Utilization of palm kernel expeller (PKE), a palm oil milling by-product, may be diversified through the exploitation of its protein component. The PKE protein could be effectively extracted using an alkaline
solution and followed by enzymatic hydrolysis to produce PKE protein hydrolysates or crude PKE peptide. The extraction of PKE protein was successfully carried out using an alkaline solution at pH11, at ratio of 1:10 (g/ml), PKE powder to alkaline solution with continuous shaking, 150 rpm, in a water bath operating at 50°C for 30 min. The extracted protein powder (PKEP) had 68.50±3.08% crude protein, 0.54±0.03% fat and 0.73±0.02% ash. The freeze-dried PKEP was re-suspend in particular buffer and hydrolyzed with proteolytic enzymes (Alcalase® 2.4L, Flavourzyme® 500MG, pepsin or trypsin) to obtain PKEP hydrolysate (PKEPH). The effect of enzyme concentration (0, 2, 4, 6, 8 & 10%) and time of hydrolysis (0, 6, 12, 24, 48 h) was studied to determine the most efficient hydrolytic conditions. Results showed that all enzymes tested were capable of hydrolyzing the PKEP and producing hydrolysates with different degree of hydrolysis (DH%). At 8.0% concentration, Alcalase®2.4L hydrolyzed PKEP into the highest DH (75.96%) hydrolysate (PKEPH) after 1h hydrolysis. Although only with 2.0% Alcalase 2.4 L concentration, it was sufficient to produce PKEP hydrolysate of 81.35% DH %, but it required 12 h to hydrolyze the protein. Pepsin was relatively the least efficient protease to hydrolyze the PKEP.
This study aimed to determine the amount of the fish (Oreachromi sp, Clarias sp. and Pangasius sutchii) consumption in Malaysia; the quantity of heavy metal residues (arsenic, cadmium, mercury and plumbum) in the fish and the level of the risk exposure. About 1440 respondents from six main production districts were randomly interviewed and the body weight of the respondents was also measured. A total of 240 ready to eat fish from food premises were also stratified randomly sampled where each sample was weighted to determine the average weight of one serving unit sold at food premises. The heavy metal residues were analyzed using Inductively Coupled Plasma–Optical Emission Spectrometer (ICP-OES) Optima 4300 DV (German). The level of heavy metals risk exposure was calculated as the percentage value of ’Provisional Tolerable Weekly Intakes’ (PTWI) and recalculated using computer programme @Risk 4.5 Excel (Palisade, USA). The result showed that 60.3% of the respondents consumed the fish. The level of heavy metal risk exposures were calculated as very low i.e. 0.14% (As), 0.31% (Cd), 0.09% (Hg) and 0.78% (Pb).
Halal is a term that describes substances that are deemed ‘pure and clean’ which Muslims are
allowed to consume according to Islamic law. The industrialization of food processing in the
20th and 21st centuries has exposed Muslims community to various ingredients such as blood
plasma, transglutaminase and gelatin introduced in meatballs and surimi product. Muslims
are facing difficulties to ascertain which products are permitted or not under the Islamic law.
Thus, this paper is to give knowledge of non-halal ingredients being introduced in meatballs
and surimi products for consumers, researchers and policy makers. Local halal logo issued by
Department of Islamic Development Malaysia (JAKIM) is needed to imply that all ingredients
used in the food production and processing are Syariah compliance. The scientific evidence
to substantiate any claim on Halal issue was developed based on several methods including
PCR-based methods with different mitochondria and chromosomal DNA (MtDNA and cDNA)
primers, real-time PCR with different probes and DNA binding agent, loop-mediated isothermal
amplification (LAMP) with different primers developed, PCR- RFLP, ELISA and etc.
Megabiodiversity of Malaysian’s flora and fauna which include microorganism could be conserved and served as alternative source indigenous yeast, the leavening agent of commercial bread making. This study was conducted in attempt to exploit the potential of Saccharomyces cerevisiae strains isolated from 30 different local fruits and plant parts as a leavening agent in bread making. The enrichment was carried out by fermenting the plant samples in medium containing Grape Must at 25°C for 10 days following by isolation of tentative yeasts at 30°C for 3 to 5 days. 20 out of 30 samples tested showed the presence of yeasts was then selected for identification of S. cerevisiae strains through biochemical and physiological tests. Of the 20 yeast strains examined, 13 strains were identified as S. cerevisiae and potentially used as leavening agent in bread making where 5 strains namely SN3, SMK9, SDB10, SRB11 and SS12 showed better fermentative performance compared to commercial strains. Thus, indicated that the local fruits and plant parts could be the potential source of indigenous S. cerevisiae strains for leavening agent in bread making.
The study was conducted to detect the porcine DNA in pharmaceutical products in local market using polymerase chain reaction (PCR) and southern-hybridization on the biochip. A total of 113 (n=113) of hard (82 samples) and soft gel (31 samples) capsules from pharmaceutical products were purchased and tested for the presence of porcine DNA for Halal authentication. All capsules were gelatin-based purchased from local over the counter (OTC) markets. Of all samples tested, 37.2% (42/113) contained porcine DNA. While, none porcine DNA band was detected for 62.8% (71/113) of capsules tested. All samples which were positive toward porcine DNA were imported pharmaceutical products with none Halal logo. Results in the presence study demonstrated that the PCR techniques and southern-hybridization on the biochip is suitable tool for monitoring the Haram component in highly processed product of soft and hard capsule.