فهرست مطالب سیدعلی مرتضوی

The increasing growth of cardiovascular diseases, high blood pressure, and hardening of the vessel walls as well as obesity in many countries has made low-fat and low sodium pizza cheese one of the subjects of study all over the world. The effects of four important independent variables including inulin (0-0.025 %), pre-gelatinized starch (0-0.5 %), NaCl (0.35-1%), and KCl (0.35-1%) were studied. The fat content of imitation pizza cheese was significantly decreased to 11.91% with the increased levels of inulin and starch substitution (p<0.05). Also, its moisture and pH values were significantly different (p < 0.05). The increased levels of pre-gelatinized starch and inulin reduced hardness (from 5.04 to 3.55) and adhesiveness (from 4368.89% to 1640.54%), however, increased cohesiveness (from 0.365 to 0.43) and springiness (from 0.456 to 0.545). NaCl and KCl increased the hardness of the product. Inulin and starch led to decrease the a* value. The b* value decreases with the increase of inulin and increases with the increase of modified starch. The formulation containing 0.19% inulin, 0.4% pre-gelatinized starch, 0.35% NaCl, and 0.50% KCl was found as the optimal formulation for low-fat imitation cheese. Results of scanning electron microscope (SEM) images revealed that inulin crystals were accumulated in the continuous phase, which this can lead to important changes in the sensory and textural properties. The study concludes that inulin or starch can be used to replace up to 3.6% of fat in the imitation pizza cheese and 0.35% NaCl-0.50% KCl to lower the sodium content of the product.

Native starches have limited use in the food industry owing to their insolubility in cold water and lack of reactivity. Native starches are susceptible to chemical, physical, and enzymatic modification. This article examines cold plasma as one of the physical mechanisms of starch modification. The structure of each system is analyzed, and the effects of cold plasma at atmospheric pressure on the functional, thermal, molecular, morphological, and physicochemical aspects of various starches researched by different researchers are described. Changes in the characteristics of DBD plasma-modified starch are primarily caused by the depolymerization and cross-linking of amylose and amylopectin side chains. The molecular weight, viscosity, and gelatinization temperature decrease after DBD plasma treatment. The plasma etching of starch granules improves their surface energy and hydrophilicity. Cold plasma is an alternate approach for changing starch characteristics; it may be inferred.

Today, the extraction and use of biologically active compounds from agricultural and food wastes has received much attention. In the present research, the effect of enzyme treatment, ultrasound and the combined effect of enzyme treatment and ultrasound on the extraction of phenolic compounds of sour grape wastes was done so that 2 pectinase enzymes (Pectinex Ultracolor and Pectinex Yildamesh) at levels of 10, 20 and 30 mg/kg and ultrasound (times 10, 25 and 40 minutes) and (sound intensity 30, 60 and 90%) were used. The effect of enzyme treatment, ultrasound and the combined effect of enzyme treatment and ultrasound were investigated. According to the obtained results, the highest extraction efficiency belonged to Yaldemesh enzyme and with increasing sound intensity, the extraction efficiency increased significantly. On the other hand, increasing the extraction time led to an increase in extraction efficiency (p≤0.01). So that the highest extraction efficiency was observed in the sample extracted by Yaldemesh enzyme and under ultrasound at 90% sound intensity for 40 minutes (p≤0.01). According to the obtained results, the highest flavonoid, total phenol and antioxidant activity (DPPH, FRAP, ABTS) belonged to Yaldemesh enzyme, and with increasing sound intensity, antioxidant activity increased significantly (p≤0.01). On the other hand, increasing the extraction time led to a significant increase in antioxidant activity (p≤0.01). The highest antioxidant activity belonged to the sample extracted by Yaldemesh enzyme and subjected to ultrasound at a ultrasound intensity of 90% for 40 minutes and was introduced as the best treatment.

In this study, the effect of edible coating based on Lallemantia iberica seed mucilage (LISM) with different contents (0, 0.5, 1, 1.5 and 2% vol/vol) of Citrus paradise essential oil nanoemulsion (CPN) was investigated on the microbial, chemical, and sensory qualities of lamb slices during cold storage. The antimicrobial results showed that at the end of the storage period, the lowest number of total viable bacteria (6.26 log CFU/g), psychrotrophic count (3.28 log CFU/g), Escherichia coli (0.95 log CFU/g), Staphylococcus aureus (0.87 log CFU/g) and fungi (1.12 log CFU/g) were observed in LISM+2% CPN sample. The highest and lowest pH at the end of the storage period were related to uncoated samples (6.42) and LISM+2%CPN (5.65). The amount of peroxide number and thiobarbituric acid in the control and LISM+2%CPN samples were 11.60 meq O2/kg and 1.20 mg MDA/kg and 5.40 meq O2/kg and 0.59 mg MDA/kg, respectively, after 9 days of cold storage. The meat color (L*, a*, b*) was also preserved by edible coating containing C. paradise essential oil nanoemulsion (LISM+CPN). The addition of nanoemulsion in edible coating increased sensory scores such as aroma, color, texture, and overall acceptance of lamb slices, especially on the last day of cold storage. The obtained results suggest the LISM+CPN edible coating as a solution for retarding the chemical and microbial spoilage of lamb slices.

