KR100894323B1 - Method for Producing Available Recombinant Protein by Culturing Adventitious Root of Transformed Plants - Google Patents

Abstract

The present invention relates to a method for mass production of involuntary roots of plants using bioreactors, and to a method for mass production of useful recombinant proteins from the roots and hair roots of transformed plants. According to the method of the present invention, by using the appropriate induction medium and the appropriate concentration of plant growth regulators to induce the root or hair roots from the plant, and liquid culture in the bioreactor to produce a large amount of root or hair roots, which is useful It is possible to stably produce a large amount of recombinant protein.

Abdominal root, hairy root, plant expression vector, transformation, bioreactor

Description

Method for Producing Available Recombinant Protein by Culturing Adventitious Root of Transformed Plants}

The present invention relates to a method for mass production of involuntary roots of plants using bioreactors, and to a method for mass production of useful recombinant proteins from the roots and hair roots of transformed plants.

Recently, plants have attracted attention as mass production systems of medical and industrial proteins. This is because it can be easily harvested and processed by using the existing agricultural foundation established, and thus a large amount of desired biomass can be secured. In addition, unlike bacteria, which were mainly used as protein expression systems, plants have eukaryotic protein synthesis pathways where post-detox modification processes are essential for the activity of mammalian proteins (Cabanes-Macheteau et al ., Glycobiolgy 9: 365-). 372 (1999)), the protein expressed in the plant is almost the same as the protein expressed in the mammal, unlike the protein expressed in bacteria.

In general, foreign proteins derived from animals were mainly produced using animal cell lines, but there were high maintenance costs and difficulties in mass expression and separation and purification. In order to compensate for these disadvantages, a technique for separating and purifying glycoproteins having large-scale expression and biological activity using E. coli has been introduced. Less produced or produced polypeptides do not form a stable tertiary structure, are easily degraded, and also have a problem in that they are aggregated in an inactive form and exist as an inclusion body in cells.

Therefore, a method of using a transgenic plant obtained by introducing a gene involved in producing a recombinant protein useful for a plant using the advantages of a plant as a production system of a target protein has been widely used.

The production system of useful recombinant protein using plants can be largely divided into four types. The first is to use the protein expressed in the leaves, the second is to use seeds of grains and beans, the third is to use fruits and fruits, and finally to use cotton and oil seeds. All of these have their advantages, but all have problems in terms of environmental impacts that are emerging. The first problem that is currently emerging in the field of plant genetic engineering is that the growth of the plant is unstable and inhibited by the surrounding environment when the plant is grown, and the yield may be lowered. Plants can be contaminated. Of course, there have been no reports of serious problems through scientific analysis. However, in the case of genetically engineered soybeans or corn, there are some environmental problems in the production of foreign protein expressing plants produced by plant genetic engineering. It is likely to be raised.

Rice is used for food by almost 95% of Asia's population, and is the most balanced diet in the world with more than 50% of the population. Rice has been one of the most difficult crops to genetically manipulate, but it has recently emerged as a model for research into plant genomes, plant pathology, genetic engineering and expression (Christou, Plant Mol. Biol ., 35: 197-203). , (1997); Tang et al ., Planta ., 208: 552-63, (1999). Rice, a monocotyledonous plant, is a model of monocotyledonous plants because of its small genome size and easy tissue culture, and after the publication of Hiei et al ., A transgenic system was developed by Agrobacterium tumutation (Hiei et al ., Plant J. , 6: 271-82, (1994); Aldemita and Hodges, Planta , 199: 612-7, (1996)).

Therefore, there is a need to develop a system capable of stably producing a large amount of foreign recombinant protein while solving the above-mentioned problems by proliferating large amounts of malformed or hairy roots of transformed plants in a bioreactor.

Throughout this specification, numerous citations are referenced and citations are indicated. The disclosures of the cited documents are hereby incorporated by reference in their entirety, so that the level of the technical field to which the present invention belongs and the contents of the present invention are more clearly explained.

The present inventors have made efforts to prevent the inhibition of growth due to the external environment and not to contaminate the external environment, and as a result, have developed a method capable of mass-producing plant roots and hairy roots of plants that can be used as a host of useful recombinant protein production. The present invention was completed by developing a system capable of stably mass-producing useful recombinant proteins by propagating the absorptive and hairy roots of a transgenic plant prepared by Agrobacterium trimmers or Agrobacterium risogenes in a bioreactor.

