Abstract
Summary
Both 3H-thymidine and small 32P-labeled elements of heavy density 32P2H 15N-Bacillus subtilis 168+ DNA were covalently incorporated into macromolecular DNA of genetically transformable R1 Diplococcus pneumoniae. The 3H and 32P markers in the DNA extracted from D. pneumoniae both assumed the position of light density doublestranded DNA on CsCl isopycnic equilibrium centrifugation when the DNA was untreated or shortened by sonication prior to centrifugal analysis, and of light density single-stranded DNA when first denatured by heat.
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