肝脏微粒体无机焦磷酸 - 葡萄糖磷酸转移酶、葡萄糖6 - 磷酸酶和无机焦磷酸酶的生物调节。禁食对合成和水解活性的不同影响。 - Suppr

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超能文献

Biological regulation of liver microsomal inorganic pyrophosphate-glucose phosphotransferase, glucose 6-phosphatase, and inorganic pyrophosphatase. Differential effects of fasting on synthetic and hydrolytic activities.

作者信息

Nordlie R C, Arion W J, Hanson T L, Gilsdorf J R, Horne R N

出版信息

J Biol Chem. 1968 Mar 25;243(6):1140-6.

PMID:4296409

Abstract

摘要

相似文献

Biological regulation of liver microsomal inorganic pyrophosphate-glucose phosphotransferase, glucose 6-phosphatase, and inorganic pyrophosphatase. Differential effects of fasting on synthetic and hydrolytic activities.肝脏微粒体无机焦磷酸 - 葡萄糖磷酸转移酶、葡萄糖6 - 磷酸酶和无机焦磷酸酶的生物调节。禁食对合成和水解活性的不同影响。

J Biol Chem. 1968 Mar 25;243(6):1140-6.

Some properties of variously activated microsomal glucose-6-phosphatase, inorganic pyrophosphatase and inorganic pyrophosphate-glucose phosphotransferase. Shift in pH optimum.不同激活状态下微粒体葡萄糖-6-磷酸酶、无机焦磷酸酶和无机焦磷酸-葡萄糖磷酸转移酶的一些特性。最适pH值的变化。

Biochim Biophys Acta. 1967 May 16;139(1):138-47. doi: 10.1016/0005-2744(67)90120-9.

Effects of cetyltrimethylammonium bromide on catalytic properties of kidney microsomal glucose-6-phosphatase, inorganic pyrophosphate-glucose phosphotransferase and inorganic pyrophosphatase activities.十六烷基三甲基溴化铵对肾微粒体葡萄糖-6-磷酸酶、无机焦磷酸-葡萄糖磷酸转移酶及无机焦磷酸酶活性催化特性的影响。

Biochim Biophys Acta. 1969;191(3):636-43. doi: 10.1016/0005-2744(69)90356-8.

Activation in vitro of glucose-6-phosphatase, inorganic pyrophosphate-glucose phosphotransferase and related enzymes: relationship to microsomal membrane structure.葡萄糖-6-磷酸酶、无机焦磷酸-葡萄糖磷酸转移酶及相关酶的体外激活：与微粒体膜结构的关系

Biochim Biophys Acta. 1969;193(2):260-7. doi: 10.1016/0005-2736(69)90187-4.

METABOLISM OF INORGANIC PYROPHOSPHATE. II. THE PROBABLE IDENTITY OF MICROSOMAL INORGANIC PYROPHOSPHATASE, PYROPHOSPHATE PHOSPHOTRANSFERASE, AND GLUCOSE 6-PHOSPHATASE.无机焦磷酸的代谢。II. 微粒体无机焦磷酸酶、焦磷酸磷酸转移酶和葡萄糖6-磷酸酶可能的同一性

J Biol Chem. 1964 Dec;239:4041-6.

Parallel changes in vivo in microsomal inorganic pyrophosphatase, pyrophosphate-glucose phosphotransferase and glucose 6-phosphatase activities.微粒体无机焦磷酸酶、焦磷酸-葡萄糖磷酸转移酶和葡萄糖6-磷酸酶活性在体内的平行变化。

Biochim Biophys Acta. 1966 May 26;121(1):102-9. doi: 10.1016/0304-4165(66)90352-7.

Liver microsomal inorganic pyrophosphate-glucose phosphotransferase and glucose-6-phosphatase. Effects of diabetes and insulin administration in kinetic parameters.肝脏微粒体无机焦磷酸 - 葡萄糖磷酸转移酶和葡萄糖 - 6 - 磷酸酶。糖尿病及胰岛素给药对动力学参数的影响。

Biochim Biophys Acta. 1970 Jan 14;198(1):66-75. doi: 10.1016/0005-2744(70)90033-1.

Liver microsomal glucose 6-phosphatase, inorganic pyrophosphatase, and pyrophosphate-glucose phosphotransferase. IV. Effects of adrenalectomy and cortisone administration on activities assayed in the absence and presence of deoxycholate.

J Biol Chem. 1965 Sep;240(9):3479-84.

Activation of rat-liver microsomal glucose 6-phosphatase, inorganic pyrophosphatase and inorganic pyrophosphate-glucose phosphotransferase by hydroxyl ion.

Biochim Biophys Acta. 1966 Nov 15;128(2):344-50. doi: 10.1016/0926-6593(66)90181-0.

LIVER MICROSOMAL GLUCOSE 6-PHOSPHATASE, INORGANIC PYROPHOSPHATASE, AND PYROPHOSPHATE-GLUCOSE PHOSPHOTRANSFERASE. II. KINETIC STUDIES.肝脏微粒体葡萄糖6-磷酸酶、无机焦磷酸酶和焦磷酸-葡萄糖磷酸转移酶。II. 动力学研究。

J Biol Chem. 1964 Sep;239:2752-7.

引用本文的文献

Free fatty acid-induced PP2A hyperactivity selectively impairs hepatic insulin action on glucose metabolism.游离脂肪酸诱导的 PP2A 过度活跃选择性地损害肝脏对葡萄糖代谢的胰岛素作用。

PLoS One. 2011;6(11):e27424. doi: 10.1371/journal.pone.0027424. Epub 2011 Nov 7.

Glucose-6-phosphatase activity in fed rat liver.喂食大鼠肝脏中的葡萄糖-6-磷酸酶活性

Biochem J. 1990 Mar 1;266(2):619-20.

On the involvement of a glucose 6-phosphate transport system in the function of microsomal glucose 6-phosphatase.关于6-磷酸葡萄糖转运系统在微粒体6-磷酸葡萄糖酶功能中的作用

Mol Cell Biochem. 1975 Feb 28;6(2):75-83. doi: 10.1007/BF01732001.

Glucose-6-phosphatase (EC 3.1.3.9) and esterase (EC 3.1.1.1) activities of microsomes prepared from perfused rat livers after partial outflow block or phalloidin poisoning.部分流出道阻塞或鬼笔环肽中毒后，从灌注大鼠肝脏制备的微粒体的葡萄糖-6-磷酸酶（EC 3.1.3.9）和酯酶（EC 3.1.1.1）活性。

Naunyn Schmiedebergs Arch Pharmacol. 1975;288(1):87-96. doi: 10.1007/BF00501816.

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