In the present investigation, the purification of β-galactosidase synthesized from Bacillus safensis (JUCHE 1), a new strain isolated from casein whey, has been considered. Broth harvested after 28 h (100.8 × 103s) was first centrifuged, and the sedimented cell pellet was sonicated to isolate intracellular β-galactosidase. After sonication, the intracellular fluid was subjected to microfiltration (MF) (0.2 × 10-6m) and ultrafiltration (UF) (300 kg mol-1) in series using a flat-sheet poly(ether sulfone) (PES) membrane in a novel rotating-disk membrane module. In the present investigation, four-stage discontinuous diafiltration (DD) at a constant volume concentration factor (VCF = 2) was carried out. Hydrodynamic studies were conducted to determine the appropriate stirrer speed, transmembrane pressure (TMP), and membrane rotation speed. Finally, β-galactosidase was purified based on the principle of salting-out upon addition of 40% (w/v) ammonium sulfate, followed by dialysis using a 1 kg mol-1membrane. Subsequently, purified β-galactosidase was characterized using ortho-nitrophenyl-β-galactoside (ONPG) and lactose as substrates. © 2013 American Chemical Society.

Purification and characterization of β-galactosidase synthesized from bacillus safensis (JUCHE 1)

Sudip Chakraborty
Validation
;
Enrico Drioli
Supervision
;
2013-01-01

Abstract

In the present investigation, the purification of β-galactosidase synthesized from Bacillus safensis (JUCHE 1), a new strain isolated from casein whey, has been considered. Broth harvested after 28 h (100.8 × 103s) was first centrifuged, and the sedimented cell pellet was sonicated to isolate intracellular β-galactosidase. After sonication, the intracellular fluid was subjected to microfiltration (MF) (0.2 × 10-6m) and ultrafiltration (UF) (300 kg mol-1) in series using a flat-sheet poly(ether sulfone) (PES) membrane in a novel rotating-disk membrane module. In the present investigation, four-stage discontinuous diafiltration (DD) at a constant volume concentration factor (VCF = 2) was carried out. Hydrodynamic studies were conducted to determine the appropriate stirrer speed, transmembrane pressure (TMP), and membrane rotation speed. Finally, β-galactosidase was purified based on the principle of salting-out upon addition of 40% (w/v) ammonium sulfate, followed by dialysis using a 1 kg mol-1membrane. Subsequently, purified β-galactosidase was characterized using ortho-nitrophenyl-β-galactoside (ONPG) and lactose as substrates. © 2013 American Chemical Society.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/366620
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