Abstract
Three-phase partitioning (TPP) was used to purify invertase from Baker's yeast ( Saccharomyces cerevisiae) in a single step. The influence of various process parameters like ammonium sulfate concentration, crude extract to t-butanol ratio and pH on invertase partitioning is investigated in order to enhance the purification fold degree and activity recovery of invertase. Under optimized conditions (50%, w/v, ammonium sulfate saturation, 1:0.5 crude extract to t-butanol ratio and pH 4.0), the invertase was purified to 15-fold with 363% activity recovery. The enzyme obtained from TPP showed considerable purification on sodium dodecyl polyacrylamide gel electrophoresis with a molecular weight of 52 kDa. The optimum temperature and pH were determined as 60 °C and pH 6.0, respectively. The purified enzyme was also very stable at a pH range of 4.0–6.5 and temperature range of 4–50 °C. The K m and V max values were calculated from Lineweaver–Burk plot as 0.19 M and 29.8 U, respectively.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
