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1
The metabolism of glyoxylate by human- and rat-liver mitochondria.人和大鼠肝脏线粒体对乙醛酸的代谢
Biochem J. 1962 Oct;85(1):163-71. doi: 10.1042/bj0850163.
2
Mitochondrial hydroxyproline metabolism: implications for primary hyperoxaluria.线粒体羟脯氨酸代谢：对原发性高草酸尿症的影响。
Am J Nephrol. 2005 Mar-Apr;25(2):171-5. doi: 10.1159/000085409. Epub 2005 Apr 21.
3
Oxalate synthesis in mammals: properties and subcellular distribution of serine:pyruvate/alanine:glyoxylate aminotransferase in the liver.哺乳动物中草酸盐的合成：肝脏中丝氨酸：丙酮酸/丙氨酸：乙醛酸转氨酶的特性及亚细胞分布
Mol Urol. 2000 Winter;4(4):333-40.
4
L-alanine-glyoxylate aminotransferase II of rat kidney and liver mitochondria possesses cysteine S-conjugate beta-lyase activity: a contributing factor to the nephrotoxicity/hepatotoxicity of halogenated alkenes?大鼠肾脏和肝脏线粒体中的L-丙氨酸-乙醛酸转氨酶II具有半胱氨酸S-共轭β-裂解酶活性：这是卤代烯烃肾毒性/肝毒性的一个促成因素吗？
Biochem J. 2003 Nov 15;376(Pt 1):169-78. doi: 10.1042/BJ20030988.
5
The subcellular distribution of rat liver L-alanine-glyoxylate aminotransferase in relation to a pathway for glucose formation involving glyoxylate.大鼠肝脏L-丙氨酸-乙醛酸氨基转移酶的亚细胞分布与涉及乙醛酸的葡萄糖生成途径的关系。
Biochem J. 1972 Mar;127(1):155-65. doi: 10.1042/bj1270155.
6
Purification and properties of peroxisomal pyruvate (glyoxylate) aminotransferase from rat liver.大鼠肝脏过氧化物酶体丙酮酸（乙醛酸）氨基转移酶的纯化及性质
Biochem J. 1978 Nov 1;175(2):765-8. doi: 10.1042/bj1750765.
7
Subcellular distribution of pyruvate (glyoxylate) aminotransferases in rat liver.大鼠肝脏中丙酮酸（乙醛酸）氨基转移酶的亚细胞分布
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8
Characteristics of hepatic alanine-glyoxylate aminotransferase in different mammalian species.不同哺乳动物物种中肝脏丙氨酸-乙醛酸氨基转移酶的特征
Biochem J. 1978 Jan 1;169(1):113-22. doi: 10.1042/bj1690113.
9
Metabolism of glyoxylate, the end product of purin degradation, in liver peroxisomes of fresh water fish.淡水鱼肝过氧化物酶体中嘌呤降解终产物乙醛酸的代谢
Biochem Biophys Res Commun. 1996 Dec 13;229(2):603-6. doi: 10.1006/bbrc.1996.1850.
10
Primary hyperoxalurias: disorders of glyoxylate detoxification.原发性高草酸尿症：乙醛酸解毒障碍
Biochim Biophys Acta. 2012 Sep;1822(9):1453-64. doi: 10.1016/j.bbadis.2012.03.004. Epub 2012 Mar 14.