One of the common adulterations in milk and dairy products, is the addition of low-priced vegetable oils such as palm oil in order to increase the profitability of products. Therefore, there is an urgent need to develop accurate, fast and reliable identification techniques to protect consumers against this type of adulteration. The aim of the present study was DNA barcoding with real-time PCR as a reliable method for detecting palm oil fraud with levels of 2, 3, 4, 5, 10, 30, 50 and 100 % and positive and negative control samples in yogurt. According to the results, the highest and lowest concentrations of DNA extracted belonged to the palm oil sample of 100 % and 3% , respectively, while among all samples, the concentration of DNA extracted in sesame oil and then in the control oil sample was lower. It was determined from other samples. The lowest and highest adsorption rates (10mm) between the samples were control oil (excluding palm) and 100 % palm oil, respectively. There was no significant difference in absorption rate between 4%, 5% and sesame oil samples. The range for detecting palm oil adulteration was from 0.05% to 100% palm oil. LOQ and LOD were 0.1 % and 0.05 % of palm oil, respectively.

Oxidation reactions and microorganisms’ activity are considered as the most important factors affecting the quality of food products. Recently, in the light of the inefficiency of some chemical preservatives against microorganisms and the presence of toxic residues in food products, the use of natural antimicrobials and antioxidants has been increased. Natural antimicrobial compounds have the potential to control microbial contamination and reduce the use of antibiotics. Plant essential oils are natural compounds with the potential to be used as active ingredients in the food, pharmaceutical, and cosmetic industries. Various studies have shown that essential oils have antifungal, antibacterial, antiviral, and antioxidant activity. The essential oils are considered as superb preservatives with various biological functions. Essential oils are generally recognized as safe product (GRAS) which can be used as an alternative to synthetic additives.Grapefruit (Citrus paradisi) peel and fruit contain active ingredients such as acids, flavonoids, vitamin C, and potassium, and its essential oil is composed of terpenic hydrocarbons, such as citral, limonene, citronelal, and geraniol. Although plant essential oils have antimicrobial and antioxidant properties, one of the main problems of these natural compounds is their high volatility and instability. In this context, nanoemulsion formulations are frequently used to increase the stability and efficiency of these biologically active compounds. This study is therefore aimed to nanoemulsifying the grapefruit essential oil and evaluate its antioxidant and antimicrobial properties.

β-carotene, linoleic acid, ABTS (2,2’-Azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt), and DPPH (2,2-diphenly-1-picrylhydrazyl) were purchased from Sigma-Aldrich Co. (USA). Mueller Hinton Broth (MHB) and Mueller Hinton Agar (MHA) were supplied from Merck Co. (Darmstadt, Germany). Grapefruit peel was dried at ambient temperature and then powdered. The obtained powder was then transferred to a Clevenger device containing 750 ml of distilled water to perform the distillation extraction (3 h). The resulting grapefruit essential oil was stored at 4 °C until use. Grapefruit essential oil was prepared using the hydrodistillation method, and then nanoemulsified. The antioxidant activity of the nanoemulsified essential oil was investigated by DPPH and ABTS  radical scavenging activity and beta-carotene/linoleic bleaching test. The nanoemulsified essential oil or methanolic (control) was mixed with DPPH solution and the mixture was then stored at ambient temperature for 30 min, in a dark place. The control sample was prepared by methanol. The absorbance of the samples was measured at 517 nm. To determine the ABTS-RS activity, the nanoemulsified essential oil was briefly charged with methanolic ABTS radical cation solution and the resulting mixture was left at room temperature for 30 min. Afterward, the absorbance was read at 734 nm. A spectrophotometric method was applied to monitor β-carotene/linoleate solution bleaching in the presence of the nanoemulsified essential oil. To do this, the absorbance of the solution was recorded at 490 nm after 120 min against the control sample at time zero and after 120 min. Antibacterial effect of the grapefruit essential oil nanoemulsion was also evaluated against Escherichia coli ATCC 25922, Salmonella typhi ATCC 6539, Pseudomonas aeruginosa ATCC 27853, Listeria innocua ATCC 33090, Staphylococcus aureus ATCC 25923, Bacillus cereus ATCC 14579, Bacillus subtilis ATCC 23857, Streptococcus pyogenes ATCC 19615, and Staphylococcus epidermidis ATCC 12228, based on disk diffusion agar, well diffusion agar, minimum inhibitory concentration, and minimum bactericidal concentration.

