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Plant Tissue Culture
Plant Tissue Culture
Li, Hsin
https://pl-pl.bakker.com/
CONTENTS
01 Abstract
02 Introduction
04 Result
05 Conclusion
06 References
Abstract
• The purpose of this study was investigated that effect of activated carbon (AC) a
nd light on in vitro proliferation of Dendrobium spp.. AC is often added to the me
dium to improve the plant growth, and the light also is the most important factors
affecting plant growth. For this study the 0.5 -1cm nodal explants were used and c
ultivated in MS medium additive different AC concentrations and given light or d
ark environments to explore its effects for the proliferation and plantlet growth.
Introduction of Dendrobium
• Is a fairly large genus under Orchidaceae.
• Dendrobium is usually divided into spring and autumn
• Native all over Asia,
• Growth on the trunk or tree hole.
• Colors are very diverse, but mainly white and reddish purple.
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https://jardinage.ooreka.fr/plante/voir/1473/den
Introduction of Heuchera micrantha
• Drought-tolerant and adaptable
• Growth divided into four stages, spring to summer for the growth period, autumn f
or mature period, winter for dormancy period, blooming in spring or in autumn.
• Daylight : Compared with general orchids, it need more daylight.
• Growth temperature is 18-30 ℃, but sometime even can grow well when the temp
erature more than 30 ℃.
• Reproduction: TC, cuttings, buds.
Introduction of activated carbon (AC)
Function
• Inhibit or promote bud and stem growth.
• Speed up reproduction .
• Establish a darkened environment to improve rooting.
• Adsorption some undesirable or inhibit substance.
• Prevent plant browning
Material and method
Take the young stem, cut from the top buds where down to 3-4 nodes, and remove t
e the growth.
MS medium formula (A soulation)
Material and method - Plant material
Stems were washed with 75% ethanol to remove surface contamination and then
sterilized by 1% sodium hypochlorite and one drop of Tween-20 then shaking tub
e by 10 minutes to sterilize.
The stems were then rinsed three times with sterile distilled water in laminar flow
to remove minor amounts of disinfection liquid. and cut the stems for use in vitro.
Material and method - Culture media and con
ditions
For germinating, the seeds were cultured in mugs on 10 ml of ½ MS medium, w
photoperiod provided.
Method
Method - Experimental design
AC concentration
NO add AC Add 1g/l AC Add 2g/l AC
Light
environments
• D+AC/ D-AC
(L= light environments, D= dark environments.)