• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    Method of regeneration of cultivars from immature embryos. …<??>It comprises three steps… - formation of embryogenic callouses in a medium containing a cytokinin-type hormone,… - culturing of the callouses in a medium of the same nature as that above,… - culturing of the plantlets. …<??>Application to sunflower cultivars.
    公开号:SU1727514A3
    申请号:SU874203619
    申请日:1987-10-29
    公开日:1992-04-15
    发明作者:Фрейссине Жорж；Фрейссине Мартин
    申请人:Рон-Пуленк Агрошими (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to biotechnology, in particular to the cultivation of plants in vitro, more specifically, it relates to a method for regenerating sunflower plants from immature embryos by means of samatic embryogenesis,
    A number of works on the regeneration of sunflower plants are known. So, it is known to obtain regenerants from the segments of salts and hypothyls, shoot apexes.
    The disadvantage of this method is the low yield of regenerative with high labor intensity of cultivation /
    There is also known a method of regeneration of sunflower shoots from immature embryos.
    However, this method is not satisfactory; un- stable production of re-rattling plants.
     A known method for producing regenerants of sunflower from immature embryos by their preliminary explantation and the production of fertile plants from them.
    However, this method does not allow mass regeneration of plants due to the low multiplication factor when using this method.
    The purpose of the invention is to increase the yield of regenerants, as well as the higher frequency of formation of zones of embryo-rfog.
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    The goal is achieved by using three successive stages: the first stage is the formation of embryogenic calli from cells or tissues by cultivation in a nutrient inducing medium containing a hormone; the second stage of cultivation of embryogenic calli for their growth, from development and their germination in a medium containing a hormone; in certain cases, the third stage, consisting in cultivation that allows the growth and development of plants; The first two steps are carried out in the same nature medium, and this medium contains pitotine kin type hormone without harmonic auxin.
    Plant tissues, from where the explants can be extracted to produce somatic embryos, originate from Hellanthus annuus sunflower cultivators, used mainly in breeding programs. As an example, 8 cultivators (varieties), HA 89, HA 290, HA 291, HA 300, HA 303, T 76, PT 26 and Giant Gray stripe HA Grade 89 comes from Dade Florida Florida, Grade HA 290, HA 291. AT 300. AT 303, T 76, and PT 26 originate from Scedtec International I he California, and Giant Gray stripede northrup Kind seeds California.
    Explants originate from plants cultivated in the greenhouse and subjected to controlled fertilization. A preferred explant for callus production is an undeveloped germ. Underdeveloped embryos with pericarp are isolated from sunflower heads, when they are 4-21 days old, their size is usually 0..1-5 mm. Underdeveloped embryos of a considerable size can be cut into several equal parts according to a plane passing along the axis of the feather of the embryonic root, which multiplies the number of clones obtained from a single embryo.
    The invention according to the invention is carried out as follows.
    The varieties of sunflower AT 89, AT 290, AT 291. AT 300. AT 303, T 76, PT26 and Giant Gray Stripe are cultivated in a greenhouse (26 ° C, 40,000 lux, photoperiod 15 hours a day) and subjected to controlled fertilization. Underdeveloped embryos are removed 4–21 days after pollination. Grains separated from the heads are sterilized by immersing for 20 minutes in a solution of lava water with 3 ° CI, to which a few drops of wetter are added, then washed 3 times with sterile distilled water. The embryos are then isolated under aseptic conditions, cut in known cases and placed
    on the first Wednesday - the medium of induction of embryos.
    This first medium includes mineral salts, vitamins, amino acids, sucrose, and a hormone in an amount sufficient for dl. callus formation. Mineral salts include salts of macronutrients and salts of oligo-elements. The macronutrients used in this first medium can be chosen, for example, among the following compounds: magnesium sulfate, calcium chloride, potassium monophosphate, potassium nitrate and ammonium nitrate. The following oligogase-based salts include: boric acid, manganese sulphate, zinc sulphate, sodium molybdan, copper (II) sulphate, cobalt chloride, potassium iodide, and chelate ma-ELTC. This combination of mineral salts is known under the name Murashige and Skoog (MS).
    Preferred quantities of macronutrients and oligo elements on. 1 l of medium is as follows: mg: 370 heptahydrated magnesium sulfate, 440 dihydrated calcium chloride, 170 dihydration potassium monosulfate, 1900 potassium nitrate, 1650 ammonium nitrate, 6.2 boric acid, 22.3 tetrahydrated manganese sulfate, 8.6 heptahydrated zinc sulfate, 0.25 molybdate dihydrated sodium. 0.025 pentahydrated copper (II) sulfate, 0.025 hexahydrate cobalt chloride, 0.83 potassium iodide, 36.7 iron chelate-Na-ETLC.
