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二氨基二苯砜在由卢氏分枝杆菌和麻风分枝杆菌制备的无细胞叶酸合成系统中的抑制活性及作用模式。一项比较研究。

Inhibitory activity and mode of action of diaminodiphenylsulfone in cell-free folate-synthesizing systems prepared from Mycobacterium lufu and Mycobacterium leprae. A comparison.

作者信息

Kulkarni V M, Seydel J K

出版信息

Chemotherapy. 1983;29(1):58-67. doi: 10.1159/000238174.

Abstract

Cell-free folate synthesizing extracts have been isolated from Escherichia coli, Mycobacterium lufu, Mycobacterium smegmatis (ATCC 607) and Mycobacterium leprae, and the inhibitory power of diaminodiphenylsulfone (DDS) in such cell-free systems on the synthesis of dihydropteroic acid has been determined. M. lufu and M. leprae extracts show very similar high sensitivities against DDS. Mode of action studies seem to indicate that the observed high sensitivity of M. lufu and M. leprae as compared to E. coli can be solely attributed to a high affinity for the dihydropteroic acid synthetase. A dihydropteroic acid analog formation where DDS is incorporated instead of p-aminobenzoic acid--as has been observed in E. coli--could not be detected.

摘要

已从大肠杆菌、鲁氏分枝杆菌、耻垢分枝杆菌(美国典型培养物保藏中心607)和麻风分枝杆菌中分离出无细胞叶酸合成提取物,并测定了二氨基二苯砜(DDS)在这种无细胞体系中对二氢蝶酸合成的抑制能力。鲁氏分枝杆菌和麻风分枝杆菌提取物对DDS表现出非常相似的高敏感性。作用方式研究似乎表明,与大肠杆菌相比,观察到的鲁氏分枝杆菌和麻风分枝杆菌的高敏感性可能完全归因于对二氢蝶酸合成酶的高亲和力。未检测到如在大肠杆菌中所观察到的那样,DDS取代对氨基苯甲酸形成二氢蝶酸类似物的情况。

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