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软骨中鸟氨酸脱羧酶和多胺的存在情况。

Occurrence of ornithine decarboxylase and polyamines in cartilage.

作者信息

Conroy P D, Simms D M, Pointon J J

出版信息

Biochem J. 1977 Feb 15;162(2):347-50. doi: 10.1042/bj1620347.

DOI:10.1042/bj1620347
PMID:15559
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1164607/
Abstract

The activity of ornithine decarboxylase was investigated in cartilage from chick embryos, rabbits, rats and human foetuses. The enzyme activity in these cartilages was of the same order as the detected in other body tissues. Ornithine decarboxylase activity in chick-embryo cartilage and liver was the same when compared on the basis of total soluble tissue protein. The cartilage enzyme exhibited a pH optimum of 6.5 and a Km for ornithine of 0.16mM. Ornithine decarboxylase activity in chick-embryo pelvic leaflets was maintained at the value in vivo for up to 22h when the isolated tissue was incubated in a modified Waymouth's medium (MB 752/1) at 37 degrees C. After addition of cycloheximide to the incubation medium, ornithine decarboxylase activity declined, with a half-life of 40 min. The concentrations of the polyamines spermidine and spermine in chick-embryo pelvic cartilage and rabbit costal cartilage were of the same order as the concentrations detected in other tissues.

摘要

对鸡胚、兔、大鼠和人类胎儿软骨中的鸟氨酸脱羧酶活性进行了研究。这些软骨中的酶活性与在其他身体组织中检测到的活性处于同一水平。以总可溶性组织蛋白为基础进行比较时,鸡胚软骨和肝脏中的鸟氨酸脱羧酶活性相同。软骨酶的最适pH为6.5,鸟氨酸的Km为0.16mM。当分离的鸡胚骨盆叶在改良的威茅斯培养基(MB 752/1)中于37℃孵育时,其鸟氨酸脱羧酶活性在体内水平维持长达22小时。在孵育培养基中加入环己酰亚胺后,鸟氨酸脱羧酶活性下降,半衰期为40分钟。鸡胚骨盆软骨和兔肋软骨中多胺亚精胺和精胺的浓度与在其他组织中检测到的浓度处于同一水平。

相似文献

1
Occurrence of ornithine decarboxylase and polyamines in cartilage.软骨中鸟氨酸脱羧酶和多胺的存在情况。
Biochem J. 1977 Feb 15;162(2):347-50. doi: 10.1042/bj1620347.
2
Polyamines and enzymes of polyamines metabolism in the cartilage during embryonic development.胚胎发育过程中软骨内的多胺及其多胺代谢酶
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Cancer Res. 1975 Dec;35(12):3618-22.
4
Effect of suramin (Bayer 205) on renal ornithine decarboxylase activity and polyamine concentrations in rats.苏拉明(拜耳205)对大鼠肾脏鸟氨酸脱羧酶活性和多胺浓度的影响。
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Ornithine decarboxylase and polyamines in liver and kidneys of rats on cyclical regimen of protein-free and protein-containing diets. Relationship to deoxyribonucleic acid synthesis in liver.采用无蛋白饮食和含蛋白饮食周期性方案的大鼠肝脏和肾脏中的鸟氨酸脱羧酶和多胺。与肝脏中脱氧核糖核酸合成的关系。
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[Synthesis of polyamines in the rat liver during thermal injury].[热损伤时大鼠肝脏中多胺的合成]
Vopr Med Khim. 1982 Nov-Dec;28(6):71-5.

引用本文的文献

1
Polyamine and differentiation: induction of ornithine decarboxylase by parathyroid hormone is a good marker of differentiated chondrocytes.多胺与分化:甲状旁腺激素诱导鸟氨酸脱羧酶是分化软骨细胞的良好标志物。
Proc Natl Acad Sci U S A. 1980 Mar;77(3):1481-5. doi: 10.1073/pnas.77.3.1481.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
THE ESTIMATION OF DEOXYRIBONUCLEIC ACID IN THE PRESENCE OF SIALIC ACID: APPLICATION TO ANALYSIS OF HUMAN GASTRIC WASHINGS.在唾液酸存在的情况下对脱氧核糖核酸的估计:在人胃冲洗液分析中的应用。
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SPERMIDINE, SPERMINE, AND RELATED AMINES.亚精胺、精胺及相关胺类
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[Amino acid determination on paper chromatograms].[纸色谱法测定氨基酸]
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Studies on the biosynthetic pathway of polyamines in rat liver.大鼠肝脏中多胺生物合成途径的研究。
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On the purification of L-ornithine decarboxylase from rat prostate and effects of thiol compounds on the enzyme.大鼠前列腺L-鸟氨酸脱羧酶的纯化及硫醇化合物对该酶的影响
J Biol Chem. 1971 Mar 25;246(6):1725-32.
7
Stimulation of ornithine decarboxylase activity in rat tissues by growth hormone and by serum growth factor from rats infested with spargana of Spirometra mansonoides.生长激素及曼氏迭宫绦虫裂头蚴感染大鼠血清生长因子对大鼠组织中鸟氨酸脱羧酶活性的刺激作用。
Biochim Biophys Acta. 1972 Sep 15;279(2):377-86. doi: 10.1016/0304-4165(72)90156-0.
8
The natural history of amine oxidases.胺氧化酶的自然史。
Rev Physiol Biochem Pharmacol. 1974;70:83-148. doi: 10.1007/BFb0034294.
9
Amine synthesis in rapidly growing tissues: ornithine decarboxylase activity in regenerating rat liver, chick embryo, and various tumors.快速生长组织中的胺合成:再生大鼠肝脏、鸡胚及多种肿瘤中的鸟氨酸脱羧酶活性
Proc Natl Acad Sci U S A. 1968 Aug;60(4):1420-7. doi: 10.1073/pnas.60.4.1420.
10
Polyamines: a high correlation with cell replication.多胺:与细胞复制高度相关。
FEBS Lett. 1975 Jan 15;50(1):1-4. doi: 10.1016/0014-5793(75)81026-x.