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ELUTION DIAGRAM OF CYTOCHROME-C FROM ION-EXCHANGE MAGNETIC NANOPARTICLES. FERMENTATION PROFILE OF Pichia pastoris : PRODUCTION OF RECOMBINANT DROSOMYCIN. ADSORPTION ISOTHERM OF DROSOMYCIN FERMENTATION BROTH ON MAGNETIC NANOPARTICLES. SUMMARY OF DROSOMYCIN PURIFICATION USING
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ELUTION DIAGRAM OF CYTOCHROME-C FROM ION-EXCHANGE MAGNETIC NANOPARTICLES
FERMENTATION PROFILE OF Pichia pastoris: PRODUCTION OF RECOMBINANT DROSOMYCIN
ADSORPTION ISOTHERM OF DROSOMYCIN FERMENTATION BROTH ON MAGNETIC NANOPARTICLES
SUMMARY OF DROSOMYCIN PURIFICATION USING MAGNETIC NANOPARTICLES
SDS GEL ELECTROPHORESIS USING MAGNETIC NANOPARATICLES: ELUTION PROFILES OF DROSOMYCIN
COMPARISON OF MAGNETIC NANOPARTICLES WITH OTHER PURIFICATION SCHEMES
NEW CONCEPT IN INCREASING OXYGEN TRANSFER RATE USING MAGNETIC NANOPARTICLES Magnetic particle Oleic Acid 20 nm 30-50 nm • Low amount of coating • Very high interfacial areas • Readily recovered by magnetic filtration
Aqueous solution of FeCl2 and FeCl3 NH4OH 80ºC Oleic acid coating Hitenol coating SYNTHESIS OF MAGNETIC NANO-PARTICLES • Fast (30 min) simple synthesis (stirred tank) • Inexpensive, readily available materials
MASS TRANSFER CHARACTERIZATION IN BIOREACTORS: SULFITE OXIDATION air to mass spec Di = 10cm HL = 14.5cm [SO32-] = 0.67M [Cu2+] = 1x10-3 M VTOTAL = 20L VWORKING = 5.5L Dtank = 22cm
OXYGEN MASS TRANSFER COEFFICIENT VERSUS GASSED POWER PER UNIT VOLUME IN 20-LITER BIOREACTOR Ф: particle wt%
OXYGEN MASS TRANSFER IN E. coli FERMENTATIONS • Seed culture • - 100 ml LB in 500 ml shake flask • - overnight culture at 37 oC, 220rpm • Fermentation culture (7.5 L fermentor) • - inoculation volume: 10% (v/v) • - initial fermentation volume: 3 L • - temperature: 37 oC • - agitation speed: 600 rpm • - pH = 6.8-6.9, adjusted by 4 M (NH4OH:NaOH = 2:2)
SUMMARY OF OXYGEN TRANSFER COEFFICIENT IN E. COLI FERMEMENTATION WITH AND WITHOUT MAGNETIC NANOPARTICLES
SUMMARY AND CONCLUSIONS • Micro-Bioreactors Will Began to Have Impacts in Biotechnology Processes • Reducing Time in Process Development • Strain Selection • Medium Development • Product Quality in Mammalian Cell Culture • Nano-Technology Has Definite Future • Product Purification • Over-Coming Transport Barriers • Oxygen Transfer • Biocatalysis and Co-Factor Regeneration