[Home ] [Archive]   [ فارسی ]  
:: Main :: About :: Current Issue :: Archive :: Search :: Submit :: Contact ::
Main Menu
Home::
Journal Information::
Articles archive::
For Authors::
For Reviewers::
Registration::
Contact us::
Site Facilities::
::
Search in website

Advanced Search
..
Receive site information
Enter your Email in the following box to receive the site news and information.
..
Indexing




..
:: Volume 1, Issue 3 (10-2025) ::
Journalaer 2025, 1(3): 75-86 Back to browse issues page
Comparative effect of butyric acid alone and with endogenous quorum quencher bacteria on biochemical parameters of Acanthopagrus arabicus
Simak Salehipour Bavarsad * , Takavar Mohammadian , Preeta Kochanian , Vahid Yavari , Mansour Torfi mozan zadeh
Abstract:   (1077 Views)
Introduction: Considering the significance of Acanthopagrus arabicus in Iran, characterized by its carnivorous nature and robust digestive system adapted for high-protein diets, there culture a necessity for the use of dietary supplements such as acidifier probiotics. This study was undertaken to investigate the impact of administering quorum quencher probiotics independently and in conjunction with the acidifier butyric acid on the alterations in biochemical parameters in A. arabicus.
Materials & Methods: A total of 360 fish fry, with an average weight of 15±3.2 gr, were randomly assigned to eight experimental treatments, each repeated three times. Over a period of 60 days, all fish groups were fed with the experimental diet. The treatments included: 1. Treatment A: Food with 0.5% butyric acid per Kg. 2. Treatment B: Bacillus cereus with quorum quenching properties (cfu g-1 108) per kg of ration. 3. Treatment C: B. thuringiensis with quorum quenching properties (108 cfu g-1) per Kg of diet (B). 4. Treatment D: B. cereus and B. thuringiensis with quorum quenching properties (108 cfu g-1) per Kg of diet (C). 5. Treatment E: B. cereus with quorum quenching property (108 cfu g-1) along with 0.5% butyric acid per Kg of food. 6. Treatment F: B. thuringiensis with quorum quenching properties (108 cfu g-1) along with 0.5% butyric acid per Kg of food. 7. Treatment G: B. cereus and B. thuringiensis with quorum quenching properties (108 cfu g-1) along with 0.5% butyric acid per Kg of food. 8. Control Treatment H: Food without acidifying probiotics. The control group received daily commercial food with 42% protein, including 100% fish meal.
Results: The consumption of diets containing a combination of B1 and B2 probiotics with butyric acid (Treatment G) and the group fed with the combination of probiotic B1 with butyric acid (Treatment F) resulted in a significant increase in glucose, triglyceride, cholesterol, and creatine phosphokinase in fish serum. Additionally, protein levels in fish serum increased, particularly in treatments containing Bacillus B1, Bacillus B2, and butyric acid alone, and the combination of both probiotics (Treatment D) compared to the control group. A substantial increase in albumin was observed in groups containing the combination of B1 and B2 bacilli along with butyric acid (Treatment D) and groups B and E. Moreover, the calcium content in the blood serum of fish fed with probiotic compound B2 (Treatment C) was higher than other treatments, especially the control group (H).
Conclusion: In summary, the combination of probiotics with butyric acid, along with the combination of B1 and B2 probiotics, has led to significant improvements in glucose, protein, albumin, cholesterol, triglyceride, calcium, and creatine phosphokinase enzyme activity.
