CN103749158A - Micro-grafting method for acer palmatum and acer paimatum under tissue culture condition - Google Patents

Micro-grafting method for acer palmatum and acer paimatum under tissue culture condition Download PDF

Info

Publication number
CN103749158A
CN103749158A CN201410006369.3A CN201410006369A CN103749158A CN 103749158 A CN103749158 A CN 103749158A CN 201410006369 A CN201410006369 A CN 201410006369A CN 103749158 A CN103749158 A CN 103749158A
Authority
CN
China
Prior art keywords
acer
micro
micrografting
scion
stock
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201410006369.3A
Other languages
Chinese (zh)
Other versions
CN103749158B (en
Inventor
郑超
马建华
王小辉
吴佳川
朱晓菲
沈香兰
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sichuan Qicai Forestry Co., Ltd.
Original Assignee
VIMA MANUFACTURE ASSOCIATION
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by VIMA MANUFACTURE ASSOCIATION filed Critical VIMA MANUFACTURE ASSOCIATION
Priority to CN201410006369.3A priority Critical patent/CN103749158B/en
Publication of CN103749158A publication Critical patent/CN103749158A/en
Application granted granted Critical
Publication of CN103749158B publication Critical patent/CN103749158B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Abstract

The invention discloses a micro-grafting method for acer palmatum and acer paimatum under a tissue culture condition. The method includes sowing acer palmatum seeds in greenhouses to culture the acer palmatum; selecting acer palmatum which grows healthily as rootstock; manufacturing explants by acer paimatum branches; performing induction culture on auxiliary buds and exercising seedlings; cutting the exercised acer paimatum auxiliary buds to be used as scions and performing micro-grafting on the scions; culturing, exercising and transplanting micro-grafted seedlings to obtain micro-grafted acer paimatum seedlings which grow healthily. The method has the advantages that operation is simple, large quantities of acer paimatum micro-grafted seedlings can be acquired in a short period of time without constraints of environmental factors such as the seasons, the temperatures and the climate, regenerated plants cultured by the method are stable in genetic character and short in nursery period, are healthy and grow vigorously, and the survival rate of the regenerated plants can reach 85% at least.