The results showed that the nanoemulsion of grapefruit essential oil had a remarkable antioxidant effect of 42.27 mg/ml, 33.27 mg/ml and 54.54%, respectively, based on DPPH, ABTS, and beta-carotene-linoleic acid bleaching tests. According to disk diffusion agar and well diffusion agar results, the lowest inhibition zone was related to E. coli and the highest inhibition zone was observed in L. innocua. The minimum inhibitory concentration for L. innocua and S. aureus (the most sensitive bacteria) was 25 mg/ml, and E. coli, S. typhi, and P. aeruginosa had the highest inhibitory concentration. Also, the lowest bactericidal concentration was related to L. innocua and S. aureus bacteria and the highest concentration was observed for E. coli, S. typhi and P. aeruginosa. The nanoemulsified essential oil generally exhibited greater antibacterial activity against Gram-positive species. This could be mainly due to the difference in the cell wall composition of Gram-positive bacteria in comparison to Gram-negative; Gram-positive bacteria have a thicker mucopeptide layer in their cell wall, while Gram-negative bacteria have only a thin layer of mucopeptide and the wall structure is mainly composed of lipoprotein and lipopolysaccharide, thereby leading to a higher resistant to antibacterial agents According to the results, grapefruit essential oil nanoemulsion can be used as a natural antioxidant and antimicrobial agent to control oxidation reactions and the growth of spoilage and pathogenic microorganisms.

Dairy sludge is one of the main and inexpensive wastes of the dairy industry, which contains the nutrients necessary for the growth of lactic acid bacteria (LAB) to produce microbial metabolites, and for its efficient use, optimization of fermentation conditions is critical. In order to optimize the production of dry biomass, three independent variables of dairy sludge concentration (5, 12.5 and 20%), pH (6, 7 and 8) and the inoculation rate of Lactobacillus fermentum strain 4-17 (1, 3 and 5%) were used. Before fermentation, the cell growth and morphology of this bacterium were examined in order to determine the function of the growth rate and confirm the presence of bacteria in this medium. The independent variables were optimized using response surface method (RSM) with central composite design (CCD) in order to maximize dry biomass production by this bacterium. The optimization results showed that the maximum amount of dry biomass production related to the optimal treatment included 20% dairy sludge concentration, 1% inoculation rate and pH 8. Also, according to the results, the dairy sludge substrate is suitable for the fermentation of this bacterium. As a result, the effect of dairy sludge bed concentration and pH on dry biomass production by this bacteria was very significant.

Starch is the most abundant carbohydrate in legumes. On the other hand, due to its non-reactive nature and insolubility in cold water, natural leguminous starch has limited use in the food industry. Natural legume starch can be modified by chemical, physical, and enzymatic methods. Modified legume starches have gained importance in the food industry due to their improved functional properties. Ultrasound is one of the physical methods of starch modification examined in this article. Also, ultrasound is increasingly used as a green technology for the physicochemical modification of food systems. This study aims to investigate the effect of ultrasonic treatment (bath-probe) on the functional, rheological, thermal, morphological, and crystal structure characteristics of modified starch samples. The change in the properties of ultrasonically modified starch is mainly due to the depolymerization of amylose and amylopectin chains. After ultrasound treatment, molecular weight, viscosity, and crystallinity decrease; Therefore, it can be concluded that ultrasound is an alternative technology for modifying the properties of leguminous starch.

Tooth decay is one of the most common problems in the world, which is caused by the growth of biofilm and acid production by them. Many solutions have been used to solve this problem. However, due to the increase in antibiotic resistance of microorganisms and the increasing need for antimicrobial substances, efforts are being made to use natural antimicrobial substances. Lactoferrin is a protein in milk and saliva with antimicrobial and anti-biofilm properties. In this research, lactoferrin was encapsulated by nanoliposomes to increase its antimicrobial properties. In order to measure the effect of lactoferrin on the number of bacteria in the polymicrobial biofilm and acid production, each of the free substances or nanoliposomes in 4 concentrations (0, 1.5, 3, 6 mg/ml) in the Active Attachment biofilm model with saliva and culture medium was incubated.The results showed that lactoferrin nanocoating increased the ability to inhibit biofilm and acid production by this bacterium due to the slow release of lactoferrin from liposomes. When increasing the concentration of free and nanoliposomal lactoferrin to a concentration of 3 mg/ml, a significant decrease in the number of bacteria in the biofilm was observed compared to the control sample (P<0.01). However, increasing the concentration of free lactoferrin again increased the number of bacteria in the biofilm. Meanwhile, nanoliposomal lactoferrin at a concentration of 6 mg/ml still caused a decrease in bacteria in the biofilm, which was insignificant compared to the concentration of 3 mg/ml (P>0.01). From the obtained results, it can be concluded that nanoliposomal lactoferrin can be used to design products related to oral and dental health.

Today various sweeteners are competing with sucrose in food market. They are creating acceptable sweetness and preserving technological and sensory properties of the product. In this study enzymatic sorghum malt use as sucrose replacer in gluten-free rice cake production. For this purpose, moisture, specific volume, porosity, crust color values, firmness and sensory properties were evaluated. The results showed that with increasing substitution of sucrose by enzymatic sorghum malt, moisture content and a* increased. However, falling the moisture content in sample containing malt flour were lower than control during the storage (1week) was with the lapse of time a week after bake a cake, malt flour contains less moisture loss in samples from the control samples. The results also showed enzymatic sorghum malt increased the softness of texture and able to prevent hardening of the texture during storage. In addition, the results indicated that the sample that 40% sucrose had been replaced with malt flour had the highest porosity, specific volume and L* value. Also this sample was equal in sweetness to control and the judges taste the sample was superior in other features. Thus, according to the results we can say that an enzymatic sorghum malt can be used as a natural sweetener, especially in celiac disease is needed products.