    The first medium also contains vitamins such as nicotinic acid, thiamine, pyridoxine, myo-inositol, and an amino acid such as alanine, glutamine, serine, tryptophan, cysteine, and preferably glycine. The preferred amounts of vitamins and amino acids per liter of medium are mg: 0.5 nicotinic acid, 0.1 thiamine hydrochloride, 0.5 pyridoxine hydrochloride, 100 myo-inositol, 2 glycine.
    The first medium may also contain an additive of vitamin and amino acids. This additive is not necessary for the formation of somatic embryos, but it increases their frequency. In this case, the preferred amounts of vitamins and amino acids per liter of medium are, mg: 0.5 nicotinic acid, 0.1 thiamine hydrochloride, 0.5 pyridoxine hydrochloride, 4000 myonositol, 1000 1-alanine, 800 1-glutamine, 160 1-serine, 50 tryptophan, 10 1-cysteine; 2 glycine.
    The sucrose contained in the first medium is in the amount of 8-12%, preferably 9%.
    The hormone of the first medium, the choice of which is characteristic of the invention of the pit &amp; A new type, for example, kinetin or 6-benzylaminopurine, and preferably the latter. Amounts of 0.5-1 mg per liter of medium are generally suitable. Agar, Phytagar or Gelrite is used to create a solid medium. A final concentration of 0.6% for Phytagar or 0.3% for Gelrite gives good results. The pH of the medium can vary from 5.0 to 6.3 V, preferably 5.0. .
    The medium is sterilized in an autoclave with the exception of hormones that are sterilized by filtration through a microporous membrane.
    Underdeveloped embryos, isolated as described above, are placed on this first medium, cultured for about 2-3 weeks in the dark at 26 ° C. During this period, zygotic embryos develop and somatic embryos appear at the hypocotyl level and on the inner surface of the seeds in the case of the PA 291 stump & variety (AP) cultivar. Then the somatic embryos can be isolated and placed in the second medium-sprout growth medium. Embryogenic callus or isolated germs are cultivated in the second medium for 2–8 weeks at 26 ° C and in the light (1500 lx) with a photoperiod of 12–16 hours on 1 day, preferably 16 hours on 1 day. During this period, the embryos germinate and the sprouts formed develop in known cases of the root.
    The second medium, like the first, contains mineral salts, vitamins / amino acid, sucrose and hormone. Mineral salts include salts of macronutrients and salts of oligo-elements. Macronutrients, oligoelements, vitamins and amino acids are the same as in the first medium, and identical concentrations without additions. Sucrose is present in an amount preferably below this first medium, for example 2-4%, preferably 3%.
    The hormone used is cytoninin, preferably identical or different from the first medium, preferably 6-benzylamine purine. Amounts of 0.1-0.5 mg per sheet are usually suitable. Phytagar or Gelrite agar is used to create a solid medium. A final concentration of 0.6% for Phytagar and 0.3% for Gelrite gives good results. The medium is sterilized as before, pH of the medium is 5.0-6.8, preferably pH 5.0.
    After 2-5 weeks of being in the second medium, the isolated somatic embryos germinate and turn into sprouts of 2-5 cm. Sprouts that have developed roots can be planted in the ground, sterile
    a mixture of peat, vermiculite, fine sand (3: 2: 1) contained in Jibbi pots. The pots are placed in a tank. zapoppemny wet sand, and covered with a thick plastic bag to maintain a high degree of humidity. The entire set is placed in a climatic chamber with a temperature of 15 ° C (6000 lk) with a photoperiod of 12–16 hours on 1 day, preferably 15 hours on 1 day. After 10 days, the plants are placed in larger pots and cultivated in a greenhouse at 26 ° C (40,000 l K) with a photoperiod of 12–16 hours on 1 day, preferably 15 hours on 1 day.
    5 Plants that have not developed roots
     can be grafted on young plants cultivated in the greenhouse according to the classical method or placed for a period of 10-20 days on rooting medium or
    0 third Wednesday.
