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脆弱拟杆菌超氧化物歧化酶中的体内金属取代

In vivo metal substitution in Bacteroides fragilis superoxide dismutase.

作者信息

Chen Y, Gregory E M

机构信息

Department of Biochemistry and Nutrition, Virginia Polytechnic Institute and State University, Blacksburg 24061-0308.

出版信息

Free Radic Res Commun. 1991;12-13 Pt 1:313-8. doi: 10.3109/10715769109145800.

Abstract

Bacteroides fragilis, an obligate anaerobe, synthesizes an azide-inhibitable iron-containing superoxide dismutase when grown in complex medium. Cells grown anaerobically in complex media containing desferrioxamine (Desferal, Ciba-Geigy) and graded concentrations of Mn synthesize the azide-resistant manganese-containing SOD. The fraction of MnSOD activity in dialyzed cell extracts increased progressively as the Mn concentration in the medium increased. The fraction of MnSOD activity also increased in extracts of cells grown in the medium with 1 mM Mn but with graded concentrations of desferrioxamine (0-10 micromolar). The SOD activity in the cells grown under the various conditions varied but not in a causal relationship with either Mn or desferrioxamine concentration. Electrophoresis revealed that the SOD activity in cells grown in the absence or presence of 1 mM Mn migrated with the same relative mobility and exhibited identical activity patterns when examined separately or as a mixture. These data are consistent with substitution of Mn for Fe in the B. fragilis apoprotein under anaerobic conditions and support the model of a single protein binding either Fe or Mn.

摘要

脆弱拟杆菌是一种专性厌氧菌,当在复合培养基中生长时,它会合成一种对叠氮化物敏感的含铁超氧化物歧化酶。在含有去铁胺(去铁敏,汽巴 - 嘉基公司)和不同浓度锰的复合培养基中厌氧培养的细胞,会合成对叠氮化物有抗性的含锰超氧化物歧化酶(MnSOD)。随着培养基中锰浓度的增加,透析后的细胞提取物中MnSOD活性的比例逐渐增加。在含有1 mM锰但去铁胺浓度不同(0 - 10微摩尔)的培养基中生长的细胞提取物中,MnSOD活性的比例也增加。在各种条件下生长的细胞中的超氧化物歧化酶(SOD)活性有所不同,但与锰或去铁胺浓度没有因果关系。电泳显示,在不存在或存在1 mM锰的情况下生长的细胞中的SOD活性,具有相同的相对迁移率,并且单独检测或作为混合物检测时,呈现相同的活性模式。这些数据与厌氧条件下脆弱拟杆菌脱辅基蛋白中的铁被锰取代一致,并支持单一蛋白质结合铁或锰的模型。

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