Journals / Ankara Üniversitesi Veteriner Fakültesi Dergisi / 2018 / Cilt: 65 - Sayı: 2

Tavşan böbrek arginaz aktivitesi için optimal şartların belirlenmesi

Determination of optimal conditions for activity of arginase in kidney of rabbit

Pages
109–113
Publication Date
2022-10-12
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

It was found to be preincubation temperature 53 °C, preincubation period is 15 minutes, incubation period is 10 minutes and optimum pH is 10.1 in NaHCO3-NaOH buffer for arginase in rabbit kidney tissue.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Optimum conditions for arginase in kidney tissue may differ from those for arginase of liver.
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Key Findings & Data:In the present study, the kidneys of six New Zealand rabbits aged 1 year old were used.
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Conclusion & Impact:It was found to be preincubation temperature 53 °C, preincubation period is 15 minutes, incubation period is 10 minutes and optimum pH is 10.1 in NaHCO3-NaOH buffer for arginase in rabbit kidney tissue.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Optimum conditions for arginase in kidney tissue may differ from those for arginase of liver. Because optimum conditions for measuring arginase activity in rabbit kidney tissue were not determined, it was aimed to optimize arginase of rabbit kidney tissue and compare it with arginase of liver. In the present study, the kidneys of six New Zealand rabbits aged 1 year old were used. It was found to be preincubation temperature 53 °C, preincubation period is 15 minutes, incubation period is 10 minutes and optimum pH is 10.1 in NaHCO3-NaOH buffer for arginase in rabbit kidney tissue. Enzyme achieved its highest activity at 1 mM MnCl2concentration. Km of arginase in rabbit kidney tissue for L-arginine was measured as 12.5 mM. It was determined that Mn+2 ions and preincubation at 53 °C were essential for the activation of the enzyme. As a result, optimal conditions for the kidney arginase were found to be different from those for the liver arginase. Our study indicates that arginases encoded by separate gene loci may have different optimal conditions

Özet

Böbrek dokusundaki arginazın optimum şartları karaciğer arginazınınkinden farklı olabilir. Tavşan böbrek dokusundaki arginazın ölçülmesi için optimum şartlar tespit edilmediğinden böbrek dokusundaki arginazın optimize edilmesi ve karaciğer arginazınınki ile karşılaştırılması amaçlanmıştır. Çalışmada bir yaşında 6 adet Beyaz Yeni Zelanda Tavşanı'nın böbrek dokuları kullanıldı. Tavşan böbrek doku arginazı için preinkübasyon ısısı 53°C, preinkübasyon zamanı 15 dakika, inkübasyon zamanı 10 dakika, en uygun tampon NaHCO3-NaOH tamponu ve optimum pH 10.1 şeklinde tespit edilmiştir. Enzimin aktivitesi, 1 mM MnCl2 konsantrasyonunda en yüksek değere ulaşmıştır. Tavşan böbrek dokusu arginazının L-arginine karşı olan Km'i 12.5 mM olarak bulunmuştur. Enzimin aktive olması için Mn+2 iyonları ve 53 °C' de preinkübasyon gereklidir. Böbrek arginazı için tayin edilen optimum şartlar karaciğer arginazınınkinden farklı olarak bulundu. Yapılan çalışma, ayrı gen lokusları tarafından kodlanan arginazların farklı optimum şatlara sahip olduğunu göstermektedir

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Cite This Article

ERİŞİR, M., ŞENGÜL, B. (2022). Tavşan böbrek arginaz aktivitesi için optimal şartların belirlenmesi. Ankara Üniversitesi Veteriner Fakültesi Dergisi, Cilt: 65 - Sayı: 2, 109–113. https://ajindex.com/articles/444599

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References (14)

  1. Aminlari M, Shahbazkia HR, Esfandiari A (2007): Distribution of arginase in tissues of cat (Felis catus). J Feline Med Surg, 9 (2), 133-139
  2. Benzer F, Temizer Ozan PS (2002): The levels of arginase enzyme activity in sheep with fasciolasis and some biochemical properties of arginase in liver tissue. FÜ Sağ Bil Vet Derg, 16 (2), 217-222
  3. Colombo JP, Konarska L (1984): Arginase. In: Bergmayer GM. (Editor). Methods of Enzymatic Analysis. 3rd Edition, Weinheim: Vertag Chemie, 285-294
  4. Dabir S, Dabir P, Somvanshi B (2005): Purification, properties and alternate substrate specificities of arginase from two different sources: Vigna catjang cotyledon and buffalo liver. Int J Biol Sci, 1 (3), 114-122
  5. Dabir S, Dabir P, Somvanshi B (2006): The kinetics of inhibition of Vigna catjang cotyledon and buffalo liver arginase by L-proline and branched-chain amino acids. J Enzyme Inhib Med Chem, 21 (6), 727-731
  6. Demir F, Ozan G, Temizer Ozan PS (2015): Ratlara uygulanan kurşun asetatın karaciğer arginazına etkisi ve enzimin bazı kinetik özellikleri. FÜ Sağ Bil Vet Derg, 29 (1), 37-43
  7. Erdem N, Erişir M (2013): Tavşan Karaciğer Arginazının Optimize Edilmesi ve Dokulardaki Dağılımı. FÜ Sağ Bil Vet Derg, 27 (2), 81-86
  8. Erişir M, Aydilek N, Aksakal M (2005): Effect of Vitamin E on Arginase Activity in the Liver and Kidneys of Testesterone Treated and Castrated Rabbits. Acta Vet Brno, 74, 527-531
  9. Erişir M, Beytut E, Ozan TS, et al. (2003): Effects of dietary vitamin E and Selenium on Arginase Activity in the liver, kidney and heart of rats treated with high doses of glucocorticoids. Cell Biochem Funct, 21, 331-335
  10. Erişir M, Erçel E, Yılmaz S, et al. (2005): Evaluation of optimal conditions for arginase activity in streptozotocin induced diabetic rats. Vet Med-Czech, 50, 69-76
  11. Erişir M, Nazıroğlu M, Taşdemir B, et al. (2006): Effect of a dietary combined vitamin C and E supplementation on the liver, kidneys and brain arginase activity in nonpregnant and pregnant rats with streptozotocin-induced diabetes. Revue Med Vet, 157, 445-449
  12. Erişir M, Tamser M, Taşdemir, et al. (2006): Ovariektomili Ratlara Estradiol 17-β ve Vitamin E Verilmesinin Arginaz Aktivitesi Üzerine Etkisi. Kafkas Üniv Vet Fak Derg, 12 (1), 31-35
  13. Geyer JW, Dabich D (1971): Rapid method for determination of arginase activity in tissue homogenates. Anal Biochem, 39, 412-417
  14. Glass RD, Knox WE (1973): Arginase isozymes of rat mammary gland, liver, and other tissues.