Keywords: Probiotics, Quorum quencher bacteria, Butyric acid, Acanthopagrus arabicus, Biochemical parameters
Full-Text [PDF 1053 kb]   (411 Downloads)    
Type of Study: Research | Subject: Special
Received: 2025/09/6 | Accepted: 2025/10/2 | Published: 2025/10/2
References
1. 1. Mohammadian, T., Momeni, H., Mesbah, M., Tabandeh, M.R. and Khosravi, M., 2020. Effect of different levels of dietary acidifier “sodium diformate” on the innate immune system and expression of growth and immunological related genes in Salmo trutta caspius. Aquaculture Nutrition. 26(6): 2074-2085.‌ https://doi.org/ 10.1111/anu.13148
2. 2. Hosseini, S.A., Alishahi, M., Rastiannasab, A., Salahi Ardakani, M.M. and Mohammadpour, M., 2023. The effect of bivalent vaccine, streptococcus/yersinios on some of the blood and Immunologic factors in rainbow trout, Oncorhynchus mykiss. Journal of Animal Environment. 15(1): 213-220.‌ (In Persian) doi: 10. 22034/AEJ.2021.268851.2451
3. 3. Alishahi, M., Gholami, S. and Feli, F., 2021. Antiparasitic effects of Lawsonia inermis, Satureja khuzestanica and Citrullus colocynthis on fish parasite: Ichthyophthirius multifiliis. Journal of Animal Environment. 13(4): 185-192.‌ (In Persian) doi: 10.22034/ AEJ.2021.261673.2427
4. 4. Aalamifar, H., 2020. Dietary butyric acid improved growth, digestive enzyme activities and humoral immune parameters in Barramundi (Lates calcarifer). Aquaculture Nutrition. 26(1): 156-164.‌ https://doi.org/10.1111/anu. 12977
5. 5. Ahire, J.J., Mokashe, N.U. and Chaudhari, B.L., 2019. Effect of dietary probiotic Lactobacillus helveticus on growth performance, antioxidant levels, and absorption of essential trace elements in goldfish (Carassius auratus). Probiotics and antimicrobial proteins. 11(2): 559-568. doi: 10.1007/s12602.018.9428.5
6. 6. Ahmadifar, E., Moghadam, M.S., Dawood, M.A. and Hoseinifar, S.H., 2019. Lactobacillus fermentum and/or ferulic acid improved the immune responses, antioxidative defence and resistance against Aeromonas hydrophila in common carp (Cyprinus carpio) fingerlings. Fish & shellfish immunology. 94: 916-923.‌ doi: 10.1016/j.fsi.2019.10.019
7. 7. Al‐Dohail, M.A., Hashim, R. and Aliyu‐Paiko, M., 2011. Evaluating the use of Lactobacillus acidophilus as a biocontrol agent against common pathogenic bacteria and the effects on the haematology parameters and histopathology in African catfish Clarias gariepinus juveniles. Aquaculture Research. 42(2): 196-209. https:// doi.org/10.1111/j.1365-2109.2010.02606.x
8. 8. Ansari, R., Gul, B., Khan, D.J. and Weber, M.A., 2007. Potential of halophytes as source of edible oil. Journal of Environment Environments. 68(2): 315-321.‌ (In Persian)
9. 9. Barton, B.A., Schreck, C.B. and Barton, L.D., 1987. Effects of chronic cortisol administration and daily acute stress on growth, physiological conditions, and stress responses in juvenile rainbow trout. Diseases of aquatic organisms. 2(3): 173-185.
10. 10. Bhatt, S., Gething, P.W., Brady, O.J., Messina, J.P., Farlow, A.W., Moyes, C.L. and Hay, S.I., 2013. The global distribution and burden of dengue. Nature. 496(7446): 504-507. doi: 10.1038/nature12060
11. 11. Banaee, M., Mehrpak, M., Hagi, B.B.N. and Noori, A., 2015. Amelioration of cadmium-induced changes in biochemical parameters of the muscle of Common Carp (Cyprinus carpio) by Vitamin C and Chitosan. International Journal of Aquatic Biology. 3(6): 362-371.
