Lindley T E, Scheiderer C L, Walsh P J, Wood C M, Bergman H L, Bergman A L, Laurent P, Wilson P, Anderson P M
Department of Biochemistry, University of Minnesota-Duluth, Duluth, Minnesota 55812, USA.
J Biol Chem. 1999 Oct 15;274(42):29858-61. doi: 10.1074/jbc.274.42.29858.
The tilapia fish Oreochromis alcalicus grahami from Kenya has adapted to living in waters at pH 10.5 by excreting the end product of nitrogen metabolism as urea rather than as ammonia directly across the gills as occurs in most fish. The level of activity in liver of the first enzyme in the urea cycle pathway, carbamoyl-phosphate synthetase III (CPSase III), is too low to account for the observed high rates of urea excretion. We report here the surprising finding that CPSase III and all other urea cycle enzyme activities are present in muscle of this species at levels more than sufficient to account for the rate of urea excretion; in addition, the basic kinetic properties of the CPSase III appear to be different from those of other known type III CPSases. The sequence of the CPSase III cDNA is reported as well as the finding that glutamine synthetase activity is present in liver but not in muscle. This unusual form of adaptation may have occurred because of the apparent impossibility of packaging the needed amount of urea cycle enzymes in liver.
来自肯尼亚的罗非鱼奥利亚罗非鱼已经适应了生活在pH值为10.5的水域中,它通过将氮代谢的终产物以尿素的形式排出,而不是像大多数鱼类那样直接通过鳃以氨的形式排出。尿素循环途径中的第一种酶——氨甲酰磷酸合成酶III(CPSase III)在肝脏中的活性水平过低,无法解释观察到的高尿素排泄率。我们在此报告一个惊人的发现,即该物种的肌肉中存在CPSase III和所有其他尿素循环酶活性,其水平足以解释尿素排泄率;此外,CPSase III的基本动力学特性似乎与其他已知的III型CPSases不同。报告了CPSase III cDNA的序列,以及谷氨酰胺合成酶活性存在于肝脏而非肌肉中的发现。这种不寻常的适应形式可能是因为在肝脏中包装所需数量的尿素循环酶显然是不可能的。