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. 1971 Jul;68(7):1639-43.
doi: 10.1073/pnas.68.7.1639.

Role of exonuclease and beta protein of phage lambda in genetic recombination. V. Recombination of lambda DNA in vitro

Role of exonuclease and beta protein of phage lambda in genetic recombination. V. Recombination of lambda DNA in vitro

E Cassuto et al. Proc Natl Acad Sci U S A. 1971 Jul.

Abstract

The sequential action of lambda exonuclease and polynucleotide ligase upon redundant joint molecules is sufficient to produce intact polynucleotide chains and heat-stable, biologically active molecules of lambda DNA, whereas the action of ligase alone is insufficient. These results (a) confirm the previously described mechanism of single-strand assimilation, including a subsidiary mechanism by which the further action of lambda exonuclease is arrested when a redundant strand is completely assimilated, and (b) represent a simulation of the steps in genetic recombination that follow the formation of biparental complexes (synapsis). lambda exonuclease is postulated to catalyze a concerted reaction that includes exposure of complementary sequences, formation of heteroduplex regions, and elimination of redundant branches.

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References

    1. J Biol Chem. 1967 Feb 25;242(4):679-86 - PubMed
    1. J Mol Biol. 1967 Jun 28;26(3):537-40 - PubMed
    1. J Mol Biol. 1967 Nov 28;30(1):147-64 - PubMed
    1. J Biol Chem. 1968 Sep 10;243(17):4556-63 - PubMed
    1. Proc Natl Acad Sci U S A. 1969 Oct;64(2):573-7 - PubMed