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Effect of Streptococcal Extracellular Nuclease on the Carrier Activity of RNA for Streptolysin S
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Upon digestion with a streptococcal extracellular nuclease, yeast RNA yielded acid-insoluble core having increased carrier activity for streptolysin S. The carrier activity was found in minor fractions of the core which were eluted from a DEAE-cellulose column at higher salt concentrations. Upon gel filtration through a Sephadex G-75 column, the effective component (Fr. I) was eluted earlier than bulk oligonucleotides (Fr. II). Nucleotide composition (in mol %) of Fr. I was AMP: 21.8; GMP: 55.1; CMP: 8.2; UMP: 14.9, whereas that of Fr. II was AMP: 38.0; GMP: 33.1; CMP: 8.0; UMP: 20.9. Chromatographic patterns of SLS complex induced by Fr. I were similar to those of the toxin formed in the presence of active fraction prepared from RNase I core. Hemolytic activity of the latter complex was, like the former, unaffected by streptococcal nuclease treatment. The carrier activity of DNA digested with the nuclease was also investigated.
Title: Effect of Streptococcal Extracellular Nuclease on the Carrier Activity of RNA for Streptolysin S
Description:
Upon digestion with a streptococcal extracellular nuclease, yeast RNA yielded acid-insoluble core having increased carrier activity for streptolysin S.
The carrier activity was found in minor fractions of the core which were eluted from a DEAE-cellulose column at higher salt concentrations.
Upon gel filtration through a Sephadex G-75 column, the effective component (Fr.
I) was eluted earlier than bulk oligonucleotides (Fr.
II).
Nucleotide composition (in mol %) of Fr.
I was AMP: 21.
8; GMP: 55.
1; CMP: 8.
2; UMP: 14.
9, whereas that of Fr.
II was AMP: 38.
0; GMP: 33.
1; CMP: 8.
0; UMP: 20.
9.
Chromatographic patterns of SLS complex induced by Fr.
I were similar to those of the toxin formed in the presence of active fraction prepared from RNase I core.
Hemolytic activity of the latter complex was, like the former, unaffected by streptococcal nuclease treatment.
The carrier activity of DNA digested with the nuclease was also investigated.
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