Abstract
High performance liquid chromatography was used for the purification of ribosomal proteins derived from the halophilic archaebacteriumHalobacterium marismortui. Separation was performed using size exclusion chromatography, reversed phase and ion-exchange chromatography. For reversed phase separation several solvent systems were te sted including isopropanol and acetonitrile. Tris/citrate buffer containing 30% N,N-dimethylformanide was employed in combination with a DEAE-anoin-exchanger.
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