Accordingly, it is an object of the present invention to provide a method for mass production of abscess root of monocotyledonous or dicotyledonous plants using a bioreactor.

It is also an object of the present invention to provide a method for mass production of useful recombinant protein from the root of the transformed plant using a bioreactor.

Another object of the present invention is to provide a method for mass-producing a useful recombinant protein from hairy root of a transgenic plant using a bioreactor.

According to one aspect of the present invention,

(i) germinating seeds of monocotyledonous or dicotyledonous plants;

(Ii) inducing callus by inoculating the cotyledon section or hypocotyl of the germinated seed in a callus induction medium to which plant growth regulator is added;

(Iii) propagating suspension cultured cells by liquid culturing the callus using a liquid suspension culture medium;

(Iii) inoculating adventitious root by inoculating the callus of step (ii) or the suspension cultured cell of step (iii) in an adventitious root induction medium; And

(Iii) It provides a method of mass production of the root muscle of monocotyledonous or dicotyledonous plants using a bioreactor comprising the step of culturing the root of the roots in large quantities using a bioreactor (bioreactor).

Hereinafter, the method of the present invention will be described in detail step by step.

I. Germinating seeds of monocotyledonous or dicotyledonous plants

One that can be used as a tissue culture material of a plant is seed, leaf, stem or leaf disease. Such materials can be obtained from various parts of the plant, but the most preferred material is to use seeds. The seed is preferably sterilized beforehand using a disinfectant such as chlorine (especially sodium hypochloride) or the like.

According to a preferred embodiment of the present invention, the medium to be used for germination of seeds is a nutritional basic medium, energy sources and vitamins such as MS (Murashige and Skoog), B5 (Gamberg), LS, N6 (Gupfa and Durzan) and White, etc. Including but not limited to. The energy source is more preferably a saccharide, most preferably sucrose. In addition, the vitamin preferably includes nicotinic acid, thiamine, pyridoxine and the like. Meanwhile, the germination medium of the present invention may further include MES (2- (N-Morpholino) ethanesulfonic acid Monohydrate), which serves to buffer the pH change, and may further include agar as a solid support. The plant growth regulator is not added to the germination medium of the present invention. Seed germination is carried out under suitable dark / light conditions using a suitable medium.

II. Inducing callus by inoculating cotyledon sections or hypocotyls of germinated seeds on callus induction medium to which plant growth regulators are added

The medium for inducing callus from germinated sterile material is MS or N6 medium, wherein plant growth regulators IAA (Indoleacetic acid), IBA (Indolebutyric acid), NAA (Naphthalene acetic acid) and 2,4-D Auxins selected from the group consisting of (2,4-dichlorophenoxyacetic acid) are added and the callus is induced by treating 0.01-5 ppm, preferably 0.1-5 ppm of oxins. According to a preferred embodiment of the present invention, the callus induction effect is best when the 2,4-D 0.5-5 ppm treatment.

III. Propagating suspension cultured cells by liquid culturing the callus using a liquid suspension culture medium.

Suspension culture cell proliferation step by liquid culture of callus is a liquid suspension culture medium using MS, WPM (Lloyd and McCown) or SH (Schenk and Hilderandt) medium, the cell inoculation amount is 8-12%, preferably It is effective to set it to 10%. In order to continuously obtain a large amount of cells in algebraic growth period, subcultured at two-week intervals results in more than doubled bioweight after four weeks of culture.

IV. Inducing adventitious root by inoculating callus or suspension cultured cells in inferior root muscle-inducing medium

Inducement of inferior root muscle can be induced directly from callus or from liquid suspension cultured cells. -5 ppm added mB5 (modified Gamberg), MS (Murashige and Skoog); Induce negative roots by culturing in 1/2 MS, B5 (Gamberg), Schenk and Hild ebrandt (SH), Linsmair-Skoog (LS) or Gupfa and Durzan (N6) medium. In this case, it is most effective to add 2,4-D 0.01-1 ppm and NAA 0.01-1 ppm to the MS MS or N6 medium or 0.01-1 ppm NAA to the MS medium or N6 medium. to be.

V. Amount of Abdominal Muscle Mass Production Using a Bioreactor                     

Suspension cultured cells can be grown in bioreactors to produce large amounts of malaria. The bioreactor capable of culturing the suspension cultured cells in the method of the present invention may use any reactor known in the art. Preferably, there is a plate, flask, or air lift bioreactor for suspension cell culture, more preferably an air float bioreactor. The culture of suspension cultured cells is also not affected by the specific culture, and a closed system, a batch culture or an open system, an air lift culture is used.