Poultry and meat products are the largest sources of non-typhoid salmonella infections in most countries. Studies have shown that raw foods of animal origin, especially poultry and its products, are the main source of contamination of kitchens and restaurants. In terms of growth conditions, these microorganisms are resilient bacteria and easily adapt to their environmental conditions. Salmonella has been known to cause intestinal disease for many years and has been reported as the most important cause of food poisoning. According to Iranian and international standards, there should be no S. enteritidis or S. typhimurium in 25 grams of food. DNA-based methods for the identification and differentiation of Salmonella serovars have been designed and applied using specific primers at the genus and serovar levels. Therefore, they can be used as useful and rapid screening tests, as well as to supplement or replace conventional biochemical and serological tests. Real-time PCR, with the most accurate and reliable results using a fluorescence probe, which of course has a high cost. In this method, sequence specific fluorescence probes are used, and as a result, in the target molecule, screening and determination the presence or even the concentration of specific sequences is possible. Therefore, even in the presence of other types of nucleic acid molecules, the results are obtained quickly and have a high level of specificity. Under these conditions, if specific probes with different florescence dyes are used, even multiple targets can be detected in a single PCR reaction. The aim of this study was to identify S. enteritidis or S. typhimurium by PCR and Salmonella spp. by real time PCR method in poultry products. 

In total, 45 samples of poultry products, including chicken breast, liver and gizzard (15 samples each) were purchased from different regions of Mashhad and from various companies and transferred to the laboratory in accordance with hygienic standards. For each sample, 25 g of tissue was isolated and homogenized under sterile conditions and DNA extraction was then performed using a DNA extraction kit. The extracted DNA was evaluated by agarose gel electrophoresis. The purity and quantity of DNA extracted from each sample was examined by spectrophotometry method. In the next step, in order to identify the genus Salmonella, the samples were examined by real time PCR. In this method we used an internal control to ensure that negative results are not false negative due to inhibitors. The results of real time PCR showed that out of 45 samples, nine samples were infected with Salmonella. Then, these nine samples were evaluated for Salmonella typhimurium and Salmonella enteritidis infection by conventional PCR method. 

The results showed that out of nine samples that were positive in real time PCR test, seven samples were contaminated with Salmonella typhimurium, of which five samples were related to chicken breast and two to liver. Regarding Salmonella enteritidis infection, out of nine samples, only one sample was contaminated, which was related to chicken breast. Conventional methods have been traditionally used to enumerate target bacteria in food. However, these methods have some limitations and require considerable time and labor. Previous studies have already shown that real time PCR is more effective than conventional bacteriological methods for the detection of Salmonella spp. In a study by Whyte et al. (2002) The presence of Salmonella was assessed by traditional culture methods and by a Salmonella-specific polymerase chain reaction (PCR) test. Salmonella was recovered from 16% of samples using traditional culture methods. In contrast, the PCR assay proved to be more sensitive and detected Salmonella DNA in 19% of the examined samples (Whyte et al. 2002). Results of PCR with specific primers showed that reactions in real time PCR with general primers of Salmonella spp. were done correctly. Despite of accuracy and speed of real time PCR to detect DNA of microorganisms, further studies are developed to have more advantages. Loop-mediated isothermal amplification (LAMP) showed a higher sensitivity of Salmonella detection in compare to qPCR (Vichaibun & Kanchanaphum, 2020). Although LAMP could detect trace amount of Salmonella DNA but primer design for this reaction is very difficult. However, it is important to highlight that non-viable cells can be detected by real time PCR or other DNA-based methods, which does not occur in traditional methods of culture and isolation that require viable cells for quantification (Zeng et al., 2016).

Microbial quality of raw milk is very important in two respects. First, milk consumption itself plays a very significant role in people's food tables and its high microbial load endangers consumer health. Second, if the microbial quality of milk is not suitable, from a technology point of view, milk-derived products will not have a good quality. In this project, which has been carried out in collaboration with Pegah Golestan Company, the separation process (with separators) and double bactofugation was used to reduce microbial load with the aim of reducing milk heating (in order to reduce the nutritional value as a result of heat). Milk samples used for lactic cheese production in Golestan province were examined in 2020 and 2021. After the process, total microbial counting, aerobic and anaerobic spores were counted. The results showed that by using this method, the total microbial load, aerobic and anaerobic spores of the collected milks were reduced to an acceptable level throughout the year without decreasing the microbial quality of the produced cheese during the storage period. On the other hand, the process of separation and bactofugation produces dairy sludge. Normally, dairy sludge is removed every 20 minutes, which was performed in separator and bactofuge1 to 21 minutes to reduce dairy sludge.

