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The morphogenic potential of Siberian potato cultivars in tissue cultures. / Ibragimova, S. M.; Romanova, A. V.; Myzgina, G. Kh et al.

In: Вавиловский журнал генетики и селекции, Vol. 22, No. 3, 01.01.2018, p. 316-320.

Research output: Contribution to journalArticlepeer-review

Harvard

Ibragimova, SM, Romanova, AV, Myzgina, GK & Kochetov, AV 2018, 'The morphogenic potential of Siberian potato cultivars in tissue cultures', Вавиловский журнал генетики и селекции, vol. 22, no. 3, pp. 316-320. https://doi.org/10.18699/VJ18.366

APA

Ibragimova, S. M., Romanova, A. V., Myzgina, G. K., & Kochetov, A. V. (2018). The morphogenic potential of Siberian potato cultivars in tissue cultures. Вавиловский журнал генетики и селекции, 22(3), 316-320. https://doi.org/10.18699/VJ18.366

Vancouver

Ibragimova SM, Romanova AV, Myzgina GK, Kochetov AV. The morphogenic potential of Siberian potato cultivars in tissue cultures. Вавиловский журнал генетики и селекции. 2018 Jan 1;22(3):316-320. doi: 10.18699/VJ18.366

Author

Ibragimova, S. M. ; Romanova, A. V. ; Myzgina, G. Kh et al. / The morphogenic potential of Siberian potato cultivars in tissue cultures. In: Вавиловский журнал генетики и селекции. 2018 ; Vol. 22, No. 3. pp. 316-320.

BibTeX

@article{215834f2a7534a84871497772b78c5fd,
title = "The morphogenic potential of Siberian potato cultivars in tissue cultures",
abstract = "Potato is an important crop widely cultivated throughout the world. It is prone to several pathogenic fungi, viruses, and bacteria, which cause severe economic loss every year. Recent advances in plant biotechnology have made it possible to produce resistant cultivars by plant genome editing. This approach allows crop modifications that would be difficult to obtain by conventional breeding techniques. A successful and reproducible plant system requires a responsive in vitro regeneration system. Three Siberian potato cultivars - Kemerovchanin, Tuleevsky, and Sapho - and two control cultivars - Golubizna and Nikulinsky - were chosen for in vitro response tests. The stem explants were excised from in vitro grown plantlets. Their stem explants were incubated on Murashige & Skoog (MS) medium supplemented with 1 mg/L trans-zeatin, 0.1 mg/L IAA, and 10 mg/L GA3 with vitamins (medium P1). All the stages of cultivation up to obtaining full-fledged regenerant plants were carried out on medium P1. Every two weeks the explants were transferred to fresh nutrient media. All cultivars formed calluses but differed in terms of callus formation and in callus type. With further cultivation on the medium of the same composition, morphogenesis was observed: shoots formed on wound surfaces of the stem explants. Cultivars Tuleevsky, Kemerovchanin, and Golubizna showed high regeneration ability (73-97.7 %), while that of Sapho (63 %) was poor. All the Siberian cultivars were variable with regard to their morphogenic potentials. Root formation was observed in the shoots within 7 days on hormone-free MS. In the control (hormone-free medium), stem explants of all cultivars did not form calluses or develop shoots on the wound surfaces. The protocol described here is simple and efficient. It can be applied to other potato cultivars.",
keywords = "Biotechnology, Breeding, Cultivars, Potato, Regeneration in vitro, Solanum tuberosum L., Stem explants",
author = "Ibragimova, {S. M.} and Romanova, {A. V.} and Myzgina, {G. Kh} and Kochetov, {A. V.}",
note = "Publisher Copyright: {\textcopyright} 2018 AUTHORS.",
year = "2018",
month = jan,
day = "1",
doi = "10.18699/VJ18.366",
language = "English",
volume = "22",
pages = "316--320",
journal = "Вавиловский журнал генетики и селекции",
issn = "2500-0462",
publisher = "Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences",
number = "3",

}

RIS

TY - JOUR

T1 - The morphogenic potential of Siberian potato cultivars in tissue cultures

AU - Ibragimova, S. M.