At this time, N6 or 1/2 MS medium is the most effective medium for culture of root muscle, and it is essential to add about 0.1-5 ppm of NAA to induce the root muscle in cultured cells. In addition, the density of the cells at the time of inoculation is adjusted to 0.1-0.5% of the total amount of the medium, and then maintained in the same medium for 3-5 weeks culture, it is possible to differentiate the root muscle.

For the incubation of rice arrhythmia using a bioreactor, the initial inoculation amount is about 0.5% when cultivating rice arrhythmia in a 5 L air-incubated bioreactor, and the medium is supplied every 7 days, when the culture roots start to entangle. This method is much more effective than the one batch culture, where the inoculum of 0.5-2.0 cm in length will increase the fresh weight at harvest.

According to another aspect of the invention, the invention

(Vi) Agrobacterium tumefaciens , which is inserted into the genomic DNA of plant cells and contains a vector having a gene sequence encoding a useful recombinant protein, is infected with the cotyledon or hypocotyl of a monocot or dicotyledonous plant. Making a step;

(Ii) regenerating the cotyledons or hypocotyls of the infected plants in a regeneration medium containing plant growth regulators to form shoots;

(Iii) rooting the regenerated shoots in a rooting medium containing plant growth regulator NAA to form a transgenic plant;

(Iii) germinating seeds of the transgenic plant;

(Iii) adding callus induction medium and plant growth regulator to induce callus from the seed of the germinated transgenic plant;

(Iii) propagating suspension cultured cells by liquid culture of callus;

(Iii) inducing arrhythmia from the callus of step (iii) or the suspension cultured cell of step (iii); And

(Iii) providing a method for mass-producing a useful recombinant protein from the root of the transformed plant, comprising culturing the root of the root of the transformed plant in a large amount using a bioreactor.

Hereinafter, the method of the present invention will be described in detail step by step.

I. Infecting cotyledon or hypocotyl of monocot or dicotyledonous plants with Agrobacterium tumefaciens embedded in a genomic DNA of a plant cell and containing a vector having a gene sequence encoding a useful recombinant protein.

In the present invention, all tissues generated from germination of seeds may be used, but preferably cotyledons and hypocotyls are used, and most preferably cotyledons are used. In the case of obtaining cotyledons from germinated seeds, it is preferable to completely remove the growth point and to collect them. In addition, it is preferable that the cotyledons use the whole uncut cotyledons.

Transformation of plant cells, especially rice cells, is carried out with Agrobacterium tumerization incorporating Ti plasmids (Depicker et al ., Plant cell transformation by Agrobacterium plasmids.In Genetic Engineering of Plants, Plenum Press, New York, 1983 ).

Agrobacterium trimers have a huge (about 200,000 base pairs) plasmid called Ti plasmid. When the bacteria come into contact with the plant cells, fragments called T DNA (approximately 23,000 base pairs) are transferred from the Ti plasmid into the nucleus of the plant cells and integrated into one of the plant's chromosomes during transformation. do. This phenomenon is a rare example of the transfer of DNA from nucleated organisms to nucleated organisms.

T DNA encodes an enzyme that converts plant metabolites into two classes of compounds important for bacteria. The first class is the plant hormones auxin and cytokinin. They promote the proliferation of transformed cells, resulting in crown bone tumors. The second class, called opines, is a group of amino acids that are not normally seen and serve as a food source for bacteria. Opin is produced in high concentrations in the tumor and secreted into the environment. Opines are metabolized only by Agrobacterium, and enzymes are also encoded somewhere on the Ti plasmid. As such, these bacteria monopolize the useful nutrients by converting them into forms that are useless in some other organisms.

As a vector having a gene sequence encoding a useful recombinant protein, a binary vector system is more preferably used (An et al ., Binary vectors.In Plant Gene Res. Manual, Martinus Nijhoff Publisher, New York, 1986). ). Such binary vectors include, for example, pBin19, pRD400 or pRD320, and the like, and pRD400 was used in the preferred embodiment of the present invention.

