Gelatine obtained from fish skin has become a potential source of preparing nanoparticles and
encapsulation of bioactive compounds. Within these fish skin, gelatine nanoparticles show
potent benefits for application in pharmaceutical and cosmetic industry. The encapsulated
bioactive ingredients within nanoparticles have improved bioavailability, delivery properties,
and solubility of the nutraceuticals within the human body and blood stream. Many of such
bioactive peptides (biopeptides) are potent antioxidants; and as oxidative stress is the main
cause of the onset of various chronic diseases, encapsulation of antioxidant biopeptides within
fish gelatine nanoparticles could be a potential remedy to prevent or delay the onset of such
diseases and for better health prospects. The purpose of the present work was to prepare a
simple, safe, and reproducible novel food delivery nanoparticle system encapsulating a desirable antioxidant biopeptide. An optimisation study was conducted to produce a desirable size
of gelatine nanoparticles which showed a higher encapsulation efficiency of an antioxidant
biopeptide. Sunflower biopeptide was chosen as the antioxidant biopeptide, as the activity of
this protein hydrolysate is quite high at DPPH of 89% and FRAP assay of 968 µm/L. Tilapia
fish was used as gelatine source at an average yield of the process at 10% wt/wt. Effects of
parameters such as pH, biopeptide concentration, and cross-linking agent ‘glutaraldehyde’ on
the size, stability, and encapsulation efficiency on the nanoparticles were studied. The average
diameter of the biopeptide loaded gelatine nanoparticle was between 228.3 and 1,305 nm.
Encapsulation efficiency was 76% at an optimal pH of 2, glutaraldehyde concentration of 2
mL, and biopeptide concentration of 0.1 mg/mL exhibited DPPH at 92% and FRAP assay of
978 µm/L. To understand the absorption of sunflower biopeptide in stomach, blood stream,
and biopeptide release of the gelatine nanoparticles, biopeptide loaded gelatine nanoparticles
were subjected to simulated gastrointestinal conditions mimicking human stomach and
intestine; and showed peptide release of 0.1464 and 0.277 mg/mL upon pepsin and pancreatin
digestion, respectively.
Watermelon waste materials remained one of the important food grade agro-wastes generated by most hospitality industries in Southeast Asia and particularly in Malaysia. Jam was prepared from watermelon rind with different flavours (vanilla, pineapple, strawberry, lemon and no flavour). Five different samples were prepared at various compositions T₁ (50-50), T₂ (80-20), T₃ (60-40), T₄ (40-60) and T₅ (20-80) of rind and sugar. T₁ (50-50) gave the best jam set. Ten man panel (trained) evaluated the jam for its sensory characteristics and physicochemical analysis. Sensory evaluation conducted among five flavours was significantly different at (p>0.05). Chemical analysis showed that ascorbic acid reduced greatly among all treatments during three month storage. Soluble sugar and pH also decreased gradually for T₁ (from 4.96 to 4.40), T₂ (from 4.92 to 4.21), T₃ (from 4.74 to 4.11), T₄ (from 4.62 to 4.51) and T₅ (from 4.52 to 4.25) upon storage. Strawberry flavoured jam was most acceptable by the panel.
Optimization of the process conditions of mixed culture of bacidiomycete fungi for improved protein enrichment of fruit peels is necessary to ease replication and scale-up processes. Sixday fermentation period and temperature of 32°C were optimum for elevated protein synthesis and enzyme activities (78.99 units/ml for α-amylase and 0.36 units/ml for cellulase). A highly significant quadratic model obtained from Face Centered Central Composite Design (FCCCD) described the process optimization. Linear effect of pH and inoculum size were significant (p < 0.05) while pH and moisture content (MC) interact significantly. 70.2% MC, pH 5.4 and 6.1% inoculum were the optimum level for a maximum crude protein synthesis of 198.77 mg/g. The crude protein contained essential and non-essential amino acid at a comparable level with other bioprocessed materials that are currently used as animal feed supplement.
