Abstract
The original observation that extracts of liver contain considerable gluta- mine-hydrolysing activity was reported by Krebs in 1935 [1]. Errera [2] demonstrated that the major part of the glutaminase activity was dependent on added phosphate and was located in the particulate fraction of the liver. Definitive evidence that glutaminase is a mitochondrial enzyme was first obtained by Guha [3]. Liver extracts also contain a phosphate-independent glutamine-hydrolysing activity located in the supernatant fraction [2, 4–6]. This activity is stimulated by maleate and represents a partial reaction of γ -glutamyltransferase (EC 2.3.2.2) [7]. In a careful reinvestigation of the characteristics of glutamine hydrolysis in rat liver extracts, Horowitz and Knox [8] showed that 90% of the glutamine hydrolysing activity was phosphate-de- pendent and located in the mitochondria and was thus catalysed by the enzyme now classified as glutaminase (EC 3.5.1.2)
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References
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Mcgivan, J.D., Bradford, N.M., Verhoeven, A.J., Meijer, A.J. (1984). Liver Glutaminase. In: Häussinger, D., Sies, H. (eds) Glutamine Metabolism in Mammalian Tissues. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-69754-8_8
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DOI: https://doi.org/10.1007/978-3-642-69754-8_8
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