Binary vectors used in the present invention are basically (a) the origin of replication acting in plant cells; (b) a promoter capable of promoting transcription in plant cells; (c) a structural gene sequence encoding a foreign protein functionally linked to said promoter; And (d) a polyadenylic signal sequence that operates in plant cells to form polyadenyls at the 3 ′ end of RNA. In addition, the vector may further include antibiotic genes (such as carbenicillin, kanamycin, spectinomycin, hygromycin, etc.) as selection markers. Meanwhile, the vector may additionally include a gene encoding a reporter substance (luciferase, β-glucuronidase, etc.).

Promoters that can be used in the binary vector include, for example, the cauliflower mosaic virus 35S promoter, the 1 'promoter, the 2' promoter or the nopaline synthase (nos) promoter or a root specific promoter derived from a host plant. Meanwhile, the structural gene sequence encoding the foreign protein is determined according to the desired trait to be obtained.

According to a preferred embodiment of the present invention, a promoter suitable for the present invention may be any one commonly used in the art for gene introduction of a plant, for example, the Coliflora Mosaic Virus (CaMV) 35S promoter , Nopaline synthase (nos) promoter, pigwarm mosaic virus 35S promoter, sugacran basilisform virus promoter, commelina yellow mottle virus promoter, ribulose-1,5-bis-phosphate carboxylase small subunit ( ssRUBISCO) photoinducible promoter, rice cytosol triosphosphate isomerase (TPI) promoter, phosphate induced promoter or root specific promoter or sugar induced promoter, adenine phosphoribosyltransferase (APRT) promoter and octopain of arabidopsis Synthase promoters.

Optionally, the vector further comprises a gene encoding a reporter molecule (eg, luciferase and β-glucuronidase). In addition, the vectors of the present invention are selected as antibiotic markers (e.g. neomycin, carbenicillin, kanamycin, spectinomycin and hygromycin, etc.) and resistance genes (e.g. neomycin phosphotransferase ( nptII ), hygro Mycin phosphotransferase ( hpt ) and the like).

Infection of plant cells by Agrobacterium incorporating the above-described vectors can employ conventional methods known in the art. For example, by co-culturing by immersing the cotyledons collected so that growth points are excluded, Agrobacterium is infected with cotyledons. Co-cultures preferably include acetosyringone, which is intended to help transform Agrobacterium into plants.

Identification of transformants produced by the methods of the invention can be carried out by methods known in the art. For example, by performing PCR using DNA samples isolated from tissues of transgenic rice, foreign genes inserted into the genome of rice by transformation can be easily identified. Transformants can also be identified by Southern blotting and Northern blotting (Maniatis et al ., Molecular Cloning, L Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 1989). On the other hand, if the vector used to introduce the gene has a β-glucuronidase gene, a part of the leaf tissue into which the gene is introduced is selected from X-gluc (5-Bromo-4-Chloro-3-Indole-β-D- By immersing in a substrate solution such as Glucuronic Acid), the color development can be easily observed by visual observation (Jefferson, Plant Mol. Biol. Rep. , 5: 387 (1987)).

II. Regrowing cotyledons or hypocotyls of infected plants in regeneration media containing plant growth regulators to form shoots

The regeneration medium for regenerating cotyledon or hypocotyl of infected plants to form shoots is preferably selected from the group consisting of BA, kinetin, zeatin and GA3, more preferably BA. The plant growth regulator added to the regeneration medium is preferably selected from the group consisting of BA, NAA and IAA, more preferably using BA. BA is preferably added at 0.1-5 ppm, more preferably 0.5-2 ppm.

III. Regenerating shoots are rooted in rooting medium containing plant growth regulator NAA to form transformed plants.

The rooting medium from which the regenerated shoots can be rooted to produce a transformed plant is preferably selected from the group consisting of NAA, IAA, IBA, and 2,4-D, more preferably NAA. The NAA is preferably added at 0.01-5 mg / l and more preferably 0.01-1 mg / l relative to the total rooting medium. In a preferred embodiment of the present invention, the rooting medium contains a plant growth regulator NAA, antibiotic kanamycin and a certain amount of agar, the NAA is added in a dose of 0.01-1 mg / L at 25 ± 1 ℃ and 8,000 Transgenic plants were formed by incubation at lux, 16/8 hours (day / night).

IV-iii. Mass culturing the root muscle from the seed of the transgenic plant using a bioreactor

Germinating seeds of transgenic plants, inducing callus from germinated seeds, proliferating suspension cultured cells by liquid culture of callus, inducing negative roots from callus or suspension cultured cells, The step of culturing is carried out in the same manner as described in the method for mass production of arrhythmia from the plants described above.