    The third medium includes mineral salts, vitamins and sucrose. Mineral salts include salts of macronutrients and salts of oli elements. Used in this third
    5 The macro elements can be selected among the following compounds magnesium sulfate, calcium chloride, monosodium phosphate. potassium nitrate and ammonium sulfate. Among the salts on the basis of oligoelements, you can
    They include boric acid, manganese sulfate, zinc sulfate, sodium molybdate, copper sulfate (II), cobalt chloride, potassium iodide, and Fe-Na-ETLK chelate. This combination of mimeral salts is known as B
    5 5. Preferred amounts of macroelements and oligoelements per 1 liter of the medium are as follows: 250 heptahydrated magnesium sulfate, 150 dihydrated calcium chloride, 169 mono-hydrated
    0 monosodium phosphate, 3000 potassium nitrate, 3 boric acid, 13.2 tetrahydrated manganese sulfate, 2. heptahydrated zinc sulfate, –0.25 sodium dihydration molybdate, 0.025
    5 pentahydrated copper (II) sulfate, 0.025 hexahydrate cobalt chloride, 0.75 potassium iodide, 40 Fe-Na chelate
    edtk
    Third Wednesday also contains vitamins.
    0 This is nicotinic acid, thiamine, pyridoxin, and myo-inositol. Preferred amounts of vitamins per liter of medium are mg: 1 nicotinic acid, 10 thiamine hydrochloride, 1 pyridoxine hydrochloride, and 100
    5 myo-inositol.
    The third medium also contains sucrose and activated carbon and / or auxin type hormone. Sucrose is, for example, in the amount of 1-2%. preferably 1%, and activated carbon in an amount
    0.1%. If you use a hormone instead of activated carbon, then choose 3-indole-acetic acid in doses of OJ-0.2 mg per 1 liter. Agar Phytagar or Gel rite. USE to create a solid medium. A final concentration of 0.5% for Phytagar and 0.25% for Gelrite is sufficient. The pH of the medium may range from 5.0 to 6.0 and preferably be 5.0. The medium is sterilized in an autoclave.
    Plants are cultivated in this medium for 2-3 weeks at 26 ° C in the light (1500 lk) with a T2-SchV photoperiod of 1 day, preferably 16 hours on 1 day. The plants form roots and can be planted in the ground.
    Plants obtained by this method can be phenrtypically different from the starting material due to in vitro stress. The plants are pollinated by hand and kept until the seeds are harvested. Several units of grains are planted to analyze new sunflower plants and select possible interesting mutants, which are then involved in a variety breeding program;
    Example 1, Preparation of stock solutions
    a.Math B5 solution. The B5 mother liquor, concentrated tenfold, is prepared by dissolving a bag with B5 medium without sucrose Flow Laboratories (contains B5 mineral salts, 1 mg nicotinic acid, 1 mg pyridixin — H01, 10 Ml of triamine. HCI and 100 mg of inositol. In final concentrations) in 100 ml (final volume) distilled in deionized water. The mother liquor is divided into 100 ml aliquots and stored at -20 ° C.
    b. The mother solution BAP. A solution of BAP with 1 g / l is prepared by dissolving 100. mg of b-benzylaminopurine in a few ml of 0.15 and HCI, heating slightly, and diluting with 100 ml of distilled and deionized water. This solution is sterilized by filtration through a 0.2 micron Mlnisart NML membrane (Sartortus) before adding it to the first and second media.
    Century A. A1 solution A solution of A1A with 0.2 g / l is prepared by dissolving 20 mg of 3-inductacetic acid in a few millimeters of pure ethanol and diluting 100 ml of distilled and deionized water. This solution is sterilized by filtration through a Mlnlsart NML 0.2 μm membrane (Sartorlus) before adding to the third medium.
     The addition of vitamin and amino acids according to Chandler and BEARD.
    The initial solution of vitamin and amino acids, twenty times concentrated, is prepared by dissolving a set of 30 g of myo-inocetol, 10 g of L-alanine, 8 g of L-glutamine, 1.6 g of L-serine, 0.5 L-tryptophan and 0.1 g L-cysteine in 500 ml (final volume) of distilled and deionized water. The stock solution is divided into 50 ml aliquots and stored at -20 ° C. PRI mme R 2. Preparation n -
    a. First environment or environment of induction of an embryo. The medium is prepared by dissolving pectin with Murashlge and Skoog medium without sucrose Flow Laboratories, contains mineral salts MS 0.1 mg thiamine, HCI 0.5 mg nicotinic acid, 0.5 mg pyridoxine.
    HCI, 2 mg of glycine and 100 mg of inositol and 90-120 g of sucrose in distilled and deionized water. After a possible addition of 50 ml of vitamin and amino acid supplements, the pH is adjusted to 5.0 with 0.1
    n the sodium hydroxide solution, the volume is brought to 1 l and after adding 6. g Phytagar (Clbco) or 3 g Gelrite (Kelco) the mixture is kept in an autoclave for 20 minutes at 120 psi. When the mixture has cooled, it is added
    0.5-1 ml of a solution of BAP (2.2-4.4 µmol) sterilized as described above. The mixture is then poured into Petri dishes.
    b. The second medium or sprout growth medium. The second medium is prepared identical.
