The production of phytase in a recombinant E.coli using the pBAD expression system was optimized using response surface methodology with full-factorial faced centered central composite design. The ampicilin and arabinose concentration in the cultivation media and the incubation temperature were optimized in order to maximize phytase production using 2 3 central composite experimental design. With this design the number of actual experiment performed could be reduced while allowing eludidation of possible interactions among these factors. The most significant parameter was shown to be the linear and quadratic effect of the incubation temperature. Optimal conditions for phytase production were determined to be 100 µg/ml ampicilin, 0.2 % ar...
Abstract Phytase production by Pichiapastoris was used as a case to study the mechanism and strategy...
The function of chitinase as a chitin digestive enzyme has attracted the attention as one of the pot...
The gene encoding for phytase from ASUIA279 has been successfully cloned and expressed in pichia pas...
The production of phytase in a recombinant E.coli using the pBAD expression system was optimize...
The production of phytase in a recombinant E.coliusing thepBAD expression system wasoptimized using ...
The medium for recombinant phytase production by E. coli BL21 was optimized using response surface m...
The medium for recombinant phytase production by E. coli BL21 was optimized using response surface m...
An efficient fermentation process for the production of phytase was developed by statistical optimiz...
An efficient fermentation process for the production of phytase was developed by statistical optimiz...
An efficient fermentation process for the production of phytase was developed by statistical optimiz...
Screening for the important variables is part of the optimization study of enzyme production. It is ...
The recombinant Escherichia coli BL21(DE3) that carries a thermostable phytase gene from Bacillussp....
Due to several biological characteristics, bacterial phytases have considerable potential in commerc...
Response surface methodology was used to optimize critical process variables in the production of ca...
Factorial designs and second order response surface methodology (RSM) for medium optimization were e...
Abstract Phytase production by Pichiapastoris was used as a case to study the mechanism and strategy...
The function of chitinase as a chitin digestive enzyme has attracted the attention as one of the pot...
The gene encoding for phytase from ASUIA279 has been successfully cloned and expressed in pichia pas...
The production of phytase in a recombinant E.coli using the pBAD expression system was optimize...
The production of phytase in a recombinant E.coliusing thepBAD expression system wasoptimized using ...
The medium for recombinant phytase production by E. coli BL21 was optimized using response surface m...
The medium for recombinant phytase production by E. coli BL21 was optimized using response surface m...
An efficient fermentation process for the production of phytase was developed by statistical optimiz...
An efficient fermentation process for the production of phytase was developed by statistical optimiz...
An efficient fermentation process for the production of phytase was developed by statistical optimiz...
Screening for the important variables is part of the optimization study of enzyme production. It is ...
The recombinant Escherichia coli BL21(DE3) that carries a thermostable phytase gene from Bacillussp....
Due to several biological characteristics, bacterial phytases have considerable potential in commerc...
Response surface methodology was used to optimize critical process variables in the production of ca...
Factorial designs and second order response surface methodology (RSM) for medium optimization were e...
Abstract Phytase production by Pichiapastoris was used as a case to study the mechanism and strategy...
The function of chitinase as a chitin digestive enzyme has attracted the attention as one of the pot...
The gene encoding for phytase from ASUIA279 has been successfully cloned and expressed in pichia pas...