Thus, the root of the mass produced transgenic plant expresses a useful recombinant protein, it is possible to produce a useful recombinant protein in large quantities by using the method of the present invention. Separation of useful recombinant proteins from the root can be carried out through conventional methods known in the art.

In addition, according to another aspect of the present invention,

( Iii ) infecting plant root segments with Agrobacterium rhizogenes comprising an Ri plasmid with a gene encoding a useful recombinant protein;

(Ii) inducing hairy root from infected root sections;

(Iii) inducing callus from hairy root using callus inducing medium and plant growth regulator;

(Iii) inducing somatic embryos by transferring the callus to in-flight embryo media;

(Iii) inducing the transgenic plant by culturing somatic embryos in germination medium and regeneration medium; And

(Iii) a method of mass-producing a useful recombinant protein from the parental root of a transgenic plant, comprising liquid culture of the parental root of a transgenic plant in a bioreactor.

Hereinafter, the method of the present invention will be described in detail step by step.

I. Infecting plant root fragments with Agrobacterium rhizogenes comprising a Ri plasmid with a gene encoding a useful recombinant protein

Agrobacterium lyzogenes causes hairy root disease in dicotyledonous plants, has a large plasmid called Ri plasmid, and the T-DNA portion of the Ri plasmid is transferred to the plant nucleus in the same manner as the T-DNA of the Ti plasmid. At the site of Agrobacterium risogenes infection, hairy muscle, an abnormal tumor, is produced.

Root slices of plants for infecting Agrobacterium risogenes are preferably aseptically treated and cut to a size of about 20 mm to facilitate infection. In a preferred embodiment of the present invention, Agrobacterium risogenes ATCC 15834 was used as the Agrobacterium risogenes containing Ri plasmid, and inoculated at a concentration of 1 × 10 ⁸ cells / ml.

Methods for infecting Agrobacterium risogenes to root slices of plants include the commonly used electroporation, the use of polyethylene glycol, or the injection using a microscopic syringe under a microscope. Can be used.

II. Inducing hairy root from infected root sections                     

MS medium is most preferred as a medium for inducing hairy root from infected root sections, and according to a preferred embodiment of the present invention, the hairy root derived from MS medium is cut and transferred to a medium to which carbenicillin and kanamycin are added. After removal, hairy roots are induced by transferring to hairy root growth medium without the antibiotic and incubating for 2 months.

III. Inducing callus from hairy root using callus induction medium and plant growth regulator

MS or N6 medium is used as a callus induction medium for inducing callus from hairy roots, wherein the plant growth regulator is selected from the group consisting of IAA, IBA, NAA, and 2,4-D. Treatment with 0.1-10 ppm, preferably 0.1-5 ppm induces callus. According to a preferred embodiment of the present invention, as a result of inducing embryonic callus from hairy root, the embryo formation rate was 13.2% after 4 weeks and 39.5% after 12 weeks, according to the method of the present invention. Formation rate was found to be very high.

Ⅳ. Inducing somatic embryos by transferring the callus to in-flight embryo culture medium

The medium for inducing somatic embryos from callus is selected from the group consisting of BA, kinetin, zeatin and GA3, with zeatine or GA3 being preferred. According to the method of the present invention, the induction rate of somatic embryos from callus was found to occur 26 times per callus.

Ⅴ. Inducing transgenic plants by culturing somatic embryos in germination and regeneration media

In the step of inducing transgenic plants from the somatic embryos, the concentrations of BA and NAA, which are plant growth regulators, are very important, so that they can be re-differentiated at a low level of 0.01-2 ppm. The seedlings thus produced are vigorously developed in roots and are suitable for culturing hairy roots using a bioreactor.

Ⅵ. Liquid culture of hairy roots of transformed plants in a bioreactor

According to the method of the present invention, in liquid culture of hairy roots of transgenic plants, the added plant growth regulator has the highest rate of hairy root growth when IAA is used at 0.5 ppm.

Since the parental muscles that are mass-produced in this way contain a large amount of useful recombinant proteins, the method of the present invention enables mass production of useful recombinant proteins from parental roots of transgenic plants. It is preferable to use a conventional method known in the art as a method for separating useful recombinant protein from the hair root of the plant.

The method of the present invention is applied to various monocotyledonous or dicotyledonous plants, preferably rice ( Oryza sativa ), barley ( Hordum sativum ), wheat ( Triticum aestivum or Triticum vulgare ), potatoes ( Solanum tuberosum ), sweet potatoes ( Ipomoea batatas ), Cucumis sativus and melon ( Cucumis melo ) are selected from the group consisting of, and most preferably applied to rice.

