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哈德酸对盘基网柄菌生长及腺苷酸琥珀酸合成酶活性的影响。

Effect of hadacidin on growth and adenylosuccinate synthetase activity of Dictyostelium discoideum.

作者信息

Rossomando E F, Maldonado B, Crean E V

出版信息

Antimicrob Agents Chemother. 1978 Sep;14(3):476-82. doi: 10.1128/AAC.14.3.476.

Abstract

The growth of the eucaryotic microorganism Dictyostelium discoideum in liquid culture was completely inhibited by the aspartic acid analog hadacidin (N-formylhydroxyamino-acetic acid). Growth arrest occurred both in chemically defined medium and in complex growth medium containing aspartic acid and AMP precursors such as adenine and adenosine. Although these compounds could not overcome the effect of hadacidin, growth was restored if cells were washed and resuspended in fresh growth medium. Additional experiments showed that D. discoideum contains adenylosuccinate synthetase, the enzyme which catalyzes the synthesis of adenylosuccinate from IMP, aspartic acid, and GTP in the de novo biosynthesis of purines. A partially purified preparation of this enzyme was obtained, and the effect of hadacidin on its activity was studied. We found that maximum inhibition of the D. discoideum activity occurs at a ratio of aspartic acid to hadacidin of 5:1, suggesting that the affinity of the drug for this enzyme is less than for the enzyme from rabbit muscle and plants but greater than for that from Escherichia coli. The effect of the drug can be overcome by a 10-fold excess of aspartic acid, suggesting that the drug acts as a competitive inhibitor. A comparison of the adenylosuccinate synthetase activity levels at various stages of growth showed that its specific activity decreases about 60% as cells enter the stationary growth phase, and decreases about 75% after starvation for 2 h. Further studies showed that in cells treated with hadacidin the rate of uptake of exogenous nutrients is reduced about 75% and that these cells are more resistant to rupture by osmotic shock. While the results of this study are consistent with the proposal that growth arrest is contingent upon inhibition of adenylosuccinate synthetase activity, they also suggest that, as a consequence of this inhibition, some physiological properties of the cell have been altered.

摘要

天冬氨酸类似物哈德酸(N-甲酰羟基氨基乙酸)可完全抑制真核微生物盘基网柄菌在液体培养基中的生长。在化学成分明确的培养基以及含有天冬氨酸和腺嘌呤、腺苷等AMP前体的复合生长培养基中,均会出现生长停滞。尽管这些化合物无法克服哈德酸的作用,但如果将细胞洗涤后重悬于新鲜的生长培养基中,生长即可恢复。额外的实验表明,盘基网柄菌含有腺苷酸琥珀酸合成酶,该酶在嘌呤的从头生物合成中催化由IMP、天冬氨酸和GTP合成腺苷酸琥珀酸。我们获得了该酶的部分纯化制剂,并研究了哈德酸对其活性的影响。我们发现,当天冬氨酸与哈德酸的比例为5:1时,盘基网柄菌的活性受到最大抑制,这表明该药物对这种酶的亲和力低于对兔肌肉和植物中的酶,但高于对大肠杆菌中的酶。10倍过量的天冬氨酸可克服该药物的作用,这表明该药物起竞争性抑制剂的作用。对生长各个阶段的腺苷酸琥珀酸合成酶活性水平进行比较表明,随着细胞进入稳定生长期,其比活性降低约60%,饥饿2小时后降低约75%。进一步的研究表明,在用哈德酸处理的细胞中,外源营养物质的摄取速率降低约75%,并且这些细胞对渗透休克破裂更具抗性。虽然本研究的结果与生长停滞取决于腺苷酸琥珀酸合成酶活性抑制的观点一致,但它们也表明,由于这种抑制作用,细胞的一些生理特性发生了改变。

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