12. 12. Boopathi, S., 2017. Stigmatellin Y-An anti-biofilm compound from Bacillus subtilis BR4 possibly interferes in PQS-PqsR mediated quorum sensing system in Pseudomonas aeruginosa. Bioorganic & medicinal chemistry letters. 27(10): 2113-2118.‌ doi: 10.1016/j. bmcl.2017.03.074
13. 13. Carmichael, G.J., Wedemeyer, G.A., McCraren, J.P. and Millard, J.L., 1983. Physiological effects of handling and hauling stress on smallmouth bass. The Progressive Fish-Culturist. 45(2): 110-113. https://doi. org /10.1577/1548-8659
14. 14. Cheng, P., Ji, B., Gao, L., Zhang, W., Wang, J. and Liu, T., 2013. The growth, lipid and hydrocarbon production of Botryococcus braunii with attached cultivation. Bioresource technology. 138: 95-100.‌ doi: 10.1016/j.biortech.2013.03.150
15. 15. Chu, W., Liu, Y., Hu, Y., Zhang, J., Zhong, L. and Chi, S., 2020. Sodium butyrate supplementation in high soybean meal diets for juvenile rice field eel (Monopterus albus): Effects on growth, immune response and intestinal health. Aquaculture. 88: 65-75.‌ doi: 10.1016/j.fsi.2019.02.064
16. 16. Costas, B., Aragão, C., Dias, J., Afonso, A. and Conceição, L.E., 2013. Interactive effects of a high quality protein diet and high stocking density on the stress response and some innate immune parameters of Senegalese sole Solea senegalensis. Fish Physiology and Biochemistry. 39(5): 1141-1151.‌ doi: 10.1007/s10695-0 13-9770-1
17. 17. Dai, J., Li, Y., Yang, P., Liu, Y., Chen, Z., Ou, W. and Mai, K., 2018. Citric acid as a functional supplement in diets for juvenile turbot, Scophthalmus maximus L.: Effects on phosphorus discharge, growth performance, and intestinal health. Aquaculture. 495: 643-653.‌ https:// doi.org/10.1016/j.aquaculture.2018.04.004
18. 18. Das, A., Paul, T., Ghosh, P., Halder, S.K., Das Mohapatra, P.K., Pati, B.R. and Mondal, K.C., 2015. Kinetic study of a glucose tolerant β-glucosidase from Aspergillus fumigatus ABK9 entrapped into alginate beads. Waste and Biomass Valorization. 6: 53-61.‌ doi: 10.1007/s12649-014-9329-0
19. 19. Defoirdt, T., Boon, N., Bossier, P. and Verstraete, W., 2004. Disruption of bacterial quorum sensing: an unexplored strategy to fight infections in aquaculture. Aquaculture. 240(1-4): 69-88. doi: 10.1016/j. aquaculture.2004.06.031
20. 20. Defoirdt, T., Boon, N., Sorgeloos, P., Verstraete, W. and Bossier, P., 2007. Alternatives to antibiotics to control bacterial infections: luminescent vibriosis in aquaculture as an example. Trends in biotechnology. 25(10): 472-479.‌ doi: 10.1016/j.tibtech.2007.08.001
21. 21. Defoirdt, T., Boon, N., Sorgeloos, P., Verstraete, W. and Bossier, P., 2008. Quorum sensing and quorum quenching in Vibrio harveyi: lessons learned from in vivo work. The ISME journal. 2(1): 19-26.‌ doi: 10.1038/ ismej.2007.92
22. 22. De las Heras, V., Martos-Sitcha, J.A., Yúfera, M., Mancera, J.M. and Martínez-Rodríguez, G., 2015. Influence of stocking density on growth, metabolism and stress of thick-lipped grey mullet (Chelon labrosus) juveniles. Aquaculture. 448: 29-37. doi: 10.1016/j. aquaculture.2015.05.033