Hereinafter, the present invention will be described in more detail with reference to Examples. These examples are only for illustrating the present invention more specifically, and the scope of the present invention is not limited to these examples according to the gist of the present invention.

Example 1 Disinfection and Germination of Samples

Rice is a short grain cultivated in Korea and used japonica Ilmi rice (Dongjin rice) for the experiment. First, the seeds were disinfected in 5% NaOCl solution for 15 minutes, and then washed three times for 15 minutes with sterile distilled water. Subsequently, germinated medium containing 1/2 MS (Murashige & Skoog medium including Minimal Salts), 2% sucrose and 0.6% agar was incubated for 4 days at 25 ± 1 ° C. under dark conditions. Then, only seedlings without main leaves were selected, cotyledon slices and hypocotyls were collected and used for the following experiment.

Example 2 Callus Induction

Cotyledon fragments generated in the above example were selected and inoculated in a medium containing plant growth regulators to observe the callus proliferation state. At this time, the culture medium used was MS medium, and plant growth regulators were made from indoleacetic acid (IAA), indolebutyric acid (IABA), naphthalene acetic acid (NAA) or 2,4-D (2,4-dichlorophenoxyacetic). acid) was treated stepwise from 0.1 ppm to 10 ppm.

As a result, the callus proliferation effect was excellent when 2,4-D and NAA were treated, and the callus proliferation effect was found to be excellent when 2,4-D was treated with 0.5-5.0 ppm. Callus mainly occurred in the upper part of the culture after thickening of the tissue, but when it was separated and cultured three times or more at 4 weeks intervals, fast growing callus was obtained. Table 1 shows the results of callus growth according to the treated plant growth regulator and its concentration.

Effect of Callus Formation on Growth Regulators division Concentration (ppm) 0.1 0.5 One 2 3 4 5 10 IAA One 2 6 6 5 5 5 One IBA 4 5 6 6 4 6 6 2 NAA 7 13 10 9 7 6 6 5 2,4-D 10 14 13 12 12 11 11 8

Example 3: Suspension Cultured Cell Proliferation in Callus

The growth rate was relatively fast and white or pale yellow callus was crushed with a scalpel, and then suspended in liquid culture medium and subcultured at about 1 month intervals. At this time, the cell mass was removed with gauze during passage for continuous passage. It was effective to adjust the initial cell inoculation amount to 10% of the total amount of the medium in liquid suspension culture, and it was observed that the bioweight increased more than three times after 4 weeks of culture.

As a result of using N6 medium in liquid suspension culture, there was almost no difference between the medium in increasing cell growth, but MS medium was observed to be rather good. In order to continuously obtain a large amount of cells in the algebraic growth period, it is preferable to perform the subculture at intervals of two weeks.

Example 4: Induction of Abdominal Muscle

The growth rate was relatively fast and white or pale yellow callus were selected and grown in solid medium for 2 weeks, and then induced root muscle. Induction of abscess muscle was carried out by a general plant tissue culture method.

The culture medium contained 2,4-D and NAA as growth regulators in MS, 1/2 MS, B5 (Gamberg), Schenk and Hildebrandt (SH), LS, White, N6 or Gresshoff and Doy medium (GD) medium. Medium added with -5 ppm was used.

In the case of callus, it was effective to incubate a mass of 1-1.5 cm in diameter, in which culture medium was added 0.5-5 ppm of 2,4-D and 0.5-1 ppm of NAA in 1/2 MS medium or N6 medium. It was most effective to add 0.5-1 ppm of NAA to MS medium or N6 medium. The results are shown in Table 2 below.

Nerve root induction in callus (unit :) badge 2,4-D concentration (ppm) NAA concentration (ppm) 0.5 One 5 0.5 One 5 MS 5 7 2 8 7 One 1/2 MS 8 8 3 15 14 3 B5 - - - - - - SH - - - - - - LS - - - 2 2 - White One One - 3 3 - N6 8 8 2 12 11 One GD - - - 2 2 -

Example 5: Induction of Abdominal Muscle in Suspension Cultured Cells

Using the same medium and plant growth regulators as in Example 4 to induce the root muscle from suspension cultured cells. As a result, it was essential to add about 0.5-5 ppm of NAA in 1/2 MS medium, and the density of cells at the time of inoculation was adjusted from 0.1% to 0.5% of the total volume of the medium, and then in the same medium for 4-6 weeks of culture. It was necessary to maintain the differentiation of the root muscle.

