GB2201572A - Process for in vitro propagation of potato - Google Patents

Process for in vitro propagation of potato Download PDF

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Publication number
GB2201572A
GB2201572A GB08803408A GB8803408A GB2201572A GB 2201572 A GB2201572 A GB 2201572A GB 08803408 A GB08803408 A GB 08803408A GB 8803408 A GB8803408 A GB 8803408A GB 2201572 A GB2201572 A GB 2201572A
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GB
United Kingdom
Prior art keywords
media
shoots
pieces
cultures
rooted
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.)
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Application number
GB08803408A
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GB8803408D0 (en
Inventor
Gyorgy Molnar
Ferenc Foglein
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Novotrade Rt
Original Assignee
Novotrade Rt
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Publication date
Application filed by Novotrade Rt filed Critical Novotrade Rt
Publication of GB8803408D0 publication Critical patent/GB8803408D0/en
Publication of GB2201572A publication Critical patent/GB2201572A/en
Withdrawn legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01HNEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
    • A01H4/00Plant reproduction by tissue culture techniques ; Tissue culture techniques therefor
    • A01H4/005Methods for micropropagation; Vegetative plant propagation using cell or tissue culture techniques

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Cell Biology (AREA)
  • Developmental Biology & Embryology (AREA)
  • Botany (AREA)
  • Environmental Sciences (AREA)
  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
  • Hydroponics (AREA)
  • Cultivation Receptacles Or Flower-Pots, Or Pots For Seedlings (AREA)

