EFFICIENT in vitro PROPAGATION OF Amaranthus viridis L. USING NODE EXPLANTS

Hyperhydricity is a frequently problem in plants during in vitro culture and affected micropropagation of plants. To develop an efficient in vitro regenerated system without hyperdydricity, we demonstrated the effect of different disinfected agents (mercuric chlorite and hypochlorite), growth regul...

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Main Authors: Tour Jan, Ikram Ullah, Bilal Muhammad, _ Tariq, Ali Mansoor, Zaheer Ullah, Muhammad Asif Nawaz
Format: Article
Language:English
Published: University of Life Sciences in Lublin - Publishing House 2020-08-01
Series:Acta Scientiarum Polonorum: Hortorum Cultus
Subjects:
Online Access:https://czasopisma.up.lublin.pl/index.php/asphc/article/view/2218
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author Tour Jan
Ikram Ullah
Bilal Muhammad
_ Tariq
Ali Mansoor
Zaheer Ullah
Muhammad Asif Nawaz
author_facet Tour Jan
Ikram Ullah
Bilal Muhammad
_ Tariq
Ali Mansoor
Zaheer Ullah
Muhammad Asif Nawaz
author_sort Tour Jan
collection DOAJ
description Hyperhydricity is a frequently problem in plants during in vitro culture and affected micropropagation of plants. To develop an efficient in vitro regenerated system without hyperdydricity, we demonstrated the effect of different disinfected agents (mercuric chlorite and hypochlorite), growth regulators, their concentrations and combinations, Agar, pH, ammonium nitrate (NH4NO3) and number of subcultures. Mercuric chlorite at 0.07% and exposing time (9–10 min) was appropriate for hygienic culture. The shoots induced by Benzyladnine (BA) alone or in combination with α-Naphthaleneacetic acid (NAA) exhibited maximum multiplication with symptoms of hyperhydricity than those induced by Kinetin alone or in combination with NAA. Hyperhydricity was also reduced by increasing the concentration of agar, pH and elimination of NH4NO3 from the macroelements of Murashig and Skoog (MS) medium. Repeated subcultures affected both multiplication and hyperhydricity. The multiplication of shoots increased from parental culture up to 5th subculture and thereafter declined in 6th subculture. Although shoot hyperhydricity were observed from 1st subculture (19%) and then increased up to 85% in 6th subculture. This increased in hyperhydricity could be due to the remaining influence of hormones. In shoots of 5th subculture the content of chlorophyll (dark green) were higher than shoots of 6th subculture.
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spelling doaj.art-5fdea0d6c4464323b946c0c3ec6dc10d2023-12-12T07:51:33ZengUniversity of Life Sciences in Lublin - Publishing HouseActa Scientiarum Polonorum: Hortorum Cultus1644-06922545-14052020-08-0119410.24326/asphc.2020.4.4EFFICIENT in vitro PROPAGATION OF Amaranthus viridis L. USING NODE EXPLANTSTour Jan0Ikram Ullah1Bilal Muhammad2_ Tariq3Ali Mansoor4Zaheer Ullah5Muhammad Asif Nawaz6Plant Tissue Culture Laboratory Department of Botany, University of Malakand, Dir Lower, KP, PakistanPlant Tissue Culture Laboratory Department of Botany, University of Malakand, Dir Lower, KP, PakistanPlant Tissue Culture Laboratory Department of Botany, University of Malakand, Dir Lower, KP, PakistanPlant Tissue Culture Laboratory Department of Botany, University of Malakand, Dir Lower, KP, PakistanPlant Tissue Culture Laboratory Department of Botany, University of Malakand, Dir Lower, KP, PakistanPlant Tissue Culture Laboratory Department of Botany, University of Malakand, Dir Lower, KP, PakistanDepartment of Biotechnology, SBBU, Sheringal, Dir Upper, KP, Pakistan Hyperhydricity is a frequently problem in plants during in vitro culture and affected micropropagation of plants. To develop an efficient in vitro regenerated system without hyperdydricity, we demonstrated the effect of different disinfected agents (mercuric chlorite and hypochlorite), growth regulators, their concentrations and combinations, Agar, pH, ammonium nitrate (NH4NO3) and number of subcultures. Mercuric chlorite at 0.07% and exposing time (9–10 min) was appropriate for hygienic culture. The shoots induced by Benzyladnine (BA) alone or in combination with α-Naphthaleneacetic acid (NAA) exhibited maximum multiplication with symptoms of hyperhydricity than those induced by Kinetin alone or in combination with NAA. Hyperhydricity was also reduced by increasing the concentration of agar, pH and elimination of NH4NO3 from the macroelements of Murashig and Skoog (MS) medium. Repeated subcultures affected both multiplication and hyperhydricity. The multiplication of shoots increased from parental culture up to 5th subculture and thereafter declined in 6th subculture. Although shoot hyperhydricity were observed from 1st subculture (19%) and then increased up to 85% in 6th subculture. This increased in hyperhydricity could be due to the remaining influence of hormones. In shoots of 5th subculture the content of chlorophyll (dark green) were higher than shoots of 6th subculture. https://czasopisma.up.lublin.pl/index.php/asphc/article/view/2218agarAmarinthus viridisHgCl2hyperhydricitypHsubcultures
spellingShingle Tour Jan
Ikram Ullah
Bilal Muhammad
_ Tariq
Ali Mansoor
Zaheer Ullah
Muhammad Asif Nawaz
EFFICIENT in vitro PROPAGATION OF Amaranthus viridis L. USING NODE EXPLANTS
Acta Scientiarum Polonorum: Hortorum Cultus
agar
Amarinthus viridis
HgCl2
hyperhydricity
pH
subcultures
title EFFICIENT in vitro PROPAGATION OF Amaranthus viridis L. USING NODE EXPLANTS
title_full EFFICIENT in vitro PROPAGATION OF Amaranthus viridis L. USING NODE EXPLANTS
title_fullStr EFFICIENT in vitro PROPAGATION OF Amaranthus viridis L. USING NODE EXPLANTS
title_full_unstemmed EFFICIENT in vitro PROPAGATION OF Amaranthus viridis L. USING NODE EXPLANTS
title_short EFFICIENT in vitro PROPAGATION OF Amaranthus viridis L. USING NODE EXPLANTS
title_sort efficient in vitro propagation of amaranthus viridis l using node explants
topic agar
Amarinthus viridis
HgCl2
hyperhydricity
pH
subcultures
url https://czasopisma.up.lublin.pl/index.php/asphc/article/view/2218
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AT tariq efficientinvitropropagationofamaranthusviridislusingnodeexplants
AT alimansoor efficientinvitropropagationofamaranthusviridislusingnodeexplants
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