Overexpression of Adenosine Deaminase in Escherichia coli

  • Jo, Young-Bae (Division fo Biological Science, Pusan National University, Pusan 609-735) ;
  • Baik, Hyung-Suk (Division fo Biological Science, Pusan National University, Pusan 609-735) ;
  • Bae, Kyung-Mi (Division fo Biological Science, Pusan National University, Pusan 609-735) ;
  • Jun, Hong-Ki (Corresponding author, Division fo Biological Science, Pusan National University, Pusan 609-735)
  • Published : 1999.10.01

Abstract

To overexpress E. coli ADA in host strain E. coli M15, the expression plasmid pQEADD was constructed. To analyze the expression characteristics of ADA, a time course of the expression was first examined. The protein was not detected in no inducted in no induction samples. After the addition of IPTG, a band corresponding to the expected size of ADA was appeared. Its molecular weight was about 36,000 dalton. Maximum expression level was revealed when the cell cultured for 3∼4hrs after induction. This result indicated that the efficient expression of add can be achieved by induction at early logarithmic phase. The effect of different IPTG concentration on the degree of ADA expression was investigated. The expression levels of add were not largely affected by IPTG concentration. Location of overexpression ADA was checked out. A protein band corresponding to the ADA was seen in only crude extract B(insoluble protein). This result suggests that ADA is in E. coli M15. The molecular weight of ADA estimated by SDS-PAGE was approximately 36,000 Da.

Keywords