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Abstract |
Application
of Flow Cytometry for Estimation of Nuclear DNA Content in Elaeis
A method was established and proposed to be the standard protocol for
estimating the genome size of oil palm [Elaeis guineensis and
its intraspecific hybrids, E. oleifera and oleifera
x guineensis (O x G) interspecific hybrids]. The method used
is laser-sourced flow cytometry. Oil palm Frond -1 leaflets, LBO1 lysis
buffer and Glycine max cv. Polanka (as external standard) were used
for the DNA content estimation. The 2C DNA contents of E. guineensis
for the different fruit types were: dura (D) = 4.10 ± 0.20, pisifera
(P) = 3.64 ± 0.28 and tenera (DxP) = 3.83 ± 0.31 pg. A
simple average gave the DNA content for E. guineensis as 3.86 ±
0.26 pg.
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CO2/CH4
AND O2/N2 Kinetic Selectivities of Oil Palm
Shell-Based Carbon Molecular Sieves
Carbon molecular sieves (CMS) have become an interesting area of adsorption
due to their microporous nature and favourable separation factor on
size and shape selectivity basis for many gaseous systems. In this
work, CMS were prepared from locally available oil palm shell by thermal
treatment of carbonization followed by steam activation, then benzene
deposition. The carbonization of dried palm shell at 900°C for
1 hr followed by steam activation at 30-420 min produced activated
carbons with various degrees of burn-off. The highest micropore surface
area and micropore volume of the activated samples were obtained at
53.2% burn-off. This sample was found suitable to be used as precursor
for CMSs production in the deposition step. Subsequent benzene deposition
onto activated samples at temperatures from 600oC-900oC for various
benzene concentrations resulted in a series of CMS with different
O2/N2 and CO2/CH4 kinetic
selectivities.
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Enzymatic
Synthesis and Characterization of Palm-Based Kojic Acid Ester
Kojic acid ester was synthesized from acyl donor (fatty acid/palm oil)
and kojic acid by esterification using lipase as a biocatalyst in an
organic medium. Analysis of the product using GC and FTIR showed the
presence of kojic acid ester. The gas chromatography-mass spectrometry
(GC-MS) analysis and 1H-NMR and 13C-NMR spectral
data confirmed the molecular structure of the kojic acid ester. Among
the enzymes tested, lipase from Pseudomonas cepacia gave the highest
synthetic specific activity. Oleic acid was found to be the best substrate
with which to produce the ester in acetonitrile. The optimum conditions
for the synthesis of kojic acid derivatives using Pseudomonas
cepacia lipase were time, 24 hr, temperature, 50°C, amount of enzyme,
0.15 g, solvent of log P = -0.33, mole ratio of 4 (kojic acid/oleic
acid), with no added water, no control of water activity and oleic acid
as substrate.
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Efficacy
of Single and Mixed Treatments of Trichoderma harzianum as
Biocontrol Agents of Ganoderma Basal Stem Rot in Oil Palm
Two Trichoderma harzianum strains (FA 1132 and FA 1166) were
tested as biocontrol agents for basal stem rot in oil palm seedlings
artificially infected with the causal pathogen, Ganoderma boninense.
The treatment was carried out by applying a Trichoderma-infused
surface mulch and periodic applications of a conidial soil drench made
from spore suspensions of the respective Trichoderma strains.
A disease severity index (DSI) ranging from 0 to 100 was used to assess
the disease severity. A single strain application of T. harzianum,
FA 1132 gave the best disease suppression with the lowest DSI of 28.35
compared to the infected, non-treated control plants that gave the highest
DSI of 86.67. However, FA 1166 as a single application was ineffective,
so was the mixture of the two strains. The biological control property
of Trichoderma was shown to be strainspecific and not species-specific.
In addition, it was found that applying the mixed inocula significantly
decreased the performance of FA1132, the choice strain.
