The Production of Alkaline Protease from a Recombinant Strain Expressed Apr
- DOI
- 10.2991/icmsa-15.2015.77How to use a DOI?
- Keywords
- Alkaline Protease, Recombinant, Optimization, Activity.
- Abstract
The alkaline protease gene, Apr, from Bacillus licheniformis 2709 was cloned into an expression vector pET - 28b(+). The pET-28b(+) - Apr was expressed in a high expression strain E. coli BL21. In order to develop and optimize mathematical model of protease activity, three variables were investigated, including peptone concentration (6 g/L to 10 g/L), incubation time (16 h to 32 h) and agitation frequency (150 r/min to 240 r/min), by response surface methodology (RSM). The protease produced by recombinant strain with optimal protease activity was predicted to be obtained at: the peptone concentration 8.08 g/L, the incubation time 24.25 h and the agitation frequency 180.14 r/min. Under the optimal condition, the protease activity achieved 1125.81 U/mL.
- Copyright
- © 2015, the Authors. Published by Atlantis Press.
- Open Access
- This is an open access article distributed under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/).
Cite this article
TY - CONF AU - Mei-Shuo Zhang AU - Ya-Nan Yang AU - Xue-Nan Li AU - Song-Yi Lin PY - 2014/06 DA - 2014/06 TI - The Production of Alkaline Protease from a Recombinant Strain Expressed Apr BT - Proceedings of the 2015 International Conference on Material Science and Applications PB - Atlantis Press SP - 427 EP - 431 SN - 2352-541X UR - https://doi.org/10.2991/icmsa-15.2015.77 DO - 10.2991/icmsa-15.2015.77 ID - Zhang2014/06 ER -