Description

Your micro-grafting method of Acer palmatum gold under a kind of condition of tissue culture
Technical field
The invention belongs to plant micro-grafting method technical field, be specifically related to your micro-grafting method of Acer palmatum gold under a kind of condition of tissue culture.
Background technology
Aceraceae ( aceraceae) maple genus ( acer) the common general term maple of plant, custom claims again " maple " or " maple ".Whole world maple has kind more than 200, is distributed in Asia, Europe, North America and Africa northern.China has more than 160 to plant, and accounts for the more than 75% of whole world sum, and all there is distribution all parts of the country, the main product Yangtze river basin and on the south each provinces and regions.Maple can be used as construction timber, paper making raw material, medicine extraction, iundustrial oil and nectariferous plant.Tree-like abundant, the attitude of some maple graceful, leaf abundant, leaf look changeable, is described as world-renowned ornamental foliage plant.
Acer palmatum (Acer paimatum) is called refined maple, is that Aceraceae maple belongs to, and is ornamental tree species famous and precious in urban look.Originate in Yangtze River in China basin, also there is distribution in Japan, the Korea peninsula.China is mainly distributed in each province, the Yangtze river basin, is born in the border or sparse woods on the following mountain region of height above sea level 1200m, hills more.Shank Acer defoliation small arbor, high about 8m, bark Dark grey, annual shoot purple or pale purple green; Perennial branch light gray, purple or darkviolet.Acer palmatum happiness is warm, humid climate and half cloudy environment, and intolerant to waterlogging is more drought-enduring, in the isolated planting of direct sunlight place, subjects to a day bright evil summer; Fit and be born in soil fertile, moistening and that draining is good, cold resistance is not strong, acidity, neutrality and calcareous soil all can adapt to, because it has high ornamental value, the performance of urban look is had to considerable effect, the places such as Middle Isolated Grassland of Highway, park, square, greenbelt in little residential region its graceful figure that is seen everywhere is the good ornamental tree species of competitively cultivating in recent years.Countries in the world are introducing and planting already, and mutation and modification are a lot.Japan's Acer palmatum is cultivated more than 450 reward leaf kinds at present.
Jin Gui (Acer palmatum ' katsura ') has another name called: " card Soviet Union " is that the variation of Acer palmatum gardens one of is planted.Spring young leaves glassy yellow, edge is orange red, summer, blade became light greenly to yellowish green, autumn, leaf color became again bright orange to orange.Blade is mostly 5 and splits, and splits deeply, and there is shallow tooth at edge.Its vertical growth, plant type is compact.Jin Gui is a very attracting maple kind, but it is very difficult for breeding, and cuttage root-taking rate is low, and tissue culture propagation technical system is not also set up at present, and seed germination rate is low, and production quantity does not far reach the market demand.
Micrografting refers under condition of tissue culture the technology that stock and scion are carried out to grafting, if can set up your micrografting system of Acer palmatum gold under condition of tissue culture, can reach the object of carrying out throughout the year the expensive seedling of the fast numerous gold of short-term.By By consulting literatures, aspect the golden expensive group training of Acer palmatum micrografting, have not been reported.
Summary of the invention
object of the present invention is to overcome the deficiencies in the prior art, provide the Acer palmatum gold under a kind of condition of tissue culture your micro-grafting method, the method is simple to operate, can within short-term, obtain the expensive grafting of a large amount of gold, and be not subject to the restriction of season, temperature, weather, the expensive plant stabilization characteristics of genetics of gold that the method is cultivated, plant be healthy, it is vigorous to grow, growing-seedling period is short, survival rate is high.
The object of the invention is to be achieved through the following technical solutions: your micro-grafting method of Acer palmatum gold under a kind of condition of tissue culture, it comprises the following steps:
S1. obtaining of stock: sow Acer palmatum seed and cultivate in booth seedbed, when Acer palmatum plant strain growth to 30~40cm height, choose the plant of robust growth as stock;
S2. obtaining of scion: gather the expensive branch of gold that diameter is 2.5~3.5mm in fine day, being cut into length is the explant that 3.5~4.5cm trains for group with the stem section of 2 buds, explant is seeded on inducing culture and is cultivated, until golden your explant bud, moved into booth hardening 3~4d during in half germinating, the axillalry bud cutting after hardening is scion, while noting cutting, scion needs band portion xylem, and scion length is 0.8~1.2cm; Wherein, described inducing culture is MS+6-BA 0.5mg/L+IAA 0.8mg/L+ sucrose 20g/L+ agar 6g/L; Under the bud of described explant bud, position retains the stem that length is 4.5~5.5mm;
