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利用无细胞细菌提取物进行诱变叠氮化物代谢物的体外合成。

In vitro synthesis of a mutagenic azide metabolite by cell-free bacterial extracts.

作者信息

Owais W M, Kleinhofs A, Nilan R A

出版信息

Mutat Res. 1981 Dec;84(2):239-46. doi: 10.1016/0027-5107(81)90193-7.

Abstract

Cell-free extracts of Salmonella typhimurium synthesize a mutagenic azide metabolite from sodium azide and O-acetylserine. S. typhimurium mutant DW379 (O-acetylserine sulfhydrylase-deficient) extracts were neither able to carry out this reaction not produce the mutagenic azide metabolite in vivo. The in vitro reaction was inhibited by sulfide but not by L-cysteine. The catalytic activity responsible for the mutagenic metabolite synthesis was stable to brief heating up to 55 degrees C and had a pH optimum between 7-7.4. These results suggest that the enzyme O-acetylserine sulfhydrylase catalyzes the reaction of azide with O-acetylserine to form a mutagenic azide metabolite.

摘要

鼠伤寒沙门氏菌的无细胞提取物能从叠氮化钠和O-乙酰丝氨酸合成一种诱变叠氮代谢物。鼠伤寒沙门氏菌突变体DW379(缺乏O-乙酰丝氨酸巯基酶)的提取物既不能进行此反应,也不能在体内产生诱变叠氮代谢物。体外反应受到硫化物的抑制,但不受L-半胱氨酸的抑制。负责诱变代谢物合成的催化活性在高达55摄氏度的短暂加热下稳定,最适pH值在7 - 7.4之间。这些结果表明,O-乙酰丝氨酸巯基酶催化叠氮化物与O-乙酰丝氨酸反应形成诱变叠氮代谢物。

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