Description

Process for the increase the efficiency of in vitro vegetative propagation of potato.
The invention relates to a process for increase the efficiency of in vitro phase of vegetative propagation of potato.
Several methods have been developed for the in vitro vegetative propagation of potato. We have worked out a complex method which can be applied for the economical mass-production of the potato 'a propagation material in great quantities and it is suitable for the production of different propagation materials (rooted cuttings, minitubers and small tubers, No. of Hungarian patent appl.: 1160/54.).
During the application of the above mentioned invention we have found that shoots are growing and multiplying better in liquid media than on solid media.
Propagation of shoots in liquid media is preferable for getting rooted plants. In addition to this we have planned experiments for the further propagation of the rooted plants propagated by liquid culture. As a result of these experiments we. have worked out such a method which is much more efficient for the in vitro propagation compared with the earlier ones.
The essential point of this method is that the rooted plants produced in liquid media, for further cultivation in glasshouses or for production of in vitro minitubers, are propagated in such a, way that those are divided for shoots and rooted shoot-pieces at first and both parts - the shoots and rooted shoot-pieces - are placed on fresh nutritive media. The further propagation of shoots grown in liquid media is increasing the efficiency of propagation, but the essential new step of this method is the use of the rooted shootpieces for further propagation and this step can increase five times the rate of multiplication and next to this, one can spare a lot of time.
According to a variant of this invention both - the shoots and the rooted shoot-pieces - are placed in liquid media so cultures grown from shoots are identical to the original rooted cultures and those can be used for minituber production or can be~,placed into glasshouses or can be propagated on the above written way, while cultures grown from the rooted shoot-pieces can be used preferably for foundation of in vitro minituber cultures.
According to another variant of this invention only the shoots are placed in liquid media and grown further to get rooted cultures, while the rooted shoot-pieces are placed on solid media and within a short time the rooted pieces are producing several new shoots which are good for further propagation.
The rooted shot-pieces cultivated on solid agar media are suitable not only for in vitro propagation, but also for green-house planting since they are equivalent to the cultures grown on liquid media.
According to a further variant of the process both the rooted shoot-pieces and the shoots were placed onto solid media. From the rooted shoot-pieces great amount of new shoots were developed while the shoots placed onto solid media has grown uninterrupted root-system. Both of the cultures may be used as described above, i.e. may be further propagated under in vitro conditions, in vitro minitubers maybfnduced on them, and may be planted into green-house.
This last mentioned process is the preferred variant of our invention since in this process less propagation material is necessary than in the process using liquid media, and shoots may be developed from all buds of the shoot-pieces, which may be cut short.
The rooted culture grown on agar media may be planted into the soil together with the media.
During the examination of the utilization possibilities of the solid agar media it has been established that the solid media may be used also in thinner layer than usual, about in a layer of 1 cm.
The root-system of the cultures grown in such media is more favourable in respect of both the in vitro propagation and planting into the soil.
The time-spareing is the result of two factors: 1. The arrangementef shoots in liquid media needs less time compared with the case of the solid media.
2. The rooted shoot-pieces can be placed on to the fresh liquid or solid media with one movement because of the adjacent roots.
The following examples illustrate the invention.
The composition of the nutritive media used by us is the following: Potato nutritive media Solid, maintaining and propagating media: NH4N03 1600 mg Mesoinosit 100 mg KN03 1900 mg Thiamine HCl 0,5 mg CaCl2.2H20 440 mg Pyridoxine HCl 1,0 mg MgS04.7H20 370 mg Nicotinic acid 5,0 mg Na2-EDTA+FeS04.7H20 25 mg Panthotene acid 2,5 mg H3604 6,2 mg Naphtylacetic acid 0,OOlmg MnS04.4H20 22,3 mg Sacharose 30 g ZnS04.4H20 8,6 mg Agar 6,5 g KI 0,83 mg pH 5,7 Na2Mo04.2H20 0,25 mg CuS04.5H20 0,025 mg CoCl2.6H20 0,025 mg Liquid rooting media: as above, without agar.
Example 1.
The shoots of the potato cultures grown on solid media were cut and approx. 10 pieces of it were placed in a 400 ml flask containing 20 ml liquid media and were cultured approx. for two weeks under 22 0C 16 hours 3000 lux illumination. Under these conditions 20-25 new shoots and adjacent roots are developing. The rooted culture is removed with a forceps from the flask under steril condition, the shoots are cut and placed into 2-3 flasks containing fresh nutritive media and the remaining rooted shoot- pieces are placed in a new liquid media. Cultures prepared in this way were grown for 2 weeks and were induced for minituber production and after 2-3 months - in average - 50 mini tubers can be produced by them.
Cultures developed from the cutted shoots can be used - on the above written way - for propagation, can be transplanted into glasshouses or minitubers can be induced by them.
Using the process detailed above one can produce 50% more cultures within the same time as one uses cultures grown on solid media.
Example 2.
Shoots of cultures grown on solid media (the composition of it is written above) were cut and approx. 10 pieces of it were placed into a 400 ml flask containing 20 ml liquid media and were cultured approx. for 2 weeks under 22 C 16 hours 3000 lux illumination. Under these conditions cultures were developing 20-20 new shoots and adjacent roots. The rooted cultures were removed with steril forceps, shoots were cut and placed into 2-3 flasks containing fresh liquid media. Cultures grown in liquid media were used for further propagation, minituber induction or were planted out into glasshouses. The rooted shoot-pieces placed on solid media were developing new shoots within 2 weeks, which are suitable for foundation of 3-4 new cultures.
Using the process detailed above one can produce 5 times more cultures within the same period as if one is only using cultures grown on solid media for propagation and a lot of time can be spared.

Claims (8)

What we claim is:
1. A process for the increase the efficiency of in vitro vegetative propagation of potato, characterized in that, the rooted cultures grown in liquid media can be propagated fully by dividing them for shoots and rooted shoot -pieces.
2. The process as claimed in claim 1, characterized in that, both parts - the shoots and the rooted shoot-pieces are propagated further in liquid media.
3. The process as claimed in claim 1, characterized in that, the shoots are propagated further in liquid media, the rooted shoot-pieces are propagated further on solid media.
4. The process as claimed in claim 1, characterized in that both the shoots and the rooted shoot-pieces are propagated on solid agar media.
5. The process as claimed in any one of claims 1 to 4, characterized in that, the process can be repeated several times.
6. The process as claimed in any one of claims 1 to 3 and 5 characterized in that, cultures developed from shoots grown in liquid media can be used for minituber induction and/or further propagation and/or planting into glasshouses.
7. The process as claimed in claim 1 or 2, characteriz in that, cultures developed from rooted shoot-pieces grown in liquid media can be used for minituber induction.
8. The process as claimed in claim 1 or 3 or 4, characterized in that, cultures developed from rooted shoot -pieces grown on solid media can be used for propagation of new cultures.
GB08803408A 1987-02-16 1988-02-15 Process for in vitro propagation of potato Withdrawn GB2201572A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
HU87595A HU204946B (en) 1987-02-16 1987-02-16 Method for increasing the effectiveness of "in vitro" vegetative propagation of potato