S3. micrografting: the stock that step S1 is obtained is blocking apart from root 4.5~5.5cm place, with micrografting cutter, at stock truncation surface place, vertically split out the otch that the degree of depth is 1.2~1.8cm, by the formation layer alignment stock of step S2 gained scion, in insertion otch, with plastic seal membrana oralis bale packing interface, obtain micrografting seedling;
S4. cultivate: micrografting seedling is planted in basin, be placed in canopy and cultivate; Keeping humidity in canopy is >=90%, and temperature is 23~28 ℃, cultivates 18~22d;
S5. acclimatization and transplants: the micrografting seedling that above-mentioned cultivation is survived moves in another canopy, and slowly reduce humidity and shift out golden your micrografting seedling to outer humidity.
The invention has the beneficial effects as follows:
1. the present invention utilizes propagation by grafiting know-why, by methods such as your axillalry bud of tissue culture and inducement gold, Multiple Buds, within compared with short-term, obtained the expensive scion of a large amount of gold and carried out micrografting, obtained a large amount of Jin Guimiao, set up golden your group training micrografting propagation technique system, for the expensive breeding of gold provides a new way.
2. utilize the inventive method graft seedling growth can obtain whole plant in 20~30 days, really realize high efficiency quick breeding.The regeneration plant stabilization characteristics of genetics that the method is cultivated, plant be healthy, it is vigorous to grow, growing-seedling period is short, survival rate can reach more than 85%.
3. because the obtaining of the obtaining of the inventive method stock, scion, micrografting, cultivation and acclimatization and transplants are to realize, be not therefore subject to the restriction of the envirment factors such as season, weather and temperature under artificial control.
Accompanying drawing explanation
Fig. 1 is for cultivating the expensive micrografting seedling of the gold schematic diagram of 15 days;
Fig. 2 is for cultivating the expensive micrografting seedling of the gold schematic diagram of 20 days;
Fig. 3 is for cultivating the expensive micrografting seedling of the gold schematic diagram of 30 days;
Fig. 4 is the expensive micrografting seedling of the gold after acclimatization and transplants schematic diagram.
Embodiment
Below in conjunction with embodiment, the present invention will be further described, and protection scope of the present invention is not limited to the following stated.
embodiment 1:your micro-grafting method of Acer palmatum gold under condition of tissue culture, it comprises the following steps:
S1. obtaining of stock: sow Acer palmatum seed and cultivate in booth seedbed, during to 30cm height, choose the plant of robust growth as stock until Acer palmatum plant strain growth;
S2. obtaining of scion: gather the expensive branch of gold that diameter is 2.5mm in fine day, being cut into length is the explant that 3.5cm trains for group with the stem section of 2 buds, explant is seeded on inducing culture and is cultivated, until golden your explant bud, moved into booth hardening 3d during in half germinating, the axillalry bud cutting after hardening is scion, while noting cutting, scion needs band portion xylem, and scion length is 0.8cm; Wherein, described inducing culture is MS+6-BA 0.5mg/L+IAA 0.8mg/L+ sucrose 20g/L+ agar 6g/L; Under the bud of described explant bud, position retains the stem that length is 4.5mm;
S3. micrografting: the stock that step S1 is obtained is blocking apart from root 4.5cm place, with micrografting cutter, at stock truncation surface place, vertically split out the otch that the degree of depth is 1.2cm, by the formation layer alignment stock of step S2 gained scion, in insertion otch, with plastic seal membrana oralis bale packing interface, obtain micrografting seedling;
S4. cultivate: micrografting seedling is planted in basin, be placed in canopy and cultivate, as shown in Figure 1, Figure 2, Figure 3 shows; Keeping humidity in canopy is 90%, and temperature is 23 ℃, cultivates 18d;
S5. acclimatization and transplants: the micrografting seedling that above-mentioned cultivation is survived moves in another canopy, and slowly reduce humidity in canopy and shift out golden your micrografting seedling to extraneous humidity, as shown in Figure 4.
embodiment 2:your micro-grafting method of Acer palmatum gold under condition of tissue culture, it comprises the following steps:
S1. obtaining of stock: sow Acer palmatum seed and cultivate in booth seedbed, during to 40cm height, choose the plant of robust growth as stock until Acer palmatum plant strain growth;
