Abstract:
Sansevieria trifasciata is a common perennial plant native to West Africa and
specifically found in Nigeria and Congo. It is commonly known as “Snake plant”
and “Mother-in-law‟s tongue”. S. trifasciata is a versatile and valuable plant with a
wide distribution, distinctive morphology, and several practical benefits, including
air purification and less maintenance, contributing to its popularity as an indoor and
outdoor ornamental plant. It is a great challenge to produce planting materials
through traditional propagation techniques due to the increased demand. Therefore,
it will be vital to develop a cost-efficient protocol for in vitro propagation of S.
trifasciata. At the first phase of surface sterilisation, the explants from fully
expanded young leaves were treated with 70% (v/v) ethanol for 5 min following
five different Clorox™ concentrations (10%, 15%, 20%, 25%, and 30%) separately,
each for 20 minutes. Surface sterilisation of leaf explants could not be optimized in
Phase I due to severe microbial contamination. Therefore, in Phase II surface
sterilisation, leaf explants were treated with three different exposure times of 70%
(v/v) ethanol and 30% Clorox™ for 30 minutes. Explants treated with 70% (v/v)
ethanol for 20 min followed by 30% Clorox™ for 30 min showed optimised surface
sterilisation, resulting in 100% explants survival, 2 weeks following incubation.
Cultures were maintained in hormone-free media for two weeks at standard
conditions to allow root and shoot elongation. Later, those were transferred to a
media supplemented with different concentrations of BAP (1 mg/l, 2 mg/l, 3 mg/l)
while maintaining the hormone-free media as the standard. After 10 weeks of
incubation, media supplemented with 3 mg/l BAP showed a significantly higher
mean number of shoots (4.35 ± 0.67) and mean length of shoots (1.38 ± 0.25 cm)
compared to all other treatments. The study demonstrated that the treatment with
70% ethanol (20 min) and 30% Clorox™ (30 min) successfully sterilised the leaf
explants of S. trifasciata and 3 mg/l of BAP markedly improved the multiplication
and growth of shoots, highlighting the significance of developing an optimized
surface sterilization and appropriate growth regulation for a successful in vitro
propagation.
