جستجوی مقالات مرتبط با کلیدواژه « Tilapia » در نشریات گروه « پزشکی »
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Background
Tilapia Piscidin 4 (TP4) showed potential anti-tumor effects against various cancer cells. Lycosine-1 (LYC1), is another Antimicrobial Peptides (AMP) from spider venom with targeted penetration to cancer cells without any adverse effects on normal cells. The aim of this study was to produce a soluble recombinant fusion peptide in order to diminish the cytotoxicity of TP4 against normal cells.
MethodsIn order to express of TP4-LYC-1, TP4, and LYC1 in fusion to the inteins1/2 of pTWIN-1 vector, induction condition was optimized to earn soluble peptides. Autocleavage induction of inteins1/2 was performed based on IMPACT® manual and their effect on cell viability of HeLa and HUVEC cells was surveyed by MTT assay.
ResultsThe best condition for accessing the most soluble peptide in fusion to the inteins was approximately similar for all three peptides (0.1 mM of IPTG, at 22°C). After the induction of self-cleavage of inteins, a band in 3, 3, and 6 kDa was observed on tricine- SDS-PAGE. The IC50 values of TP4-LYC1 and TP4 against HeLa cells were calculated as 0.83, and 2.75 μM, respectively.
ConclusionIn the present study, a novel chimeric peptide, TP4-LYC1, was successfully produced. This fusion protein can act as a safe bio-molecule with potent cytotoxic effects against cancer cells, but the penetration ability and determination of cell death mechanism must be performed in order to have more precise view on the apoptosis induction of this recombinant peptide.
Keywords: Cell survival, HeLa cells, Inteins, Spider venoms, Tilapia} -
Background
Preserving the quality and safety of fish and its products is a critical concern for food industry. In the present study, the effect of green tea extract and olive leaves extract-based preservative coatings on chemical, microbial, and sensory quality of wild type Nile tilapia (Oreochromis niloticus) was determined during pre-freezing ice and subsequent frozen storage.
MethodsForty-eight ponds raised tilapia, freshly caught in April, 2021, which were divided into three groups: group CT with no coating, group GTE with green tea extract-based coating, and group OLE with olive leaves extract-based coating. Fish samples in all groups were kept in ice for five days (1±2 °C) and then subjected to freezing (-18±2 °C) for 105 days. Chemical (moisture, ash, protein, fat, Total Volatile Basic-Nitrogen (TVB-N), pH) and microbial (Aerobic Plate Count (APC), Total Coliform (TC), Faecal Coliform (FC), Escherichia coli) parameters as well as sensory attributes (appearance, odour, acceptability, flesh color, Total Quality Index (TQI)) of tilapia in all groups were analysed after five days of ice storage and 15, 45, 75, and 105 days of frozen storage.
ResultsAPC of tilapia treated with preservative coatings remained below the permissible limit (<5×105 Colony Forming Unit (CFU)/g) throughout the storage period. After five days, content of TVB-N in untreated samples of tilapia was 32.94±2.30 mg/100 g compared to 5.05±2.19 and 7.24±2.89 mg/100 g in tilapia treated with green tea and olive leaves extract-based coating, respectively. Fat content of untreated tilapia was significantly (p<0.05) reduced to 0.05±0.01% at the end of the study period from the the initial content of 0.24±0.04%. However, the tilapia treated with preservative coatings achieved significantly (p<0.05) lower scores of TQI compared with the untreated one owing to the coloration of fish with extract solution.
ConclusionGreen tea extract and olive leaves extract-based coatings can, therefore, be used to improve fish quality and safety during storage. However, there is a need to change consumer’s perception about the sensory attributes of fish.
Keywords: Edible Films, Tilapia, Food Safety, Quality Control, Plant Extracts} -
Background
Few studies have been published about the quality of freshwater fish in Algeria. This study determined the chemical composition and the fatty acid of six species of freshwater fish cultivated in the North region of Algeria (Nile tilapia, red tilapia, common carp, Algerian barb, crucian carp, and mirror carp) as well as the nutritional quality of the lipids in these freshwater fish species.
MethodsOne hundred and ten freshwater fish were randomly caught in the spring of 2021 from Achor Ali farm (Jijel), Beni-Haroun Dam (Mila), and EL-Agrem Dam (Jijel) from Algeria. Moisture, ash, protein, lipid, and fatty acids were measured according to standard laboratory procedures and protocols of previous studies. Statistical analysis was performed using ANOVA (XLSTAT 2014), and the pair wise comparison of the means was done by Tukeys test at the 5% significance level (p<0.05).