    In the first medium, a solution of a combination of a bag with medium M, 30 g of sucrose and 6 g of Phytagar or 3 g of Gelrite in 1 l of water are added, after keeping in an autoclave, 0.1-0.5 ml of sterile BAP
    (0.44-2.2 μmol). The medium is poured into planteon cups (Flow Laboratories).
    c. Third environment or rooting medium. The third medium is prepared by adding 1020 g of sucrose per 100 ml of the initial solution.
    B5, in distilled and deionized water. The pH was adjusted to 5.0 with 0.1 n. sodium hydroxide solution, then the volume is made up to 1 l and a mixture of 0.5 g of Phytagar and 1 g of alkylated coal is added. After
    passing the autoclave, the medium is poured into the mason jars. If one wants to use a third medium containing A1A, then activated carbon is not consumed during the preparation of this third medium. After
    Passing the autoclave to the cooled medium, add 0.5-1 ml of sterile solution A1A (0.57-1.14 µmol). Wednesday poured in an identical manner in the Mason jars.
    The liquid variant of the third medium includes only mineral salts in 5 m of 1% sucrose, at pH 5.0. The mixture is divided into 10 ml fractions into glass tubes containing bridges of filter paper, according to the method described
    CHANDLER and BEARD, then kept in an autoclave.
    EXAMPLE 3. Underdeveloped embryos with their pericarps are separated from the sunflower head (Hellanthus annuus, variety T76B) when they reach a size of 0.5-1.5 mm. The grains are sterilized for 20 minutes in a solution of cavel water at 3 ° C and rinsed with distilled water. The immature embryos are separated from their shells and placed in petri dishes on the first medium. The first medium was obtained as described, with 90 g / l sucrose and 0.5 mg / l B of AR (2.2 μmol) .:
    Petri dishes are incubated in the dark for 3 weeks in order to result in the formation of somatic embryos.
    In this stage, the somatic embryos that have begun to germinate are separated from the zigotic embryo and placed on a second medium in Planteon cups. The second medium, prepared as described above, contains 0.1 mg BAP per liter or 0.44 μmol. The embryos are cultivated in the light for 3 weeks and they are differentiated by sprouts.
    Sprouts 2–5 cm high are then transferred to a third medium to initiate root formation. The third medium, prepared as described above, preferably contains 10 g of sucrose. In the event of a medium being stoned, an additive of 1 g / l of activated carbon removes the residual effect of BAP in the previous environment of MAENE. AND DEBERGH, Plant CEII Tissue Organ Culture and favors the rapid growth of roots. After about 2 weeks, sprouts can be planted in the ground.
    If the sprouts began to develop roots on the second medium, they can be brought into contact with the third liquid medium, according to the technique described. CHNDLER and BEARD. This device allows you to significantly develop the root system and avoid damage to the roots during the landing on the ground .:
    Example 4. Underdeveloped embryos of HeJianthus annuus HA 89 are selected when they reach a growth of 0.1-0.5 mm, with endosperm on the first Wednesday. The first medium contains 90 g of sucrose and 0.5 mg of BAP per 1 liter or 2.2 μmol. After 3 weeks in the dark, somatic embryos are isolated and placed on the first fresh medium all the time in the dark. Secondary somatic embryos are formed on isolated embryos. After 3 weeks in the dark, secondary somatic embryos are isolated and placed on a second medium. The second medium contains 30 g of charose and 0.1 mg per 1 liter (0.44 μmol).
    Sprouts that develop. can then be transferred to a third kind of liquid 5, or subjected to wild rooting for rooting, then transplanted to the ground.
    Example 5. The underdeveloped embryos of Helianthus annuus, a species of HA 89 from 0, are collected 21 days after pollination, they are 5 mm in size. They are separated from their shells and, before being deposited on the first medium, are cut into four equal parts longitudinally according to two perpendicular flat 5 cm between them and the feather of the primary root parallel to the axis. In this case, the first medium contains 90 g of sucrose and 1 mg of BAP per liter. After 3 weeks in the dark, the somatic nuclei are isolated and placed 0 on the second medium. The second medium contains 30 g of sucrose and 0.5 mg of BAP per liter.