Example 6: Rice root muscle culture using small scale bioreactor

The root muscles derived from cultured cells and callus were generally about 2-7 cm in length, and the number of root muscles was about 40 to 60. This sample was used to examine the effects of speculum on growth in order to find the optimal conditions for continuous production in small bioreactors. It could be observed. The initial inoculation amount was about 0.5% when culturing rice arrhythmia in a 5 L air-incubated bioreactor, and the medium supply was added in 7-day increments when the cultured root muscle began to entangle. It is more effective than the batch culture method. Rice roots grown in a 5 L air lift bioreactor were subcultured to a 20 L air float bioreactor four weeks after culture.

Example 7 Introduction of Vectors for Expression of Foreign Proteins in Plants

Seeds of rice were germinated in the same manner as in Example 1 to obtain cotyledon fragments therefrom. A plant binary vector, pRD400, was introduced into Agrobacterium tuberization GV3101 (Mp90) containing Ti plasmid by conjugation or transformation ( Plant-cell-rep. , 15 (11): 799 -803 (1996). Agrobacterium trimmers GV3101 (Mp90) (Hamid et al ., Plant Cell Reports 15 (11): 799-803, 1996) were super broth: 37 g / l Brain heart infusion broth (Difco), 0.2% Sucrose, pH 5.6) was incubated for 18 hours, and then the cotyledon slices were immersed in the culture and mixed for 10 minutes. Then, Agrobacterium tumer for 3 days in coculture medium [Murashige & Skoog medium including Gamborg B5 vitamins) containing 2 mg / L BAP (6-benzylaminopurine) at 25 ° C. Sections and cotyledons were cocultured. The cotyledons were then subjected to a cleanup step to remove bacteria, and the cotyledons were cultured on a medium based on MSB5, MES 0.5 g / l, 3% sucrose and 0.4% pitagel, with 2 mg / l BA and 500 mg / l carbenicillin, Kanamycin was added at different concentrations and incubated at 25 ± 1 ° C. and 8,000 lux, 16 hours / 8 hours (day / night) for 4 weeks.

Subsequently, the differentiated shoots were transferred to a rooting medium containing a certain amount of NAA (0, 0.01 and 0.1 mg / l), kanamycin 100 mg / l and a certain amount of agar (0.4%, 0.6% and 0.8%) at 25 ± 1 ° C. And 8,000 lux, 16 hours / 8 hours (day / night) incubated in the conditions of the subject was estimated as a transformant was analyzed using the method of Example 8 below.

Example 8: Identification of Transgenic Plants

Identification of the transformant in Example 7 was carried out as follows:

Example 8-1: GUS Analysis

Confirmation of the gene expression of the plant obtained in Example 7 was carried out as follows: beta-glucuronidase (β- glucuronidase, GUS) After harvesting the leaves to confirm the expression of the reporter gene, GUS analysis solution 200 μl of (X-gluc (5-Bromo-4-Chloro-3 3-Indole-β-D-Glucuronic Acid), 1 mg / ml) is placed in a container with leaves and thoroughly vacuumed using a vacuum. The vacuum was maintained until it was. After that, the appearance of color was visually observed to confirm the introduction and expression of the gene.

Example 8-2 PCR Analysis

Isolation of plant genomic DNA for PCR analysis was extracted by Edwards method (Edward et al., Nucleic Acids Research 19 (6): 1349, 1991). The primers used in the PCR analysis correspond to the nucleotide sequence of the Kan gene of the vector in the Agrobacterium turmeration, and the forward primers are shown in SEQ ID NO: 1 (5'-AGA CCA GTT GAG ATT AGG CCA G-3 '), And the reverse primer is the sequence set forth in SEQ ID NO: 2 (5'-GCC TCA TGC AAC CTA ACA GA-3'). PCR reaction was performed by Taq polymerase, total denaturation at 96 ° C. for 2 minutes, denaturation at 94 ° C. for 1 minute, connection at 55 ° C. for 1 minute, and polymerization at 72 ° C. for 2 minutes, 35 times. After extending the reaction at 72 ° C. for 10 minutes, the reaction product was analyzed on a 1.0% agarose gel.