In this study, first, the hydraulic flow by combining the gabion structure with a vertical drop and then the effect of porosity and length of the gabion structure on the energy dissipation values were investigated. For two modes of simple vertical drop and gabion, a total of 260 experiments including two heights of 15 and 20 cm drop, three porosities of 40, 45, and 50 percent, and eight different gabion lengths with a flow range of 150 to 800 liters per minute were performed. The results showed that in all the studied models, with increasing the relative critical depth parameter of the flow, the energy dissipation decreases and the relative downstream depth increases. The integration of the gabion structure caused the energy dissipation and the Froude number downstream to increase and decrease, respectively. On average, in all models, the use of gabions increased 57% of the energy dissipation of the current compared to the simple vertical drop and reduced the range of the landing number from 3.5-8.7 to 0.52-2.5. The flow regime passing through the vertical drop gabion physical models includes inflow, transient, and overflow, of which the Inflow regime plays a Major contribution in energy dissipation. For a constant relative length, increasing the porosity of the gabion structure increases the volume of water passing through the porous medium and the energy dissipation of the flow, In contrast for a constant porosity, increasing the relative length of the gabion structure has little effect on the energy dissipation.

Essential oils and extracts of black cumin have been attracted researchers in the field of protection of raw and processed food due to their antimicrobial and antioxidant compounds. In the current study, the chemical composition, antibacterial and antioxidant properties of black cumin essential oil extracted by Clevenger and ultrasound assisted (frequencies 37 and 80 kHz and 70 and 100% power) methods were performed and the optimization of extraction conditions according to the chemical properties of the essential oil. Antibacterial properties of black cumin essential oil against E.coli and S.aureus were measured by measuring the minimum inhibitory concentration and the minimum lethal concentration of pathogenic bacteria using micro-plate method. The antioxidant activity of essential oil was measured by examining the percentage of DPPH free radical scavenging. The results of analysis of black cumin essential oil by GCMS showed that the main composition of black cumin essential oil extracted by Clevenger method was γ-terpene with 30.03% and in ultrasound method was 31.04%. The highest efficiencies of essential oils and extracts obtained by Clevenger method were 2.04 and 0.75%, respectively, and in ultrasound method (80/100) for essential oils and extracts were 2% and 1%, respectively. The results showed that S.aureus was the most sensitive and E.coli the most resistant bacteria to cumin essential oil. Therefore, it can be stated that the extraction of black cumin essential oil by ultrasound method (80/100) could have the greatest effect on the extraction of essential oils and extracts and can be used to protect food against various systems. Benefit from oxidative and microorganisms that cause infections and food poisoning.

The purpose of this study was to evaluate the free radical scavenging activity, yogurt starters counts and sensory characteristics (color, flavour, consistency, overall acceptance) of low-fat probiotic yogurt enriched with different levels of hydroalcoholic extract of Ferulago angulata (F.angulata) and microalgae Spirulina platensis (S. platensis) for 21 days at refrigerated temperature and predicting the experiments results by Artificial neural network (ANN). In order to predict the experiments results, the multilayer perceptron neural network with two inputs (extract concentration, storage time) and one output using MATLAB R2013a software was used. About free radical scavenging activity (DPPH) of probiotic yogurt samples, the R2 was determined to be 0/989. Over time, by the 14th day, the free radical scavenging activity was increased and then decreased. F. angulata extract had a greater impact on this activity. For L. bulgaricus and S. thermophilus, R2 were 0/99 and 0/97 respectively. Treatments containing S. platensis extract had a higher count of these strains in comparsion with F. angulata extract. while the starter cultures count in the final day was determined to be more than the minimum number in probiotic yogurt (107 cfu/ml). R2 for color, flavor, consistency, and overall acceptance were 0/93, 0/98, 0/98, and 0/97 respectively, while the treatments containing S. platensis extract showed higher sensory scores in comparsion with F. angulata extract. The results showed that using a network with 10 neurons in the hidden layer and by the active hyperbolic sigmoid function and the data percentage used for training / test / evaluation is 60/ 15 / 20, probiotic yogurt can be predicted. The sensitivity analysis of optimal neural network showed the importance of predicting the parameters of extract concentrations and storage time on the changes of physicochemical, microbial and sensory characteristics of probiotic yogurt. It can be said ANN is a powerful tool for predicting the quality of probiotic yogurt.

Gamma aminobutyric acid (GABA) is a non-protein bioactive compound that can be effective in controlling many diseases such as Alzheimerchrs, hypertension, stress, etc. The main stimulus for the production of GABA is the enzyme glutamic acid decarboxylase (GAD), which is highly active in lactic acid bacteria. Also, the presence of monosodium glutamate (MSG) can act as a substrate for this enzyme and increase its activity. In this study, the production potential of gamma aminobutyric acid by Lactobacillus brevis PML1 in MRS medium was investigated. In order to optimize the fermentation process, culture medium containing MSG (1, 3 and 5%) was examined at 24, 48 and 72 hours. after fermentation, thin layer chromatography method was used to identify GABA produced by bacteria. Spectrophotometric method was used to quantify the bands in thin layer chromatography. The results of studies at the level of 95% significance showed that the optimal treatment included a culture medium containing 5% monosodium glutamate and a time of 72 hours at 37 ° C, in which the amount of GABA production was approximately 300 ppm; Therefore, the desired strain not only has the potential to produce gamma aminobutyric acid under normal conditions (control sample) but also by adding different percentages of monosodium glutamate to the culture medium, the amount of this production can be increased.