ResultsRegarding freshwater fish species, fatty acid profiles were discovered to have 38.94 to 57.75% Saturated Fatty Acids (SFAs), 29.35 to 46.63% Monounsaturated Fatty Acids (MUFAs), and 6.79 to 26.55% Polyunsaturated Fatty Acids (PUFAs). Common carp was a rich resource of Eicosapentaenoic Acid and Docosahexaenoic Acid (EPA+DHA) (5.38%); the highest concentration of ω-3 was recorded in crusian carp (10.63%); and Nile tilapia contained significant levels of ω-6 PUFA. Results demonstrated that the examined freshwater fish species appeared to have a good nutritional value and be a source of important fatty acids with positive effects on consumer health. On the other hand, results revealed low levels of PUFAs.
ConclusionThe examined freshwater fish species appeared to have a good nutritional value, but, it is important to provide diets rich in fatty acids, in particular PUFAs, to these freshwater fish to improve the nutritional quality of their lipids.
Keywords: Fatty Acids, Unsaturated, Tilapia, Docosahexaenoic Acid, Eicosapentaenoic Acid, Algeria} -
مقدمه
آبزیان به دلیل کالری و پروتیین بالا و همچنین وجود چربی غیراشباع امگا 3 از اهمیت بسزایی در سبد غذایی برخوردارند. در مراحل مختلف از زمان صید تا رسیدن به دست مصرف کننده، همواره ممکن است بسیاری از آبزیان از جمله ماهی به برخی از میکروارگانیسم های بیماری زا آلوده شوند و در نهایت مسمومیت شدید را برای افراد ایجاد نمایند. در پژوهش حاضر به بررسی ثبت و شناسایی ژن های توکسیک استافیلوکوکوس اوریوس جدا شده از ماهی تیلاپیا با تکنیک Multi plex PCR پرداخته شده است.
مواد و روش هاتعداد کل نمونه ها 42 عدد (21 عدد نمونه ماهی تازه و 21 عدد نمونه ماهی منجمد) مدنظر قرار گرفته شد. ابتدا پس از آماده سازی نمونه های مورد بررسی به ترتیب استافیلوکوکوس اوریوس جدا شد و به صورت کشت سطحی در محیط برد پارکر مورد بررسی قرار گرفت، سپس تست کوآگولاز انجام شد و در مرحله بعد با استخراج DNA ژن انتروتوکسیک شناسایی شد. در نهایت توالی یابی ژن به صورت اتوماتیک و دستگاهی انجام گرفت.
یافته هایافته های به دست آمده نشان داد، 9/92 درصد از کل نمونه های مورد بررسی (21 عدد ماهی تیلاپیا تازه و 18 عدد ماهی منجمد) فاقد باکتری استافیلوکوکوس اوریوس بودند و 1/7 درصد از کل نمونه ها آلوده به باکتری استافیلوکوکوس اوریوس شدند. نتایج بررسی تست کوآگولاز نیز نشان داد، هر سه نمونه ماهی منجمد مورد بررسی، کوآگولاز مثبت بودند. پس از بررسی ژن های تولید کننده انتروتوکسیک (SEA، SEB، SEC، SED، SEE و SEG) در بین سه نمونه منجمد آلوده به باکتری استافیلوکوکوس مشاهده شد که تنها در یک نمونه منجمد، ژن انتروتوکسیک SEA وجود داشت.
نتیجه گیرینتایج نشان داد با توجه به هزینه کم و زمان بسیار کوتاه تر مورد نیاز برای شناسایی ژن های استافیلوکوکوس اوریوس با روش Multiplex PCR، این روش ابزار قدرتمندی برای مطالعه ژنوتیپ های جدایه های استافیلوکوک می باشد. بنابراین با استفاده از این روش می توان به ارتقا سطح سلامت غذایی در جامعه به خوبی پرداخت.
کلید واژگان: استافیلوکوکوس اورئوس, ژن, ماهی تیلاپیا, Multiplex PCR}IntroductionAquatic animal products are considered very important food items in the food basket regarding their high calorie, protein, and omega-3 unsaturated fat. Many aquatic animals, including fish, may always be infected with pathogenic microorganisms at various stages, from hunting to purchasing. Eventually, these factors would cause severe poisoning in humans. The present study investigates the registration and identification of Staphylococcus aureus’s toxic genes isolated from tilapia using the Multiplex PCR technique.
Materials and MethodsThe sample size included 42 subjects (21 fresh fish samples and 21 frozen fish samples). First, after preparing the samples, Staphylococcus aureus was isolated and examined as surface culture in Baird-Parker medium. Next, a Coagulase test was performed, and the enterotoxin gene was identified by DNA extraction. Finally, gene sequencing was carried out automatically and systematically.