Media components such as wheat flour, MgSO4 and particle size were screened by Placket Burman design (PBD) while the operating range was fixed by one-factor-at-a-time method (OFAT), primarily for the enrichment of cassava peels as animal feed. Optimization of the selected media components was carried out using Face–Centered Central Composite Design (FCCCD) of the Response Surface Methodology (RSM) and the responses were measured in term of protein and lignin contents. Statistical analysis of the result showed that the quadratic term of wheat flour and the interaction between wheat flour and particle size were highly significant (P
Gelatin from fish skin is known to be an alternative source for mammalian gelatin. However, it has weaker properties compared to bovine and porcine gelatin, which limits its use in the industry. The conventional method for fish gelatin extraction requires long production time and could cause serious water pollution and chemical treatments are often being used to enhance the yield of fish gelatin and its properties but it may affect the amino acid content of the gelatin. In this regard, High-Pressure Processing (HPP) is a novel method suggested for fish gelatin extraction. The HPP method is classified as green technology as it requires low electricity throughout the process. This study will discuss the impact of HPP the technique gelatin extracted from fish skin. Skins from four types of fish, namely red tilapia (Oreochromis niloticus), black tilapia (Oreochromis mossambicus), grouper (Epinephelus areolatus) and threadfin bream (Nemipterus tambuloides), were used. High pressure was applied at either pretreatment in citric acid solution or during thermal extraction; and the pressure was maintained at 250 MPa with pressure holding time of 10 minutes and 18 hours of water extraction. Gelatin extract from traditional acid-base method was prepared as a standard for comparison. The study found that there was an increment in the yield of gelatin and the concentration of gelatin extract, and the pre-treatment time was also reduced.
Extraction of gelatin using traditional acid-base pretreatment method has several limitations
such as time consuming and causes serious water pollution. Chemical treatment often being used
as an alternative process to overcome the weaknesses of the conventional method. However,
excessive chemical elements would damage the structure of the gelatin due to its high sensitivity
to the acid content. High Pressure Processing (HPP) is a novel and environmental friendly
method that has been suggested to assist gelatin extraction. Pressurization during pretreatment
could reduce the extraction time and amount of acid used. It also has a potential in enhancing the
properties of the gelatin extract and increasing the gelatin yield. In this research, One-Factor-
at-Time (OFAT) and optimization study were done to determine the optimum parameters for
extraction of gelatin assisted by HPP from red tilapia skin. Four parameters; applied pressure,
pressure holding time, ratio of acid to skin and extraction time have been selected for the OFAT
design and concentration of the gelatin extract and percentage of yield gelatin were evaluated.
From OFAT, optimum technical parameters for response surface optimization design were 250
MPa pressure, 7.5 ml of acid to 1 g of skin and 12 hours extraction time. Pressure holding
time was fixed for 10 min. FCCCD has been used for optimization study. Results from the
data shows that the optimum conditions for gelatin extraction from red tilapia skin were 250
MPa for pressure, 10 min of pressure holding time, 7.5 ml of acid for 1 g of skin and 12 hours
of extraction time while the maximum concentration and yield were 19.51 mg/ml and 32.04%
(320.4 mg/g), respectively. These findings proved that HPP could increase the concentration
and the yield of the gelatin while reducing the chemical waste and shortening the extraction
process.
Lycopene is a well-known carotenoid, causing red color of fresh tomatoes. The significance of lycopene as antioxidant agent and coloring in the cosmetics, and its use in pharmaceutical and food industries has expanded in the recent years. Extraction of lycopene was improved effectively under solid state fermentation process; whereby, cellulase produced from the fermentation process was employed to degrade the cell-wall constituents, which facilitated the release of intracellular contents. The optimum conditions for the fermentation process were determined using Response Surface Methodology (RSM). The Facecentered Central Composite Design (FCCD) was employed to investigate the effects of three independent factors: moisture content in the range of 60 to 80 %, inoculum size ranging between 5 to 15% while the incubation time was set at 2, 3 and 4 days. Twenty runs of experiment were conducted and each one was repeated three times. The obtained data was analyzed using the Design Expert software v.6.0.8. Regression analysis showed that 94.56% of the variation was explained by the software. Under the optimized conditions, the highest lycopene yield was 307.2 µg/g when the moisture content was 80%, the inoculum size was 15% in 4 incubation days. The experimental values agreed with the predicted values, thus proving stability of the model used and the success of RSM. This study showed as to how fermentation can improve the extraction process by comparing the result with the control (extraction without fermentation) which was 0.8 µg/g.
Solid state bioconversion (SSB) of Ulva seaweed for protein enrichment was conducted over 7-days using Phanerochaete chrysosporium (P. chrysosporium). One-factor-at-a-time (OFAT) optimization of process parameters revealed 70% for moisture content, 9% for inoculum size and 7% for minerals. Optimum substrate depth in 1 kg reactor was 12 mm and the protein increased from 88.51 mg/g to 107.89 mg/g. Fourier transformation infrared spectroscopy (FTIR) analysis showed modifications in the polysaccharide resulting from SSB. Soluble and reducing sugars concentrations improved by 168.88% (from 33.74±0.51 mg/g to 90.72±1.38 mg/g) and 198.95% (from 0.13±0.05 mg/g to 0.40±0.01 mg/g), while total carbohydrate reduced to 107.15±1.21 mg/g from initial concentration of 109.39±1.33 mg/g.