    Sprouts that develop can then be transferred to a third medium (liquid or geared) for rooting, then planted in the ground. Sprouts that do not have roots can be grafted to a young plant according to the method described by HABEIMANN and WaLl.acn.
    Examples 6-27. The examples given give combinations that can be implemented using various descriptions: examples.
    The proposed method allows mass regeneration of plants of the sunflower from immature embryos by somatic embryogenesis.
    The table presents the results of studies on the effect of the method on various sunflower lines. 0 Formula of invention
    1. The method of regeneration of sunflower plants, comprising three consecutive stages, with the first stage
    5 provides for the production of embryogenic calli and somatic omririoids from the explant, followed by their growth or modified Murashige – Skoog nutrient medium, the second stage - the formation of seedlings and their development in a plant on the modified Murashige – Skoog nutrient medium and the third stage - the formation and growth of roots from plants obtained in a nutrient medium containing sources
    5 nitrogen, phosphorus, potassium, carbon, trace elements, vitamins and growth stimulants, characterized in that, in order to increase the yield of regenerants, immature embryos are used as explants from 4 to 21 days of age in size of 0.1-5 mm .
    the first stage is carried out on a nutrient medium in the presence of 2.2-4.4 mol / l 6-benzylaminopurine, 0.5 mg / l nicotinic acid, 0.1 mg / l thiamine hydrochloride, 0.5 mg / l pyridoxine hydrochloride, 100 mg / l of myo-isositol, 2 mg / l of glycine. When the content of sucrose is 9-12%, the second stage is carried out in the presence of 0.44-4.4 mmol / l of 6-benzylaminopurine, 0.5 mg / l nicotinic acid, 0.1 mg / l thiamine hydrochloride, 0.5 mg / l pyridoxine chlorohydrate, 100 mg / l myocositol, 2 mg / l glycine, with a sucrose content of 3%, the third stage is carried out at 1 mg / l modified nicotinic acid , 10 mg / l thiamine hydrochloride, 1 mg / l pyridoxine hydrochloride, 100 mg / l myoositol, 0.1-0.2 mg / l indolyl-3-uksuu acid, with a sucrose content of 1-2%, while after the second stage, the resulting plants are grafted, 2. The method according to claim 1. j tl is based on the fact that, in order to increase
    frequency of formation of zones of embryo-4 morphogenesis; in the first stage, 3900 mg / l are added to the nutrient medium
    myoinositol, 1000 mg / l L-elanida, 160
    mg / l L-serine, 800 mg / l L-glutamine, 50
    mg / l L-tryptophan, 10 mg / l L-cysteine.
    3. Method according to paragraphs. 1 and 2, which is also distinguished by the fact that they use lines of sunflower T 76, PT26, HA 89, HA 291, Giant Gray Strlne.
    4. Method according to paragraphs. 1-3, I differ from the fact that after the second stage of the plant,
    having roots, they are planted in the ground and incubated in a climate chamber at 15 ° C, illumination intensity of 6000 lux with a 15-hour photoperiod.
    权利要求:
    Claims (5)
    [1]
    The invention relates to biotechnology, in particular to the cultivation of plants in vitro, more specifically it relates to a method for the regeneration of sunflower plants from immature embryos by somatic embryogenesis.
    A number of works on the regeneration of sunflower plants are known. So, it is known to obtain regenerants from segments of cotyledons and hypotyle, shoot apexes.
    The disadvantage of this method is the low yield of regenerative with a high complexity of cultivation /
    There is also known a method of regenerating sunflower shoots from immature embryos.
    However, this method does not provide stable production of regenerated plants.
    A known method for producing sunflower retoperlites from immature embryos by preliminary explantation and obtaining fertile plants from them.
    However, this method does not allow to obtain mass regeneration of plants due to the low reproduction rate when using this method.
    The purpose of the invention ·· increase the yield of regenerants, as well as increasing the frequency of formation of zones of embryomorphogenesis.
    1727514 AZ
    This goal is achieved by using three successive stages: the first stage of the formation of embryogenic calli from cells or tissues by cultivation in a nutrient inducing medium containing hormone: the second stage of culturing embryogenic calli for their growth, from development and their germination in a medium containing hormone: in known cases, the third stage, consisting in cultivation, which allows for the growth and development of plants; the first two stages are carried out in an environment of the same nature and this environment contains the hormone pitokinin type without auxin harmonic.
