CN109295075B

CN109295075B - NfOCP1 drought-resistant gene, amino acid sequence coded by same and application thereof in improving plant drought resistance

Info

Publication number: CN109295075B
Application number: CN201811285409.7A
Authority: CN
Inventors: 叶水烽; 高宁宁; 吴金红; 罗利军
Original assignee: SHANGHAI AGROBIOLOGICAL GENE CENTER
Current assignee: SHANGHAI AGROBIOLOGICAL GENE CENTER
Priority date: 2018-10-31
Filing date: 2018-10-31
Publication date: 2021-04-20
Anticipated expiration: 2038-10-31
Also published as: CN109295075A

Abstract

The invention belongs to the field of genetic engineering, and particularly relates to an NfOCP1 drought-resistant gene, an amino acid sequence coded by the gene and application of the gene in improving plant drought resistance, wherein the NfOCP1 drought-resistant gene is derived from Nostoc flagelliforme, a nucleotide sequence of the gene is shown as a sequence table SEQ ID NO.1, and an amino acid sequence coded by the gene is shown as a sequence table SEQ ID NO.2, and is used for improving the drought resistance of plants, particularly rice.

Description

NfOCP1 drought-resistant gene, amino acid sequence coded by same and application thereof in improving plant drought resistance

Technical Field

The invention belongs to the field of genetic engineering, and particularly relates to an NfOCP1 drought-resistant gene from Nostoc flagelliforme and an amino acid sequence coded by the same, which are used for improving the drought resistance of plants, particularly rice.

Background

Nostoc flagelliforme (Nostoc flagelliforme) is mainly distributed in arid or semiarid desert regions of the northern hemisphere and is often stressed by abiotic factors such as extreme drought, large temperature difference, high-concentration saline and alkaline, nutrient deficiency, UV-B radiation and the like. Stress factors may cause a range of damage to cells including nucleic acid damage, protein damage, membrane lipid damage, etc., thereby disrupting normal cellular metabolism. After long-term environmental selection and adaptation of self structural functions, nostoc flagelliforme has evolved a series of physiological, ecological and molecular mechanisms to resist various adversities. Therefore, nostoc flagelliforme has become one of the best materials for researching stress adaptation mechanism and discovering stress resistance genes.

Under strong light, blue algae are susceptible to photooxidative stress. Singlet oxygen is the major active oxygen form of photooxidative stress, has high reactivity, attacks and oxidizes proteins, lipids and accountants, and in particular can stimulate the degradation of D1 protein in the photosynthetic system PSII, resulting in photooxidative damage and photoinhibition (Kirilovsky, 2015). In plants, carotenoids can be directly used as substrates for singlet oxygen, thereby reducing the concentration of singlet oxygen in the photosynthetic reaction center and alleviating photooxidative stress. In cyanobacteria, it is mainly completed by Orange Carotenoid Protein (OCP) (Kirilovsky, 2015). Under natural conditions, light inhibition often occurs in the upper leaves of plants at noon on a fine day, and when strong light and other environmental stress factors, such as drought, high temperature, and the like, exist at the same time, light inhibition is aggravated and occurs even at low light intensity.

China is a country with frequent natural disasters, water resources are relatively poor, and the water resources are extremely unevenly distributed in geography and space time, so that the agriculture in China is often subjected to drought to cause grain yield reduction. Rice is one of the most important grain crops in China, nearly half of fresh water resources in China are consumed in production of the rice, the water-saving and drought-resisting performance of crops such as rice and the like is improved, and the rice is a major demand (Luo, 2010) for guaranteeing the grain safety and ecological safety in China and guaranteeing the sustainable development of agriculture. At present, the transgenic technology is widely applied to the cultivation of drought-resistant rice, and the adopted strategy is to express drought-induced or drought-resistant related genes in the rice. Therefore, the method has very important significance for cloning and excavating the drought-resistant gene of the nostoc sphaeroides and applying the gene to biological genetic engineering.

Disclosure of Invention

In view of the above, the present invention aims to provide an NfOCP1 drought-resistant gene derived from nostoc flagelliforme, which is obtained based on nostoc flagelliforme drought stress transcription, and the expression level of the gene is obviously increased under the drought stress (fig. 1).

The invention further aims to provide application of the NfOCP1 drought-resistant gene in improving plant drought resistance, particularly application in rice.