This study aimed at investigating the presence of alkaloids and other chemical constituents in Datura stramonium (Saikaran, Jimson weed). All parts of the plant were dried, crushed and then underwent extraction by soxhlet and maceration methods. The solvents used in these methods were normal hexane (nonpolar) and ethanol (polar). Thin Layer Chromatography (TLC) and FTIR techniques were used to analyse the chemical components of jimson weed. The results showed the presence of hyoscine in all plant parts while atropine in the seeds only. The best separation was found to be when the solvent system was acetone: water: ammonia (90:07:03). Maceration method is the best and cost effective procedure for extraction.
Considerable attention has been directed to nanoparticles based on gelatin biopolymer due to its numerous available active group sites for attaching target molecules and acting as a drug or nutraceutical delivery system aiming to improve the therapeutic effects and also to reduce the side effects of formulated drugs as gelatin is a natural biodegradable biocompatible polymer, nontoxic, readily available, cheap and is used in parental formulations. With mammalian gelatin (pig and cow) as the major source of gelatin production, alternatives are required due to sociocultural and health concerns to maintain halal status. This paper aims at reviewing fish skin gelatin from warm water species which can provide a potential alternative source of gelatin with almost the same rheological properties as mammalian gelatin and is a beneficial way to use fish waste such as skin, bones and fin which is generally discarded. The study also entails a lot of research being done in the field of nanoencapsulation of gelatin with various nutraceuticals as well as drug and gene therapy. There is an especially increasing interest in encapsulating biopeptides within gelatin nanoparticles in the functional food industry due to their role in preventing or delaying the onset of various diseases, food fortification, improvement of food quality, increase in shelf life, targeted peptide delivery and hence can be used as additives in food products. This review also attempts to provide an overview of the application of gelatin nanoparticles in nanoencapsulation in the food industry.
Abiotic stress factors are the main limitation to plant growth and yield in agriculture. Orange sweet potatoes may become major sources of carotenoids in the diet, but the extent of environmental and genetic influences on plant carotenoid biosynthesis are poorly understood. Carotenoid biosynthesis is regulated by several factors such as water, light, pathogen, salinity, nutrients and is susceptible to geometric isomerisation in the presence of oxygen, light and heat which causes colour loss and oxidation. The main problems associated with carotenoid accumulation arise from the inherent instability of pigments. In this study carotenoid biogenesis is investigated in sweet potato callus culture as a potential model system for carotenogenesis by analysing the effects of environmental stress agents such as NaCl (for salt tolerance), PEG (for drought tolerance), salicylic acid (for pathogen stress or disease resistance) and nutrient strength towards carotenoid content and composition. Results of this study revealed that the bioactive compounds detected in orange sweet potato callus were α-carotene, β-carotene, lutein and zeaxanthin. Not surprisingly, the response of sweet potato callus culture to such environments appeared to be highly light dependent. Another factor is the activity of functional enzymes and candidate enzymes that regulate carotenoid biosynthesis, which will determine type and quantity of individual carotenoids. By understanding the environmental factors that affected carotenoid biosynthesis, it should be possible to enhance the amount and type of carotenoid that accumulates in sweet potato tubers. In conclusion, in vitro callus culture is suggested as a successful new alternative approaches to enhance or enrich certain carotenoids through controlled environment.
Carotenoid content in plants differs due to several factors such as cultivar, maturity, climate, locality and storage. Improving the nutritional values of sweet potato is an important breeding goal and understanding the regulation, genetics and inheritance of carotenoid biosynthesis are vital to achieve this. Environmental conditions can have a marked influence on the accumulation of carotenoids in sweet potato tubers. Little is known about the effects of location, post-harvest storage time and harvesting season particularly on carotenoid biosynthesis. Therefore, this study aimed to investigate the effects of growing location, harvesting season and storage time on carotenoid biosynthesis in orange sweet potato tuber flesh. The results showed that orange sweet potato tubers contained α-carotene and β-carotene in the first and second harvesting season (year 2011 and 2012), whereas lutein and zeaxanthin were detected only in the third harvesting season (year 2013). Analysis of carotenoid profiles of the orange sweet potato tubers grown in three different locations confirmed that the harvesting season had a major effect on the total carotenoid content and the individual carotenoid compounds. The post-harvest storage time of sweet potato tubers also appears to have distinct effects on carotenoid biosynthesis, the magnitude of the effects being dependent on the storage time, harvesting season and location. The results of this study will help to understand the effects of location, year of harvesting season and storage time on carotenoid accumulation in orange sweet potato tubers.