S2. obtaining of scion: gather the expensive branch of gold that diameter is 3.5mm in fine day, being cut into length is the explant that 4.5cm trains for group with the stem section of 2 buds, explant is seeded on inducing culture and is cultivated, until golden your explant bud, moved into booth hardening 4d during in half germinating, under gnotobasis, the axillalry bud cutting after hardening is scion, and while noting cutting, scion needs band portion xylem, and scion length is 1.2cm; Wherein, described inducing culture is MS+6-BA 0.5mg/L+IAA 0.8mg/L+ sucrose 20g/L+ agar 6g/L; Under the bud of described explant bud, position retains the stem that length is 5.5mm;
S3. micrografting: the stock that step S1 is obtained is blocking apart from root 5.5cm place, with micrografting cutter, at stock truncation surface place, vertically split out the otch that the degree of depth is 1.8cm, by the formation layer alignment stock of step S2 gained scion, in insertion otch, with plastic seal membrana oralis bale packing interface, obtain micrografting seedling;
S4. cultivate: micrografting seedling is planted in basin, be placed in canopy and cultivate, as shown in Figure 1, Figure 2, Figure 3 shows; Keeping humidity in canopy is 92%, and temperature is 28 ℃, cultivates 22d;
S5. acclimatization and transplants: the micrografting seedling that above-mentioned cultivation is survived moves in another canopy, and slowly reduce humidity in canopy and transplant golden your micrografting seedling to extraneous humidity, as shown in Figure 4.
embodiment 3:your micro-grafting method of Acer palmatum gold under condition of tissue culture, it comprises the following steps:
S1. obtaining of stock: sow Acer palmatum seed and cultivate in booth seedbed, during to 35cm height, choose the plant of robust growth as stock until Acer palmatum plant strain growth;
S2. obtaining of scion: gather the expensive branch of gold that diameter is 3mm in fine day, being cut into length is the explant that 4cm trains for group with the stem section of 2 buds, explant is seeded on inducing culture and is cultivated, until golden your explant bud, moved into booth hardening 3.5d during in half germinating, the axillalry bud cutting after hardening is scion, while noting cutting, scion needs band portion xylem, and scion length is 1cm; Wherein, described inducing culture is MS+6-BA 0.5mg/L+IAA 0.8mg/L+ sucrose 20g/L+ agar 6g/L; Under the bud of described explant bud, position retains the stem that length is 5mm;
S3. micrografting: the stock that step S1 is obtained is blocking apart from root 5cm place, with micrografting cutter, at stock truncation surface place, vertically split out the otch that the degree of depth is 1.5cm, the formation layer alignment stock by the scion of step S2 gained, inserts in otch, with plastic seal membrana oralis bale packing interface, obtain micrografting seedling;
S4. cultivate: micrografting seedling is planted in basin, be placed in canopy and cultivate, as shown in Figure 1, Figure 2, Figure 3 shows; Keeping humidity in canopy is 95%, and temperature is 25 ℃, cultivates 18~22d;
S5. acclimatization and transplants: the micrografting seedling that above-mentioned cultivation is survived moves in another canopy, and slowly reduce humidity in canopy and shift out golden your micrografting seedling to extraneous humidity, as shown in Figure 4.
embodiment 4:your micro-grafting method of Acer palmatum gold under condition of tissue culture, it comprises the following steps:
S1. obtaining of stock: sow Acer palmatum seed and cultivate in booth seedbed, during to 38cm height, choose the plant of robust growth as stock until Acer palmatum plant strain growth;
S2. obtaining of scion: gather the expensive branch of gold that diameter is 3.5mm in fine day, being cut into length is the explant that 3.5cm trains for group with the stem section of 2 buds, explant is seeded on inducing culture and is cultivated, until golden your explant bud, moved into booth hardening 3d during in half germinating, under gnotobasis, the axillalry bud cutting after hardening is scion, and while noting cutting, scion needs band portion xylem, and scion length is 0.9cm; Wherein, described inducing culture is MS+6-BA 0.5mg/L+IAA 0.8mg/L+ sucrose 20g/L+ agar 6g/L; Under the bud of described explant bud, position retains the stem that length is 4.8mm;
S3. micrografting: the stock that step S1 is obtained is blocking apart from root 5.2cm place, with micrografting cutter, at stock truncation surface place, vertically split out the otch that the degree of depth is 1.7cm, by the formation layer alignment stock of step S2 gained scion, in insertion otch, with plastic seal membrana oralis bale packing interface, obtain micrografting seedling;
S4. cultivate: micrografting seedling is planted in basin, be placed in canopy and cultivate, as shown in Figure 1, Figure 2, Figure 3 shows; Keeping humidity in canopy is 93%, and temperature is 26 ℃, cultivates 22d;
S5. acclimatization and transplants: the micrografting seedling that above-mentioned cultivation is survived moves in another canopy, and slowly reduce temperature of shed and humidity is transplanted golden your micrografting seedling to ambient temperature and humidity, as shown in Figure 4.