    Plant tissues from which explants can be extracted to produce somatic embryos come from Hellanthus annuus sunflower cultivators, used mainly in breeding programs. As an example, we used 8 cultivators (cultivars), HA 89, HA 290, HA 291, HA 300, HA 303. T 76, RT 26 and GiantGray stripe HA 89 comes from Dade Counts Florida, varieties HA 290, HA 291, HA 300, HA 303, T 76, and PT 26 are descended from Scedtec International I he California, and Giant Gray stripede northrup Kind seeds California.
    Explants come from plants cultivated in a greenhouse and are subjected to controlled fertilization. The preferred explant for the production of callus is an underdeveloped germ. Underdeveloped embryos with pericarp are isolated from the heads of sunflowers, when they are 4-21 days old, their size is usually 0.1-5 mm. Underdeveloped embryos of a significant size can be cut into several equal parts according to a plane along the axis of the feather of the germinal root, which multiplies the number of clones obtained from one germ.
    Method 6 according to the invention is as follows.
    Sunflower varieties HA 89, HA 290, HA 291. HA 300, HA 303, T 7b, PT 26 and Giant Gray Stripe are cultivated in a greenhouse (26 ° C, 40,000 lux. Photoperiod 15 hours on 1 day) and subjected to controlled fertilization. Underdeveloped embryos are recovered 4-21 days after pollination. The grain separated from the heads is sterilized by immersion for 20 min in a solution of javell water at 3 ° CI, into which several drops of a wetting agent are added. then washed 3 times with sterile ’distilled water. The embryos are then isolated under aseptic conditions; in known cases, they are cut and placed in the first medium — the medium of induction of the embryos.
    This first medium includes mineral salts, vitamins, amino acids, sucrose and the hormone in an amount sufficient for. callus formation. Mineral salts include salts of macronutrients and salts of oligoelements. The macronutrients used in this first medium can be selected, for example, from the following compounds: magnesium sulfate, calcium chloride, potassium monophosphate, potassium nitrate and ammonium nitrate. The salts based on oligoelements include: boric acid, manganese sulfate, zinc sulfate, sodium molybdan, copper (II) sulfate. Cobalt chloride ·, potassium iodide and iron chelate-No-CRTK. This combination of mineral salts is known as Murashige and Skoog (MS).
    Preferred amounts of macronutrients and oligoelements on. 1 liter of medium is as follows, mg: 370 heptahydrated magnesium sulfate. 440 dihydrated calcium chloride, 170 dihydrative potassium monosulfate, 1900 potassium nitrate, 1650 ammonium nitrate, 6.2 boric acid, 22.3 tetrahydrated manganese sulfate. 8.6 heptahydrated zinc sulfate. 0.25 dihydrated sodium molybdate. 0.025 pentahydrated copper (II) sulfate, 0.025 hexahydrated cobalt chloride, 0.83 potassium iodide. 36.7 iron chelate Na-ETLC.
    The first medium also contains vitamins such as nicotinic acid, thiamine, pyridoxine, myo-inositol, and an amino acid such as alanine, glutamine, serine, tryptophan, cysteine, and preferably glycine. Preferred amounts of vitamins and amino acids per 1 liter of medium are, mg: 0.5 nicotinic acid, 0.1 thiamine hydrochloride, 0.5 pyridoxine hydrochloride, 100 myo-inositol, 2 glycine.
    The first medium may also contain vitamin and amino acid supplements. This supplement is not necessary for the formation of somatic embryos, but it increases their frequency. In this case, the preferred amounts of vitamins and amino acids per 1 liter of medium are, mg: 0.5 nicotinic acid, 0.1 thiamine hydrochloride, 0.5 pyridoxine hydrochloride, 4000 myionositol, 1000 1-alanine, 800 1-glutamine, 160 1- serine, 50 tryptophan, 10 1-cisgein; 2 glycine.
    Sucrose contained in the first medium is present in an amount of 8-12%, preferably 9%.
    The hormone of the first medium, the choice of which is a characteristic of the invention 5
    172751Ί.
    pitsquinine type, for example kinetin or 6-benzylaminopurine, and preferably the latter. Usually, quantities of 0.5-1 mg per 1 liter of medium are suitable. Agar. Phytagar or Gelrite is used to create a solid 5 medium. A final concentration of 0.6% for Phytagar or 0.3% for Gelrite gives good results. The pH of the medium may vary from 5.0 to 6.3, preferably 5.0. . 10
    The medium is sterilized in an autoclave, with the exception of hormones, which are sterilized by filtration through a microporous membrane.