The above object of the present invention is achieved by the following technical solutions:

on the first hand, the NfOCP1 drought-resistant gene is derived from Nostoc flagelliforme, the nucleotide sequence of the NfOCP1 drought-resistant gene is shown as SEQ ID NO.1, the sequence length is 441bp, and the sequence specifically comprises:

ATGACTTACACAGCTGATGAAGCAACAAAACCAGCTTTAGAAACTTTTCAAGGCTTTGA TGTAGATACTCAGCTAGCCCTACTTTGGTTCGGTTATCTTGATCTTAAAGAGCAGCTAAA CCCAGCACCTCCTGAAAGCGTAGAAGCTATAGCTAAAGCAGTGTTTGACCAAATCCAAG AGTTGTCTCAAGAAGAGCAACTGCAAGCACAACGGGACATTATTAATGGTGCAAGCCA AACCTATAATAGTCTAAGTCCCAATGCTAAATTAGACGTTTGGCTACTGCTGGCACAAGG AATGGACAATGGAAGCGTCATCCAAGTACCGTCCGACTATCAACTACCTGGTGAAACGG ATGAATTTGTCGCATTGATCAAAAAGCTAGAGTTTGAGCAGCGCGTTAATTTTATGTTGA GTGTGGTGCAAGGGTTCGGTAGTTAA, respectively; the coded amino acid sequences are 146, as shown in SEQ ID NO.2, and specifically include:

MTYTADEATKPALETFQGFDVDTQLALLWFGYLDLKEQLNPAPPESVEAIAKAVFDQIQELS QEEQLQAQRDIINGASQTYNSLSPNAKLDVWLLLAQGMDNGSVIQVPSDYQLPGETDEFVA LIKKLEFEQRVNFMLSVVQGFGS。

in a second aspect, the use of the NfOCP1 drought-resistant gene for improving drought resistance of a plant, wherein the plant is rice.

According to the sequence of the NfOCP1 drought-resistant gene, the NfOCP1 drought-resistant gene and any interested DNA or homologous DNA thereof are obtained by directly adopting a PCR (polymerase Chain reaction) technology through amplification from genome, mRNA and cDNA, and an expression vector carrying the NfOCP1 drought-resistant gene can be introduced into prokaryotic bacterial cells and plant cells by using Ti plasmids, plant virus vectors, direct DNA transformation, microinjection, electroporation and other conventional biotechnology methods. By separating and applying the DNA fragment containing the NfOCP1 drought-resistant gene in the Nostoc flagelliforme, the drought-resistant capability of escherichia coli and rice under drought conditions can be enhanced.

The invention has the beneficial effects that: the germination test is carried out on wild type seeds and NfOCP1 gene-transferred rice T2 seeds, after 10 days of culture in 1/2MS culture medium added with 120mM mannitol, the average plant height of the wild type is 6.15cm of small buds, the growth vigor of a transgenic line is obviously superior to that of a wild type control, and the average plant heights of 4 transgenic families respectively reach 11.68cm, 10.44cm, 12.41cm and 14.4 cm. The fact that the overexpression of the NfOCP1 gene in rice indeed improves the drought resistance of transgenic plants is shown.

Drawings

FIG. 1 is a graph comparing the expression of NfOCP1 gene in the water-loss transcriptome of Nostoc flagelliforme in example 1.

FIG. 2 is the expression analysis of NfOCP1 gene under water loss stress in example 1.

FIG. 3 is the SDS-PAGE result of prokaryotic expression of NfOCP1 gene in example 2, wherein ck is the negative control of empty vector, and 1, 2, 3, 4, 5, 6 are 6 clones of recombinant plasmid pGEX-NfOCP 1.

FIG. 4 is the results of the stress on prokaryotic expression in example 2. pGEX is the empty vector and NfOCP1 is the recombinant plasmid. Wherein, FIG. 4A is a graph of the experimental result under the control condition of normal culture, FIG. 4B is a graph of the experimental result under the condition of adding sorbitol, and FIG. 4C is a graph of the experimental result of simultaneously adding IPTG and sorbitol.

FIG. 5 is a diagram of the plant overexpression vector ub-06 selected in the present invention.

FIG. 6 is a graph showing the expression level of the rice line transformed with NfOCP1 gene in example 3.

FIG. 7 shows the plant height statistics of the NfOCP1 transgenic rice lines OE-1, OE-3, OE-7, OE-8 and wild-type WT in example 4 after 10 days of growth on 120mM mannitol-added plates (7A); growth performance of OE-1, OE-3, OE-7, OE-8 and wild-type WT after 10 days of growth in plates supplemented with 120mM mannitol (7B).

