Natural phosphorylation of group A streptococcal pyrogenic exotoxin type C.

Abstract:

:Group A streptococcal pyrogenic exotoxin (SPE) type C, produced by strain T18P grown in the presence of 32P, was separated from culture supernatant fluids by using alcohol precipitation. The resulting toxin (EtOH-1) contained 3 X 10(6) to 5 X 10(6) cpm of 32P per milligram of protein. The radiolabel migrated with SPE C during isoelectric focusing in polyacrylamide gels (pI 6.7) and double immunodiffusion, in which the toxin formed a line of identity with highly purified SPE C when reacted with hyperimmune antisera raised against SPE C. The EtOH-1 radiolabeled toxin was pyrogenic and had the capacity to enhance host susceptibility to lethal endotoxin shock. EtOH-1 toxin lost both radiolabel and biological activity after being treated with alkaline phosphatase. The nonspecific lymphocyte mitogenicity of purified unlabeled SPE C was stimulated by adenosine monophosphate but not adenosine, adenosine diphosphate, or adenosine triphosphate. Adenosine monophosphate may function as a cofactor of SPE C and contribute the phosphate group required for biological activity.

journal_name

Infect Immun

journal_title

Infection and immunity

authors

Schlievert PM,Bettin KM,Watson DW

doi

10.1128/IAI.26.2.585-589.1979

keywords:

subject

Has Abstract

pub_date

1979-11-01 00:00:00

pages

585-9

issue

2

eissn

0019-9567

issn

1098-5522

journal_volume

26

pub_type

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