As a result, a 0.5 kb DNA band corresponding to the Kan gene was observed in the transformant of the present invention and confirmed that the transformant was transformed.

Example 9: Hairy Muscle Induction

Rice roots were harvested and the surface of the roots was sterilized for 10 minutes with 70% ethanol and 7% sodium chlorate for 15 minutes, washed three times with sterile water and cut into 20 mm size. Agrobacterium lysogenes (ATCC 15834) diluted to 1 × 10 ⁸ cells / ml with sterile distilled water was inoculated on the surface of the rice root sections, and densified in MS medium to which 300 mg / L of Celltaxime was added. And incubated in the dark at 27 ° C. The induced hair roots were cut and transferred to a medium containing 500 mg / l of carbenicillin and 25 mg / l of kanamycin to remove bacteria, followed by hairy root growth medium without antibiotics (MSB5, 3% sucrose, MES, IAA). ) Were incubated for 2 months to induce hairy roots.

Example 10 Callus Induction in Hairy Roots

The reddish hairy root was made into 10 mm sections, and 20 aliquots were placed in callus induction medium, and then embryos were induced by incubating for 12 weeks at 24 ° C. As a result of measuring the number of callus forming embryos by anatomical microscope, the rate of embryo formation was 13.2% after 4 weeks and 39.5% after 12 weeks.

Somatic embryos were induced by transferring 10 induced callus to somatic embryo induction medium for 60 days. Somatic embryo induction rate was 26 embryos per callus.

Somatic embryos with seedling induced cotyledon were cultured in germination medium for 2 months to germinate, seedlings were obtained, and then transferred to regeneration medium (1/2 MS medium) to induce stems and roots. A month later, 33% of plants had normal stems and roots, and 67% had roots but poor stems.

Example 11: Liquid Culture of Hairy Roots

Hair growth rate of the hair roots produced in Example 6 was repeated in a small scale bioreactor presented in Example 6 in a medium in which the IAA concentration of the hair root root culture medium was adjusted to 0, 0.1, 0.5, and 1 ppm. Was highest at 0.5 ppm IAA.

As described above, the present invention provides a method of mass production of the adipocytes of the plant using an air incubation bioreactor, a method of mass production of the useful recombinant protein from the root of the transformed plant and the mass production of the useful recombinant protein from the parent root of the transformed plant Provide a method.

According to the method of the present invention, it is possible to stably produce a large amount of foreign protein by proliferating the roots of plants in a bioreactor in a large amount while preventing the inhibition of growth due to the external environment and also without contaminating the external environment.

Having described the specific part of the present invention in detail, it is apparent to those skilled in the art that such a specific technology is only a preferred embodiment, and the scope of the present invention is not limited thereto. Therefore, the substantial scope of the present invention will be defined by the appended claims and equivalents thereof.

<110> NEXGEN BIOTECHNOLOGIES, INC. <120> Method for Producing Available Recombinant Protein by Culturing          Adventitious Root and Hairy Root of Transformed Plants <130> dp-2004-0539 <160> 2 <170> KopatentIn 1.71 <210> 1 <211> 22 <212> DNA <213> Artificial Sequence <220> <223> forward primer for Kan <400> 1 agaccagttg agattaggcc ag 22 <210> 2 <211> 20 <212> DNA <213> Artificial Sequence <220> <223> reverse primer for Kan <400> 2 gcctcatgca acctaacaga 20  

Claims (18)

delete delete delete delete delete delete delete delete (i) germinating seeds of a plant selected from the group consisting of rice ( Oryza sativa ), barley ( Hordum sativum ), wheat ( Triticum aestivum or Triticum vulgare ), potatoes ( Solanum tuberosum ) and sweet potatoes ( Ipomoea batatas ); (Ii) inducing callus by inoculating the cotyledon section or hypocotyl of the germinated seed in a callus induction medium to which plant growth regulator is added; (Iii) propagating suspension cultured cells by liquid culturing the callus using a liquid suspension culture medium; (Iii) inoculating adventitious root by inoculating the callus of step (ii) or the suspension cultured cell of step (iii) in an adventitious root induction medium; And (Iii) incubating the induced root muscle of 0.5-2 cm length at a dose of 0.1-0.5% of the total amount of the medium and feeding the medium every 7 days to incubate in a large amount using a bioreactor. Method of mass production of abscess root monocotyledonous or dicotyledonous plants using a bioreactor comprising a. delete delete delete delete delete delete delete delete delete