RU1824115C - Method of multiplication of viccinium vitis-idaea l in vitro - Google Patents

Method of multiplication of viccinium vitis-idaea l in vitro

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Publication number
RU1824115C
RU1824115C SU914910564A SU4910564A RU1824115C RU 1824115 C RU1824115 C RU 1824115C SU 914910564 A SU914910564 A SU 914910564A SU 4910564 A SU4910564 A SU 4910564A RU 1824115 C RU1824115 C RU 1824115C
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RU
Russia
Prior art keywords
agar
vitro
idaea
explants
lingonberry
Prior art date
Application number
SU914910564A
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Russian (ru)
Inventor
Евгений Антонович Сидорович
Елена Николаевна Кутас
Original Assignee
Центральный Ботанический Сад Ан Бсср
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Application filed by Центральный Ботанический Сад Ан Бсср filed Critical Центральный Ботанический Сад Ан Бсср
Priority to SU914910564A priority Critical patent/RU1824115C/en
Application granted granted Critical
Publication of RU1824115C publication Critical patent/RU1824115C/en

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  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

Использование в селцгком хоз йстве и биотехнологии, в чж.тносги, дл  получени  посадочного материала брусники. Сущность изобретени : экспланты брусники культивируют на агаризованной среде Андерсона , содержащей в своем составе 100 мг/л мезоинозита, 80мг/л аденин сульфата, 0.4 мг/л тиамина, 0,4 мг/ индолилуксусной кислоты. 15,0 мг/л изопентениладенина, 30 г/л сахарозы и 7 г/л агара. Культивируют на этой среде до образовани  каллусной ткани и последующей регенерации из нее побегов , которые пересаживают дл  укоренени  на субстрат, представл ющий собой смесь торфа и перлита в соотношении 1:1 соответственно .Use in agriculture and biotechnology, in particular, to obtain lingonberry planting stock. SUMMARY OF THE INVENTION Lingonberry explants are cultured on Anderson's agar medium containing 100 mg / l mesoinositol, 80 mg / l adenine sulfate, 0.4 mg / l thiamine, 0.4 mg / indolylacetic acid. 15.0 mg / l of isopentenyladenine, 30 g / l of sucrose and 7 g / l of agar. It is cultivated on this medium until callus tissue is formed and subsequent shoots are regenerated from it, which are transplanted for rooting on a substrate, which is a mixture of peat and perlite in a 1: 1 ratio, respectively.

Description

Изобретение относитс  к технологии клонального микроразмножени  растений. Область применени : сельское и лесное хоз йство , цветоводство, пищева  и медицинска  промышленность.The invention relates to a technology for clonal micropropagation of plants. Scope: agricultural and forestry, floriculture, food and medical industry.

Целью изобретени   вл етс  разработка нового способа размножени  брусники обыкновонной в культуре in vitro.The aim of the invention is to develop a new method for the propagation of lingonberry ordinary in vitro culture.

Это достигаетс  путем пролиферации каллуса и последующей регенерации из него растений на питательной среде Андерсона , содержащей следующие добавки: мезоинозит 100 мг/л аденин сульфат 80 мг/л, тиамин 0,4 мг/л, индилилуксусна  кислота 4 мг/л, изопентениладенин 15 мг/л, сахароза 30 г/л, агар 7 г/л Укоренение побегов провод т на субстрате, состо щем из меси торфа и перлита в соотношении 1:1,This is achieved by the proliferation of callus and the subsequent regeneration of plants from it on Anderson's nutrient medium containing the following additives: mesoinositol 100 mg / l adenine sulfate 80 mg / l, thiamine 0.4 mg / l, indilyl acetic acid 4 mg / l, isopentenyladenine 15 mg / l, sucrose 30 g / l, agar 7 g / l. Rooting of shoots is carried out on a substrate consisting of a mixture of peat and perlite in a ratio of 1: 1,

Дл  получени  калпуса использовали семена брусники о ик-новенной. Стерилизацию их пронп/ 1пи п ( / растворегипохлорита Са с последующим промыванием в трех сменах стерильной воды по 15 мин в каждой. Затем семена высаживали на твердую агаризованную среду Андерсона и куль- тивировали при температуре 26°С, относительной влажности воздуха 56%, фотопериоде 16ч.In order to obtain calpus, lingonberry seeds were used. Sterilization of their pronp / 1pi n / solution of Ca hypochlorite followed by washing in three shifts of sterile water for 15 minutes each. Then the seeds were planted on Anderson's solid agar medium and cultivated at a temperature of 26 ° C, relative humidity 56%, photoperiod 16h .

