Studying the Effect of Adding Local Ginger as an Antimicrobial Growth in Frozen Chicken Meat
DOI:
https://doi.org/10.59992/IJSR.2023.v2n7p1Keywords:
Pathogenic Microbes, Ginger, Chicken MeatAbstract
This study aimed to identify the effect of adding local ginger powder at a rate of 5, 7 and 10% and fresh local ginger at a rate of 7% on the numbers of pathogenic microbial in chicken meat discs manufactured in a laboratory and preserved under freezing conditions -12 °C for 15, 30 and 60 days. The bacteriological analysis conducted on the chicken frozen tablets included the total number of bacteria, coliform bacteria, Psychrotrophic bacteria, Staphylococcus aureus bacteria and numbers of fungi and yeasts. The results of bacteriological analysis indicated a decrease in most types of the numbers of pathogenic microbes in chicken meat discs preserved under freezing conditions at -12°C when adding concentrations of 5, 7 and 10% of ginger powder and fresh ginger at a rate of 7%. Where the inhibitory effect was on the total numbers of bacteria, coliform bacteria Psychrotrophic bacteria and Staphylococcus aureus bacteria, the number of fungi and yeasts at a concentration of 5% of dry ginger powder during the 15day storage period where a decrease was observed from 6.166, 4.873, 4.477, 5.493 and 4.814 log10 cfu/g to 5.985, 3.982, 2.229, 4.926 and 4.642 log10 cfu/g respectively. The resulted showed an increase in the frozen storage period to 30 days the microbial content had a significant effect at a significant level of P < 0.05 as it was in the control treatment 5.655, 4.362, 5.638, 5.022 and 4.892 log10 cfu/g when adding dry ginger at a concentration of 5%, the numbers were 5.474, 3.741, 2.162, 4.527 and 5.031 log10 cfu/g respectively. It was observed that the total number of bacteria, coliform bacteria, Psychrotrophic bacteria, Staphylococcus aureus bacteria and numbers of fungi and yeasts increased in the control treatment at 60 day of frozen storage were 4.963, 4.537, 5.827, 4.676 and 4.472 log10 cfu/g, while when adding dry ginger at a concentration of 5%, inconstancy was seen in most of the pathogenic microbial numbers were 4.782, 3.692, 2.316, 3.746 and 4.738 log10 cfu/g respectively. The results also showed a decrease in most of the numbers of pathogenic bacteria by adding concentrations of 7 and 10% of dry ginger powder during 60 days on the total number of bacteria from 4.409 to 4.603log10 cfu/g and coliform bacteria from 3.978 to 3.833 log10cfu/g and Psychrotrophic bacteria from 2.116 to 1.151 log10cfu/g and Staphylococcus aureus bacteria from 4.424 and 3.967 log10 cfu/g and numbers of fungi and yeasts from 3.636 to 2.742 log10 cfu/g respectively. Also, the results showed that adding a concentration of 7% of fresh ginger during the storage period of 60 days had the highest inhibitory effect on the total numbers of bacteria, coliform bacteria Psychrotrophic bacteria and Staphylococcus aureus bacteria, the number of fungi and yeasts which recorded 4.084, 3.551, 1.962, 4.028 and 2.768 log10 cfu/g respectively compared to the control sample, which were 4.963, 4.537, 5.827, 4.472 and 4.676 log10 cfu/g respectively.
References
1- البكوش، العماري علي (2003). دراسة مسحية على الجودة الميكروبية لأقراص اللحم المفروم (الهمبرجر) داخل مدينة طرابلس وضواحيها. رسالة ماجستير. قسم علوم الأغذية، كلية الزراعة، جامعة طرابلس، طرابلس، ليبيا.
2- الراوي، خاشع محمود وخلف الله ؛ عبد العزيز محمد. 1980. تصميم وتحليل التجارب الزراعية. مطابع جامعة الموصل، الموصل، العراق.
3- التميمي، سالم صالح؛ أبو المعالي، رأفت أحمد (2011). تأثير الزنجبيل في أعداد الأحياء المجهرية وإطالة مدة الحفظ للبيركر المختبري المصنع من لحم البقر. المجلة العراقية لبحوث السوق وحماية المستهلك، جامعة بغداد، بغداد، العراق، المجلد 6،العدد 3.
4- جواد، رأفت عبد المحسن محمد (2011). دراسة التأثير التثبيطي للمستخلصات المائية والزيتية والكحولية لبذور نبات الحبة السوداء على انواع مختارة من البكتيريا المرضية. مجلة ابحاث البصرة (العلميات) ( 5(37): 2695-1817.
5- فاضل، مراتب عبد القادر؛ حميد، رفاه رزوق ؛ حميش، موسى جاسم (2017).التركيب الكيميائي والتغذوي لرايزومات الزنجبيلZingiber officinale L. . مجلة تكريت للعلوم الصرفة، المجلد 22، العدد 3.
6- منظمة الصحة العالمية، 2017 .مقاومة مضادات الميكروبات في إقليم شرق المتوسط، المكتب إلاقليمي لشرق المتوسط، القاهرة، مصر.
