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酸性磷脂抑制大肠杆菌中染色体DNA复制起始因子DnaA蛋白的DNA结合活性。

Acidic phospholipids inhibit the DNA-binding activity of DnaA protein, the initiator of chromosomal DNA replication in Escherichia coli.

作者信息

Makise Masaki, Mima Shinji, Katsu Takashi, Tsuchiya Tomofusa, Mizushima Tohru

机构信息

Faculty of Pharmaceutical Sciences, Okayama University, Okayama 700-8530, Japan.

出版信息

Mol Microbiol. 2002 Oct;46(1):245-56. doi: 10.1046/j.1365-2958.2002.03161.x.

Abstract

In order to initiate chromosomal DNA replication in Escherichia coli, the DnaA protein must bind to both ATP and the origin of replication (oriC). Acidic phospholipids are known to inhibit DnaA binding to ATP, and here we examine the effects of various phospholipids on DnaA binding to oriC. Among the phospholipids in E. coli membrane, cardiolipin showed the strongest inhibition of DnaA binding to oriC. Synthetic phosphatidylglycerol containing unsaturated fatty acids inhibited binding more potently than did synthetic phosphatidylglycerol containing saturated fatty acids, suggesting that membrane fluidity is important. Thus, acidic phospholipids seem to inhibit DnaA binding to both oriC and adenine nucleotides in the same manner. Adenine nucleotides bound to DnaA did not affect the inhibitory effect of cardiolipin on DnaA binding to oriC. A mobility-shift assay re-vealed that acidic phospholipids inhibited formation of a DnaA-oriC complex containing several DnaA molecules. DNase I footprinting of DnaA binding to oriC showed that two DnaA binding sites (R2 and R3) were more sensitive to cardiolipin than other DnaA binding sites. Based on these in vitro data, the physiological relevance of this inhibitory effect of acidic phospholipids on DnaA binding to oriC is discussed.

摘要

为了在大肠杆菌中启动染色体DNA复制,DnaA蛋白必须同时结合ATP和复制起点(oriC)。已知酸性磷脂会抑制DnaA与ATP的结合,在此我们研究了各种磷脂对DnaA与oriC结合的影响。在大肠杆菌膜中的磷脂中,心磷脂对DnaA与oriC的结合表现出最强的抑制作用。含有不饱和脂肪酸的合成磷脂酰甘油比含有饱和脂肪酸的合成磷脂酰甘油更有效地抑制结合,这表明膜流动性很重要。因此,酸性磷脂似乎以相同的方式抑制DnaA与oriC和腺嘌呤核苷酸的结合。与DnaA结合的腺嘌呤核苷酸不影响心磷脂对DnaA与oriC结合的抑制作用。迁移率变动分析表明,酸性磷脂抑制了含有多个DnaA分子的DnaA-oriC复合物的形成。DnaA与oriC结合的DNase I足迹分析表明,两个DnaA结合位点(R2和R3)比其他DnaA结合位点对心磷脂更敏感。基于这些体外数据,讨论了酸性磷脂对DnaA与oriC结合的这种抑制作用的生理相关性。

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