AU - Romanova, A. V.

AU - Myzgina, G. Kh

AU - Kochetov, A. V.

N1 - Publisher Copyright: © 2018 AUTHORS.

PY - 2018/1/1

Y1 - 2018/1/1

N2 - Potato is an important crop widely cultivated throughout the world. It is prone to several pathogenic fungi, viruses, and bacteria, which cause severe economic loss every year. Recent advances in plant biotechnology have made it possible to produce resistant cultivars by plant genome editing. This approach allows crop modifications that would be difficult to obtain by conventional breeding techniques. A successful and reproducible plant system requires a responsive in vitro regeneration system. Three Siberian potato cultivars - Kemerovchanin, Tuleevsky, and Sapho - and two control cultivars - Golubizna and Nikulinsky - were chosen for in vitro response tests. The stem explants were excised from in vitro grown plantlets. Their stem explants were incubated on Murashige & Skoog (MS) medium supplemented with 1 mg/L trans-zeatin, 0.1 mg/L IAA, and 10 mg/L GA3 with vitamins (medium P1). All the stages of cultivation up to obtaining full-fledged regenerant plants were carried out on medium P1. Every two weeks the explants were transferred to fresh nutrient media. All cultivars formed calluses but differed in terms of callus formation and in callus type. With further cultivation on the medium of the same composition, morphogenesis was observed: shoots formed on wound surfaces of the stem explants. Cultivars Tuleevsky, Kemerovchanin, and Golubizna showed high regeneration ability (73-97.7 %), while that of Sapho (63 %) was poor. All the Siberian cultivars were variable with regard to their morphogenic potentials. Root formation was observed in the shoots within 7 days on hormone-free MS. In the control (hormone-free medium), stem explants of all cultivars did not form calluses or develop shoots on the wound surfaces. The protocol described here is simple and efficient. It can be applied to other potato cultivars.

AB - Potato is an important crop widely cultivated throughout the world. It is prone to several pathogenic fungi, viruses, and bacteria, which cause severe economic loss every year. Recent advances in plant biotechnology have made it possible to produce resistant cultivars by plant genome editing. This approach allows crop modifications that would be difficult to obtain by conventional breeding techniques. A successful and reproducible plant system requires a responsive in vitro regeneration system. Three Siberian potato cultivars - Kemerovchanin, Tuleevsky, and Sapho - and two control cultivars - Golubizna and Nikulinsky - were chosen for in vitro response tests. The stem explants were excised from in vitro grown plantlets. Their stem explants were incubated on Murashige & Skoog (MS) medium supplemented with 1 mg/L trans-zeatin, 0.1 mg/L IAA, and 10 mg/L GA3 with vitamins (medium P1). All the stages of cultivation up to obtaining full-fledged regenerant plants were carried out on medium P1. Every two weeks the explants were transferred to fresh nutrient media. All cultivars formed calluses but differed in terms of callus formation and in callus type. With further cultivation on the medium of the same composition, morphogenesis was observed: shoots formed on wound surfaces of the stem explants. Cultivars Tuleevsky, Kemerovchanin, and Golubizna showed high regeneration ability (73-97.7 %), while that of Sapho (63 %) was poor. All the Siberian cultivars were variable with regard to their morphogenic potentials. Root formation was observed in the shoots within 7 days on hormone-free MS. In the control (hormone-free medium), stem explants of all cultivars did not form calluses or develop shoots on the wound surfaces. The protocol described here is simple and efficient. It can be applied to other potato cultivars.

KW - Biotechnology

KW - Breeding

KW - Cultivars

KW - Potato

KW - Regeneration in vitro

KW - Solanum tuberosum L.

KW - Stem explants

UR - http://www.scopus.com/inward/record.url?scp=85047759949&partnerID=8YFLogxK

U2 - 10.18699/VJ18.366

DO - 10.18699/VJ18.366

M3 - Article

AN - SCOPUS:85047759949

VL - 22

SP - 316

EP - 320

JO - Вавиловский журнал генетики и селекции

JF - Вавиловский журнал генетики и селекции

SN - 2500-0462

IS - 3

ER -

ID: 13668681