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兔肝脏中胆红素和对硝基苯基葡萄糖醛酸苷的形成。

The formation of bilirubin and p-nitrophenyl glucuronides by rabbit liver.

作者信息

Tomlinson G A, Yaffe S J

出版信息

Biochem J. 1966 May;99(2):507-12. doi: 10.1042/bj0990507.

Abstract
  1. Glucuronide formation of bilirubin and p-nitrophenol in vitro with excess of UDP-glucuronic acid by UDP-glucuronyltransferase from livers of young and adult rabbits was studied. 2. The development of UDP-glucuronyltransferase for the two substrates followed a markedly different pattern during maturation of young rabbits, p-nitrophenol-conjugation ability being much higher at birth than that for bilirubin. 3. Mg(2+) increased bilirubin conjugation, but inhibited p-nitrophenyl glucuronide formation. 4. p-Nitrophenol acted as a potent non-competitive inhibitor for bilirubin conjugation but bilirubin did not affect p-nitrophenyl glucuronidation. 5. The enzyme for bilirubin conjugation was inactivated at pH9 during treatment with snake venom, whereas in the same preparation the activity of the corresponding enzyme for p-nitrophenol was enhanced. In addition, some solubilization of the latter enzyme could be achieved by this method. 6. The possibility of the existence of more than one enzyme system for the formation of O-glucuronides is discussed.
摘要
  1. 研究了用来自幼年和成年兔肝脏的UDP-葡萄糖醛酸转移酶在体外使胆红素和对硝基苯酚与过量UDP-葡萄糖醛酸形成葡萄糖醛酸苷的情况。2. 在幼兔成熟过程中,两种底物的UDP-葡萄糖醛酸转移酶的发育遵循明显不同的模式,出生时对硝基苯酚结合能力比对胆红素的结合能力高得多。3. Mg(2+) 增加胆红素结合,但抑制对硝基苯基葡萄糖醛酸苷的形成。4. 对硝基苯酚是胆红素结合的强效非竞争性抑制剂,但胆红素不影响对硝基苯基葡萄糖醛酸化。5. 在用蛇毒处理期间,胆红素结合酶在pH9时失活,而在同一制剂中,相应的对硝基苯酚酶的活性增强。此外,通过这种方法可以实现后一种酶的部分溶解。6. 讨论了存在一种以上O-葡萄糖醛酸苷形成酶系统的可能性。

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