Medicinal properties of Malaysian Curcuma caesia have not been studied extensively, even though it has been used as a traditional remedy. This study examined the effects of various extraction temperatures (30, 40, 50, 60, 70oC) using a high frequency (40 kHz) ultrasonic extraction method, time (30,60,90 and 120 minutes), pH (1,2,3,4,5,6,7,8,9,10) on the extraction yield of total phenolics and DPPH (2,2-diphenyl-1-picrylhydrazyl) scavenging activities from C. caesia rhizome. Extraction was most efficient at pH 6.0, while the extraction time of 30 minutes and temperature of 60oC was the best in terms of total phenolics content and DPPH scavenging activity. This study is important due to its ability to improve extraction of total phenolics compound using ultrasonic extraction method while maintaining a relatively high DPPH scavenging activity of the extracts.
Bioprotein is one of the useful products obtained from biotechnology invention. It is a promising replacement for the commercial fish feed supplement. In this study, the enrichment of the bioprotein content after solid state fermentation using palm kernel cake and seaweed by the white rot fungus: Phanerochaete chrysoporium and yeast: Candida utilis was carried out. The growth media components were selected from 11 types of media using Plackett-Burman design (hereinafter PBD) and were optimized by one-factor-at-a-time (OFAT) method with bioprotein concentration (mg/g) as the response. From the screening result using PBD, three media components, namely K2HPO4, CuSO4.5H2O and MnSO4.H2O were selected for further optimization using OFAT method because of their positive contributions to the response. The final results showed that 5.0 g/L K2HPO4, 3.0 g/L CuSO4.5H2O and 0.1 g/L MnSO4.H2O were there to be the optimum media constituents with 9.0 g/L, MgSO4.7H2O, 0.1 g/L, CaCl2.H2O, 3.0 g/L FeSO4.7H2O and 3.0 g/L peptone as fixed compositions. At this optimum concentration, the protein increment of 11% was observed as compared to the results determined in the screening using PBD. The study revealed the benefits of using mixed cultures in improving the protein concentrations which can be used as nutritious fish feed.
Gelatin is one of the most widely used food ingredients, with wide applications in the food
industry. It was reported that 41% of the gelatin produced in the world is sourced from pig
skin, 28.5% from bovine hides and 29.5% from bovine bones. However, factors such as the
outbreak of BSE (a.k.a. mad cow disease) and increasing demand for non-mammalian gelatin
for halal and kosher food markets have revived interest in gelatin replacers from plant sources.
In this study, we have successfully extracted valuable pectin—as gelatin replacer--from various
types of plant wastes. Pectin is a high value functional food ingredient widely used as a gelling
agent and stabilizer. It is also an abundant, ubiquitous and multifunctional component of the
cell walls of all land plants. Mango peel was screened as the ideal source for high-yield (36.6%)
pectin of satisfactory quality. The results indicate that citric acid was the best solution for
recovery of pectin from mango peels. An extraction temperature of 90°C and pH 2 provided
the optimum conditions for maximum yield of pectin. The resulting crude mango peel pectin
(CMPP) was analyzed for physicochemical parameters. The results indicated values for ash
content (0.0412%), moisture content (0.303%), viscosity (45.18%), galacturonic acid content
(36.8-37.2-40%) and degree of esterification (38.3-41%). Following analysis of its gelling
properties and sensory evaluation, CMPP has good potential to be applied in the food industry
as a low-methoxyl pectin and a cheap source of gelatin replacer for jam preparations.
Large quantities of agro-based liquid wastes are produced every year and their disposal is often a problem for industries. In light of that, in this study prudent effort was done to screen the agro-industrial wastes - pineapple waste (PAW) and palm oil mill effluent (POME) for valuable biophenols product. Three different solvents; ethanol, acetone and distilled water were screened in order to enhance the process. All experiments were performed using fixed process conditions of solid to solvent ratio, temperatures, time and agitation speed. Effectiveness of extraction process to produce biophenol was based on high amount with more activity. POME was selected as potential source with biophenol content of 125.42 mg/L GAE.
