commonly referred to as "phytosterol" ie sitosterol
(better known as beta-sitosterol), stigmasterol and
campesterol proved to be found in some high plant
species. Some research results show that phytosterol
can reduce total cholesterol and LDL cholesterol in
the blood. Certain types of sterol compounds such as
ergosterol, can be found in low level plants such as
yeasts and fungi (Harborne, 1998).
Bangun-BAngun contains phenolic, terpenoids,
chlorophyll, nitrogen, vitamins, and secondary
metabolites that function as antioxidants,
antimicrobials, anti-inflammatory, antitumor,
antimutagen, anticancer, and diuretics (Sahay et al.,
2011). Chlorophyll or pigment main plant is widely
used as a food supplement that is useful to help
optimize metabolic functions, immune system,
detoxification, relieve inflammation (inflamatorik)
and balance the hormonal system. Chlorophyll also
stimulates blood formation because it provides the
basic ingredients of the hemoglobin-forming agent.
This is due to the chlorophyll structure resembling
blood hemoglobin with a difference in the nucleating
atoms of the core of its porphyrin ring (Setiari and
Nurchayati, 2009).
Efforts to assemble superior varieties can be done
through plant breeding activities and one of the
determinants of the success of the superior variety
assembly program is the availability of genetic
diversity. Efforts to generate genetic diversity can be
done through domestication, exploration,
hybridization, polyploidization, mutation, or other
techniques and to support breeding activities requires
an attempt to assess genetic diversity. There are
several methods that can be used to assess genetic
diversity, one with morphology and cytology
analysis, so that the genetic and phenetic information
of an individual can be known (Suntoro, 1983).
Based on the above description the authors are
interested to know the differences of vegetative
growth characteristics, sterol content and chlorophyll
from some plant wake accession.
2 MATERIAL AND METHODS
This research was conducted at the screen house of
Faculty of Agriculture, University of Sumatera Utara,
Medan with height of place ± 25 meter above sea
level. The plant material was collected from 5
locations namely Medan (Krakatau) which is a wild
plant, and the garden yard of the people of Medan
(Tuntungan), Sibolangit, Brastagi and Simalungun.
Part of the plant taken is a whole plant, namely the
roots and canopy plants or branches of plants that
have touched the ground and have roots. After
collection of plant material next the plant is planted in
polybag, where this plant will be used as plant source
for propagation. The plant material used in this
research is cuttings of shoots of Bangun-Bangun
plants from Medan (Krakatau), Medan (Tuntungan),
Sibolangit, Simalungun and Brastagi. Plant parts used
for propagation are plant shoots, where in the shoot
cuttings for all accessions are uniformed as 5 leaves
open, and stem diameter uniformed for each
accession. The cuttings to be used are removed all the
leaves and the base of the cuttings are cut near the
leaf's armpits.
Other materials used are compost, water, top soil,
polybag, scissors, label, methanol, chloroform, acetic
anhydride, concentrated sulfuric acid, and standard β-
sitosterol. Tools used include analytical scales, ovens,
and water baths. The instrument used was UV-Vis
Spectrophotometer 25 Lambda.
The research used non factorial Randomized Block
Design (RBD) with 5 treatments and 6 replications.
Factor of treatments was accession plant (A) which
consists of 5 types, namely: A1 : plant origin Medan
(Krakatau); A2 : plants from Medan (Tuntungan);
A3: plant origin Sibolangit; A4: plant origin
Simalungun; and A5 : plant origin Brastagi.
2.1 Implementation of Research
Planting medium used is a mixture of soil and cow
manure with a ratio of 1: 1 and stirred evenly and then
put into polybags. Planting media is then arranged on
the experimental grounds. Planting is done by
planting shoots cuttings into the planting medium that
has been perforated then pressed to become more
dense then watered with clean water. Watering is
done every day or if needed by looking at the
condition of planting media in the field. Harvesting
was done after the plant aged 8 week after culture.
The harvested crop has a minimum of two branches
and the leaves of the lower plants begin to turn
yellow. Parameter observation was number of leaves
(strands), root length (cm), fresh weight of shoot per
plant (g), dry weight of shoot per plant (g), shoot/root
ratio (g). Determination of dry weight was done by
drying ovenkan top of the plant that has been
calculated the weight of fresh crown at 70ºC for 48
hours to obtain a constant dry weight
2.2 Sterol Content
Determination of sterol levels is done by Liebermann-
Burchard test used to determine the presence of
triterpenoid and sterol compounds in the material.