ResultsThe results suggested that 92.9% of the total samples (21 fresh tilapia and 18 frozen fish) had no Staphylococcus aureus, and 7.1% of the samples were infected with Staphylococcus aureus. The coagulase test results also suggested that all three frozen fish samples were coagulase positive. Examining enterotoxin-producing genes (SEA, SEB, SEC, SED, SEE, and SEG) among three frozen samples infected with Staphylococcus bacteria revealed SEA enterotoxin gene only in one frozen sample.
ConclusionThe results showed that due to the low cost and much shorter time required to identify toxic Staphylococcus aureus genes using Multiplex PCR, this method is highly effective in studying the genotypes of Staphylococcus isolates. Therefore, by using this method, one can improve the food health level in the society.
Keywords: Gene, Multiplex PCR, Staphylococcus aureus, Tilapia} -
The present study aimed to investigate the effects of freezing speed and time on the deterioration indices such as Total Volatile Basic Nitrogen (TVB-N), Peroxide Value (PV), Thiobarbituric acid value (TBA), and pH, as well as the histological changes. Eighty Nile tilapias (Oreochromis niloticus) with approximate weight of 700 ± 50 g were caught from the saline water fish in research centre of Yazd, Iran in 2012. Then, the fillets were harvested and exposed to slow and quick freezing at 0.2 cm/h speed in the freezer at -18 °C during 18 hours, and 0.8 cm/h speed at -30 °C for 25 minutes, respectively. Finally, the fillets were transferred to -18 °C freezer where they were kept for 180 days. Based on the results, the changes in TVB-N, PV, TBA, pH and histological changes were less dramatic in the samples treated by quick freezing, compared to the slow freezing samples (p≤0.5).
Keywords: Chemical Quality, Freezing, Histological Change, SEM, Tilapia} -
زمینه و هدف
کیفیت نامناسب آب و وجود آلاینده هایی همچون نیترات نقره در آب می تواند باعث ایجاد استرس در ماهیان شده و با کاهش عملکرد ایمنی ماهیان سبب به خطر افتادن سلامتی آنها گردد. هدف از انجام مطالعه حاضر تعیین تاثیر سطوح مختلف پربیوتیک قارچ صدفی (Pleurotus ostreatus) بر شاخص های ایمنی سرم ماهی تیلاپیا مواجهه شده با سم نیترات نقره بود.
روش هاتعداد 120 بچه ماهی تیلاپیا به مدت 42 روز در 4 گروه آزمایشی (هر گروه: 10عدد ماهی) با 3 تکرار شامل تیمار 1) شاهد، فاقد پربیوتیک قارچ صدفی، تیمار 2) غذای حاوی 0/05، تیمار 3) غذای حاوی 0/1 و تیمار 4) غذای حاوی 0/2 درصد پربیوتیک قارچ صدفی تقسیم شدند. به هر کدام از گروه ها غلظت 0/5ppm سم نیترات نقره به مدت 16 روز اضافه گردید. در پایان شاخص های بیوشیمیایی ماهیان در سرم سنجش شد.
یافته هاشاخص های بیوشیمیایی سرم در گروه های تغذیه شده با قارچ صدفی (0/05، 0/1 و 0/2 درصد پربیوتیک قارچ صدفی) که در معرض سم نیترات نقره بودند، با گروه شاهد اختلاف معنی داری داشتند (0.05>P). استفاده از قارچ صدفی اثر مثبتی بر شاخص های بیوشیمیایی سرم داشت و در میان این شاخص ها؛ بر سطح آنزیم AST، آلبومین، گلوکز و پروتئین کل اثرات بهتری را نشان داد.
نتیجه گیریاین مطالعه نشان داد که سطح 0/2 درصد پربیوتیک قارچ صدفی، می تواند تا حدی اثر سم نیترات نقره را در ماهی تیلاپیا خنثی کند.
کلید واژگان: پربیوتیک, نیترات نقره, ماهی تیلاپیا, قارچ صدفی}Background and AimInadequate quality of water and the presence of contaminants such as silver nitrate in water can cause stress in fish and endanger their life by reducing the immune system function. The aim of this study was to determine the effect of different prebiotic levels of oyster mushroom (Pleurotus ostreatus) on some immune parameters of tilapia serum exposed to silver nitrate toxin.
Methods120 tilapia were treated for 42 days in 4 groups with 3 replications (n=10). These groups were 1) control, no oyster mushroom prebiotics, 2) food containing 0.05%, 3) food containing 0.1% and 4) food containing 0.2% prebiotic oyster mushrooms. Silver nitrate toxin with a concentration of 0.5 ppm was added to each group for 16 days. Finally, the biochemical parameters of fish in serum were measured.