Malaysia has a rich diversity of medicinal plants and some of them inhibit xanthine oxidase (XO), which can be introduced as new natural sources of gout medication and a substitute for synthetic xanthine oxidase inhibitors (XOI). The degree of XO inhibitory activity was determined by measuring the absorbance spectrophotometrically at 295 nm, which is associated with uric acid formation. Our preliminary screening study had employed the use of distilled water, 70% methanol and absolute ethanol to extract XOI from twenty parts of five plant species, namely, Averrhoa carambola, Carica papaya, Dimocarpus longan malesianus, Manilkara zapota and Salacca zalacca. These plants were selected based on their frequent medicinal usages by local folks. The results have shown that an aqueous extract of Carica papaya mature leaves has promising activity to inhibit XO up to 75.68 ± 0.1%. Statistical experimental design were employed to optimize the selected sample (dried Carica papaya leaves: distilled water) on extraction of XOI and the maximum XOI percentage of 86.93 ± 1.9% was obtained, which exhibited only 6.76% less than the activity exhibited by allopurinol (93.69 ± 0.2%), a commercial XOI. The comparison was made between allopurinol and optimized extract on the basis of IC50concentrations. Allopurinol showed IC50 value of 3.74 μg/ml that is considerably lower as compared to the optimized sample (4.33 μg/ml).
Pollutants, especially heavy metals like cadmium, Chromium, lead and mercury, play a significant role in causing various water-borne diseases to humans. This study evaluates the sorption properties of bioactive constituents of Moringa oleifera seeds for decontamination of cadmium at laboratory scale. The performance of the bioactive constituent extracted by salt extraction method was enhanced by process optimization with various concentration of bioactive dosages, agitation speed, contact time, pH and heavy metal concentrations. Statistical optimization was carried out for evaluating the polynomial regression model through effect of linear, quadratic and interaction of the factors. The maximum removal of cadmium was 72% by using 0.2 g/l of bioactive dosage.
Biological treatment of sewage treatment plant (STP) sludge by potential pure bacterial culture (Bacillus sp.) with optimum process conditions for effective biodegradation and bioseparation was carried out in the laboratory. The effective and efficient bioconversion was evaluated with the treatment of pure bacterial culture and existing microbes (uninnoculated) in sludge. The optimum process conditions i.e., temperature, 40 degrees C; pH, 6; inoculum, 5% (v/v); aeration, 1 vvm; agitation speed, 50 rpm obtained from the previous studies with chemical oxygen demand COD at 30 mgL(-1) were applied for the biological treatment of sludge. The results indicated that pure bacterial culture (Bacillus sp.) showed higher degradation and separation of treated sludge compared to treatment with the existing mixed microbes in a stirred tank bioreactor. The treated STP sludge by potential pure bacterial culture and existing microbes gave 30% and 11%; 91.2% and 59.1; 88.5% and 52.3%; 98.4% and 51.3%; 96.1% and 75.2%; 99.4% and 72.8% reduction of total suspended solids (TSS, biosolids), COD, soluble protein, turbidity, total dissolved solids (TDS) and specific resistance to filtration (SRF), respectively within 7 days of treatment. The pH was observed at 6.5 and 4 during the treatment of sludge by pure culture and existing microbes, respectively.
Forty-six bacterial strains were isolated from nine different sources in four treatment plants namely Indah Water Konsortium (IWK) sewage treatment plant (STP), International Islamic University Malaysia (IIUM) wastewater treatment plant-1,-2 and -3 to evaluate the bioconversion process in terms of efficient biodegradation and bioseparation. The bacterial strains isolated were found to be 52.2% (24 isolates) and 47.8% (22 isolates) in the IWK and IIUM treatment plants, respectively. The results showed that higher microbial population (9-10 x 10(4) cfu/mL) was observed in the secondary clarifier of IWK treatment plant. Among the isolates, 23 isolates were gram-positive bacillus (GPB) and gram-positive cocci (GPC), 19 isolates were gram-negative bacillus (GNB) and gram-negative cocci (GNC), and the rest were undetermined. Gram-negative cocci (GNC) were not found in the isolates from IWK. A total of 15 bacterial strains were selected for effective and efficient sludge bioconversion. All the strains were tested against sludge (1% total suspended solids, TSS) to evaluate the biosolids production (TSS% content), chemical oxygen demand (COD) removal and filtration rate (filterability test). The strain S-1 (IWK1001) showed lower TSS content (0.8% TSS), maximum COD removal (84%) and increased filterability (1.1 min/10 mL of filtrate) of treated sludge followed by the strains S-11, S-14, S-2, S-15, S-13, S-7, S-8, S-4, S-3, S-6, S-12, S-16, S-17 and S-9. The pH values in the fermentation broth were affected by the bacterial cultures and recorded as well. Effective bioconversion was observed during the first three days of sludge treatment.