Claims (3)

1. your micro-grafting method of the gold of the Acer palmatum under condition of tissue culture, is characterized in that, it comprises the following steps:
S1. obtaining of stock: sow Acer palmatum seed and cultivate in booth seedbed, when Acer palmatum plant strain growth to 30~40cm height, choose the plant of robust growth as stock;
S2. obtaining of scion: gather the expensive branch of gold that diameter is 2.5~3.5mm in fine day, being cut into length is the explant that 3.5~4.5cm trains for group with the stem section of 2 buds, explant is seeded on inducing culture and is cultivated, until golden your explant bud, moved into booth hardening 3~4d during in half germinating, the axillalry bud cutting after hardening is scion, while noting cutting, scion needs band portion xylem, and scion length is 0.8~1.2cm;
S3. micrografting: the stock that step S1 is obtained is blocking apart from root 4.5~5.5cm place, with micrografting cutter, at stock truncation surface place, vertically split out the otch that the degree of depth is 1.2~1.8cm, by the formation layer alignment stock of step S2 gained scion, in insertion otch, with plastic seal membrana oralis bale packing interface, obtain micrografting seedling;
S4. cultivate: micrografting seedling is planted in basin, be placed in canopy and cultivate; Keeping humidity in canopy is >=90%, and temperature is 23~28 ℃, cultivates 18~22d;
S5. acclimatization and transplants: the micrografting seedling that above-mentioned cultivation is survived moves in another canopy, and slowly reduce humidity in canopy and shift out golden your micrografting seedling to extraneous humidity.
2. your micro-grafting method of the gold of the Acer palmatum under a kind of condition of tissue culture according to claim 1, is characterized in that, inducing culture described in step S2 is MS+6-BA 0.5mg/L+IAA 0.8mg/L+ sucrose 20g/L+ agar 6g/L.
3. your micro-grafting method of the gold of the Acer palmatum under a kind of condition of tissue culture according to claim 1, is characterized in that, under the bud of the bud of explant described in step S2, position retains the stem that length is 4.5~5.5mm.
CN201410006369.3A 2014-01-07 2014-01-07 Micro-grafting method for acer palmatum and acer paimatum under tissue culture condition Active CN103749158B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410006369.3A CN103749158B (en) 2014-01-07 2014-01-07 Micro-grafting method for acer palmatum and acer paimatum under tissue culture condition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410006369.3A CN103749158B (en) 2014-01-07 2014-01-07 Micro-grafting method for acer palmatum and acer paimatum under tissue culture condition

Publications (2)

Publication Number Publication Date
CN103749158A true CN103749158A (en) 2014-04-30
CN103749158B CN103749158B (en) 2015-07-01

Family

ID=50516618

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410006369.3A Active CN103749158B (en) 2014-01-07 2014-01-07 Micro-grafting method for acer palmatum and acer paimatum under tissue culture condition

Country Status (1)

Country Link
CN (1) CN103749158B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104429635A (en) * 2014-11-17 2015-03-25 苏州市新巷农艺科技园 Grafting propagation method for albo-purpurascens
CN105519434A (en) * 2015-12-30 2016-04-27 四川禾木本业农林科技有限公司 A tissue cultured seedling micrografting method for acer palmatum 'orange dream'
CN106417025A (en) * 2016-10-14 2017-02-22 山西农业大学 Test tube micro-grafting method for seedless grape embryo-rescued malformed plantlets

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2080780C1 (en) * 1994-05-11 1997-06-10 Всероссийский научно-исследовательский институт сельскохозяйственной биотехнологии РАСХН Clonal plant micro propagation method
CN102792857A (en) * 2012-08-16 2012-11-28 江苏省林业科学研究院 Acer palmatum twig grafting propagation method
CN103004593A (en) * 2012-12-11 2013-04-03 浙江农林大学 Thin-shell pecan tissue culture bud micro grafting method
CN103053346A (en) * 2013-01-25 2013-04-24 河南省木本饲料工程技术研究中心 Micrografting method for tetraploid acacia
CN103477983A (en) * 2013-09-06 2014-01-01 巴中市光雾山植物研究所 Acer palmatum Sangokaku tissue culture propagation process

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2080780C1 (en) * 1994-05-11 1997-06-10 Всероссийский научно-исследовательский институт сельскохозяйственной биотехнологии РАСХН Clonal plant micro propagation method
CN102792857A (en) * 2012-08-16 2012-11-28 江苏省林业科学研究院 Acer palmatum twig grafting propagation method
CN103004593A (en) * 2012-12-11 2013-04-03 浙江农林大学 Thin-shell pecan tissue culture bud micro grafting method
CN103053346A (en) * 2013-01-25 2013-04-24 河南省木本饲料工程技术研究中心 Micrografting method for tetraploid acacia
CN103477983A (en) * 2013-09-06 2014-01-01 巴中市光雾山植物研究所 Acer palmatum Sangokaku tissue culture propagation process