ResultsSerum biochemical parameters in the control group were significantly different from the groups fed with oyster mushrooms (0.05, 0.1 and 0.2% oyster mushroom prebiotics) that were exposed to silver nitrate toxin (P<0.05). The use of oyster mushrooms prebiotics had a positive effect on serum biochemical parameters; more effects were observed on AST, albumin, glucose and total protein levels.
ConclusionThis study showed that the level of 0.2% prebiotic oyster mushroom can partially neutralize the effect of silver nitrate toxin in tilapia.
Keywords: Prebiotic, Silver nitrate, Tilapia, Pleurotus ostreatas} -
مقدمهژلاتین از کلاژن پوست و استخوان جانوران بدست می آید و درصنایع غذایی، داروسازی، لوازم آرایشی و بهداشتی به طور وسیع مورد استفاده قرار می گیرد. با توجه به اهمیت حلال بودن ژلاتین مصرف شده در این محصولات، تولید و عرضه ژلاتین حلال از نظر تجارت جهانی حایز اهمیت است. امروزه حلیت محصولات ژلاتینی تنها از نظر منشا خوک یا گاو کنترل می شود، ولی در مواردی که منشا کپسول یا مکمل ها از ژلاتین ماهی و آبزی باشد، تشخیص آن ها صورت نمی گیرد.روش کاربا استفاده از بانک های اطلاعاتی و مطالعات بیوانفورماتیکی، پرایمرهای اختصاصی برای تیلاپیا، سالمون، کوسه و میگو طراحی شدند. سپس بهینه سازی روش PCR انجام شد. نهایتا DNA استخراج شده از کپسول ها، کلاژن و مکمل ها با پرایمرهای اختصاصی هرگونه تکثیر و بر روی ژل آگارز رویت شد.یافته هاواکنش PCR با پرایمرهای اختصاصی تیلاپیا، سالمون، کوسه و میگو به ترتیب باندهای 113، 122، 200 و 132 جفت بازی را روی ژل آگارز نشان داد. اختصاصیت، پایداری و تکرارپذیری روش برای هر جفت پرایمر تایید شد. سپس PCR با DNA- های استخراج شده از کپسول های ژلاتینی و کلاژن نیز منشا آبزیان را تایید کرد.نتیجهدر این مطالعه برای اولین بار شناسایی منشا کلاژن و کپسول های ژلاتینی با استفاده از پرایمرهای اختصاصی تیلاپیا، سالمون، کوسه و میگو با روش PCR صورت گرفت. نتایج نشان داد پرایمرهای اختصاصی قادر به تکثیر باند مورد انتظار و شناسایی منشا می باشند. لذا با این روش می توان در مدت زمان کوتاهی حلیت موارد مذکور را قبل از ورود به کشور بررسی، تایید یا رد کرد.کلید واژگان: کپسول های ژلاتینی, تیلاپیا, سالمون, کوسه, میگو, روش PCR}IntroductionGelatin is made from the collagen of the skin and bones of animals and is widely used in food, pharmaceutical, cosmetics. Given the importance of the halal status of gelatin used in these products, the production and supply of halal gelatin are important in terms of global trade. Today, the solubility of gelatinous products is controlled for the origin of pigs or cattle, but in cases where the capsules or supplements are from fish and aquatic gelatin, they are not detected.MethodsSpecific primers for tilapia, salmon, sharks and shrimp were designed using databases and Bioinformatics studies. Then the PCR method was optimized. Finally, the DNA extracted from the capsules, collagen and supplements were amplified with specific primers and displayed on agarose gel.ResultsPCR reaction with specific primers of tilapia, salmon, shark and shrimp showed 113, 122, 200 and 132 bp bands on agarose gel, respectively. The specificity, stability and repeatability of the method were confirmed for each pair of primers. PCR with DNA extracted from gelatin and collagen capsules also confirmed the origin of aquatic animals.ConclusionIn this study, for the first time, the origin of collagen and gelatin capsules were identified using specific primers of tilapia, salmon, shark and shrimp and PCR. The results showed that specific primers are able to amplify the expected band and identify the source. Therefore, with this method, the solubility of the mentioned cases can be checked, approved or rejected in a short period of time before entering the country.Keywords: Gelatin capsules, Tilapia, Salmon, Shark, Shrimp, PCR method}
