Purification Of Hydrogenase Research Articles

Strategies for reliable and improved large-scale production of Pyrococcus furiosus with integrated purification of hydrogenase I

The hyperthermophilic archaeon Pyrococcus furiosus is an interesting organism for research and application, especially owing to its unique NADPH-dependent hydrogenase I. However, mass production of P. furiosus through fermentation is susceptible to fault because of its sensitivity to oxygen, a short exponential and stationary phase and a rapid cell lysis in typical cultivation process. In this study, significant improvement for pilot plant scale production processes for P. furiosus biomass was made by investigations of the fermentation process with subsequent hydrogenase I enzyme purification. Scale-up in a 300-L stirred tank bioreactor was successfully achieved. A repeated-batch cultivation process with high reproducibility and productivity was realized. Furthermore, the enzyme hydrogenase I was purified, and its activity tested and verified. The improvements in this production process for the production of large amount of P. furiosus biomass and hydrogenase I have been achieved, especially by successfully implementing the following key measures and steps: unsterile cultivation setup, skipping typical intermediate preculture and inoculation steps, accelerating the cultivation process by defining an optimal state of the inoculation, optimal time point of biomass harvesting and finally by choosing a one-step purification procedure for enzyme recovery.

Proteolytic resistance and its utilization in purification of hydrogenase from Thiocapsa roseopersicina

The effect of various proteinases on the hydrogenase from Thiocapsa roseopersicina has been studied by activity measurements accompanied with electrophoretic separation of the protein components. The native enzyme cannot be digested by the following proteinases: thermolysin, subtilisin, trypsin, papain, pepsin, proteinase-K, pronase E, Bacillus subtilis proteinase, Staphylococcus aureus strain V8 proteinase under standard conditions for optimal proteolytic cleavage. Pretreatments which commonly make resistant proteins accessible to proteolysis have been found ineffective in destabilizing the hydrogenase. The native hydrogenase is readily cleavable and inactivated by CNBr. Also under conditions which irreversibly inactivate the hydrogenase (boiling for 10 min) the enzyme loses its active conformation and becomes susceptible to proteolysis. The protein, as isolated, apparently contains no protective lipids or carbohydrates. The results suggest that a stable hydrogenase apoprotein structure is responsible for the proteolytic resistance. The remarkable stability of this enzyme offers new ways for its purification. A rapid and effective procedure, suitable for scale-up, has been established.

Purification of hydrogenase from Desulfovibrio desulfuricans

Purification of hydrogenase from Desulfovibrio desulfuricans