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
周艳等: "《植物微嫁接研究进展》", 《贵州科学》 *
巴中市林业局: "《七彩林业,槭树研究硕果累累》", 《HTTP://WWW.BZSLY.GOV.CN/SHOW.ASP?ID=4270》 *
曹受金等: "《美国红枫组织培养与快繁技术的研究》", 《湖北农业科学》 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104429635A (en) * 2014-11-17 2015-03-25 苏州市新巷农艺科技园 Grafting propagation method for albo-purpurascens
CN105519434A (en) * 2015-12-30 2016-04-27 四川禾木本业农林科技有限公司 A tissue cultured seedling micrografting method for acer palmatum 'orange dream'
CN106417025A (en) * 2016-10-14 2017-02-22 山西农业大学 Test tube micro-grafting method for seedless grape embryo-rescued malformed plantlets

Also Published As

Publication number Publication date
CN103749158B (en) 2015-07-01

Similar Documents

Publication Publication Date Title
CN103749124B (en) Acer palmatum overhead layering propagation method
CN103598019B (en) Grafting cultivation method of magnolia denudata and magnolia grandiflora
CN101194562B (en) Fast-growing cultivation method for moraceae ficus plants archaizing civilization design
CN103125244A (en) Cutting propagation method of golden camellia plants
CN106804379B (en) Method for promoting survival of transplanting anisetree bark in karst rocky mountain
CN103477854A (en) Acer palmatum precious tender branch cutting propagation method
CN101524042B (en) Fruit seedling cultivating technology of looking-glass trees
CN103598021B (en) Grafting cultivation domestication method for camphor trees suitable for growing in north
CN104521482A (en) Jasmine single-stem shape pot cultivating method
CN105165373A (en) Cutting seedling raising method of Davidia involucrata Baill
CN103749158B (en) Micro-grafting method for acer palmatum and acer paimatum under tissue culture condition
CN106613659B (en) Grafting cultivation method of euonymus plant golden beetle
CN105340560B (en) The introduction and cultivation method of Selaginella tamariscina
CN104160862A (en) Cuttage and field planting integrated fir cultivation method
CN108541555B (en) Transplanting nutrient medium and cultivation management method for sedum alfredii tissue culture seedlings
CN103141287B (en) Method for domesticating and culturing rubus peltatus
CN104396519A (en) Cutting propagation method for wild peanuts
CN104322357A (en) Potentilla sericea cutting propagation method
CN111972148B (en) Cutting propagation and field regression method for medicinal endangered plant Jinyun scutellaria baicalensis
CN101361457B (en) Jatropha regeneration method using excised leaf
CN107278631A (en) Powdery mildew, anthracnose and the method for cultivating landscape type Dendronenthamia japonica var.chinensis are controlled based on heteroplastic graft
CN109937722B (en) Method for rapidly propagating Chinese lizardtail ground stems
CN112136526A (en) Greenhouse castanea henryi twig cutting seedling method
CN104604542A (en) Cultivation method for honeysuckle in cold area
CN104285647A (en) Method for performing winter root cutting on Gazania splendens

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C56 Change in the name or address of the patentee
CP01 Change in the name or title of a patent holder

Address after: 610041 B 12F, Air China Century Center, No. 1, air route, Sichuan, Chengdu, Wuhou District

Patentee after: VICFARM MANUFACTURE ASSOCIATION

Address before: 610041 B 12F, Air China Century Center, No. 1, air route, Sichuan, Chengdu, Wuhou District

Patentee before: VIMA MANUFACTURE ASSOCIATION

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20190621

Address after: 635600 Tissue Culture Workshop Building of Rare and Colorful Leaf Plant Varieties in Guangwu Mountain, Sanshe, Changtan Village, Zhengzheng Town, Nanjiang County, Bazhong City, Sichuan Province

Patentee after: Sichuan Qicai Forestry Co., Ltd.

Address before: 610041 Block 12F, Air Century Center B, No. 1 Aviation Road, Wuhou District, Chengdu City, Sichuan Province

Patentee before: VICFARM MANUFACTURE ASSOCIATION