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Life
Cycle Inventory of the Production of Crude Palm Oil - A Gate to Gate
Case Study of 12 Palm Oil Mills
Life cycle inventory
(LCI) is the heart of a life cycle assessment (LCA) study. LCA is a
tool to determine the environmental impacts of a product at all stages
of its life right from cradle to grave. In order to carry out a LCA,
inventory data have to be collected and the raw data have to be extrapolated
to produce a LCI. This study has a gate to gate system boundary. The
inventory data collection starts at the oil palm fresh fruit bunch hoppers
when the fresh fruit bunches are received at the mill up till the production
of the crude palm oil in the storage tanks at the mill. For this study,
12 palm oil mills were selected. These palm oil mills were selected
based on the type of mill which were either plantation- based mills
or private mills and have different processing capacities of oil palm
fresh fruit bunches ranging from 20 t hr-1 up till 90 t hr-1.
The mills selected are all located at different zones in east and west
Malaysia basically from north, mid south, south Peninsular Malaysia
and east Malaysia. Inventory data collection consists of input and output
of materials and energy. The input data basically are inputs of raw
materials such as oil palm fresh fruit bunches, electricity, diesel,
water, fuel for boiler etc. and the output consists of the biomass wastes,
palm oil mill effluents, flue gases from stack, kernel etc. All data
were collected for duration of three months from each mill. These inventory
data were then calculated for the functional unit of every 1 t of crude
palm oil produced at the palm oil mill.
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Factors
Affecting Green Fluorescence Protein (GFP) Gene Expression in Oil Palm
After Microprojectile Bombardment
Expression of green
fluorescence protein (GFP) gene can be visualized under ultraviolet
or blue light without any substrate or co-factor addition. It has been
used to monitor transient and stable transgene expression in many plant
varieties. The effectiveness of gfp gene as a selectable marker for
oil palm transformation was evaluated through transient expression of
gfp genes in bombarded oil palm embryogenic calli and immature embryos.
Different types (version) of gfp genes which are driven by different
constitutive promoters were used to transform oil palm target tissues.
Some of the gfp genes used were targeted to specific organelle: namely
plastid, endoplasmic reticulum and mitochondria. Transient expression
of the gfp genes could be detected in oil palm tissues as early as 16
hr after bombardment. It was observed that the number of gfp expressing
cells and duration of the gfp gene expression differs from one construct
to another. The differences in the gfp constructs performance in oil
palm tissues were evaluated based on the following factors: version
of the gfp genes, promoter used to drive the gfp gene, backbone vector
and the size of the whole plasmid. The CaMV35S promoter was found to
be the most effective promoter for driving gfp gene in oil palm tissues
followed by HBT and maize ubiquitin promoter. The sGFPS65T was the most
effective version of gfp gene for oil palm tissues followed by sGFP
and mGFP5. It was also demonstrated that the pUC18 backbone vectors
was the most effective vector backbone in expressing the gfp gene in
oil palm. Finally, it was observed that the smaller the gfp vector,
the higher the number of gfp expressing cells obtained. Possible reasons
for these observations were elaborated and discussed.
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Does
the Palm Tocotrienol-Rich Fraction Induce Irritant Contact Dermatitis?
In Malaysia, the
tocotrienol-rich fraction (TRF) is used as one of the functional ingredients
in cosmetics products. The topically applied vitamin E plays a role
in protecting the skin from free radicals damage induced by the ultraviolet
radiation. The formulation of new topical products always includes
risk of unexpected cutaneous side effects in certain individuals.
Although the irritant contact dermatitis (ICD) has been reported for
many compounds including active substances in cosmetics, the local
topical ICD of TRF preparations has not been reported. This article
describes the safety evaluation of palm TRF on skin. The primary irritation
potential was assessed through animal study while the ICD was determined
using patch testing technique on healthy as well as highly sensitize
patients. The sensitization potential was evaluated using human repeated
insult patch test on healthy subjects. Results indicated that the
palm TRF did not induced any cutaneous irritation or sensitization
at 1%, 2.5% and 5%.
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