    The underdeveloped embryos isolated 15 as described above are placed in this first medium, cultivated for about 2-3 weeks in the dark at 26 ° C. During this period, zygotic embryos develop and somatic embryos appear 20 at the level of the hypocotyl and on the inner surface of the cotyledons in the case of cultivar (cultivar) PA 29’1. Then somatic embryos can be isolated and placed in the second medium — the medium of seedling growth. Em-25 bryogenic callus or isolated zaro; the breaths are cultured in the second medium for 2-8 weeks at 26 ° C and in the light (1500 lux) with a photoperiod of 12-16 hours on 1 day, preferably 16 hours on 1 day. During 30 of this period, the embryos germinate and the resulting sprouts develop in known cases. Roots.
    The second medium, like the first, contains mineral salts, vitamins, amino acid 35, sucrose and hormone. Mineral salts include salts of macronutrients and salts of oligoelements. Macronutrients, oligoelements, vitamins and amino acids are the same as in the first medium, and identical concentrations are 40 without additives. Sucrose is present in an amount preferably below such a first medium, for example 2-4%, preferably 3%.
    The hormone used is cy- 45 toninine, preferably identical or different from the first medium, preferably 6-benzylamino-purine. Usually, 0.1-0.5 mg per sheet is suitable. Phytagar agar or Gelrite is used to create a solid 50 medium. A final concentration of 0.6% for Phytagar and 0.3% for Gelrite gives good results. The medium is sterilized as before, the pH of the medium is 5.0-6.8, preferably pH 5.0. 55
    After 2-5 weeks of being in the second medium, the isolated somatic embryos germinate and turn into sprouts
    [2]
    2-5 cm. Sprouts that have developed roots can be planted in the ground, a sterile mixture of peat, vermiculite, fine sand (3: 2: 1) contained in Jibbi pots. Pots are placed in a tank filled with wet sand, and covered with a transparent plastic bag to maintain a high degree of humidity. The whole set is placed in a climatic chamber with a temperature of 15 ° C (6000 lux) with a photoperiod of 12-16 hours on 1 day, preferably 15 hours on 1 day.
    [3]
    After 10 days, the plants are placed in larger pots and cultivated in a greenhouse at 26 ° C (40,000 lux) with a photoperiod of 12-16 hours on 1 day, preferably 15 hours on 1 day. ·
    Plants that have not developed roots can be inoculated with young plants cultivated in the greenhouse, according to the classical method, or placed for 10-20 days in a rooting medium or in a third medium.
    The third medium includes mineral salts, vitamins and sucrose. Mineral salts include salts of macronutrients and salts of ol oloelements. The macronutrients used in this third medium can be selected among the following compounds magnesium sulfate, calcium chloride, monosodium phosphate. potassium nitrate and ammonium sulfate.
    [4]
    Among the salts based on oligoelements, one can name boric acid, manganese sulfate, zinc sulfate, sodium molybdate, sulfide! copper (II), cobalt chloride, potassium iodide and chelate Fe-Na-ETLK. This combination of mineral salts is known as B
    [5]
    5. Preferred amounts of macroelements and oligoelements per 1 liter of medium are the following mg: 250 heptahydrated magnesium sulfate, 150 dihydrated calcium chloride, 169 monohydrated monosodium phosphate, 3000 potassium nitrate, 3 boric acid, 13.2 tetrahydrated manganese sulfate, 2 heptahydrated zinc sulfate, · 0.25 dihydrated sodium molybdate, 0.025 pentahydrated copper (II) sulfate, 0.025 hexahydrated cobalt chloride, 0.75 potassium iodide, 40 Fe-Na EDTA chelate.
    The third medium also contains vitamins. These are nicotinic acid, thiamine, pyridoxine, and myo-inositol. Preferred amounts of vitamins per 1 liter of medium are, mg: G nicotinic acid. 10 thiamine hydrochloride, 1 pyridoxine hydrochloride and 100 myo-inositol.
    The third medium also contains sucrose and activated charcoal and / or an auxin type hormone. Sucrose is, for example, in an amount of 1-2%. preferably 1%, and activated carbon in an amount
    0.1% If you use a hormone instead of activated carbon, then choose 3-indoleacetic acid in doses of 0.1-0.2 mg per 1 liter. Phytagar agar or Gelrite. used to create a solid environment. A final concentration of 0.5% for Phytagar and 0.25% for Gelrite is sufficient. The pH of the medium can vary from 5.0 to 6.0, and is preferably 5.0. The medium is sterilized in an autoclave.
    Plants are cultivated in this medium for 2-3 weeks at 26 ° C in the light (1500 lux) with a photoperiod of 12-16 on 1 day, preferably 16 hours on 1 day. Plants form roots and can be planted in the ground.
