Abstract
Diphtheria toxin and fragment B bind to hydrocarbon-coated agaroses. Fragment A of the toxin is not adsorbed to such resins. Using Seph-C4, the toxin and fragment B can be eluted from the column after adsorption by increasing the ionic strength of the eluent. The toxin is also eluted from the Seph-C6 column, but fragment B is eluted only in the denatured form. Purification of the toxin can be achieved simply by passing the growth medium supernatant through a small size Seph-C6 column and eluting the toxin by 0.1 m NaCl. The fragments of diphtheria toxin obtained after mild trypsin treatment can be separated purely on a Seph-C4 column. The hydrophobic chromatography system may thus serve as a tool for purification of the toxin and its fragments: it may also be useful in large-scale preparations.
| Original language | English |
|---|---|
| Pages (from-to) | 71-75 |
| Number of pages | 5 |
| Journal | Analytical Biochemistry |
| Volume | 109 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1980 |
| Externally published | Yes |
Bibliographical note
Funding Information:We wish to thank Mrs. S. Gozhansky nical assistance. This work was supported from the Bat-Sheva de Rothschild to Y.N.
Funding
We wish to thank Mrs. S. Gozhansky nical assistance. This work was supported from the Bat-Sheva de Rothschild to Y.N.
| Funders |
|---|
| Bat-Sheva de Rothschild |
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