Narcissus tazetta var.
chinensis
is a perennial monocot plant that is well known for its pharmaceutical
and ornamental uses. This study aimed to understand the changes in
the primary and secondary metabolites in different in vitro tissues
of N. tazetta (callus, adventitious
root, and shoot) using high-performance liquid chromatography and
gas chromatography time-of-flight mass spectrometry. In addition,
to optimize the most efficient in vitro culture methods for primary
and secondary metabolite production, N. tazetta bulbs were used as explants and cultivated in Murashige and Skoog
(MS) medium containing different hormones at various concentrations.
In addition, the present study found suitable hormonal concentrations
for callus, adventitious root, and shoot induction and analyzed the
primary and secondary metabolites. The MS medium supplemented with
1.0 mg L–1 dicamba, 3.0 mg L–1 indole-3-butyric acid (IBA), and 3.0 mg L–1 6-benzylaminopurine
(BAP) was the most efficient media for callus, adventitious root,
and shoot induction in N. tazetta.
The tissue induced in this medium was subjected to primary (amines,
amino acids, organic acids, sugars, and sugar alcohols) and secondary
metabolite (galantamine and phenolic acids) analysis. The shoots and
roots showed the highest amounts of metabolites. This study showed
that bulb in vitro culture can be an efficient micropropagation method
for N. tazetta and the production of
primary and secondary metabolites, offering implications for the mass
production of primary and secondary metabolite compounds from N. tazetta tissues generated in vitro.