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赖氨酸脱羧酶的选择性不可逆抑制剂DL-α-二氟甲基赖氨酸对差异支原体生长的抑制作用以及尸胺(1,5-二氨基戊烷)的逆转作用。

Inhibition of growth of Mycoplasma dispar by DL-alpha-difluoromethyllsine, a selective irreversible inhibitor of lysine decarboxylase, and reversal by cadaverine (1,5-diaminopentane).

作者信息

Pösö H, McCann P P, Tanskanen R, Bey P, Sjoerdsma A

出版信息

Biochem Biophys Res Commun. 1984 Nov 30;125(1):205-10. doi: 10.1016/s0006-291x(84)80355-1.

Abstract

DL-alpha-Difluoromethyllysine was shown to be a potent inhibitor of lysine decarboxylase from Mycoplasma dispar. The inhibition appeared to be specific since neither difluoromethylornithine nor difluoromethylarginine, known to inhibit other decarboxylases, inhibited the reaction catalyzed by lysine decarboxylase in extracts of M. dispar. Inhibition was irreversible since extensive dialysis could not overcome the inhibitory effect exerted by difluoromethyllysine. Difluoromethyllysine (1 mM) also totally blocked the growth of M. dispar when added at the beginning of the growth period, while 1 mM cadaverine, the product of the reaction, reversed this inhibitory effect when added to the culture medium. When difluoromethyllysine was added during the logarithmic growth phase of Mycoplasma, it inhibited the increase of the growth; 1 mM cadaverine again partially reversed this inhibitory action.

摘要

DL-α-二氟甲基赖氨酸被证明是一种来自殊异支原体的赖氨酸脱羧酶的有效抑制剂。这种抑制作用似乎具有特异性,因为已知抑制其他脱羧酶的二氟甲基鸟氨酸和二氟甲基精氨酸均不能抑制殊异支原体提取物中赖氨酸脱羧酶所催化的反应。抑制作用是不可逆的,因为广泛透析无法克服二氟甲基赖氨酸所施加的抑制作用。当在生长初期添加时,二氟甲基赖氨酸(1 mM)也完全阻断了殊异支原体的生长,而1 mM尸胺(该反应的产物)添加到培养基中时可逆转这种抑制作用。当在支原体的对数生长期添加二氟甲基赖氨酸时,它会抑制生长的增加;1 mM尸胺再次部分逆转了这种抑制作用。

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