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A Bipartite Thermodynamic-kinetic Contribution by an Activating Mutation to RDF-independent Excision by a Phage Serine Integrase

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Specialty Biochemistry
Date 2020 Jun 2
PMID 32479633
Citations 6
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Abstract

Streptomyces phage ϕC31 integrase (Int)-a large serine site-specific recombinase-is autonomous for phage integration (attP x attB recombination) but is dependent on the phage coded gp3, a recombination directionality factor (RDF), for prophage excision (attL x attR recombination). A previously described activating mutation, E449K, induces Int to perform attL x attR recombination in the absence of gp3, albeit with lower efficiency. E449K has no adverse effect on the competence of Int for attP x attB recombination. Int(E449K) resembles Int in gp3 mediated stimulation of attL x attR recombination and inhibition of attP x attB recombination. Using single-molecule analyses, we examined the mechanism by which E449K activates Int for gp3-independent attL x attR recombination. The contribution of E449K is both thermodynamic and kinetic. First, the mutation modulates the relative abundance of Int bound attL-attR site complexes, favoring pre-synaptic (PS) complexes over non-productively bound complexes. Roughly half of the synaptic complexes formed from Int(E449K) pre-synaptic complexes are recombination competent. By contrast, Int yields only inactive synapses. Second, E449K accelerates the dissociation of non-productively bound complexes and inactive synaptic complexes formed by Int. The extra opportunities afforded to Int(E499K) in reattempting synapse formation enhances the probability of success at fruitful synapsis.

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References
1.
Fan H, Li H . Studying RecBCD helicase translocation along Chi-DNA using tethered particle motion with a stretching force. Biophys J. 2009; 96(5):1875-83. PMC: 2717269. DOI: 10.1016/j.bpj.2008.11.048. View

2.
Bai H, Sun M, Ghosh P, Hatfull G, Grindley N, Marko J . Single-molecule analysis reveals the molecular bearing mechanism of DNA strand exchange by a serine recombinase. Proc Natl Acad Sci U S A. 2011; 108(18):7419-24. PMC: 3088605. DOI: 10.1073/pnas.1018436108. View

3.
Rowley P, Smith M . Role of the N-terminal domain of phiC31 integrase in attB-attP synapsis. J Bacteriol. 2008; 190(20):6918-21. PMC: 2566186. DOI: 10.1128/JB.00612-08. View

4.
Siuti P, Yazbek J, Lu T . Synthetic circuits integrating logic and memory in living cells. Nat Biotechnol. 2013; 31(5):448-52. DOI: 10.1038/nbt.2510. View

5.
Breuner A, Brondsted L, Hammer K . Novel organization of genes involved in prophage excision identified in the temperate lactococcal bacteriophage TP901-1. J Bacteriol. 1999; 181(23):7291-7. PMC: 103692. DOI: 10.1128/JB.181.23.7291-7297.1999. View