2016
DOI: 10.4067/s0717-66432016000100014
|View full text |Cite
|
Sign up to set email alerts
|

Plant growth regulators optimization for maximize shoots number in Agave americana L. by indirect organogenesis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
3
0

Year Published

2017
2017
2024
2024

Publication Types

Select...
7
2

Relationship

1
8

Authors

Journals

citations
Cited by 13 publications
(4 citation statements)
references
References 18 publications
1
3
0
Order By: Relevance
“…Due to their cell division capacity, they are considered a good source of explants. Our results are in the range reported in other works of A. Americana, regarding the percentage of callus where the meristem was used [20,26], finding percentages ranging from 80% to 100%. However, the callus obtained in those works was of the organogenic type, which is not desirable to generate a cell suspension.…”
Section: Discussionsupporting
confidence: 87%
“…Due to their cell division capacity, they are considered a good source of explants. Our results are in the range reported in other works of A. Americana, regarding the percentage of callus where the meristem was used [20,26], finding percentages ranging from 80% to 100%. However, the callus obtained in those works was of the organogenic type, which is not desirable to generate a cell suspension.…”
Section: Discussionsupporting
confidence: 87%
“…Rooting and acclimatization of plantlets. Plantlets were rooting and acclimatization according to Reyes-Zambrano et al (2016). Two hundred and fifty plantlets with a welldeveloped root system were washed in running water to remove phytagel and transferred to unicel pots (12 • 10 cm) (one plantlet per unicel pot) containing peatmoss and agrolite mixture (1:1) for acclimatization.…”
Section: Methodsmentioning
confidence: 99%
“…In order to obtain the shoot apical meristem, the leaves, stems and roots were removed, explants were placed on MS (Murashige & Skoog) medium [19] supplemented with vitamins, sucrose (30 g/l), myo-inositol (0.228 mM), sodium phosphate (0.362 mM), phytagel (2.5 g/l), supplemented with 2,4-D (0.11 μM) and BAP (44 μM). Explants were incubated at 22°C ± 2 in continuous light [20]. The response was evaluated at eight weeks post culture and the percentage of callus induction was determined in each explant, and calculated with the following formula [21].…”
Section: Callus Induction and Proliferationmentioning
confidence: 99%