Спуст  6 недель культивировани  из колб в стерильных услови х извлекали проростки , делили их на экспланты и высаживали на ту же среду, что и семена. Через 6 недель экспланты образовали каллус с последующей регенерацией из него растенийAfter 6 weeks of cultivation, seedlings were removed from the flasks under sterile conditions, divided into explants and planted on the same medium as the seeds. After 6 weeks, the explants formed a callus with subsequent regeneration of plants from it.

Claims (1)

Формула изобретени  Способ размножени  Vaccinium vitls- Idaea L. In vitro, включающий культивирование эксплантов на агаризоеанной питательной среде до получени  р стений- регенерантов, отличающийс  тем. что экспланты культивируют на агаризованнойSUMMARY OF THE INVENTION A method for propagating Vaccinium vitls-Idaea L. in vitro, the method comprising culturing explants on an agarized nutrient medium to obtain regenerated plants. that explants are cultured on agar ЁYo 0000 IKIK ЈьЈь 01 01 среде Андерсона, содержащей в своем со-этом культивирование осуществл ют доAnderson’s medium containing in this cultivation is carried out until ставе 100 мг/л мезоинозита. 80 мг/л аденинпролиферации каллусной и регенерасульфата , 0,4 мг/л тиамина. 0.4 мг/л индо-ции из нее побегов, укоренение которыхat a rate of 100 mg / l of mesoinositis. 80 mg / l of callus and regenerate sulfate adenine proliferation, 0.4 mg / l of thiamine. 0.4 mg / l Indo-tion of shoots from it, the rooting of which лилуксусной кислоты. 15 мг/л изопентени-провод т из субстрате, состо щем из смесиlilacetic acid. 15 mg / L isopentenium is carried out from a substrate consisting of a mixture ладенина, 30 г/л сахарозы и 7 г/л агара, при5 торфа и перлита в соотношении 1 1ladenina, 30 g / l sucrose and 7 g / l agar, with 5 peat and perlite in a ratio of 1 1
SU914910564A 1991-02-12 1991-02-12 Method of multiplication of viccinium vitis-idaea l in vitro RU1824115C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU914910564A RU1824115C (en) 1991-02-12 1991-02-12 Method of multiplication of viccinium vitis-idaea l in vitro

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU914910564A RU1824115C (en) 1991-02-12 1991-02-12 Method of multiplication of viccinium vitis-idaea l in vitro

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RU1824115C true RU1824115C (en) 1993-06-30

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103999773A (en) * 2014-05-27 2014-08-27 昆明凌览生物科技有限公司 Tissue culture method of vaccinium dunalianum containing caffeoyl arbutin
CN104012411A (en) * 2014-06-09 2014-09-03 赵兰 Tissue culture method for cowberry blueberries
CN104082142A (en) * 2014-07-02 2014-10-08 江苏农林职业技术学院 Proliferation medium for Sierra cowberry blueberry tissue culture and preparation method thereof
CN109906942A (en) * 2019-04-30 2019-06-21 黑龙江省科学院自然与生态研究所 A kind of Cranberry based on three-stage culture medium quickly breeds regeneration method
CN109984043A (en) * 2019-05-15 2019-07-09 西南林业大学 It is a kind of using blade as the camphor tree leaf blueberry method for tissue culture of explant

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Gibhard К, Filedrlch M. In vitro shoot regeneration of llngonberry clones, Gartenbauwlssen-schaft 1986, vol 44, p. 170- 175. *

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103999773A (en) * 2014-05-27 2014-08-27 昆明凌览生物科技有限公司 Tissue culture method of vaccinium dunalianum containing caffeoyl arbutin
CN104012411A (en) * 2014-06-09 2014-09-03 赵兰 Tissue culture method for cowberry blueberries
CN104082142A (en) * 2014-07-02 2014-10-08 江苏农林职业技术学院 Proliferation medium for Sierra cowberry blueberry tissue culture and preparation method thereof
CN109906942A (en) * 2019-04-30 2019-06-21 黑龙江省科学院自然与生态研究所 A kind of Cranberry based on three-stage culture medium quickly breeds regeneration method
CN109906942B (en) * 2019-04-30 2021-12-07 黑龙江省科学院自然与生态研究所 Three-stage culture medium-based rapid propagation and regeneration method for cranberries
CN109984043A (en) * 2019-05-15 2019-07-09 西南林业大学 It is a kind of using blade as the camphor tree leaf blueberry method for tissue culture of explant

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