Detailed Description

The invention will now be further illustrated by reference to the following examples:

experimental procedures without specific conditions noted in the examples below, generally following conventional conditions, such as molecular cloning, Sambrook et al: the conditions described in the Laboratory Manual (New York: Cold Spring Harbor Laboratory Press, 1989), or as recommended by the manufacturer.

Example 1: cloning of Nostoc flagelliforme NfOCP1 gene

(1) Culture of Nostoc flagelliforme

Nostoc flagelliforme cultured in liquid (natural wild sample was sampled from Sunit left flag of inner Mongolia autonomous region). Homogenizing algae seed with glass homogenizer to disperse algae filament before inoculation, inoculating into 300ml BG11 culture medium for aseptic culture at 25 deg.C and light intensity of 20 + -2 μmol phosns m^-2s^-1(24h continuous illumination), shaking the algae in the morning, at noon and at night three times a day to enable the algae cells to be suspended and uniformly illuminated.

(2) DNA extraction

Grinding the nostoc flagelliforme sample cultured in the step (1) in liquid nitrogen, subpackaging the ground nostoc flagelliforme sample into 1.5mL centrifuge tubes, adding 1mL of extracting solution (100mmol/L Tris-HCl, 500mmol/L NaCl, 50mmol/L EDTA, PH8.0), 100 microliter 20% SDS, 10 microliter 10mg/mL proteinase K, and fully and uniformly mixing; cracking at 37 deg.C for 30min, and mixing once every 5 min; centrifuging at 12000rpm for 10min, collecting supernatant, adding equal volume of Tris saturated phenol, mixing, and standing at room temperature for 2 min; centrifuging at 12000rpm for 10min, collecting supernatant, adding equal volume of chloroform/isoamyl alcohol, mixing, and standing at room temperature for 2 min; centrifuging at 12000rpm for 10min, collecting supernatant, adding equal volume of chloroform, mixing, and standing at room temperature for 2 min; centrifuging at 12000rpm for 10min, collecting supernatant, adding isopropanol with equal volume, adding 3M NaAc with volume of 1/10, and mixing to obtain white filament; picking up the white filamentous precipitate with a10 microliter suction head, and washing with 70% ethanol for 2 times; air dried and dissolved by adding 30. mu.l of Buffer EB.

(3) Amplification of full-Length NfOCP1

In nostoc flagelliforme water loss transcriptome analysis, the expression of the NfOCP1 gene is obviously improved under the conditions of water loss of 10%, 30%, 50%, 70% and 90%. The full-length sequence of the NfOCP1 gene is obtained by transcriptome sequencing, and upstream and downstream primers (NfOCP1F1:5-ATGACTTACACAGCTGATGA-3, NfOCP1R 1: 5-TTAACTACCGAACCCTTG-3) are designed according to sequence information and are shown in a sequence table SEQ ID NO. 3-4.

The NfOCP1 gene is obtained by cloning from Candida phaeoides genome DNA, and the amplified product is the nucleotide sequence (1-441bp) shown in SEQ ID NO.1 of the invention through sequencing verification.

(4) Expression profiling analysis of NfOCP1 gene under dehydration treatment

The solid nostoc flagelliforme is soaked in BG11 culture medium and reaches complete saturation after 2 days. And starting dehydration treatment, sampling at 6 time points of 0%, 10%, 30%, 50%, 70% and 90% of dehydration, and grinding in liquid nitrogen. The total RNA of the Chinese cabbage is extracted by using an RNAprep Pure polyphenol polysaccharide plant total RNA extraction kit (catalog number: DP441) of TIANGEN company, the quality of the total RNA is identified by electrophoresis, and then the RNA content is determined on a spectrophotometer.

Reverse transcription to synthesize first strand cDNA

The extracted RNA sample was digested with DNaseI before reverse transcription in the following reaction scheme:

after 15min at 37 ℃ the reaction was stopped by adding 0.25. mu.L of 0.1M EDTA (to ensure a final concentration >2mM), incubating at 70 ℃ for 10min, and briefly centrifuged and placed on ice for further use.

First strand cDNA was synthesized according to the Promega reverse transcription System A3500 handbook, with the following steps:

the following reagents were added to the DNaseI digested sample in order to prepare a 20. mu.L reaction system:

incubating the reaction system at 42 ℃ for 15 min; then heating at 95 deg.C for 5min to inactivate AMV reverse transcriptase and prevent it from binding to DNA; standing at 4 deg.C or on ice for 5 min. The prepared cDNA can be used immediately or stored at-20 ℃ for use.

