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      Condensation of bacteriophage phi W14 DNA of varying charge densities by trivalent counterions.

      Biochemistry
      Bacteriophages, Chemical Phenomena, Chemistry, Cobalt, DNA, Viral, isolation & purification, Elasticity, Light, Mathematics, Nucleic Acid Conformation, Pseudomonas, Putrescine, Scattering, Radiation, Spermidine

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          Abstract

          Bacteriophage phi W14 DNA carries the hypermodified, positively charged (2+) base alpha-putrescinylthymine (puThy) and consequently exhibits a decreased average linear charge density compared to the conventional B-form DNA helix. Noting that the unusual physical characteristics may contribute to the collapse properties of this DNA and facilitate the exceptionally high density of packaging of its genome in phi W14, I used total intensity light scattering to determine in vitro the critical concentrations of spermidine (Spd, 3+) required to induce the cooperative, monomolecular collapse of wild-type and mutant phi W14 DNA samples and quasi-elastic light scattering to compare the dynamic characteristics of the compacted particles. The DNA samples carried various percentages of the modified base with average charge spacings ranging from 1.3 to 2.2 A in comparison to T4 phage DNA (1.7 A). The results are analyzed and discussed both from a general theoretical point of view according to the counterion condensation theory of Manning [Manning, G. S. (1978) Q. Rev. Biophys. 11, 179-246] and from the more specialized aspect of DNA packaging in phi W14. In accord with theory, DNAs of lower charge density require a considerably higher critical counterion concentration (up to 118 microM Spd), whereas the outside diameter of the toroidal condensates, which they form, varies only marginally. Specific ion effects were probed by substituting hexaamminecobalt(III) (Hc, 3+) for Spd. Hc appears to be more efficient than Spd: it induces the collapse of all DNA samples at only one-sixth the critical concentration of Spd, and its condensates are 30% smaller (1072-1142 A vs. 744-800 A) except for wild-type phi W14 DNA, which forms Hc-collapsed particles indistinguishable from Spd-induced condensates. Collapse occurs, again with the exception of wild-type phi W14 DNA, when approximately 89% of the charges on each DNA are neutralized by territorially bound Spd. I conclude that the driving force for condensation clearly is a function of the charge density of the DNA and that the charge distribution may be an important factor in determining the degree of neutralization at which collapse becomes possible. The sample with the lowest charge density, wild-type phi W14 DNA, does not follow the trends set by the other members of the series.(ABSTRACT TRUNCATED AT 400 WORDS)

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