Department of Biochemistry and Molecular Biology, University of North Dakota, School of Medicine and Health Sciences, Grand Forks, ND 58202, USA.
Life Sci. 2010 Sep 11;87(11-12):339-49. doi: 10.1016/j.lfs.2010.06.021. Epub 2010 Jul 21.
In a scientific career spanning from 1955 to 2000, my research focused on phosphoenolpyruvate carboxykinase and glucose-6-phosphatase. Grounded in basic enzymology, and initially pursuing the steady-state rate behavior of isolated preparations of these critically important gluconeogenic enzymes, our key findings were confirmed and extended by in situ enzyme rate experiments exploiting isolated liver perfusions. These efforts culminated in the discovery of the liver cytosolic isozyme of carboxykinase, known today as (GTP)PEPCK-C (EC4.1.1.32) and also revealed a biosynthetic function and multicomponent nature of glucose-6-phosphatase (EC3.1.3.9). Discovery that glucose-6-phosphatase possessed an intrinsically biosynthetic activity, now known as carbamyl-P:glucose phosphotransferase - along with a deeper consideration of the enzyme's hydrolytic activity as well as the action of liver glucokinase resulted in the evolution of Tuning/Retuning Hypothesis for blood glucose homeostasis in health and disease. This THEN & NOW review shares with the reader the joy and exhilaration of major scientific discovery and also contrasts the methodologies and approaches on which I relied with those currently in use.
在 1955 年至 2000 年的科学职业生涯中,我的研究重点是磷酸烯醇丙酮酸羧激酶和葡萄糖-6-磷酸酶。我的研究基于基础酶学,最初是研究这些至关重要的糖异生酶的分离制剂的稳态速率行为,我们的关键发现通过利用分离的肝灌注进行的原位酶速率实验得到了证实和扩展。这些努力最终发现了胞质溶胶同工酶的羧基激酶,即现在的(GTP)PEPCK-C(EC4.1.1.32),并揭示了葡萄糖-6-磷酸酶(EC3.1.3.9)的生物合成功能和多组分性质。发现葡萄糖-6-磷酸酶具有内在的生物合成活性,现在称为氨甲酰磷酸:葡萄糖磷酸转移酶 - 以及对酶的水解活性以及肝葡萄糖激酶的作用的更深入考虑,导致了健康和疾病中血糖稳态的调谐/重新调谐假说的发展。本 THEN & NOW 综述与读者分享了重大科学发现的喜悦和振奋,同时对比了我所依赖的方法和方法与当前使用的方法。