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A computational study of λ-lac mutants

Maria Werner et al 2009 Phys. Biol. 6 046007 (11pp)   doi: 10.1088/1478-3975/6/4/046007  Help

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Maria Werner and Erik Aurell
Department of Computational Biology, KTH—Royal Institute of Technology, Albanova University Center, SE-10691 Stockholm, Sweden
E-mail: mariawer@kth.se

Abstract. We present a comprehensive, computational study of the properties of bacteriophage λ mutants designed by Atsumi and Little (2006 Proc. Natl. Acad. Sci. 103 4558-63). These phages underwent a genetic reconstruction where Cro was replaced by a dimeric form of the Lac repressor. To clarify the theoretical characteristics of these mutants, we built a detailed thermodynamic model. The mutants all have a different genetic wiring than the wild-type λ. One group lacks regulation of PRM by the lytic protein. These mutants only exhibit the lysogenic equilibrium, with no transiently active PR. The other group lacks the negative feedback from CI. In this group, we identify a handful of bi-stable mutants, although the majority only exhibit the lysogenic equilibrium. The experimental identification of functional phages differs from our predictions. From a theoretical perspective, there is no reason why only 4 out of 900 mutants should be functional. The differences between theory and experiment can be explained in two ways. Either, the view of the λ phage as a bi-stable system needs to be revised, or the mutants have in fact not undergone a modular replacement, as intended by Atsumi and Little, but constitute instead a wider systemic change.

Received 10 June 2009, accepted for publication 11 September 2009
Published 6 October 2009

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