Publications (2)

Publication Number Publication Date
GB8803408D0 GB8803408D0 (en) 1988-03-16
GB2201572A true GB2201572A (en) 1988-09-07

Family

ID=10950343

Family Applications (1)

Application Number Title Priority Date Filing Date
GB08803408A Withdrawn GB2201572A (en) 1987-02-16 1988-02-15 Process for in vitro propagation of potato

Country Status (21)

Country Link
JP (1) JPS63279723A (en)
CN (1) CN1032448A (en)
AU (1) AU1173188A (en)
BE (1) BE1000851A4 (en)
DD (1) DD267652A5 (en)
DE (1) DE3804702A1 (en)
DK (1) DK76488A (en)
FI (1) FI880681A (en)
FR (1) FR2610785A1 (en)
GB (1) GB2201572A (en)
GR (1) GR880100088A (en)
HU (1) HU204946B (en)
IT (1) IT8819410A0 (en)
LU (1) LU87135A1 (en)
NL (1) NL8800376A (en)
NO (1) NO880663L (en)
PL (1) PL270676A1 (en)
PT (1) PT86764B (en)
SE (1) SE8800528L (en)
TR (1) TR23306A (en)
YU (1) YU30288A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5047343A (en) * 1988-04-29 1991-09-10 Wisconsin Alumni Research Foundation Microtuber propagation of potatoes
KR920001196B1 (en) * 1989-03-11 1992-02-06 한국과학기술원 Propagation of potato by microtuber using petridish
CN102257957B (en) * 2011-05-17 2012-12-19 北方民族大学 Early-maturing potato detoxification basic seedling culture medium and preparation method thereof
CN106105639A (en) * 2016-06-27 2016-11-16 安徽梅兰园林景观工程有限公司 A kind of Rhizoma Solani tuber osi implantation methods
CN109380114A (en) * 2018-11-06 2019-02-26 延边大学 A kind of method of fast-propagation potato test tube seedling

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4569914A (en) * 1982-06-28 1986-02-11 Gyogynoveny Kutato Intezet Process for the sterile micropropagation of plant material
EP0233492A1 (en) * 1986-01-29 1987-08-26 Cpc International Inc. Process for microplant propagation through increased multiple shoot formation

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR886424A (en) * 1941-04-25 1943-10-14 Process for the improvement, multiplication or cultivation of potatoes

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4569914A (en) * 1982-06-28 1986-02-11 Gyogynoveny Kutato Intezet Process for the sterile micropropagation of plant material
EP0233492A1 (en) * 1986-01-29 1987-08-26 Cpc International Inc. Process for microplant propagation through increased multiple shoot formation

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
WO A1 88/02213 *

Also Published As

Publication number Publication date
SE8800528L (en) 1988-08-17
NO880663L (en) 1988-08-17
SE8800528D0 (en) 1988-02-16
PL270676A1 (en) 1988-12-08
JPS63279723A (en) 1988-11-16
AU1173188A (en) 1988-08-18
DK76488A (en) 1988-08-17
DE3804702A1 (en) 1988-08-25
NL8800376A (en) 1988-09-16
DD267652A5 (en) 1989-05-10
FR2610785A1 (en) 1988-08-19
IT8819410A0 (en) 1988-02-15
DK76488D0 (en) 1988-02-15
CN1032448A (en) 1989-04-19
HUT46353A (en) 1988-10-28
HU204946B (en) 1992-03-30
GB8803408D0 (en) 1988-03-16
TR23306A (en) 1989-09-19
GR880100088A (en) 1988-12-16
FI880681A0 (en) 1988-02-12
NO880663D0 (en) 1988-02-15
PT86764B (en) 1992-04-30
YU30288A (en) 1989-06-30
FI880681A (en) 1988-08-17
LU87135A1 (en) 1989-09-20
PT86764A (en) 1988-03-01
BE1000851A4 (en) 1989-04-18

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