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A study of the irradiation of catalase by ionizing radiations in the presence of cysteine, cystine and glutathione.

作者信息

DALE W M, RUSSELL C

出版信息

Biochem J. 1956 Jan;62(1):50-7. doi: 10.1042/bj0620050.

DOI:10.1042/bj0620050
PMID:13293151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1274510/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/6c2386933f04/biochemj00861-0064-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/931915c24cfe/biochemj00861-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/d98b32acc8d5/biochemj00861-0063-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/96cd782fddfc/biochemj00861-0063-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/365f9755ad12/biochemj00861-0063-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/7d4053202768/biochemj00861-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/6c2386933f04/biochemj00861-0064-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/931915c24cfe/biochemj00861-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/d98b32acc8d5/biochemj00861-0063-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/96cd782fddfc/biochemj00861-0063-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/365f9755ad12/biochemj00861-0063-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/7d4053202768/biochemj00861-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46d/1274510/6c2386933f04/biochemj00861-0064-b.jpg

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1
A study of the irradiation of catalase by ionizing radiations in the presence of cysteine, cystine and glutathione.一项关于在半胱氨酸、胱氨酸和谷胱甘肽存在的情况下,过氧化氢酶受电离辐射照射的研究。
Biochem J. 1956 Jan;62(1):50-7. doi: 10.1042/bj0620050.
2
Adult T cell leukemia (ATL)-derived factor/human thioredoxin prevents apoptosis of lymphoid cells induced by L-cystine and glutathione depletion: possible involvement of thiol-mediated redox regulation in apoptosis caused by pro-oxidant state.成人T细胞白血病(ATL)衍生因子/人硫氧还蛋白可防止由L-胱氨酸和谷胱甘肽耗竭诱导的淋巴细胞凋亡:硫醇介导的氧化还原调节可能参与了由促氧化状态引起的细胞凋亡。
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Cathepsin B stability, but not activity, is affected in cysteine:cystine redox buffers.在半胱氨酸:胱氨酸氧化还原缓冲液中,组织蛋白酶B的稳定性受到影响,但活性不受影响。
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[Role of the reaction of free cysteine with peroxide compounds in the biological effect of ionizing radiations].
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引用本文的文献

1
Sulfheme formation during homocysteine S-oxygenation by catalase in cancers and neurodegenerative diseases.过氧化氢酶在癌症和神经退行性疾病中亚同型半胱氨酸 S-氧化过程中形成亚磺酸。
Nat Commun. 2016 Nov 16;7:13386. doi: 10.1038/ncomms13386.
2
Effect of cysteine on respiration and catalyse synthesis by Saccharomyces cerevisiae.半胱氨酸对酿酒酵母呼吸作用及催化合成的影响。
Biochem J. 1964 Sep;92(3):504-8. doi: 10.1042/bj0920504.
3
Synthesis of M protein by group A hemolytic streptococci in completely synthetic media during steady-state growth.

本文引用的文献

1
Convenient methods for preparing crystalline catalase from cow liver.从牛肝中制备结晶过氧化氢酶的简便方法。
J Biol Chem. 1952 Apr;195(2):703-6.
2
Purification of horse-radish peroxidase and comparison of its properties with those of catalase and methaemoglobin.辣根过氧化物酶的纯化及其与过氧化氢酶和高铁血红蛋白性质的比较。
Biochem J. 1951 Jun;49(1):88-104. doi: 10.1042/bj0490088.
3
Delayed toxicity of radiostrontium in monkeys.放射性锶对猴子的迟发性毒性。
A组溶血性链球菌在完全合成培养基中稳态生长期间M蛋白的合成。
J Bacteriol. 1968 Jan;95(1):162-8. doi: 10.1128/jb.95.1.162-168.1968.
4
Bactericidal effect of cysteine exposed to atmospheric oxygen.暴露于大气氧中的半胱氨酸的杀菌作用。
Appl Environ Microbiol. 1979 Mar;37(3):383-90. doi: 10.1128/aem.37.3.383-390.1979.
Nature. 1955 Jan 1;175(4444):33. doi: 10.1038/175033a0.
4
[Electrophoretic study on the effect of roentgen rays on watery solutions of proteins].[关于X射线对蛋白质水溶液作用的电泳研究]
Strahlentherapie. 1953;92(3):416-22.
5
Oxidation of pyrogallol to purpurogallin by crystallin catalase.晶状体过氧化氢酶催化邻苯三酚氧化为红紫素。
J Biol Chem. 1953 Nov;205(1):395-400.
6
Serum changes in diseases as determined by filter paper chromatography.通过滤纸层析法测定的疾病中的血清变化。
Exp Med Surg. 1953;11(3):230-9.
7
Studies on the mechanism of action of ionizing radiations. IX. The effect of x-irradiation on cytochrome c.电离辐射作用机制的研究。IX. X射线照射对细胞色素c的影响。
Arch Biochem Biophys. 1952 Nov;41(1):203-11. doi: 10.1016/0003-9861(52)90520-1.