1 and the Agrobacterium GV3101 bacterium liquid of step 2pCAMBIA2300 expression vector, (every liter contains the 10g Tryptones to draw an amount of YEP of adding, the 10g yeast extract, 5gNaCl)/Gent (gentamicin 25mg/L)+Kan (kantlex 50mg/L) substratum in, 28 ℃, 250rpm cultivates 36hr.22 ℃, the centrifugal 20min of 5500g, remove supernatant, with conversion medium (a large amount of compositions of 1/2 * MS (Murashigeand Skoog, 1962), 1/2 * B5 trace ingredients (Gamborg et al, 1968), 5%sucrose, 0.05%silwet-77,44nM benzylaminopurine) resuspended, adjust the OD value and reach about 0.8.The Arabidopis thaliana of just having bloomed is stood upside down in conversion medium, soak in 30 seconds, and shake gently.Take out Arabidopis thaliana, with leaf, stem, take the unnecessary globule and shake off, lie in the clean plastic tub, and cover the black out 16hr that preserves moisture with film.Open film, Arabidopis thaliana is placed under fluorescent light intensity of illumination 80～110 μ mol.m -2.s -1, and water Hogland nutritive medium (KNO 35 * 10 -3Mol/L, KH 2PO 45 * 10 -3Mol/L, MgSO 4.7H 2O 4 * 10 -3Mol/L, Ca (NO 3) 24 * 10 -3Mol/L, FeSO 47H 2O 5 * 10 -5Mol/L, Na 2-EDTA 5 * 10 -5Mol/L, MS trace ingredients (Murashige and Skoog, 1962)), treat that its Arabidopis thaliana angle fruit is withered and yellow fully, when ftractureing, gather in the crops seed.The Arabidopis thaliana seed of sterilizing is moved on the screening flat board that contains Kan (50g/ml), evenly tiling, and inhale and remove dull and stereotyped interior unnecessary water.4 ' C vernalization 2d moves in the greenhouse, guarantees intensity of illumination 80～110 μ mol.m -2.s -1The plant that has changed plasmid after about 10d over to has the Kan resistance, so cotyledon is green, hypocotyl is longer, and has grown two true leaves.Transformant is moved in the vermiculite that irrigates with nutritive medium, preserve moisture with film and spend the night, moved in the weather greenhouse in second day, culture condition is the same.T2 is for seed for results, analyzes.
4. these two kinds of transgenic line offsprings are hybridized.
5. offspring and parent are carried out the protein quantification analysis.
A) get the 50mg blade, add 100 μ l1 * PBS (KH 2PO 40.2g/l, Na 2HPO 41.15g/l, KCl0.2g/l, NaCl 8g/l) in the 1.5ml centrifuge tube, grind; 13000g, 4 ℃ are centrifugal 10 minutes; Get supernatant, standby (above process is in carrying out) on ice.
B) with reference to Bradford method (Bradford, 1976).Get 2 μ l protein samples, add 1mlBradford reagent, behind the mixing, spectrophotometric instrumentation OD 595
C) preparation of SDS-PAGE protein isolate: SDS-PAGE is with reference to " molecular cloning " (Sambrook etc., 1989): before the application of sample, sample is placed the sample loading buffer (2 * sample loading buffer: glycerine 2.4g, 1M Tris-HCl 1ml (pH6.8) that contains 50mmol/LDTT; Bromjophenol blue 0.01%, H 2O constant volume 20ml), boiled 10 minutes; Polyacrylamide gel electrophoresis under the room temperature 100V voltage reaches the bottom of gel up to indicator (bromjophenol blue) forward position.
D) protein is to shifting on the nitrocellulose filter: before the transfer, use damping fluid (39ml glycine, 48mmolTris-base, 0.037%SDS, 20% methyl alcohol) balanced gel and nitrocellulose membrane 30 minutes; Shift 1h with the half dry type electroporation under the room temperature, 3 layers of Whatman filter paper are respectively filled up in the gel both sides.
E) Protein Detection on the film: nitrocellulose membrane is immersed in the confining liquid, and 37 ℃ are slowly shaken, and seal 60 minutes (confining liquid: get 5 gram skim-milks and be dissolved in 100ml1 * PBS (containing the 0.5g sodium azide)); Again filter membrane is immersed in the lavation buffer solution 37 ℃ of washed twice, each 15 minutes; Add first antibody (antibody of anti-human granulocyte macrophage colony stimulating factor), 37 ℃ of incubations 30 minutes; Same step b) is washed three times; Add second antibody (avidin-alkaline phosphatase enzyme complex), 37 ℃ of incubations 30 minutes, washed twice; Add the substrate colour developing and observe protein band.
