Abstract
The constitutive expression of glutaryl-7-amidocephalosporanic acid (GL-7-ACA) acylase was realized. Based on it, a new plasmid pGEMKT-HPfACY with optimized RBS was constructed and transformed into E. coli JM105.After culturing in LB media, this recombinant strain reached an activity of 0.44 U/mL. This activity was twice of former one while the activity of the strain JM105/pGEMKT-HPRfACY reached as high as 2.98 U/mL using corn-steep as culture media. The acylase activity of recombinant strain hit 6.37 U/mL, using a strategy of controlling pH 7.5 by adding nutrient such as glycerin.
Original language | English (US) |
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Pages (from-to) | 140-143 |
Number of pages | 4 |
Journal | Guocheng Gongcheng Xuebao/The Chinese Journal of Process Engineering |
Volume | 8 |
Issue number | 1 |
State | Published - Jan 2008 |
Externally published | Yes |
Keywords
- 7-aminocephalosporanic acid
- Constitutive expression
- Glutaryl-7-amidocephalosporanic acid acylase