23. 23. Di Cagno, R., De Angelis, M., Limitone, A., Minervini, F., Carnevali, P., Corsetti, A. and Gobbetti, M., 2006. Glucan and fructan production by sourdough Weissella cibaria and Lactobacillus plantarum. Journal of Agricultural and Food Chemistry. 54(26): 9873-9881. doi: 10.1021/jf061393‌
24. 24. Djoussé, L., Rothman, K.J., Cupples, L.A., Levy, D. and Ellison, R.C., 2003. Effect of serum albumin and bilirubin on the risk of myocardial infarction (the Framingham Offspring Study). American Journal of Cardiology. 91(4): 485-488. doi: 10.1016/s0002-9149 (02)03256-3
25. 25. Edwards 3rd, H.M., Fernandez, S.R. and Baker, D.H., 1999. Maintenance lysine requirement and efficiency of using lysine for accretion of whole-body lysine and protein in young chicks. Poultry Science. 78(10): 1412-1417.‌ doi: 10.1093/ps/78.10.1412
26. 26. El-Fattah, A., El-Sanhoury, S.A., El-Mednay, M.H. and Abdel-Azeem, N.M., 2008). Thyroid activity, some blood constituents, organs morphology and performance of broiler chicks fed supplemental organic acids. Int. J. Poult. Sci. 7(3): 215-222.‌ doi: 10.3923/ijps.2008.215.222
27. 27. Boyd, C.E., Aaron, A., McNevin, K. and Robert, P.D., 2022. The contribution of fisheries and aquaculture to the global protein supply. Food security. 14(3): 805-827.‌ doi: 10.1007/s12571-021-01246-9
28. 28. ‌Tacon, A.G.J., 2006. Use of fishery resources as feed inputs to aquaculture development: trends and policy implications. No. 1018. Rome: Food and Agriculture Organization of the United Nations.
29. 29. Falcinelli, S., Rodiles, A., Hatef, A., Picchietti, S., Cossignani, L., Merrifield, D.L. and Carnevali, O., 2018. Influence of probiotics administration on gut microbiota core: a review on the effects on appetite control, glucose, and lipid metabolism. Journal of Clinical Gastroenterology. 52: S50-S56.‌‌ doi: 10.1097/ MCG.0000000000001064
30. 30. Fayolle, F., Rémy, M. and Ballerini, D., 1990. Effect of controlled substrate feeding on butyric acid production by Clostridium tyrobutyricum. Journal of industrial microbiology. 6: 179-183. doi: 10.1007/BF01577693
31. 31. Fu, F., Sun, F., Lu, X., Song, T., Ding, J., Gao, R. and Pei, C., 2019. A novel potential biomarker on Y263 site in human serum albumin poisoned by six nerve agents. Journal of Chromatography B. 1104: 168-175.‌ doi: 10.1016/j.jchromb.2018.11.011
32. 32. Ghose, C., Kalsy, A., Sheikh, A., Rollenhagen, J., John, M., Young, J. and Ryan, E.T., 2007. Transcutaneous immunization with Clostridium difficile toxoid A induces systemic and mucosal immune responses and toxin A-neutralizing antibodies in mice. Infection and immunity. 75(6): 2826-2832.‌ doi: 10.1128/IAI.00127-07
33. 33. Hassaan, M.S., Mohammady, E.Y., Adnan, A.M., Abd Elnabi, H.E., Ayman, M.F., Soltan, M.A. and El-Haroun, E.R., 2020. Effect of dietary protease at different levels of malic acid on growth, digestive enzymes and haemato-immunological responses of Nile tilapia, fed fish meal free diets. Aquaculture. 522: 735124.‌ https://doi.org/10.1016/j.aquaculture.2020.735 124
34. 34. Hossain, M.S., Koshio, S., Ishikawa, M., Yokoyama, S., Sony, N.M., Dawood, M.A. and Fujieda, T., 2016. Efficacy of nucleotide related products on growth, blood chemistry, oxidative stress and growth factor gene expression of juvenile red sea bream, Pagrus major. Aquaculture. 464(3): 8-16. doi: 10.1016/j.aquaculture. 2016.06.004