Filial generation has improved 63% and 70% than the parent respectively
Embodiment 2 human granulocyte macrophage colony stimulating factors close expression in rich 25 seeds at soybean varieties
1 usefulness Xho I digestion with restriction enzyme pCAMBIA3300 plasmid and human granulocyte macrophage colony stimulating factor (hGM-CSF) gene, flat with T4DNA polysaccharase benefit, with Shrimp alkaline phosphatase dephosphorylation.The hGM-CSF gene is connected with the T4 ligase enzyme with the pCAMBIA3300 carrier, spends the night.The gene end adds aaggatgagctt oligonucleotide targeting signal.
2. with XhoI digestion with restriction enzyme pCAMBIA3300 plasmid and human granulocyte macrophage colony stimulating factor (hGM-CSF) gene, flat with T4DNA polysaccharase benefit, with Shrimp alkaline phosphatase dephosphorylation.The hGM-CSF gene is connected with the T4 ligase enzyme with the pCAMBIA3300 carrier, spends the night.The gene end adds gctttcgtttac oligonucleotide targeting signal.
3. these two kinds of expression vectors are changed among the Agrobacterium LBA4404, soybean transformation closes rich 25.
A) soybean seeds is through sterilization, be placed on MSB (a large amount of compositions of MS (Murashige and Skoog, 1962)+B5 trace ingredients (Gamborg et al, 1968))+6-BA (6-benzyl aminopurine, 6-benzylaminopurine) sprouted 5 days on 0.4mg/L (PH5.8) substratum, remove terminal bud and make wound, obtain explant, (+6-BA10mg/L+IBA 0.2mg/L (PH5.8) substratum was cultivated one day in advance to be placed on MSB.
B) under the vacuum condition under the 104Pa condition of negative pressure, make up pCAMBIA3300 expression vector Agrobacterium LBA4404 in the implementation column 4 and infect 10～20 minutes (OD600nm ≈ 0.5), be placed on MSB+6-BA 1.0mg/L+IBA 0.2mg/L (PH5.8) substratum and cultivated altogether 3 days, take out and be placed on 2 weeks of degerming on MSB+6-BA0.5mg/L+IBA0.1mg/L+ cephamycin 300mg/L+ Pyocianil 300mg/L (PH=5.8) substratum.
C) explant after the degerming is placed on MSB+ kantlex 80mg/L (PH=5.8) substratum, and per 2 weeks switching is once screened to indefinite bud occurring.Excision cotyledon when being elongated to 1～2cm is to being elongated to 3～4cm.
D) downcut the indefinite bud on the explant and being placed on 1/2MSB+ kantlex 50mg/L (PH=5.8) substratum, transformed the bud root induction 15～20 days, be transplanted to big basin until obtaining the seed that transformed plant produces.
E) results T2 analyzes for seed.
4. these two kinds of transgenic line offsprings are hybridized.
5. measure human granulocyte macrophage colony stimulating factor semi-invariant in the transgenic line seed, and compare with parent before the hybridization not respectively.Proteic quantitative analysis is with the step 5 among the embodiment 1.
Filial generation has improved 68% and 76% than the parent respectively.
Embodiment 3 human granulocyte macrophage colony stimulating factors close expression in rich 42 seeds at soybean varieties
1. the structure of conversion carrier is with step 1 and step 2 among the embodiment 2.
2. will contain pCAMBIA3300 expression vector Agrobacterium LBA4404, the soybean transformation kind closes rich 42.Concrete steps are seen the step 3 of embodiment 2.
4. these two kinds of transgenic line offsprings are hybridized.
5. measure human granulocyte macrophage colony stimulating factor semi-invariant in the transgenic line seed, and compare with parent before the hybridization not respectively.Measuring method is seen the step 5 of embodiment 1.
Filial generation has improved 52% and 87% than the parent respectively.