    Plants obtained by this method may be phenotypically different from the starting material due to in vitro stress. Plants are pollinated by hand and matured until the collection of seeds. Several units of grains are planted for the analysis of new sunflower plants and the selection of possible interesting mutants, which are then involved in the program of selection of varieties;
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    同族专利:
    公开号 | 公开日
    AU601774B2|1990-09-20|
    CS276396B6|1992-05-13|
    IL84231A|1992-01-15|
    TNSN87120A1|1990-01-01|
    RO100219B1|1992-02-24|
    ES2025200B3|1992-03-16|
    CA1308255C|1992-10-06|
    PT86050B|1990-08-31|
    GR3002902T3|1993-01-25|
    KR880004738A|1988-06-27|
    DK566787D0|1987-10-29|
    DE3773836D1|1991-11-21|
    EP0266287B1|1991-10-16|
    JPS63129983A|1988-06-02|
    HUT49034A|1989-08-28|
    CN87107542A|1988-06-29|
    DK566787A|1988-05-01|
    ZA878095B|1988-04-26|
    EP0266287A1|1988-05-04|
    TR23032A|1989-02-10|
    US5017491A|1991-05-21|
    NZ222330A|1990-08-28|
    AU8040587A|1988-05-05|
    HU200070B|1990-04-28|
    IL84231D0|1988-03-31|
    AT68317T|1991-11-15|
    YU198487A|1991-10-31|
    PT86050A|1987-11-01|
    BG48561A3|1991-03-15|
    FR2605839A1|1988-05-06|
    FR2605839B1|1989-02-24|
    CN1019165B|1992-11-25|
    MA21093A1|1988-07-01|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US4038778A|1976-09-27|1977-08-02|Gte Laboratories Incorporated|Tissue culture technique for asexual plant reproduction and a medium for use therewith|
    US4354327A|1979-04-27|1982-10-19|International Paper Company|Tissue culture method for asexual propagation of pine trees and medium for use therewith|
    US4552844A|1983-06-15|1985-11-12|Stauffer Chemical Company|Plant growth medium|
    EP0160390A3|1984-04-16|1987-04-08|Sandoz Ltd.|Embryogenic callus and cell suspension of inbred corn|
    US4670392A|1984-07-27|1987-06-02|Sungene Technologies Corporation|Sunflower regeneration through embryogenesis|
    US4673648A|1984-07-27|1987-06-16|Sungene Technologies Corporation|Sunflower regeneration through organogenesis|
    US4670391A|1984-07-27|1987-06-02|Sungene Technologies Corporation|Sunflower regeneration through embryogenesis and organogenesis|EP0328424A3|1988-02-12|1992-04-29|Kyowa Hakko Kogyo Kabushiki Kaisha|Process for the production of somatic embryos|
    AU646116B2|1990-12-06|1994-02-10|Pioneer Hi-Bred International, Inc.|Sunflower plants having a high frequency of regenerability of fertile plants from isolated protoplasts and method of using same|
    EP2218775B1|1996-08-30|2015-01-28|Life Technologies Corporation|Method for producing a polypeptide in vitro in mammalian cells in a protein-free and serum-free culture medium|
    US6066787A|1997-12-18|2000-05-23|Pannar Seed Limited|Hybrid sunflower plant and seed PAN 9501|
    US6034307A|1997-12-18|2000-03-07|Pannar Seed Limited|Hybrid sunflower plant and seed pan 9612|
    CN101258806B|2007-03-08|2010-09-22|谭宾|Technique for cultivating sunflower all the year|
    US8901377B2|2010-12-03|2014-12-02|E. I. Du Pont De Nemours And Company|Method of sunflower regeneration and transformation using radicle free embryonic axis|
    CN102301960A|2011-08-18|2012-01-04|新疆康地种业科技股份有限公司|Method for establishing a Kangdi No.6 oil sunflower regeneration system|
    CN103404439B|2013-08-12|2015-11-25|南京农业大学|A kind of method of jerusalem artichoke adventitious bud inducing and plant regeneration|
    CN106414707A|2014-01-23|2017-02-15|日产化学工业株式会社|Method for producing culture medium composition|
    CN107182782B|2017-05-09|2019-06-18|三瑞农业科技股份有限公司|A method of accelerating sunflower generation process|
    CN113508753A|2021-07-26|2021-10-19|浙江省农业科学院|Method for rapid propagation and tissue culture plant regeneration of ornamental sunflower|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    FR8615299A|FR2605839B1|1986-10-30|1986-10-30|METHOD OF REGENERATING SUNFLOWER BY EMBRYOGENESIS|
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