Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1985 Jan;161(1):72-9.
doi: 10.1128/jb.161.1.72-79.1985.

Comparison of transformation mechanisms of Haemophilus parainfluenzae and Haemophilus influenzae

Comparative Study

Comparison of transformation mechanisms of Haemophilus parainfluenzae and Haemophilus influenzae

F Barany et al. J Bacteriol. 1985 Jan.

Abstract

Transformation pathways in two closely related bacterial species, Haemophilus parainfluenzae and Haemophilus influenzae, were studied. Both organisms rapidly take up transforming DNA within minutes into specialized membranous structures on the cell surface (transformasomes). DNA within transformasomes is in a protected state, inaccessible to external DNase or internal restriction and modification enzymes. However, the subsequent processing of donor DNA differs in these two organisms. In H. influenzae, linear DNA immediately undergoes degradation from one end at a constant rate, leaving a lower-molecular-weight intermediate in the transformasome. The end undergoing degradation is searching for homologous regions of the chromosome. Once pairing is initiated, the remaining lower-molecular-weight DNA exits from the transformasome, and a single strand undergoes efficient integration. In contrast, in H. parainfluenzae little degradation of donor DNA is observed, with the majority remaining intact within the transformasomes after 1 h. Thus, whereas only 10% of donor DNA molecules leave the protected state after 1 h, portions of each molecule appear to become quantitatively integrated.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Proc Natl Acad Sci U S A. 1981 Nov;78(11):7028-32 - PubMed
    1. J Bacteriol. 1975 May;122(2):443-53 - PubMed
    1. J Bacteriol. 1982 Oct;152(1):183-90 - PubMed
    1. Proc Natl Acad Sci U S A. 1982 Oct;79(20):6370-4 - PubMed
    1. Annu Rev Genet. 1982;16:169-92 - PubMed

Publication types

LinkOut - more resources