One of the most important challenges facing medical science is infectious diseases and poisoning, which in turn increases the production and consumption of new and common antibiotics. With theover use of common antibiotics, we are witnessing the spread of antibiotic-resistant microbial species, which makes the treatment of infectious diseases long and costly. Natural compounds of plant origin (essential oils and extracts) have been used to kill or at least prevent the growth of pathogenic microorganisms. These compounds, which are naturally present in plant tissues, are probably produced as part of their defense mechanisms against microbial invasion. Plant-based antimicrobials have therapeutic potential and are not only effective in treating infectious diseases, but also reduce the large number of side effects that are often associated with synthetic antimicrobials. Essential oils are complex mixtures of volatile, aromatic, low molecular weight and hydrophobic compounds present in various parts of aromatic plants, including leaves, flowers, seeds, sprouts and shoots. Among these plants, we can mention the coriander plant. Coriander (Coriandrum sativum L.) is an annual, herbaceous, aromatic plant belonging to the Apiaceae family. Coriander has a long history of nutritional and therapeutic use. This plant is a rich source of aromatic compounds and essential oils that have antibacterial, antifungal and antioxidant effects and is used in the preparation of various foods as a spice.
 
The tested coriander seeds were obtained from Khorasan Razavi province, Mashhad city. Antioxidant-free soybean oil was obtained from the Seh Gol Khorasan vegetable oil factory. Total phenolic content (TPC), Radical scavenging ability (DPPH assay), Oxidative stability index (OSI), Peroxide value (PV), Minimum inhibitory concentration (MIC) and Minimum bactericidal concentration (MBC) of essential oil were measured on a number of bacteria causing infection and food poisoning. The compositions of essential oils were identified by Gas Chromatography-Mass Spectrometry (GC-MS).
 
Most of the constituents of coriander seed essential oil were oxygen monoterpene compounds. Essential oils that have a higher percentage of oxygenated compounds are more important than other compounds in terms of aroma, strong odor, as well as antimicrobial and antioxidant power, so they are considered more valuable essential oils. Analysis of microbial test results showed that coriander seed essential oil had a relatively strong and good effect against the studied Gram-positive bacteria, so that the essential oil inhibited the growth of Staphylococcus aureus even at low concentrations. This essential oil had good antioxidant activity in the thermal stability of soybean oil. Coriander seed essential oil as an antioxidant compound was able to increase the oxidative stability of soybean oil under oxidative acceleration conditions. The results showed that total phenolic compounds were 0.161 mg GAE/100g, IC50 for essential oil was 30.981 mg/ml and thermal stability of soybean oil treated with coriander seed essential oil was 5.17 h. The results of microbial tests showed that Gram-positive bacteria was more sensitive to Coriander seed oil than Gram-negative bacteria. The most important constituents of coriander seed essential oil were Linalool (49%), Terpinolene (7%) and α-Pinene (6.8%).

In this study, wheat germ extract at different concentrations (2.5, 10 and 20%) and wheat germ extract powder produced by spray and freeze drying process method at three concentrations (0.2, 0.4 and 0.6%) was added to the ultrafiltrated white cheese and physicochemical properties of that were evaluated in thirty days during retention time. Moisture, acidity, total protein contents and antioxidant activity decreased in all samples during retention time and pH value increased during retention time. The results showed that freeze drying is a better method for preserving antioxidant compounds in wheat germ extract. Also, increasing the concentration of the wheat germ extract and powder of the wheat germ extract by both spray and freeze drying methods increased the antioxidant activity of the cheese compared to the control. Therefore, it is possible to use powdered wheat germ extract powder with freeze dryer as a functional ingredient in Ultrafiltrated White Cheese.

 Solid lipid nanoparticles and nanostructure lipid carriers were used to entrap curcumin and broaden confined knowledge of application of nanocarriers as the functional ingredients in food sectors. The effect of lipids ratio (GDS /GMS), kind of nanocarrier (SLN and NLC) and curcumin concentration (0, 0.25 and 0. 5 % (w / w) of emulsion) on the qualitative characteristics of nanocarrier were evaluated. Based on the results the massive physical structure of Curcumin and also increases the viscosity of the material dispersed phase in the presence of active, loading Curcumin in the developed nanocarrier led to significant (p<0.05) increase in nanoparticles size. DSC analyses showed that the crystalline states of produced nanocarriers were less ordered than pure materials and indicated that the curcumin was well incorporated in lipid matrices. However, our pretest showed that concentration of 5% Glycerol distearate and 0.25% Curcumin was the optimum for the production of Solid lipid nanoparticles and nanostructure lipid carriers.

