Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6491817 | Journal of Biotechnology | 2013 | 5 Pages |
Abstract
The LST-03 lipase from Pseudomonas aeruginosa LST-03 requires lipase-specific foldase for activation. Abundant expression of the active lipase was successfully accomplished with individual expression of the lipase and foldase in a heterologous host and subsequent in vitro activation. Although the activity of the native lipase from culture supernatant of P. aeruginosa LST-03 was 110Â kI.U./g, that after in vitro activation using individually expressed lipase and foldase was 228Â kI.U./g. Furthermore, the activity after in vitro activation with afterwards adding calcium ions was 359Â kI.U./g. However, the incubation of the lipase with the foldase in the presence of calcium ions resulted in a small conformational transition and low activation levels of the lipase by the foldase. The lipase showed high affinity for the foldase in the presence of calcium ions. The results indicate that in a cellular environment that contains calcium ions, the lipase would not become a hyperactive form by the foldase.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Bioengineering
Authors
Hiroyasu Ogino, Sosuke Inoue, Masahiro Yasuda, Noriyuki Doukyu,