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
. 1958 Dec 1;108(6):803-21.
doi: 10.1084/jem.108.6.803.

Studies on the bacteriophages of hemolytic streptococci. II. Antigens released from the streptococcal cell wall by a phage-associated lysin

Studies on the bacteriophages of hemolytic streptococci. II. Antigens released from the streptococcal cell wall by a phage-associated lysin

R M KRAUSE. J Exp Med. .

Abstract

The lysis of cell walls of hemolytic streptococci by a phage-associated lysin has been described. A method is presented for preparing the lysin from Group C streptococcal phage lysates. Following lysis almost all of the cell wall carbohydrate is recovered in solution. This material has the serological reactivity, physical-chemical properties, and values for nitrogen, rhamnose, and glucosamine similar to those of the carbohydrate isolated from the cell walls by the Streptomyces albus enzyme. Group C carbohydrate isolated by either enzyme inactivates Group C bacteriophage. The protein liberated by the lysin from Group A Type 6 cell walls gives a type-specific precipitin reaction with homologous rabbit antiserum. Preliminary data are presented on the ammonium sulfate fractionation and the electrophoretic separation of a protein fraction with the serological reactivity of M protein.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Exp Med. 1946 Jul 31;84(2):127-42 - PubMed
    1. J Bacteriol. 1948 Nov;56(5):683-93 - PubMed
    1. J Gen Physiol. 1951 Sep;35(1):89-118 - PubMed
    1. J Gen Microbiol. 1957 Jun;16(3):584-95 - PubMed
    1. Methods Biochem Anal. 1954;1:141-70 - PubMed