In this study, after the extraction of F.angulata and microalgae Spirulinaplatensis by ultrasound technique and ethanol (99/70 %), levels of 0/1 to 1% of both extracts were injected into milk samples, according to the formulation, and probiotic yogurt containing LactobacillusacidophilusLa-5 wasprepared. Then,determination of pH, color and probiotic count was donewithin 21 days. By increasing the storage time, the pH and syneresis values decreased and increased respectively.Treatments containing different levels of Chevil extract showed lower pH and more syneresis in comparsion with Spirulina extract. Regarding color parameters (L*a*b*), increasing the storage time until the 14th day, the lightness intensity (L*) decreased and the green intensity (a*) of the samples increased. From the 14th day until the end of period, the L* and a* values was increased and decreased respectively.Treatments containing F.angulata extract, had a less L* value and greater a* value than S. platensisextract. The b* value decreased over time, and the highest mean (more yellowness) was related to the treatments containing F.angulata extract. During cold storage until 14 d, L.acidophilus count increased significantly, and then, declined 1 logarithmic cycle, but it was more than the standard number in probiotic yogurt. Treatments containing S. platensisextract showed a higher count of L. acidophilus.The use of S. platensis extract in comparison with F.angulata extract, yielded better results in terms of pH, color and probiotic count. The use of both extracts could improve yogurt color and increase the probiotic count.

Using colostrum as natural source rich in bioactive compounds is a new approach in functional food formulations. The aim of this research was to study the effect of different levels of colostrum on the quality characteristics of beverage yogurt, containing honey and the probiotic bacteria Lactobacillus acidophilus. The treatments (T0, T1, T2, T3, T4) were prepared by adding different levels of colostrum (0, 10, 20 and 30%) to buffalo milk and then inoculated with 2% yogurt starter culture and Lactobacillus acidophilus. 5% honey was added to all treatments except control (T4). Samples were subjected to physicochemical and sensory evaluations during 21 days of storage at 4 ° C. The results showed that the effect of different levels of colostrum on the physicochemical characteristics of beverage yogurt including pH, acidity, synersis and overall acceptance was significant (p<0.05) and caused a decrease in pH (4.39 to 4.11) and an increase in acidity (95.73 to 110) during the storage. Also, increasing the level of colostrum in the treatments reduced the amount of synersis from 29.22 to 28.34. The results of sensory test showed that the overall acceptability of treatments decreased with increasing colostrum level. The viability of Lactobacillus acidophilus in treatment with 30% colostrum(T3) was counted higher than the other treatments (1.67 *108). The number of probiotic bacteria decreased by one logarithmic cycle from day 14 of storage, but for 21 days it was still in the range defined for probiotic products (1.9 * 107).

The impact of aw (0.65-0.9), temperature (15-30°C) and their interaction on the germination and radius growth of Aspergillus fumigatus isolated from cake was surveyed on Yeast Extract Glucose Chloramphenicol Agar (YGC-Agar) during 60 days as well as the capabilities of Gompertz and Logistic models for fitting data were explored. Rising aw (from 0.65 to 0.9) and temperature (from 15 to 25°C) caused significant enhancing of germination and growth rate of A. fumigatus (P < 0.05). However, in constant aws, further increasing of temperature (up to 30°C) led to meaningful decreasing of these parameters (P < 0.05). A. fumigatus did not germinate at aw 0.65. In addition, germination was observed at aw 0.7 and 0.75 only when the temperature was 15 and 25°C while the mycelium growth was not occurred at these conditions. Although the germination rate was relatively high at aw 0.8, the mycelium growth was very limited. The most amount of germination and radius growth was for aw 0.85 -0.9 and temperature 15-25°C (P < 0.05). Consequently, the optimum growth of A. fumigatus was seen at aw 0.9 and temperature 25°C and the best shelf life of cake proved at aw < 0.7. Furthermore, fitting the growth curves demonstrated the more accuracy of Logistic model rather than Gomperts model.

One of the problems with the processed meat products shelf life is the formation of yellow spots in sausages. The aim of this study was to isolate and identify the microbial agents causing yellow stain from sausage by molecular- and culture-based methods. For this purpose, 15 samples from yellow spot and separation areas of chicken sausages were sampled. A total of 44 colonies grown on the MRS, M17, YGC, and PDB culture medium were inoculated into pre-packaged cutting sausages to induce the yellow spot. Yellow spots appearance9 samples and they were characterized by both culture-based methods and sequencing of a 350 bp fragment from 16S rRNA V3 region and a 800bp fragment from 18S rRNA ITS4 region. The results of the culture-based and molecular assay showed that the main causes of the yellow spots in the chicken sausage packaged under vacuum were Enterococcus faecium, Enterococcus faecalis, Streptococcus faecium and Candida saitoana. In addition, one species of Enterococcus and one species of Candida were also identified at the genus level. Examination of yellow spotted samples also showed that the microorganisms that cause yellow spotting cause changes in pH, color indices L*, a* and b*, and syneresis compared to the control sample but the rate of change is only in the syneresis quantity and a* was significant.

