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Thesis final - after defense-7 - Jacobs University

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Chapter 3<br />

among the adsorbents were higher at low salt concentrations than at the high salt<br />

concentrations (121). The reason for this could be that at the extreme hydrophobic conditions,<br />

the hydrophobic potential of the mobile phase has covered the potential of the base supports<br />

to demonstrate according to their hydrophobicities. At low salt concentrations, the mobile<br />

phase has low hydrophobicity and the adsorption was more dependent on the hydrophobicity<br />

of the base supports.<br />

3.2.3.5. Application note<br />

This work can help those interested in the purification of proteins listed in Tables 12-14. It<br />

will simplify the work of researchers and they will not have to scout for chromatographic<br />

experiments to figure out the elution position of any tabulated protein. The protein can be<br />

purified by isocratic chromatography, without going through trial and error chromatographies.<br />

Some of the important enzymes are Pyruvate kinase (eluted at 0.6 M on Sepharose-Phenyl),<br />

Phosphoglycerate mutase 2 (eluted at 0.8 M on Toyopearl-Phenyl), Polymerase A (0 M on<br />

Source-Pheny), Methyl transferase (0.2 M on Sepharose-Phenyl), Thiosulfate sulphur<br />

transferase (0.2 M on Source-Phenyl), Enolase 2 (1.6 M on Toyopearl-Phenyl), D-serine<br />

dehydratase (0.6 M on Toyopearl-Phenyl) and Alcohol dehydrogenase (0.2 M on Sepharose-<br />

Phenyl).<br />

100

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