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DNA连接酶在复制叉处的多种作用。

Multiple roles of DNA ligase at the replication fork.

作者信息

Montecucco A, Pedrali-Noy G, Spadari S, Ciarrocchi G

机构信息

Istituto di Genetica Biochimica ed Evoluzionistica, CNR, Pavia, Italy.

出版信息

Biochim Biophys Acta. 1988 Dec 20;951(2-3):330-4. doi: 10.1016/0167-4781(88)90103-0.

Abstract

The loss of superhelical turns from a covalently closed duplex DNA exposed to bacteriophage T4 DNA ligase in the presence of AMP and Mg2+ has recently been found to be gradual and not sudden (Montecucco, A. and Ciarrocchi, G. (1988) Nucleic Acids Res. 16, 7369-7381). In this paper, we show that the AMP-dependent DNA relaxation catalyzed by human and E. coli DNA ligases also takes place according to a step-wise mechanism. DNA relaxation is inhibited by pyrophosphate, by ATP (or NAD in the case of the E. coli enzyme) and by high ionic strength and is essentially distributive with the human or T4 DNA ligases, and processive with the bacterial one. The AMP-dependent ability of DNA ligases to relax DNA might allow these enzymes to relieve possible topological complications of the nascent double helix generated by the replication of the lagging strand.

摘要

最近发现,在存在AMP和Mg2+的情况下,暴露于噬菌体T4 DNA连接酶的共价闭合双链DNA中超螺旋圈数的损失是逐渐的而非突然的(蒙特库科,A.和恰罗奇,G.(1988年)《核酸研究》16,7369 - 7381)。在本文中,我们表明,由人和大肠杆菌DNA连接酶催化的AMP依赖性DNA松弛也按照逐步机制发生。DNA松弛受到焦磷酸、ATP(对于大肠杆菌酶而言为NAD)以及高离子强度的抑制,并且对于人或T4 DNA连接酶而言基本上是分布性的,而对于细菌DNA连接酶而言是持续性的。DNA连接酶的AMP依赖性松弛DNA的能力可能使这些酶能够缓解由滞后链复制产生的新生双螺旋可能出现的拓扑复杂性。

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