35. 35. ‌Hoseinifar, S.H., Mirvaghefi, A., Merrifield, D.L., Amiri, B.M., Yelghi, S. and Bastami, K.D., 2011. The study of some haematological and serum biochemical parameters of juvenile beluga (Huso huso) fed oligofructose. Fish physiology and biochemistry. 37(1): 91-96. doi: 10. 1007/s10695-010-9420-9
36. 36. Jeon, S.M., Bok, S.H., Jang, M.K., Kim, Y.H., Nam, K.T., Jeong, T.S. and Choi, M.S., 2002. Comparison of antioxidant effects of naringin and probucol in cholesterol-fed rabbits. Clinica Chimica Acta. 317(1-2): 181-190.‌ doi: 10.1016/s0009-8981(01)00778-1
37. 37. Kavitha, P. and Rao, J.V., 2008. Toxic effects of chlorpyrifos on antioxidant enzymes and target enzyme acetylcholinesterase interaction in mosquito fish, Gambusia affinis. Environmental toxicology and pharmacology. 26(2): 192-198.‌ doi: 10.1016/j.etap.2008. 03.010
38. 38. Keck, R., Nayak, N., Lerner, L., Raju, S., Ma, S., Schreitmueller, T. and Jones, A., 2008. Characterization of a complex glycoprotein whose variable metabolic clearance in humans is dependent on terminal N-acetylglucosamine content. Biologicals. 36(1): 49-60. doi: 10.1016/j.biologicals.2007.05.004
39. 39. Khosravi, M., Sotoudeh, G., Amini, M., Raisi, F., Mansoori, A. and Hosseinzadeh, M., 2020. The relationship between dietary patterns and depression mediated by serum levels of Folate and vitamin B12. BMC psychiatry. 20: 1-8.‌ doi: 10.1186/s12888-02 0-2455-2
40. 40. Krasňan, V., Stloukal, R., Rosenberg, M. and Rebroš, M., 2016. Immobilization of cells and enzymes to LentiKats®. Applied microbiology and biotechnology. 100(6): 2535-2553. doi: 10.1007/s00253-016-7283-4
41. 41. Knudsen, K.E.B., Serena, A., Canibe, N. and Juntunen, K.S., 2003. New insight into butyrate metabolism. Proceedings of the Nutrition Society. 62(1): 81-86.‌ doi: 10.1079/PNS2002212
42. 42. Krome, C., Schuele, F., Jauncey, K. and Focken, U., 2018. Influence of a sodium formate/formic acid mixture on growth of juvenile common carp (Cyprinus carpio) fed different fishmeal replacement levels of detoxified Jatropha curcas kernel meal in practical, mixed diets. Journal of Applied Aquaculture. 30(2): 137-156. doi: 10.1080/10454438.2017.1412845‌
43. 43. Liu, X., Zhu, Y. and Yang, S.T., 2006. Butyric acid and hydrogen production by Clostridium tyrobutyricum ATCC 25755 and mutants. Enzyme and Microbial Technology. 38(3-4): 521-528. doi: 10.1016/j.enzmictec. 2005.07.008
44. 44. Liu, C.L., Wang, Y.J., Zeng, R.C., Zhang, X.M., Huang, W.J. and Chu, P.K., 2010. In vitro corrosion degradation behaviour of Mg-Ca alloy in the presence of albumin. Corrosion Science. 52(10): 3341-3347.‌ doi: 10. 1016/j.corsci.2010.06.003
45. 45. Liu, J., Yang, T., Wang, D.W., Lu, G.Q., Zhao, D. and Qiao, S.Z., 2013. A facile soft-template synthesis of mesoporous polymeric and carbonaceous nanospheres. Nature communications. 4(1): 2798.‌ doi: 10.1038/ncomms 3798
46. 46. Mohammadian, T., Monjezi, N., Peyghan, R. and Mohammadian, B., 2022. Effects of dietary probiotic supplements on growth, digestive enzymes activity, intestinal histomorphology and innate immunity of common carp (Cyprinus carpio): a field study. Aquaculture. 549(4): 737787. doi: 10.1016/j. aquaculture. 2021.737787