Quantitative analysis of Gene expression Using Takara

Premix Ex Taq^TM(Perfect Real Time) kit, and American ABI

7000 quantitative PCR instrument. A quantitative primer (NfOCP1 QF: 5-GCTGATGAAGCAACAAAACC-3; NfOCP1 QR: 5-CAAGATAACCGAACCAAAGT-3, the primer sequence is shown in a sequence table SEQ ID NO. 5-6) is designed according to the sequence of NfOCP 1. A primer was designed based on the cDNA sequence of a rice housekeeping gene actin (GenBank accession No. AY212324) as a reference gene.

Preparation of 20. mu.l reaction System:

the reaction conditions are as follows: the temperature is 95 ℃ for 30s, then the circulation is carried out for 40 times at 95 ℃ for 5s and 60 ℃ for 31s, and the Dissociation Stage is additionally arranged. Data was collected at 60 ℃ for 31s for each cycle and other detailed operations were performed according to the instrument instructions. Calculating the average CT value and the Delta CT value of the target gene and the reference gene, using 2^-ΔΔCTThe method carries out result analysis, and finally, data are imported into GraphPad prism5.0 to make a histogram of the relative expression quantity of the target gene, which is shown in figure 2.

Example 2: prokaryotic expression and stress identification of Nostoc flagelliforme NfOCP1 protein

The prokaryotic expression vector of NfOCP1 was constructed by One Step Cloning Kit recombinant technology. Using the NfOCP1 gene obtained in example 1 as template, the primer NfOCP1F 2: 5-ttccaggggcccctgggatccATGACTTACACAGCTGATGA-3, rear primer NfOCP1R 2: 5-gtcacgatgcggccgctcgagTTAACTACCGAACCCTTG-3, and the primer is shown in SEQ ID NO.7-8 of the sequence table, PCR amplification is carried out, the product is recovered and purified, and the amplified product fragment is cloned to the vector pGEX-6P-14984 through One Step Cloning Kit recombination reaction. The specific process is as follows:

(1) PCR amplification

The 20 μ L reaction was as follows:

and (3) amplification procedure: pre-denaturation at 94 ℃ for 3min, at 94 ℃ for 1min, at 56 ℃ for 45sec, at 72 ℃ for 1min, for 30 cycles, at 72 ℃ for 10 min. After the reaction, 5. mu.L of the mixture was subjected to electrophoresis.

(2) Recovery of PCR products

The DNA was purified and recovered by using a general agarose gel DNA recovery kit (Tiangen Biochemical technology Co., Ltd.).

(3) Recombination reactions

The recombination reaction was performed using One Step Cloning Kit from Nanjing Novowed Biotechnology Ltd. The method comprises the following steps:

mu.g of the circular pGEX-6P-14984 plasmid was added to 20. mu.l of the digestion reaction system and digested at 37 ℃ for 2 hr. The restriction enzymes were used in an amount of 1. mu.l each of BamHI and XhoI. After the enzyme digestion is finished, the enzyme digestion product is heated for 20min at 65 ℃ to inactivate the endonuclease. The following reaction system was prepared in an ice-water bath.

After the system is prepared, the components are mixed evenly by gently blowing and beating the components up and down for several times by a pipette and are placed at 37 ℃ for reaction for 30 min. After the reaction was completed, the reaction tube was immediately placed in an ice-water bath to cool for 5 min. Then 20. mu.l of the cooled reaction solution was added to 200. mu.l of expression-sensitive BL21 cells, and the mixture was flicked onto the tube wall and left on ice for 30 min. And (3) thermally shocking for 45-90 seconds at 42 ℃, and incubating for 2min in an ice water bath. 900. mu.l of LB medium was added and incubated at 37 ℃ for 10min for sufficient recovery. Shake the bacteria for 45min at 37 ℃. 100 mul of the bacterial solution was evenly spread on a plate containing antibiotic Amp +. The plate was inverted, cultured overnight at 37 ℃ and sequenced to obtain recombinant plasmid pGEX-NfOCP1 containing NfOCP 1.

