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[大肠杆菌来源的L-天冬酰胺酶制剂在细胞培养中的生物学特性]

[Biological properties of L-asparaginase preparations from E. coli in cell cultures].

作者信息

Kondrat'eva N A, Dobrynin Ia V, Merkulov M F

出版信息

Antibiotiki. 1978 Jan;23(1):43-5.

PMID:341799
Abstract

Non-specific cytotoxicity and specific antitumor activity of 5 preparations of L-asparaginase from E. coli were studied. Two cell line, i.e. the asparagine-dependent (Berkitt lymphoma cells) and asparagin-independent (human ovary cancer cells) were used as the test-system. Incorporation of 3H-thimidine into DNA was the criterion of the preparation effect on the cells. Preparation I with the specific activity of 60-90 IU per 1 mg of protein obtained at the first stages of purification had high non-specific cytotoxicity. Preparation II obtained after further purification of preparation I, as well as preparation II without any stabilizer with the specific activity of 200 IU/mg were not inferior to the "Bayer" preparation by their biological properties. Addition of L-asparaginase to the preparation as a stabilizer of excessive glycine (preparation IV) increased its non-specific cytotoxicity and interfered with the study of its properties in the cell systems. Mannitol (preparation V) had no effect on the biological activity of L-asparaginase preparation.

摘要

研究了5种大肠杆菌来源的L-天冬酰胺酶制剂的非特异性细胞毒性和特异性抗肿瘤活性。使用两种细胞系,即天冬酰胺依赖型(伯基特淋巴瘤细胞)和天冬酰胺非依赖型(人卵巢癌细胞)作为测试系统。3H-胸腺嘧啶核苷掺入DNA是制剂对细胞作用的标准。在纯化第一阶段获得的每1mg蛋白质比活性为60 - 90IU的制剂I具有高非特异性细胞毒性。制剂I进一步纯化后得到的制剂II以及无任何稳定剂、比活性为200IU/mg的制剂II,其生物学性质不逊色于“拜耳”制剂。向制剂中添加L-天冬酰胺酶作为过量甘氨酸的稳定剂(制剂IV)增加了其非特异性细胞毒性,并干扰了其在细胞系统中性质的研究。甘露醇(制剂V)对L-天冬酰胺酶制剂的生物学活性无影响。

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