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大肠杆菌中羟乙基噻唑的摄取:摄取的一般特性及其与硫胺素生物合成的关系

Hydroxyethylthiazole uptake in Escherichia coli: general properties and relationship between uptake and thiamine biosynthesis.

作者信息

Yamasaki H, Sanemori H, Yamada K, Kawasaki T

出版信息

J Bacteriol. 1973 Dec;116(3):1280-6. doi: 10.1128/jb.116.3.1280-1286.1973.

Abstract

Uptake of (35)S-hydroxyethylthiazole (4-methyl-5-hydroxyethylthiazole) by Escherichia coli intact cells was studied. Hydroxyethylthiazole was taken up in the presence and absence of glucose at the same rate. The uptake was almost proportional to a hydroxyethylthiazole concentration gradient up to 0.1 mM with no tendency of saturation, and reached a steady state within 2 min. When the cells were treated with 1 mM N-ethylmaleimide, about 50% inhibition of hydroxyethylthiazole uptake was observed. Hydroxyethylthiazole uptake was stimulated by the addition of hydroxymethylpyrimidine (2-methyl-4-amino-5-hydroxymethylpyrimidine), and this effect was further enhanced in the presence of glucose. For full activation of hydroxyethylthiazole uptake, 1 muM hydroxymethylpyrimidine was necessary in the presence of glucose. The rate of hydroxyethylthiazole uptake was almost linear up to 60 min in the presence of hydroxymethylpyrimidine and glucose. Hydroxymethylpyrimidine monophosphate and its pyrophosphate could not stimulate the uptake. Thiamine and 2-amino-hydroxyethylthiazole were inhibitory on hydroxyethylthiazole uptake in the presence of hydroxymethylpyrimidine and glucose. N-ethylmaleimide and 2, 4-dinitrophenol were also inhibitory. No stimulatory effect of hydroxymethylpyrimidine on hydroxyethylthiazole uptake was observed in mutant cells lacking either thiaminephosphate pyrophosphorylase or hydroxymethylpyrimidine monophosphate kinase. The possibility of direct participation of thiamine-synthesizing enzymes in hydroxyethylthiazole uptake was discussed.

摘要

研究了大肠杆菌完整细胞对(35)S - 羟乙基噻唑(4 - 甲基 - 5 - 羟乙基噻唑)的摄取情况。在有无葡萄糖存在的情况下,羟乙基噻唑的摄取速率相同。摄取量几乎与高达0.1 mM的羟乙基噻唑浓度梯度成正比,且无饱和趋势,并在2分钟内达到稳态。当细胞用1 mM N - 乙基马来酰亚胺处理时,观察到羟乙基噻唑摄取受到约50%的抑制。添加羟甲基嘧啶(2 - 甲基 - 4 - 氨基 - 5 - 羟甲基嘧啶)可刺激羟乙基噻唑的摄取,在有葡萄糖存在时这种作用会进一步增强。在有葡萄糖存在的情况下,为使羟乙基噻唑摄取完全激活,需要1 μM羟甲基嘧啶。在有羟甲基嘧啶和葡萄糖存在的情况下,羟乙基噻唑的摄取速率在60分钟内几乎呈线性。羟甲基嘧啶单磷酸及其焦磷酸不能刺激摄取。在有羟甲基嘧啶和葡萄糖存在的情况下,硫胺素和2 - 氨基 - 羟乙基噻唑对羟乙基噻唑的摄取有抑制作用。N - 乙基马来酰亚胺和2,4 - 二硝基苯酚也有抑制作用。在缺乏磷酸硫胺素焦磷酸化酶或羟甲基嘧啶单磷酸激酶的突变细胞中,未观察到羟甲基嘧啶对羟乙基噻唑摄取的刺激作用。讨论了硫胺素合成酶直接参与羟乙基噻唑摄取的可能性。

相似文献

7
Overproduction of hydroxymethylpyrimidine by a thiamine regulatory mutant of Escherichia coli.
J Vitaminol (Kyoto). 1971 Mar 10;17(1):43-8. doi: 10.5925/jnsv1954.17.43.

本文引用的文献

5
Utilization of hydroxymethylpyrimidine phosphates by a mutant strain of Escherichia coli.
J Vitaminol (Kyoto). 1970 Jun 10;17(2):64-72. doi: 10.5925/jnsv1954.17.64.
10
The uptake system of free thiamine in mutants of Escherichia coli.大肠杆菌突变体中游离硫胺素的摄取系统。
Biochem Biophys Res Commun. 1972 Apr 28;47(2):465-71. doi: 10.1016/0006-291x(72)90737-1.

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