(4) Expression of NfOCP1 protein

A single clone of the strain containing the recombinant plasmid NfOCP1 was cultured overnight at 37 ℃ in 2ml LB (containing Amp 50. mu.g/ml). Diluting overnight bacteria at a ratio of 1: 50, shake culturing at 37 deg.C to OD600 ≡ 0.6, collecting part of the liquid as un-induced control group, adding IPTG inducer to final concentration of 0.4mM as experimental group, and shake culturing at 37 deg.C for 3 hr. 1ml of each of the cells was centrifuged at 12000 g.times.30 s to harvest the pellet, which was resuspended in 100. mu.L of 1% SDS, mixed well and incubated at 70 ℃ for 10 min. Centrifuging at 12000g × 1min, collecting supernatant as sample, and performing SDS-PAGE electrophoresis, wherein the specific result is shown in FIG. 3. Wherein CK1 and CK2 are negative controls of an empty vector, and 1, 2, 3, 4, 5 and 6 are clones of 6 recombinant plasmids pGEX-NfOCP 1.

(5) Prokaryotic expression stress

And (4) shaking the bacteria until OD600 is between 0.4 and 0.6, taking pGEX empty vector as a reference, adjusting the initial OD600 of each tube to be consistent, then adding the same amount of expanded and propagated bacteria liquid into ampicillin-containing LB of various treatments, wherein the 3 treatments are respectively adding no additional reagent, adding Sorbitol (Sorbitol), adding an Inducer (IPTG) and a Sorbitol reagent. OD600 is measured by a spectrophotometer at intervals (measured at intervals of 1 h), line graphs are drawn according to statistical results, the results show that under the condition of induction without IPTG, the growth potential of the recombinant plasmid and the empty vector control bacteria is not different, after induction, the growth potential of the recombinant plasmid pGEX-NfOCP1 is better under the stress of sorbitol, and specific results are shown in figure 4, wherein figure 4A is a graph of the experimental results under the condition of normal culture control, figure 4B is a graph of the experimental results under the condition of sorbitol, and figure 4C is a graph of the experimental results with IPTG and sorbitol added at the same time.

Example 3: nostoc flagelliforme NfOCP1 overexpression transformation rice

Using the NfOCP1 gene obtained in example 1 as template, the primer NfOCP1F 3: 5-caggtcgactctagaggatccATGACTTACACAGCTGATGA-3, rear primer NfOCP1R 3: 5-gggaaattcgagctggtcaccTTAACTACCGAACCCTTG-3, the primer is shown in SEQ ID NO.9-10 of the sequence table, PCR amplification is carried out, the product is recovered and purified, the amplified product fragment is cloned to a plant overexpression vector ub-06 through One Step Cloning Kit recombination reaction, and the vector diagram of ub-06 is shown in figure 5. The specific process is as follows:

(1) PCR amplification was performed as described in example 1.

(2) The PCR product was recovered as described in example 2.

(3) Recombination reactions

The recombination reaction was carried out using One Step Cloning Kit from Nanjing Novowed Biotechnology Ltd as follows:

mu.g of the circular ub-06 plasmid was added to 20. mu.l of the digestion reaction system and digested at 37 ℃ for 2 hr. The restriction enzymes were used in an amount of 1. mu.l each of BamHI and XhoI. After the enzyme digestion is finished, the enzyme digestion product is heated for 20min at 65 ℃ to inactivate the endonuclease.

The following reaction system was prepared in an ice-water bath.

After the system is prepared, the components are mixed evenly by gently blowing and beating the components up and down for several times by a pipette and are placed at 37 ℃ for reaction for 30 min. After the reaction was completed, the reaction tube was immediately placed in an ice-water bath to cool for 5 min. Then 20. mu.l of the cooled reaction solution was added to 200. mu.l of expression-sensitive DH 5. alpha. cells, gently flicked to the tube wall, and left on ice for 30 min. And (3) thermally shocking for 45-90 seconds at 42 ℃, and incubating for 2min in an ice water bath. 900. mu.l of LB medium was added and incubated at 37 ℃ for 10min for sufficient recovery. Shake the bacteria for 45min at 37 ℃. 100 mul of the bacterial solution was evenly spread on a plate containing antibiotic Amp +. The plate was inverted, cultured overnight at 37 ℃ and sequenced to obtain plasmid u6-NfOCP1 containing NfOCP 1.

(4) Agrobacterium transformation

Adding 1 mu L u6-NfOCP1 plasmid into 100 mu L agrobacterium EHA105 competent cells, gently mixing, carrying out ice-water bath for 30min, and carrying out quick freezing and cold shock for 2min in liquid nitrogen; adding 400-800 μ LYEP culture medium (Kan)⁺) Shaking and culturing at 28 deg.C and 200r/min for 3-5 h; centrifuging at room temperature (5000r/min, 5min), retaining 100 μ L supernatant, resuspending thallus, and spreading on LA solid medium (Kan)⁺) And carrying out inverted culture at 28 ℃ for 2 days until colonies with proper sizes grow out, and selecting a monoclonal for PCR detection to obtain a positive strain.

