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SfiI endonuclease activity is strongly influenced by the non-specific sequence in the middle of its recognition site

机译:SfiI核酸内切酶 活性受非特异性序列的强烈影响 识别站点的中间

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摘要

The SfiI endonuclease cleaves DNA at the sequence GGCCNNNN↓NGGCC, where N is any base and ↓ is the point of cleavage. Proteins that recognise discontinuous sequences in DNA can be affected by the unspecified sequence between the specified base pairs of the target site. To examine whether this applies to SfiI, a series of DNA duplexes were made with identical sequences apart from discrete variations in the 5 bp spacer. The rates at which SfiI cleaved each duplex were measured under steady-state conditions: the steady-state rates were determined by the DNA cleavage step in the reaction pathway. SfiI cleaved some of these substrates at faster rates than other substrates. For example, the change in spacer sequence from AACAA to AAACA caused a 70-fold increase in reaction rate. In general, the extrapolated values for kcat and Km were both higher on substrates with inflexible spacers than those with flexible structures. The dinucleotide at the site of cleavage was largely immaterial. SfiI activity is thus highly dependent on conformational variations in the spacer DNA.
机译:SfiI核酸内切酶以GGCCNNNN↓NGGCC序列切割DNA,其中N是任何碱基,↓是切割点。识别DNA中不连续序列的蛋白质可能会受到目标位点指定碱基对之间未指定序列的影响。为了检查这是否适用于SfiI,除了5 bp间隔区的离散变异外,用相同的序列制作了一系列DNA双链体。在稳态条件下测量SfiI切割每个双链体的速率:通过反应途径中的DNA切割步骤确定稳态速率。 SfiI以比其他底物更快的速率切割其中一些底物。例如,间隔序列从AACAA到AAACA的变化导致反应速率增加了70倍。通常,具有非柔性间隔物的基板上的kcat和Km的外推值均高于具有柔性结构的基板。切割位点的二核苷酸在很大程度上不重要。因此,SfiI活性高度依赖于间隔DNA中的构象变化。

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