Claims (6)

1, a kind of raising foreign protein cumulative method in transgenic plant is characterized in that, comprises the steps:
1. use digestion with restriction enzyme pCAMBIA2300 and pCAMBIA3300 plasmid and human granulocyte macrophage colony stimulating factor hGM-CSF gene, mend flat, dephosphorylation, the carrier that hGM-CSF gene and enzyme were cut is connected with the T4 ligase enzyme, spend the night, the end of gene has KDEL endoplasmic reticulum targeting signal, and this small peptide can correctly be excised in mature peptide;
2. make up the expression vector of another kind of series with above-mentioned same method, be characterized in that the end of hGM-CSF gene has AFVY storage vacuole targeting signal, this small peptide can correctly be excised in mature peptide;
3. these two kinds of expression vectors are imported respectively among Agrobacterium GV3101 and the LBA4404, draw an amount of Agrobacterium adding and contain in the antibiotic YEP substratum, 28 ℃, 250rpm cultivates 36hr, when the OD value reaches about 0.8, begins to be used for arabidopsis thaliana transformation and soybean;
4. the offspring of these two kinds of transfer-gen plants is hybridized the offspring who obtains hybridizing;
5. offspring and parent are carried out the protein quantification analysis.
2, raising foreign protein according to claim 1 cumulative method in transgenic plant is characterized in that, step 1. in, described dephosphorylation is meant and uses alkaline phosphatase.
3, raising foreign protein according to claim 1 cumulative method in transgenic plant is characterized in that, step 3. in, described antibiotic YEP is meant: every liter contains the 10g Tryptones, 10g yeast extract, 5gNaCl.
4, raising foreign protein according to claim 1 cumulative method in transgenic plant is characterized in that, step 5. in, described offspring and parent are carried out the protein quantification analysis, implement as follows:
A) quantitative to total soluble protein, get 2 μ l protein samples, add 1mlBradford reagent, behind the mixing, spectrophotometric instrumentation OD 595
B) Protein Detection on SDS-PAGE protein isolate and the film, albumen electrophoresis in SDS-PAGE glue reaches the bottom of gel up to the indicator forward position;
C) protein shifts on nitrocellulose filter at room temperature and shifts 1h with the half dry type electroporation, and 3 layers of Whatman filter paper are respectively filled up in the gel both sides;
D) Protein Detection on the film: add first antibody, 37 ℃ of incubations 30 minutes; Wash three times; Adding second antibody, 37 ℃ of incubations 30 minutes, washed twice; Add the substrate colour developing and observe protein band.
5, raising foreign protein according to claim 4 cumulative method in transgenic plant is characterized in that described first antibody is meant: the antibody of anti-human granulocyte macrophage colony stimulating factor.
6, raising foreign protein according to claim 4 cumulative method in transgenic plant is characterized in that described second antibody is meant: avidin-alkaline phosphatase enzyme complex.
CNB200510030446XA 2005-10-13 2005-10-13 Improvement for exogenous protein accumulation in transgene plant Expired - Fee Related CN1325652C (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104754954A (en) * 2012-08-23 2015-07-01 特郎萨格以色列有限公司 Transgenic microalgae and use thereof for oral delivery of proteins
US10480002B2 (en) 2014-02-12 2019-11-19 Transalgae Israel Ltd. Algal based edible vaccines

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JPH0225952A (en) * 1988-07-14 1990-01-29 Mitsubishi Electric Corp File access system
FR2777015B3 (en) * 1998-02-23 2000-09-15 Financ De Biotechnologie METHOD AND MEANS FOR OBTAINING CELLULAR AND ANIMAL MODELS OF NEURODEGENERATIVE DISEASES

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104754954A (en) * 2012-08-23 2015-07-01 特郎萨格以色列有限公司 Transgenic microalgae and use thereof for oral delivery of proteins
US9827280B2 (en) 2012-08-23 2017-11-28 Transalgae Israel Ltd. Transgenic microalgae and use thereof for oral delivery of proteins
US11344590B2 (en) 2012-08-23 2022-05-31 Transalgae Israel Ltd. Transgenic microalgae and use thereof for oral delivery of proteins
US10480002B2 (en) 2014-02-12 2019-11-19 Transalgae Israel Ltd. Algal based edible vaccines

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