Burian Ján, Ausió Juan, Phipps Barry, Moore Susan, Dougan Douglas, Kay William
Microtek International Ltd., 6761 Kirkpatrick Crescent, Saanichton, British Columbia, V8M 1Z8, Canada.
Biochemistry. 2003 Sep 2;42(34):10282-7. doi: 10.1021/bi034341b.
The Escherichia coli plasmid pKL1 is one of the smallest bacterial plasmids. It encodes a single, autoregulating structural gene, repA, responsible for replication and copy number control. The oligomerization of RepA was previously proposed as the basis of a strategy for pKL1 copy number control. To elucidate the oligomerization properties of RepA in solution, RepA was expressed in E. coli; purified by ion exchange and hydrophobic chromatography; and examined in solution by spectrapolarimetry, light scattering, sedimentation velocity, and equilibrium ultracentrifugation. RepA behaved as a concentration-dependent equilibrium of dimers and hexamers. Conformational parameters of the RepA hexameric complex were determined. These results support the proposed autogenous regulatory model whereby RepA hexamers negatively regulate repA expression thereby affecting the copy number control of pKL1. RepA of pKL1 is the first plasmid replication initiation protein documented to be in dimeric-hexameric forms.
大肠杆菌质粒pKL1是最小的细菌质粒之一。它编码一个单一的、自我调节的结构基因repA,负责复制和拷贝数控制。RepA的寡聚化先前被认为是pKL1拷贝数控制策略的基础。为了阐明RepA在溶液中的寡聚化特性,RepA在大肠杆菌中表达;通过离子交换和疏水色谱法纯化;并通过光谱偏振法、光散射、沉降速度和平衡超速离心法在溶液中进行检测。RepA表现为二聚体和六聚体的浓度依赖性平衡。确定了RepA六聚体复合物的构象参数。这些结果支持了所提出的自调节模型,即RepA六聚体负调节repA表达,从而影响pKL1的拷贝数控制。pKL1的RepA是第一个被记录为二聚体-六聚体形式的质粒复制起始蛋白。