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This study was conducted to determine the residues of mercury (Hg), lead (Pb), copper (Cu) and cadmium (Cd) in the imported tilapia fillets. Thirty random samples from imported tilapia fillets were collected from different markets in Isfahan City, central Iran. They were analyzed using Graphite Furnace Atomic Absorption Spectrometer (Perkin Elmer 800) for Pb, Cu, Cd and flow injection mercury system (Perkin Elmer 400) for Hg. Out of the 30 tested samples, concentration of Hg, Pb, Cu and Cd in the tilapia fillets samples as mean± standard deviation were 0.083±.016, 0.638±0.067, 0.521± 0.081 and 0.136 ± 0.025 mg/kg, respectively. Among these, amounts obtained for all metals except for lead were lower than the permissible level specified by WHO (PKeywords: Heavy metals, Seafood safety, Tilapia}
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BackgroundThe current study tried to investigate the antioxidant and anti-bacterial effects of green tea and grape seed extract (with a volume of 2%) on durability of Tilapia packed in polyethylene bags, which were kept in cool temperature of 4±1 °C.MethodsPrepared fish were divided into 3 batches: 2 batches were treated by dipping for 30 min in ethanolic of green tea extract (2% v/v) and grape seed (2% v/v), respectively, while the third batch was dipped in distilled water as a control sample. The control and treated fish samples were analyzed for microbiological such as total volatile count and psychrotrophic count, and chemical such as thiobarbituric acid (TBA), and free fatty acid (FFA) values. The sensory characteristic was over a period of 20 days.ResultsThe results indicated that the two extract's treatments delayed significantly (pConclusionthe present study showed that the grape seed extract and green tea were very effective in extending the shelf life of Tilapia during refrigerated storage.Keywords: Tilapia, Grape seed, Green tea}
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مقدمهگیاهان دارویی به سبب دارا بودن ترکیبات آنتی باکتریایی طبیعی بسیار موردتوجه هستند و ایران نیز یکی از غنی ترین منابع گیاهان دارویی به شمارمی رود. هدف از این پژوهش، بررسی تاثیر آنتی باکتریایی عصاره هسته انگور برافزایش عمر ماندگاری ماهی تیلاپیا است.روش بررسیماهی ها بلافاصله پس از صید و عمل شستشو به دو بخش تقسیم شدند. یک گروه در عصاره هسته انگور (غلظت5/1%)به مدت 30 دقیقه غوطه ور و سپس در کیسه های پلی اتیلن بسته بندی گردیدند، دومین گروه نمونه ها نیز به عنوان شاهد بسته بندی و همه در دمای (1±4) درجه سانتی گراد یخچال نگهداری شدند. آزمایش های میکروبی شامل، شمارش کلی میکروب های هوازی مزوفیل (Totalcount)، باکتری های سرما گرا (PTC)، به همراه ارزیابی حسی در یک دوره 20 روزه در فواصل زمانی(2،0 ،5 ،10، 20،15)انجام شد.یافته هابر اساس نتایج حاصل، گروه حاوی عصاره به طور معنی داری (05/0P<) فساد میکروبی را نسبت به نمونه شاهد به تعویق انداخت، بطوریکه تعداد باکتری های شمارش شده در ماهی های تیمار شده با عصاره هسته انگور تا پایان دوره نگهداری کمتر از حد قابل قبول پیشنهادی (log cfu/g 7)باقی ماند.همچنین در بررسی حسی ماهیان تیمار شده با عصاره هسته انگور بالاترین کیفیت را در طول دوره نگهداری از خود نشان دادند.نتیجه گیریماهی تیمارشده با عصاره هسته انگور در این مطالعه تا انتهای دوره نگهداری قابل مصرف بود، به طوری که عصاره توانست عمر ماندگاری نمونه ها را نسبت به نمونه شاهد افزایش دهند.کلید واژگان: تیلا پیا, هسته انگور, آنتی باکتریال}Tolooe Behdasht, Volume:15 Issue: 1, 2016, PP 118 -126IntroductionMedicinal plants are highly taken into consideration due to having natural antimicrobial compounds which Iran can be introduced as one of the richest sources of medicinal plants. Hence, the purpose of this study was to determine the antibacterial activities of grape seed extract on shelf life of tilapia.MethodsThe prepared fish were divided into 2 groups: the first group was treated by dipping for 30 min in grape seed extract (1.5%v/v), and the second group was dipped in distilled water as the control sample. The control and treated fish samples were analyzed for microbiological (total count of mesophilic aerobic micro organisms, PTC) and sensory characteristictis over a perid of 20 days.ResultsThe study results indicated the extract treatment group significantly delayed (pConclusionsThe present study findings revealed that grape seed extract seemed to be extremely effective in extending the shelf life of tilapia fish fillet during the refrigerated storage.Keywords: Antibacterial, Grape seed, Tilapia}
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