(5) Callus induction: rinsing the seeds with sterile water for 15-20min, sterilizing with 75% ethanol for 1min, and sterilizing with sodium hypochlorite (1.5% effective concentration) solution under shaking for 20 min. Finally, the mixture is washed with sterile water for 5 times. The washed seeds were blotted dry with absorbent paper and inoculated in an induction callus medium and cultured in the dark at 25 ℃ for 2 weeks.

Callus induction medium: the induction medium shown in Table 1 was added with proline 0.3g, casein hydrolysate 0.6g, sucrose 30g and 2.5ml of 2,4-D (concentration 1mg/ml) to prepare a 1L solution, the pH was adjusted to 5.9, agar powder 7g was added, and the solution was sterilized at high temperature and high pressure.

(6) Subculturing: the embryogenic callus was excised, inoculated into a subculture medium, and cultured in the dark at 25 ℃ for 2 weeks.

Subculture medium: adopting the subculture medium shown in Table 1, adding 0.5g of proline, 0.6g of hydrolyzed casein protease, 30g of sucrose and 2ml of 2,4-D (concentration 1mg/ml) to prepare 1L solution, adjusting pH to 5.9, adding 7g of agar powder, and sterilizing at high temperature and high pressure.

(7) Agrobacteria dip dyeing and callus co-culture: culturing Agrobacterium, selecting positive single colony, and culturing in 1ml Agrobacterium culture solution (containing antibiotic) at 28 deg.C overnight; the above culture was added to 50ml of Agrobacterium culture medium (containing antibiotics) and cultured at 28 ℃ until OD600 became 0.6-1.0. And centrifuging the obtained agrobacterium liquid, adding the collected thalli into a suspension culture solution, and performing shake culture for 30min until OD600 is 0.6-1.0. Then placing the callus into suspension culture solution containing agrobacterium liquid, and carrying out shake culture for about 20 min. Air drying the callus on sterilized filter paper, transferring into co-culture medium, and culturing at 25 deg.C in dark for 5 d.

Suspension culture solution: using the suspension culture medium shown in Table 1, 0.08g of hydrolyzed casein, 2g of sucrose and 0.2ml of 2,4-D (concentration: 1mg/ml) were added to prepare 100ml of a solution, the pH was adjusted to 5.4, the solution was divided into two bottles (50 ml each), and the solution was sterilized by autoclaving at high temperature. 1ml of 50% glucose and 100. mu.L AS (100mM) were added before use.

Co-culture medium: the co-culture medium shown in Table 1 was used, and 0.8g of hydrolyzed casein protease, 20g of sucrose and 3.0ml of 2,4-D (concentration: 1mg/ml) were added to prepare 1L of a solution, the pH was adjusted to 5.6, 7g of agar powder was added, and high-temperature and high-pressure sterilization was carried out. 20ml of 50% glucose and 1ml of AS (100mmol/L) were added before use.

(8) Screening and culturing: after co-culturing for 3 days, selecting the good callus, transferring the callus into a screening culture medium, carrying out dark culture at 25 ℃ for 2 weeks, and screening twice. Screening a culture medium: the screening medium shown in Table 2 was used, and 0.6g of hydrolyzed casein protease, 30g of sucrose and 2.5ml of 2,4-D (concentration: 1mg/ml) were added to prepare 1L of a solution, the pH was adjusted to 6.0, 7g of agar powder was added, and high-temperature autoclaving was performed. 1ml Hn and 1ml Cn (100ppm) were added prior to use.

(9) Differentiation culture: selecting embryogenic callus, inoculating into differentiation culture medium, culturing at 24 deg.C for 16h/8h in light and dark to induce differentiation bud (4-6 weeks). Differentiation medium: adopting the differentiation culture medium shown in Table 2, adding 2.0 mg/L6-BA, 2.0mg/L KT, 0.2mg/L NAA, 0.2mg/L IAA, 1.0g of hydrolytic casein and 30g of sucrose to prepare 1L solution, adjusting pH to 6.0, adding 7g of agar powder, and sterilizing at high temperature and high pressure.

