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DL-α-(二氟甲基)精氨酸:一种强效的酶激活不可逆细菌脱羧酶抑制剂。

DL-alpha-(Difluoromethyl)arginine: a potent enzyme-activated irreversible inhibitor of bacterial decarboxylases.

作者信息

Kallio A, McCann P P, Bey P

出版信息

Biochemistry. 1981 May 26;20(11):3163-8. doi: 10.1021/bi00514a027.

Abstract

DL-alpha-(Difluoromethyl)arginine (RMI 71 897) is an irreversible inhibitor of both the biosynthetic and biodegradative arginine decarboxylases of Escherichia coli and of the biosynthetic arginine decarboxylases of Pseudomonas aeruginosa and Klebsiella pneumoniae. The Ki is close to 800 muM for the biosynthetic decarboxylase of E. coli and 140 muM for the biodegradative enzyme while the respective half-lives (t1/2) calculated for an infinite concentration of inhibitor are 1.0 and 2.1 min. The inhibitor also blocks the arginine decarboxylase activity of E. coli and Pseudomonas aeruginosa in vivo, indicating that the compound is transported into the cell. DL-alpha-Methylarginine (RMI 71 699) was found to be a competitive inhibitor of both arginine decarboxylases from E. coli. These results suggest that it may be possible to use an arginine decarboxylase inhibitor in conjunction with known inhibitors of ornithine decarboxylase to block all putrescine biosynthesis in prokaryotic cells and thus to study the effects of such inhibition in these organisms.

摘要

DL-α-(二氟甲基)精氨酸(RMI 71 897)是大肠杆菌生物合成型和生物降解型精氨酸脱羧酶以及铜绿假单胞菌和肺炎克雷伯菌生物合成型精氨酸脱羧酶的不可逆抑制剂。对于大肠杆菌的生物合成型脱羧酶,其抑制常数(Ki)接近800 μM,对于生物降解型酶,Ki为140 μM,而在抑制剂浓度无限的情况下计算出的各自半衰期(t1/2)分别为1.0分钟和2.1分钟。该抑制剂在体内也能阻断大肠杆菌和铜绿假单胞菌的精氨酸脱羧酶活性,表明该化合物可转运进入细胞。发现DL-α-甲基精氨酸(RMI 71 699)是大肠杆菌两种精氨酸脱羧酶的竞争性抑制剂。这些结果表明,有可能将精氨酸脱羧酶抑制剂与已知的鸟氨酸脱羧酶抑制剂联合使用,以阻断原核细胞中所有腐胺的生物合成,从而研究这种抑制作用对这些生物体的影响。

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