引用本文的文献

1
A weak link in metabolism: the metabolic capacity for glycine biosynthesis does not satisfy the need for collagen synthesis.代谢中的薄弱环节：甘氨酸生物合成的代谢能力无法满足胶原蛋白合成的需求。
J Biosci. 2009 Dec;34(6):853-72. doi: 10.1007/s12038-009-0100-9.
2
The synergistic decarboxylation of glyoxylate and 2-oxoglutarate by an enzyme system from pig-liver mitochondria.猪肝线粒体酶系促进乙醛酸和 2-氧戊二酸的协同脱羧作用。
Biochem J. 1967 Mar;102(3):885-97. doi: 10.1042/bj1020885.
3
The metabolism of glyoxylate by cell-free extracts of Pseudomonas sp.假单胞菌细胞无细胞提取物中乙醛酸的代谢
Biochem J. 1966 Dec;101(3):755-63. doi: 10.1042/bj1010755.
4
Sequential changes in liver and heart lipids after giving linoleate or linoleate plus pyridoxine to rats depleted of fat and pyridoxine.给缺乏脂肪和吡哆醇的大鼠喂食亚油酸或亚油酸加吡哆醇后肝脏和心脏脂质的顺序变化。
Biochem J. 1964 Aug;92(2):422-9. doi: 10.1042/bj0920422.
5
The metabolic error in primary hyperoxaluria.原发性高草酸尿症中的代谢错误。
Arch Dis Child. 1965 Oct;40(213):485-91. doi: 10.1136/adc.40.213.485.
6
Metabolism of 1-14C glyoxylate, 1-14C glycollate, 1-14C glycine and 2-14C glycine by homogenates of kidney and liver tissue from hyperoxaluric and control subjects.高草酸尿症患者和对照受试者的肾脏和肝脏组织匀浆对1-¹⁴C乙醛酸、1-¹⁴C乙醇酸、1-¹⁴C甘氨酸和2-¹⁴C甘氨酸的代谢情况。
Biochem J. 1967 Nov;105(2):701-7. doi: 10.1042/bj1050701.
7
Deficiency of 2-oxo-glutarate: glyoxylate carboligase activity in primary hyperoxaluria.原发性高草酸尿症中2-氧代戊二酸：乙醛酸羧化酶活性缺乏
Proc Natl Acad Sci U S A. 1967 Apr;57(4):1123-9. doi: 10.1073/pnas.57.4.1123.
8
Primary hyperoxaluria.原发性高草酸尿症
Biochem J. 1971 Mar;122(1):7P-9P. doi: 10.1042/bj1220007p.
9
Alternate pathways of metabolism of short-chain fatty acids.短链脂肪酸的替代代谢途径。
Bacteriol Rev. 1968 Mar;32(1):1-26. doi: 10.1128/br.32.1.1-26.1968.
10
Evidence that serum calcium oxalate supersaturation is a consequence of oxalate retention in patients with chronic renal failure.有证据表明，血清草酸钙过饱和是慢性肾衰竭患者草酸盐潴留的结果。
J Clin Invest. 1986 Jun;77(6):1888-96. doi: 10.1172/JCI112516.

本文引用的文献

1
Metabolism of labeled 2-carbon acids in the intact rat.完整大鼠体内标记二碳酸的代谢
J Biol Chem. 1951 Aug;191(2):707-17.
2
Metabolism of glycine by avian liver.禽类肝脏对甘氨酸的代谢
J Biol Chem. 1962 Jan;237:99-103.
3
Studies on experimental thiamine deficiency. Trends of keto acid formtion and detection of glyoxylic acid.实验性硫胺素缺乏症的研究。酮酸形成趋势及乙醛酸的检测。
Biochem J. 1962 Mar;82(3):429-34. doi: 10.1042/bj0820429.
4
Studies on experimental thiamine deficiency. 2. Tissue breakdown and glyoxylic acid formation.实验性硫胺素缺乏症研究。2. 组织分解与乙醛酸形成。
Biochem J. 1962 Apr;83(1):101-6. doi: 10.1042/bj0830101.
5
Synthesis of serine from glycine in mitochondrial fragments.线粒体片段中由甘氨酸合成丝氨酸
Biochim Biophys Acta. 1960 Apr 8;39:367-9. doi: 10.1016/0006-3002(60)90180-3.
6
The first glycine metabolic pool in man.人体中的首个甘氨酸代谢池。
Biochem J. 1959 Oct;73(2):277-86. doi: 10.1042/bj0730277.
7
The metabolism of D- and L- glutamic acid in the rat.大鼠体内D-谷氨酸和L-谷氨酸的代谢
J Biol Chem. 1961 Feb;236:365-9.
8
Oxidation of glyoxylic acid to oxalic acid by glycolic acid oxidase.乙醇酸氧化酶将乙醛酸氧化为草酸。
J Biol Chem. 1961 May;236:1280-4.
9
Carbon assimilation by Pseudomonas oxalaticus (OXI). 5. Purification and properties of glyoxylic dehydrogenase.草酸假单胞菌（OXI）的碳同化作用。5. 乙醛酸脱氢酶的纯化及性质
Biochem J. 1961 Mar;78(3):611-5. doi: 10.1042/bj0780611.
10
Aspects of the metabolism of glycine and of porphyrins.甘氨酸与卟啉的新陈代谢方面
Biochem J. 1961 Jan;78(1):1-10. doi: 10.1042/bj0780001.

The metabolism of glyoxylate by human- and rat-liver mitochondria.

作者信息

Crawhall J C, Watts R W

机构信息

The Medical Professorial Unit, St Bartholomew's Hospital, London, E.C. 1.

出版信息

Biochem J. 1962 Oct;85(1):163-71. doi: 10.1042/bj0850163.

DOI:10.1042/bj0850163
PMID:16748967
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1243926/
Abstract
摘要