(10) Rooting culture: when the bud grows to about 2cm, cutting off the bud, inserting the bud into a rooting culture medium, culturing at about 25 ℃ in 16h/8h in light and dark, and inducing to root. Rooting culture medium: the rooting medium shown in Table 2 was added with 30g of sucrose to prepare 1L of solution, the pH was adjusted to 5.8, 7g of agar powder was added, and the solution was sterilized at high temperature and high pressure.

(11) Culturing transformed plants: opening the test tube mouth after the root system is developed, adding sterile water to harden the seedlings for 2-3d, taking out the plants, washing the attached solid culture medium with sterile water, transferring the solid culture medium into soil, shading and avoiding wind at the beginning, and performing conventional field or greenhouse management culture after the plants are robust.

Table 1: minimal Medium component 1

Table 2: minimal Medium component 2

(12) Positive detection of overexpressing plants

Cutting the regenerated plant leaves, extracting DNA by a CTAB method, and carrying out PCR detection by using hpt specific primers (hptF: ACACTACATGGCGTGATTTCAT; hptR: TCCACTATCGGCGAGTACTTCT, the primers are shown in a sequence table SEQ ID NO. 11-12).

And (3) PCR system:

PCR reaction procedure:

(13) detection of expression level of target gene in over-expression positive plant

Get T₀And (3) replacing rice leaves, grinding in liquid nitrogen, and extracting RNA. The method comprises the following specific steps:

extraction of RNA: freezing the sample with liquid nitrogen in mortar, grinding into powder, adding 1ml TRNzol-A⁺2mL of EP tube (Tiangen Biochemical technology Co., Ltd.) was shaken thoroughly, and then left at room temperature for 5min, and then 0.2mL of chloroform was added, and after shaking vigorously for 15s, left at room temperature for 3 min; after centrifugation at 12000rpm for 10min at 4 ℃ the supernatant was transferred to a new 2mL EP tube, an equal volume of isopropanol was added to precipitate RNA, and 100. mu.L of RNase-free ddH was added₂And dissolving the O. The total RNA quality is identified by electrophoresis, and then the RNA content is determined on a spectrophotometer.

Reverse transcription to synthesize first strand cDNA

Quantitative analysis of Gene expression Using Takara

Premix Ex Taq^TM(Perfect Real Time) kit, and American ABI

7000 quantitative PCR instrument. A quantitative primer (NfOCP1 QF: 5-GCTGATGAAGCAACAAAACC-3; NfOCP1 QR: 5-CAAGATAACCGAACCAAAGT-3) is designed according to the sequence of NfOCP1, and the primer is shown as a sequence table SEQ ID NO. 5-6. A primer was designed from the cDNA sequence of a reference gene, which was a rice domestication gene actin (GenBank accession No. AY212324).

Preparation of 20. mu.l reaction System:

the reaction conditions are as follows: the temperature is 95 ℃ for 30s, then the circulation is carried out for 40 times at 95 ℃ for 5s and 60 ℃ for 31s, and the Dissociation Stage is additionally arranged. Data was collected at 60 ℃ for 31s for each cycle and other detailed operations were performed according to the instrument instructions. Calculating the average CT value and the Delta CT value of the target gene and the reference gene, using 2^-ΔΔCTThe method is used for analyzing results, and finally, data are introduced into GraphPad prism5.0 to make a histogram of the relative expression amount of the target gene, as shown in FIG. 6.

Example 4: transgenic rice T₂Shoot-period mannitol simulation drought treatment for seed generation

Over-expressing transgenic pedigree seeds were dehulled and sterilized (75% alcohol treatment for 1min, 1.5% NaClO treatment for 20min, 5 washes in sterile water), germinated on 1/2MS medium containing 50mg/L hygromycin, and wild type controls were sown one day late on 1/2MS medium without hygromycin. And selecting seeds with good germination and consistent growth vigor after 2-3 days of germination, transferring the seeds to 1/2MS culture medium containing 120mM for culture, and counting the growth condition after 10 days. The experimental result shows that after 10 days of stress culture, the average plant height of the wild type control is 6.15cm, the growth vigor of the transgenic line is obviously superior to that of the wild type control, and the average plant heights of 4 transgenic families respectively reach 11.68cm, 10.44cm, 12.41cm and 14.4 cm. Specifically, as shown in fig. 6, it is demonstrated that overexpression of NfOCP1 gene in rice indeed improves drought resistance of transgenic plants.

The above description is only for the purpose of illustrating the preferred embodiments of the present invention, and the present invention should not be limited by the disclosure of the preferred embodiments. Therefore, it is intended that all equivalents and modifications which do not depart from the spirit of the invention disclosed herein are deemed to be within the scope of the invention.

