Establishment of cell suspension cultures for plant secondary metabolites study in Barringtonia racemosa L

The present study was conducted to initiate and establish a homogeneous cell suspension culture system in Barringtonia racemosa from endosperm-derived friable calli which are useful for plant secondary metabolites study. Initiation and establishment of cell suspension cultures study were carried out...

Full description

Bibliographic Details
Published in:Journal of Engineering and Applied Sciences
Main Author: Osman N.I.; Sidik N.J.; Awal A.
Format: Article
Language:English
Published: Medwell Journals 2018
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049911343&doi=10.3923%2fjeasci.2018.3119.3124&partnerID=40&md5=8534f548647fbed185f9ea7370df3b5d
id 2-s2.0-85049911343
spelling 2-s2.0-85049911343
Osman N.I.; Sidik N.J.; Awal A.
Establishment of cell suspension cultures for plant secondary metabolites study in Barringtonia racemosa L
2018
Journal of Engineering and Applied Sciences
13
Specialissue3
10.3923/jeasci.2018.3119.3124
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049911343&doi=10.3923%2fjeasci.2018.3119.3124&partnerID=40&md5=8534f548647fbed185f9ea7370df3b5d
The present study was conducted to initiate and establish a homogeneous cell suspension culture system in Barringtonia racemosa from endosperm-derived friable calli which are useful for plant secondary metabolites study. Initiation and establishment of cell suspension cultures study were carried out by using different treatments of liquid media involving different concentrations and combinations of 2, 4-D (0.5 and 1.0 mg/L) and kinetin (0.75, 1.5 and 2.0 mg/L) plant hormones in MS (Murashige and Skoog's) medium. The difference in the treatments was formulated based on the reference treatments which produced the most optimum friable calli suitable for cell suspension cultures initiation. The treatment consisted of 1.0 mg/L 2, 4-D and 1.5 mg/L kinetin (treatment A) was found to be the most optimum treatment by considering timely mean dry cell biomass changes at every 5 days, interval with its maximum record of 16.32±0.72 g/L. The distinctive phases of cell growth involving lag, exponential and declining phases had been identified. However, no lag phase were identified from the optimum treatment while other two treatments (1.0 mg/L 2,4-D + 2.0 mg/L kinetin (treatment B) and 0.5 mg/L 2,4-D+0.75 mg/L kinetin (treatment C)) underwent lag phase during first 10 days in culture. These were followed by exponential phases which were continued and achieved the peak of highest dry cell biomass records on day 50 (treatment A and C) and 55 (treatment B). Afterwards, all treatments had shown a declining progress in mean dry cell biomass records. The findings pertaining to cell growth phases are providing a useful information on plant cellular and molecular processes studies in this species and would further be utilised in research related to plant secondary metabolites production. © Medwell Journals, 2018.
Medwell Journals
1816949X
English
Article

author Osman N.I.; Sidik N.J.; Awal A.
spellingShingle Osman N.I.; Sidik N.J.; Awal A.
Establishment of cell suspension cultures for plant secondary metabolites study in Barringtonia racemosa L
author_facet Osman N.I.; Sidik N.J.; Awal A.
author_sort Osman N.I.; Sidik N.J.; Awal A.
title Establishment of cell suspension cultures for plant secondary metabolites study in Barringtonia racemosa L
title_short Establishment of cell suspension cultures for plant secondary metabolites study in Barringtonia racemosa L
title_full Establishment of cell suspension cultures for plant secondary metabolites study in Barringtonia racemosa L
title_fullStr Establishment of cell suspension cultures for plant secondary metabolites study in Barringtonia racemosa L
title_full_unstemmed Establishment of cell suspension cultures for plant secondary metabolites study in Barringtonia racemosa L
title_sort Establishment of cell suspension cultures for plant secondary metabolites study in Barringtonia racemosa L
publishDate 2018
container_title Journal of Engineering and Applied Sciences
container_volume 13
container_issue Specialissue3
doi_str_mv 10.3923/jeasci.2018.3119.3124
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049911343&doi=10.3923%2fjeasci.2018.3119.3124&partnerID=40&md5=8534f548647fbed185f9ea7370df3b5d
description The present study was conducted to initiate and establish a homogeneous cell suspension culture system in Barringtonia racemosa from endosperm-derived friable calli which are useful for plant secondary metabolites study. Initiation and establishment of cell suspension cultures study were carried out by using different treatments of liquid media involving different concentrations and combinations of 2, 4-D (0.5 and 1.0 mg/L) and kinetin (0.75, 1.5 and 2.0 mg/L) plant hormones in MS (Murashige and Skoog's) medium. The difference in the treatments was formulated based on the reference treatments which produced the most optimum friable calli suitable for cell suspension cultures initiation. The treatment consisted of 1.0 mg/L 2, 4-D and 1.5 mg/L kinetin (treatment A) was found to be the most optimum treatment by considering timely mean dry cell biomass changes at every 5 days, interval with its maximum record of 16.32±0.72 g/L. The distinctive phases of cell growth involving lag, exponential and declining phases had been identified. However, no lag phase were identified from the optimum treatment while other two treatments (1.0 mg/L 2,4-D + 2.0 mg/L kinetin (treatment B) and 0.5 mg/L 2,4-D+0.75 mg/L kinetin (treatment C)) underwent lag phase during first 10 days in culture. These were followed by exponential phases which were continued and achieved the peak of highest dry cell biomass records on day 50 (treatment A and C) and 55 (treatment B). Afterwards, all treatments had shown a declining progress in mean dry cell biomass records. The findings pertaining to cell growth phases are providing a useful information on plant cellular and molecular processes studies in this species and would further be utilised in research related to plant secondary metabolites production. © Medwell Journals, 2018.
publisher Medwell Journals
issn 1816949X
language English
format Article
accesstype
record_format scopus
collection Scopus
_version_ 1809677907798261760