Pyrophosphate hydrolysis is an intrinsic and critical step of the DNA synthesis reaction

被引:62
作者
Kottur, Jithesh [1 ]
Nair, Deepak T. [1 ]
机构
[1] NCR Biotech Sci Cluster, Reg Ctr Biotechnol, 3rd Milestone,Faridabad Gurgaon Expressway, Faridabad 121001, India
关键词
2-DEOXYNUCLEOSIDE; 5-TRIPHOSPHATES; STRUCTURAL BASIS; POLYMERASE IV; METAL-IONS; REPLICATION; FIDELITY; PYROPHOSPHOROLYSIS; MECHANISM; RESIDUE; MOTION;
D O I
10.1093/nar/gky402
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA synthesis by DNA polymerases (dPols) is central to duplication and maintenance of the genome in all living organisms. dPols catalyze the formation of a phosphodiester bond between the incoming deoxynucleoside triphosphate and the terminal primer nucleotide with the release of a pyrophosphate (PPi) group. It is believed that formation of the phosphodiester bond is an endergonic reaction and PPi has to be hydrolyzed by accompanying pyrophosphatase enzymes to ensure that the free energy change of the DNA synthesis reaction is negative and it can proceed in the forward direction. The fact that DNA synthesis proceeds in vitro in the absence of pyrophosphatases represents a long-standing conundrum regarding the thermodynamics of the DNA synthesis reaction. Using time-resolved crystallography, we show that hydrolysis of PPi is an intrinsic and critical step of the DNA synthesis reaction catalyzed by dPols. The hydrolysis of PPi occurs after the formation of the phosphodiester bond and ensures that the DNA synthesis reaction is energetically favorable without the need for additional enzymes. Also, we observe that DNA synthesis is a two Mg2+ ion assisted stepwise associative S(N)2 reaction. Overall, this study provides deep temporal insight regarding the primary enzymatic reaction responsible for genome duplication.
引用
收藏
页码:5875 / 5885
页数:11
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