47. 47. Mohammadian, T., Ghanei-Motlagh, R., Jalali, M., Nasirpour, M., Mohtashamipour, H., Osroush, E. and Nejad, A.J., Accepted Author Version of the Manuscript: Protective effects of non-encapsulated and microencapsulated Lactobacillus delbrueckii subsp. bulgaricus in rainbow trout (Oncorhynchus mykiss) exposed to lead (Pb) via diet.‌ Probiotics Antimicrob Proteins. 12(2): 375-388. doi: 10.1007/s12602-019-09 544-7
48. 48. Morohoshi, T., Ebata, A., Nakazawa, S., Kato, N. and Ikeda, T., 2005. N-acyl homoserine lactone-producing or-degrading bacteria isolated from the intestinal microbial flora of ayu fish (Plecoglossus altivelis). Microbes and environments. 20(4): 264-268. doi: 10. 1264/ jsme2.20.264
49. 49. Navidmehr, J., Zibaei, S., Salehmoghadam, M. and Fahimi Moghaddam, F., 2011. Study on possibility of using dry milk as cholesterol source instead of horse serum for cultivation of Ureaplasma urealyticum. Iranian Journal of Medical Microbiology. 4(4): 21-29.‌ (In Persian)
50. 50. Ni, J., Wang, G., Yang, J., Gao, D., Chen, J., Gao, L. and Li, Y., 2014. Carbon nanotube-wired and oxygen deficient MoO3 nanobelts with enhanced lithium-storage capability. Journal of Power Sources. 247: 90-94. https:// doi.org/10.1016/j.jpowsour.2013.08.068
51. 51. Ooi, L.G. and Liong, M.T., 2010. Cholesterol-lowering effects of probiotics and prebiotics: a review of in vivo and in vitro findings. International journal of molecular sciences. 11(6): 2499-2522. doi: 10.3390/ijms11062499
52. 52. Partanen, K.H. and Zdzislaw, M., 1999. Organic acids for performance enhancement in pig diets. Nutrition research reviews. 12(1): 117-145.‌ doi: 10.1079/0954422 99108728884
53. 53. Prabu, D.L., Sahu, N.P., Pal, A.K., Dasgupta, S. and Narendra, A., 2016. Immunomodulation and interferon gamma gene expression in sutchi cat fish, Pangasianodon hypophthalmus: effect of dietary fucoidan rich seaweed extract (FRSE) on pre and post challenge period. Aquaculture research. 47(1): 199-218. doi: 10.1111/are.12482
54. 54. Reyshari, A., 2019. Effects of sodium diformate on growth performance, gut microflora, digestive enzymes and innate immunological parameters of Asian sea bass (Lates calcarifer) juveniles. Aquaculture Nutrition. 25(5): 1135-1144. doi: 10.1111/anu.12929
55. 55. ‌Ringø, E., Hoseinifar, S.H., Ghosh, K., Doan, H.V., Beck, B.R. and Song, S.K., 2018. Lactic acid bacteria in finfish-An update. Frontiers in microbiology. 9: 1818.‌ doi: 10.3389/fmicb.2018.01818
56. 56. Saei, M.M., Beiranvand, K., Taee, H.M. and Nekoubin, H., 2016. Effects of different levels of BioAcid Ultra on growth performance, survival, hematologichal and biochemical parameters of fingerlings rainbow trout (Oncorhynchus mykiss). Journal of Aquaculture Research and Development. 7(455): 1-5.‌ doi: 10.4172/2155-9546.1000455
57. 57. Stangl, G.I., Ulrich, E. and Manfred, K., 1998. Nickel deficiency alters nickel flux in rat everted intestinal sacs. Biological trace element research. 61: 253-262.‌ doi: 10.1093/jn/126.10.2466