Immunoglobin Y (IgY) or egg yolk antibodies have captured attention as substitutes for antibiotics against the presence of disease-causing organisms (Thomsen et al., 2016; Li et al., 2015; Pereira et al., 2019). Compared to mammalian IgG, IgY has several advantages including high yield, cost-effectiveness, and convenience (Li et al., 2015). It has been reported that the use of IgY against Helicobacter pylori can be particularly useful for prevention and treatment of diseases (Najdi et al., 2016). The growth inhibitory effect of IgY antibody is one of its crucial features (Alfarouk et al., 2019), meaning that IgY antibody could be consumed daily with no health risks. Therefore, daily consumption of IgY requires a suitable host. The ice cream is the best choice for this proposed, because this product is maintained at -18 C and ice cream composition has positive effect on the function of IgY. Therefore, we develop a new product for the prevention and treatment of Helicobacter pylori.

The Mueller-Hinton media was used for H. pylori growth. Then, 109 colonies of bacterium were inactivated by formaldehyde methods. The 3 white leghorn chickens (Animal Science Department of Ferdowsi University of Mashhad) of 16 weeks old were immunized by H. pylori and Freund’s complete adjuvant with an equal volume. The reminder immunization was done two weeks later and using of Freund’s incomplete adjuvant for stage 2. One week after the chickens received their last injection, their eggs were collected on a daily basis for eight weeks, labeled and kept at 4 °C (Pauly et al., 2011). Extraction and purification of IgY antibody from egg yolk was done using polyethylene glycol 6000 (PEG 6000) powder (Merck, Germany) according to Polson’s method (Pauly et al., 2011). The IgY production wasverified by the SDS-PAGE and Bradford methods. The specific activity of IgY antibody against H. pylori was examined by ELISA. The absorbance of each well was measured at 492 nm (Nasiri et al., 2016). The egg yolk ice cream preparation contains IgY was prepared according to the method of Herald et al (2008). For estimation of IgY shelf life in ice cream, the residual activity of IgY after freezing was measured by ELISA. The Sensory evaluation of the egg yolk ice creams was conducted by 5-point hedonic scale through surveys to assess consumers’ level of acceptance.

The purification of IgY using the SDS-PAGE method was verified correctly and the size of heavy and light chains of IgY was estimated about 65 and 27 kDa. The IgY yield in samples was 11.46 mg/ml, therefore, the high purity and yield of IgY, it could be effectively used as an ideal antibody in the food industry. The purification of IgY from egg yolk by PEG method is remarkably cost effective. The ELISA assay indicated binding of IgY to H. pylori antigen that was fixed on plates. Also, the results revealed significant differences between the control and treatment groups (P-value <0.001). The shelf life of IgY in ice cream showed that this product could be most certainly used as bio-food. ELISA analysis confirmed that IgY could remain effective in ice cream for 3 months. The activity of IgY during this period decreased about 6%, which is insignificant. The sensory features of ice cream using hedonic scale revealed that this product could be suitable for marketing, as no significant difference was found between egg yolk and vanilla ice creams. Ice cream is considered as the best candidate for production of IgY bio-foods, as it possesses the features needed to protect IgY and to increase efficiency of IgY activity. The optimum temperature for protection of ice cream was -18 °C that is utterly suitable for IgY protection. Furthermore, ice cream is consumed while cold and studies showed that IgY can remain active at temperatures of up to 80 °C and pasteurization process had no effect on IgY activity (Horie et al., 2004). Jaradat et al (2000) reported that, IgY activity was inhibited in presence of carbohydrates (sucrose, lactose and trehalose). Therefore, here, we used freeze dried egg yolk to protect IgY. Consequently, ice-cream is an ideal candidate for transferring antibodies into human body, as the particular composition of ice cream can properly protect IgY antibodies.

This study was tested to evaluate the influences of different maize starches (native, modified with sonication, pre–gelenized, Heat Resistant) replacement in batter coating, based on factorial experiments in a completely randomized design to determine the best formulation of breadcrumbs. Samples were sonicated with 70 kHz for 5 minutes and a fryer equipped with a temperature controller (150, 190 and 170 degrees centigrade) and time (1, 3 and 5 minutes) was used for frying. Quality parameters (texture, Crust color values, oil absorption, sensory properties) of chicken nugget were measured during frying.Obtained result indicated that addition of ultrasound pretreatment batters and temperature influenced in texture hardness reduction of nuggets. Oil content of whole nuggets was found to decrease significantly (P< 0.05) with frying time and temperature. Chicken nuggets with native maize starch compared to control ones showed better scores for organoleptic properties. Color evaluation in samples containing native and sonication pretreatment showed significant (P< 0.05) reduction in a* and b* values at 3 minute frying, whereas L* values were significantly (P< 0.05) increased compared to control treatments at 170 and 190° c. Samples hardness was decreased due to frying temperature.