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J Bacteriol. 1972 November; 112(2): 751-760
Copyright © 1972 American Society for Microbiology. All Rights Reserved.

Molecular Events Accompanying the Fixation of Genetic Information in Haemophilus Heterospecific Transformation

N. K. Notani1 and Jane K. Setlow2

1 Department of Microbiology, University of Tennessee, Knoxville, Tennessee 37916
University of Tennessee-Oak Ridge Graduate School of Biomedical Sciences and Biology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830

ABSTRACT

Heterospecific transformation between Haemophilus influenzae and H. parainfluenzae was investigated by isopycnic analysis of deoxyribonucleic acid (DNA) extracts of 3H-labeled transforming cells that had been exposed to 32P-labeled, heavy transforming DNA. The density distribution of genetic markers from the resident DNA and from the donor DNA was determined by transformation assay of fractions from CsCl gradients, both species being used as recipients. About 50% of the 32P atoms in H. parainfluenzae donor DNA taken up by H. influenzae cells were transferred to resident DNA, and only a small amount of the label was lost under conditions of little cell growth. There was less transfer in the reciprocal cross, and almost half of the donor label was lost. In both crosses, the transferred donor material transformed for the donor marker considerably more efficiently when assayed on the donor species than on the recipient species, indicating that at least some of the associated 32P atoms are contained in relatively long stretches of donor DNA. When the transformed cultures were incubated under growth conditions, the donor marker associated with recipient DNA transformed the donor species with progressively decreasing efficiency. The data indicate that the low heterospecific transformation between H. influenzae and H. parainfluenzae may be due partly to events occurring before association of donor and resident DNA but results mostly from events that occur after the association of the two DNA preparations.


J Bacteriol. 1972 November; 112(2): 751-760
Copyright © 1972 American Society for Microbiology. All Rights Reserved.







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