7- م. ق. خ. (2017). اللحوم المجهزة ـــــ لحم البرج المواصفة القياسية الخليجية رقم (948) هيئة التقييس لدول مجلس التعاون لدول الخليج العربية.
8- م. ق. ع. (2000). مسودة المواصفة القياسية العراقية رقم (3725) /4. الحدود الميكروبية في الأغذية – الجزء الرابع – الحدود الميكروبية للحوم ومنتجاتها. الجهاز المركزي لتقييس والسيطرة النوعية، العراق.
9- مصطفى، مصطفى رضوان (2007). الجودة المكروبيولوجية لأقراص لحم الدجاج المفروم(البيرجر) في نطاق مدينة طرابلس. رسالة ماجستير. قسم علوم وتقنية الأغذية، كلية الزراعة، جامعة طرابلس، ليبيا.
10- كريمة، فتحية عبد الرزاق (2014). استخدام الزنجبيل كمضاد طبيعي للنمو الميكروبي في أقراص اللحم المفروم المبردة. رسالة ماجستير، كلية الزراعة، جامعة طرابلس، طرابلس، ليبيا.
11- Andrew, W. C. (1992). Annual of food quality control, 4-Rev. 1-Microbiological Analysis, FAO, Food and Nutrition Paper, No. 1414 (Rev.1) . Rome, Italy.
12- An, K., Zhao, D., Wang, Z., Wu, J., Xu, Y., and Xiao, G. (2016). Comparison of different drying methods on Chinese ginger (Zingiber officinale Roscoe): Changes in volatiles, chemical profile, antioxidant properties, and microstructure. Food Chemistry, 197: 1292–1300.
13- Bauchat, L. R. and Cousin, M. A. (2001). Yeasts and molds. In: Compendium of methods for the microbiological examination of foods. Downes, F. P. ( Editor). 4th ed. PP. 209-213. American public health association. Washington. D. C, USA.
14- Daily, J. W., Zhang, X., Kim, D. S. and Park, S. (2015). Efficacy of Ginger for Alleviating the Symptoms of Primary Dysmenorrhea: A Systematic Review and Meta-analysis of Randomized Clinical Trials. Pain Medicine, 16(12):2243-55.
15- El-baroty, G. S., Abd El-Baky, H. H., Farag, R. S. and Saleh, M. A. (2010). Characterization of antioxidant and antimicrobial compound of cinnamon and ginger essential oils. African Journal of Biochemistry Research, 4(6) :167-174.
16- Eshamah, L. H., Naas, T. H., Garbaj, M. A., Azwai, S. M., Gammoudi, F.T., Barbieri, L. and Eldaghayes, I. M. (2020). Extant of pathogenic and spoilage microorganisms in whole muscle meat, meat products and seafood sold in libyan market. National library of medicine, 10(3) : 276-288.
17- Shrivastava, S. and Leelavathi, S. (2010). Preliminary Phytochemical Evaluation of Leaf Extracts of Catunaregum spinosa Thunb. International Journal of Pharmaceutical Sciences Review and Research, 3(2):114-118.
18- Supu, R. D., Diantini, A. and Levita, J. (2018). Red Ginger (Zingiber officinale var. rubrum): Its chemical constituents, pharmacological activities and safety. FitofarmakaJurnal Ilmiah Farmasi, 8 (1): 25-31.
19- Marwat, K. S., Shoaib, M., Khan, A. E., Rehman, F. H. and Ullah, H. (2015) Phytochemistry and bioactivities of Quranic plant, zanjabil-ginger (Zingiber officinale Roscoe): A review. American-Eurasian Journal of Agricultural and Environmental Sciences, 15(5):707-713.
20- Zick, S. M,, Djuric, Z., Ruffin, M. T., Litzinger, A. J, Normolle, D. P., Alrawi, S., Feng, M. R. and Brenner, D. E. (2008). Pharmacokinetics of 6-gingerol, 8-gingerol, 10-gingerol, and 6-shogaol and conjugate metabolites in healthy human subjects. Cancer Epidemiology, Biomarkers and Prevention,17:1930–1936.
21- Teleni, L., McCarthy, A. L., Vitetta, L., McKavanagh, D. and Thomson, D. (2013). "Ginger (Zingiber officinale) and chemotherapy-induced nausea and vomiting: a systematic literature review". Nutrition Review, 71(4):245–54.
22- A.O.A.C., (2005). Association of Official Analytical Chemists. Official Methods of Analysis. Microbiological Food Testing. Ch., 17. and Meat and Meat Products, Ch., 39., Washington. D. C, USA.
23- HPFB (2003). Health products and food branch Standards and guidelines for microbiological safety of food. Ottawa, Canada.
24- Nickerson, J. T., and Sinsky, A. T. (1977). Microbiology of food and food processing 3rd ed. Elsvir, New York, USA.
25- Zick, S. M,, Djuric, Z., Ruffin, M. T., Litzinger, A. J, Normolle, D. P., Alrawi, S., Feng, M. R. and Brenner, D. E. (2008). Pharmacokinetics of 6-gingerol, 8-gingerol, 10-gingerol, and 6-shogaol and conjugate metabolites in healthy human subjects. Cancer Epidemiology, Biomarkers and Prevention,17:1930–1936.
