Difference between revisions of "Part:BBa K5089008"
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The rationale for this approach is that arginine’s side chain can stabilize the deprotonated catalytic serine which in turn lowers the overall pKa of the enzyme towards acidic pH (1). Using this approach, we identified potential amino acid targets, including the S146R mutation in ABO2449. | The rationale for this approach is that arginine’s side chain can stabilize the deprotonated catalytic serine which in turn lowers the overall pKa of the enzyme towards acidic pH (1). Using this approach, we identified potential amino acid targets, including the S146R mutation in ABO2449. | ||
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+ | <b>Reference:</b><br> | ||
+ | 1. Chen, A., Xu, T., Ge, Y., Wang, L., Tang, W., & Li, S. 2019. Hydrogen-bond-based protein engineering for the acidic adaptation of Bacillus acidopullulyticus pullulanase. Enzyme and Microbial Technology, 124, 79–83. https://doi.org/10.1016/j.enzmictec.2019.01.010 | ||
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+ | __NOTOC__ | ||
+ | <partinfo>BBa_K5089008 short</partinfo> | ||
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+ | <partinfo>BBa_K5089008 SequenceAndFeatures</partinfo> |
Latest revision as of 23:20, 1 October 2024
ABO2449(S146)R is an α/β hydrolase mutant with a S146R mutation to improve enzyme stability at acidic pH. Our team designed these mutants for application in acidic compost environments but can be used by other iGEM teams that require an esterase.
We designed these mutants inspired by Chen et al. (2019) who explored amino acid substation to arginine residues within the active site of Bacillus acidopullulyticus pullulanase to shift its pH optimum to acidic pH (from pH 5.0 – 4.0). By analyzing the hydrogen bonding network involving the catalytic residues within the active site, they identified a set of residues that formed hydrogen bonds with residues that directly interact with the catalytic residue (1).
The rationale for this approach is that arginine’s side chain can stabilize the deprotonated catalytic serine which in turn lowers the overall pKa of the enzyme towards acidic pH (1). Using this approach, we identified potential amino acid targets, including the S146R mutation in ABO2449.
Reference:
1. Chen, A., Xu, T., Ge, Y., Wang, L., Tang, W., & Li, S. 2019. Hydrogen-bond-based protein engineering for the acidic adaptation of Bacillus acidopullulyticus pullulanase. Enzyme and Microbial Technology, 124, 79–83. https://doi.org/10.1016/j.enzmictec.2019.01.010
ABO2449(S146R)
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 735
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 754
Illegal NgoMIV site found at 874
Illegal NgoMIV site found at 900 - 1000COMPATIBLE WITH RFC[1000]