Sequence listing

<110> Shanghai city agricultural biological gene center

<120> NfOCP1 drought-resistant gene, amino acid sequence coded by same and application thereof in improving plant drought resistance

<130> 2018-10-29

<141> 2018-10-31

<160> 12

<170> SIPOSequenceListing 1.0

<210> 1

<211> 441

<212> DNA

<213> unknown ()

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atgacttaca cagctgatga agcaacaaaa ccagctttag aaacttttca aggctttgat 60

gtagatactc agctagccct actttggttc ggttatcttg atcttaaaga gcagctaaac 120

ccagcacctc ctgaaagcgt agaagctata gctaaagcag tgtttgacca aatccaagag 180

ttgtctcaag aagagcaact gcaagcacaa cgggacatta ttaatggtgc aagccaaacc 240

tataatagtc taagtcccaa tgctaaatta gacgtttggc tactgctggc acaaggaatg 300

gacaatggaa gcgtcatcca agtaccgtcc gactatcaac tacctggtga aacggatgaa 360

tttgtcgcat tgatcaaaaa gctagagttt gagcagcgcg ttaattttat gttgagtgtg 420

gtgcaagggt tcggtagtta a 441

<210> 2

<211> 146

<212> PRT

<213> unknown ()

<400> 2

Met Thr Tyr Thr Ala Asp Glu Ala Thr Lys Pro Ala Leu Glu Thr Phe

1 5 10 15

Gln Gly Phe Asp Val Asp Thr Gln Leu Ala Leu Leu Trp Phe Gly Tyr

20 25 30

Leu Asp Leu Lys Glu Gln Leu Asn Pro Ala Pro Pro Glu Ser Val Glu

35 40 45

Ala Ile Ala Lys Ala Val Phe Asp Gln Ile Gln Glu Leu Ser Gln Glu

50 55 60

Glu Gln Leu Gln Ala Gln Arg Asp Ile Ile Asn Gly Ala Ser Gln Thr

65 70 75 80

Tyr Asn Ser Leu Ser Pro Asn Ala Lys Leu Asp Val Trp Leu Leu Leu

85 90 95

Ala Gln Gly Met Asp Asn Gly Ser Val Ile Gln Val Pro Ser Asp Tyr

100 105 110

Gln Leu Pro Gly Glu Thr Asp Glu Phe Val Ala Leu Ile Lys Lys Leu

115 120 125

Glu Phe Glu Gln Arg Val Asn Phe Met Leu Ser Val Val Gln Gly Phe

130 135 140

Gly Ser

145

<210> 3

<211> 20

<212> DNA

<213> unknown ()

<400> 3

atgacttaca cagctgatga 20

<210> 4

<211> 18

<212> DNA

<213> unknown ()

<400> 4

ttaactaccg aacccttg 18

<210> 5

<211> 20

<212> DNA

<213> unknown ()

<400> 5

gctgatgaag caacaaaacc 20

<210> 6

<211> 20

<212> DNA

<213> unknown ()

<400> 6

caagataacc gaaccaaagt 20

<210> 7

<211> 41

<212> DNA

<213> unknown ()

<400> 7

ttccaggggc ccctgggatc catgacttac acagctgatg a 41

<210> 8

<211> 39

<212> DNA

<213> unknown ()

<400> 8

gtcacgatgc ggccgctcga gttaactacc gaacccttg 39

<210> 9

<211> 41

<212> DNA

<213> unknown ()

<400> 9

caggtcgact ctagaggatc catgacttac acagctgatg a 41

<210> 10

<211> 39

<212> DNA

<213> unknown ()

<400> 10

gggaaattcg agctggtcac cttaactacc gaacccttg 39

<210> 11

<211> 22

<212> DNA

<213> unknown ()

<400> 11

acactacatg gcgtgatttc at 22

<210> 12

<211> 22

<212> DNA

<213> unknown ()

<400> 12

tccactatcg gcgagtactt ct 22

Claims

The application of the NfOCP1 drought-resistant gene in improving the drought resistance of plants is characterized in that the nucleotide sequence of the NfOCP1 drought-resistant gene is shown as SEQ ID No.1, and the plants are rice.
2. The use of claim 1, wherein said NfOCP1 drought resistance gene is derived from Nostoc flagelliforme (Nostoc flagelliforme).
3. The use according to claim 1, wherein the NfOCP1 drought resistant gene encodes an amino acid sequence shown in SEQ ID No. 2.