58. 58. Swiatkiewicz, S. and Arczewska-Wlosek, A., 2012. Prebiotic fructans and organic acids as feed additives improving mineral availability. World's Poultry Science Journal. 68(2): 269-279. doi: 10.1017/S0043933912000 323
59. 59. Tinh, N.T.N., Asanka Gunasekara, R.A.Y.S., Boon, N., Dierckens, K., Sorgeloos, P. and Bossier, P., 2007. N-acyl homoserine lactone-degrading microbial enrichment cultures isolated from Penaeus vannamei shrimp gut and their probiotic properties in Brachionus plicatilis cultures. FEMS microbiology ecology. 62(1): 45-53.‌ doi: 10.1111/j.1574-6941.2007.00378.x
60. 60. Vahabnezhad, A. and Taghavimotlagh, S.A., 2017. Growth pattern and reproductive biology of Acanthopagrus latus from the Persian Gulf. Journal of Survey in Fisheries Sciences. 4(1)18-28. doi: 10.18331/ SFS2017.4.1.3
61. 61. Van Waarde, A., Van Dijk, P., Van Den Thillart, G., Verhagen, M., Erkelens, C., Bonga, S.W. and Lugtenburg, J., 1990. 31P-NMR studies on acid-base balance and energy metabolism of acid-exposed fish. Journal of experimental biology. 154(1): 223-236.‌ doi: 10.1242/jeb.154.1.223
62. 62. Wassef, E.A., Abdel-Momen, S.A.G., Saleh, N.E.S., Al-Zayat, A.M. and Ashry, A.M., 2017. Is sodium diformate a beneficial feed supplement for European seabass (Dicentrarchus labrax)? Effect on growth performance and health status. The Egyptian Journal of Aquatic Research. 43(3): 229-234.‌ doi: 10.1016/j.ejar. 2017.09.005
63. 63. Wei, H. and Erkang, W., 2013. Nanomaterials with enzyme-like characteristics (nanozymes): next-generation artificial enzymes. Chemical Society Reviews. 42(14): 6060-6093. https://doi.org/10.1039/C3CS35486E
64. 64. Wiegertjes, G.F., Stet, R.M., Parmentier, H.K. and van Muiswinkel, W.B., 1996. Immunogenetics of disease resistance in fish: a comparative approach. Developmental & Comparative Immunology. 20(6): 365-381.‌ doi: 10.1016/s0145-305x(96)00032-8
65. 65. Ye, J. and DeBose-Boyd, R.A., 2011. Regulation of cholesterol and fatty acid synthesis. Cold Spring Harbor perspectives in biology. 3(7): a004754. doi: 10.1101/ cshperspect.a004754
66. 66. Yilmaz, S., Ergün, S. and Yıgıt, M., 2018. Effects of dietary Farmarin® XP supplement on immunological responses and disease resistance of rainbow trout (Oncorhynchus mykiss). Aquaculture. 496: 211-220.‌ doi: 10.1016/j.aquaculture.2018.07.024
67. 67. ‌Zigová, J., 1999. Butyric acid production by Clostridium butyricum with integrated extraction and pertraction. Process Biochemistry. 34(8): 835-843.‌ doi: 10.1016/S0 032-9592(99)00007-2
Add your comments about this article
Your username or Email:

CAPTCHA



XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Salehipour Bavarsad S, Mohammadian T, Kochanian P, Yavari V, Torfi mozan zadeh M. Comparative effect of butyric acid alone and with endogenous quorum quencher bacteria on biochemical parameters of Acanthopagrus arabicus. Journalaer 2025; 1 (3) :75-86
URL: http://journalaer.com/article-1-34-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 1, Issue 3 (10-2025) Back to browse issues page
پژوهش های محیط زیست جانوری Journal of Animal Environmental Research
Persian site map - English site map - Created in 0.17 seconds with 39 queries by YEKTAWEB 4774