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大肠杆菌多胺需求型突变体在缺乏多胺的情况下生长时形成补偿性多胺。

Formation of a compensatory polyamine by Escherichia coli polyamine-requiring mutants during growth in the absence of polyamines.

作者信息

Igarashi K, Kashiwagi K, Hamasaki H, Miura A, Kakegawa T, Hirose S, Matsuzaki S

出版信息

J Bacteriol. 1986 Apr;166(1):128-34. doi: 10.1128/jb.166.1.128-134.1986.

Abstract

The amounts of normal and compensatory polyamines of polyamine-requiring Escherichia coli mutants grown in the absence of polyamines were determined. Although aminopropylcadaverine, a compensatory polyamine, was synthesized by MA135 (speB) and DR112 (speA speB), no aminopropylcadaverine or only small amounts of aminopropylcadaverine were synthesized by EWH319 (speA speB speC speD) and MA261 (speB speC), respectively. The average mass doubling times of MA135, DR112, MA261, and EWH319 grown in the absence of polyamines were 113, 105, 260, and 318 min, respectively. The correlation of these values with the sum of spermidine plus aminopropylcadaverine suggested that aminopropylcadaverine is important for cell growth in the presence of limiting amounts of normal polyamines. This hypothesis is supported by the results of aminopropylcadaverine stimulation of the in vitro synthesis of polyphenylalanine and MS2 RNA replicase and of its stimulation of the growth of MA261. For the following reasons, it was concluded that aminopropylcadaverine was synthesized preferentially from cadaverine made by ornithine decarboxylase: aminopropylcadaverine was synthesized in relatively large amounts in cells (MA135 and DR112) which possess ornithine decarboxylase; ornithine decarboxylase catalyzed the decarboxylation of lysine in vitro, and the in vivo formation of aminopropylcadaverine was inhibited by an inhibitor of ornithine decarboxylase.

摘要

测定了在缺乏多胺的情况下生长的多胺需求型大肠杆菌突变体中正常多胺和补偿性多胺的含量。虽然补偿性多胺氨丙基尸胺是由MA135(speB)和DR112(speA speB)合成的,但EWH319(speA speB speC speD)和MA261(speB speC)分别不合成氨丙基尸胺或仅合成少量氨丙基尸胺。在缺乏多胺的情况下生长的MA135、DR112、MA261和EWH319的平均质量倍增时间分别为113、105、260和318分钟。这些值与亚精胺加氨丙基尸胺之和的相关性表明,在正常多胺含量有限的情况下,氨丙基尸胺对细胞生长很重要。氨丙基尸胺对聚苯丙氨酸和MS2 RNA复制酶体外合成的刺激及其对MA261生长的刺激结果支持了这一假设。基于以下原因,得出结论:氨丙基尸胺优先由鸟氨酸脱羧酶产生的尸胺合成:在具有鸟氨酸脱羧酶的细胞(MA135和DR112)中,氨丙基尸胺合成量相对较大;鸟氨酸脱羧酶在体外催化赖氨酸脱羧,并且氨丙基尸胺的体内形成受到鸟氨酸脱羧酶抑制剂的抑制。

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