Difference between revisions of "Part:BBa K2949013"
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====1.2 Expression and purification of CA2(L203K)-C-LCTPSR protein in E.coli TB1==== | ====1.2 Expression and purification of CA2(L203K)-C-LCTPSR protein in E.coli TB1==== | ||
− | The expression of CA2(L203K)-C-LCTPSR in E.coli were detected by SDS-PAGE. The results showed that CA2(L203K)-C-LCTPSR could be successfully expressed in our chassis E.coli.(Fig. 4) | + | The expression of CA2(L203K)-C-LCTPSR in E.coli TB1 were detected by SDS-PAGE. The results showed that CA2(L203K)-C-LCTPSR could be successfully expressed in our chassis E.coli TB1.(Fig.4) |
[[File:T--AHUT China--ImproPart 04.png|350px|center|thumb|Fig.4 SDS-PAGE analysis for CA2(L203K)-C-LCTPSR cloned in pET-30a(+) and expressed in | [[File:T--AHUT China--ImproPart 04.png|350px|center|thumb|Fig.4 SDS-PAGE analysis for CA2(L203K)-C-LCTPSR cloned in pET-30a(+) and expressed in | ||
E.coli TB1<br>Lane 1: CA2(L203K)-C-LCTPSR protein expression without IPTG induction; Lane 2: | E.coli TB1<br>Lane 1: CA2(L203K)-C-LCTPSR protein expression without IPTG induction; Lane 2: |
Revision as of 17:40, 21 October 2019
Carbonic Anhydrase 2(L203K)-C-LCTASR
we constructed this new biobrick by connecting the C-terminal of the mutant human carbonic anhydrase 2 [CA2(L203K)] (BBa_K2547004) with the six-residue sulfatase submotif (LCTPSR). Formylglycine generating enzyme can selectively recognize and oxidize the cysteine residues in the sulfatase subunit of the protein terminal to form formylglycine (FGly) residues containing aldehyde groups, which can be immobilized via forming covalent bond with amino functionalized carriers (Unisil 30-100 NH2) through the Schiff base reaction.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
In order to the further improve the industrial application of CA2 for CO2 capture, basing on the existing part (BBa_K2547004) we designed last year, we have constructed a new biobrick[CA2(L203K)-C-LCTPSR](BBa_K2949013) by connecting the C-terminal of the mutant human carbonic anhydrase 2 [CA2(L203K)](BBa_K2547004) coding sequences with the six-residue sulfatase submotif(LCTPSR) in a way similar to that of CA2(L203K)-N-LCTPSR, to achieve enzyme immobilization and maintain high thermal stability and CA2 reuse by modifying its gene sequence.
1. Engineered E.coli TB1
1.1 Construction of CA2(L203K)-C-LCTPSR expression plasmid
The coding sequence of CA2(L203K)-C-LCTPSR(BBa_K2949013) was synthesized, and then cloned into pET-30a(+) expression vector.
The correctness of the obtained recombinant vector was identified by restriction enzyme digestion (Fig.2) and sequencing(Fig.3).
1.2 Expression and purification of CA2(L203K)-C-LCTPSR protein in E.coli TB1
The expression of CA2(L203K)-C-LCTPSR in E.coli TB1 were detected by SDS-PAGE. The results showed that CA2(L203K)-C-LCTPSR could be successfully expressed in our chassis E.coli TB1.(Fig.4)
We successfully co-transformed pBAD-FGE and pET-30a(+)-CA2(L203K)-C-LCTPSR into E.coli TB1 for the following CA2(L203K)-C-LCTPSR immobilization. Then the improve part of CA2(L203K)-C-LCTPSR protein was further purified through nickel column and detected by SDS-PAGE, as shown in Fig.5.
2. Identification of the function for CO2 capture
2.1 The efficiency of CA2(L203K)-C-LCTPSR protein immobilization
FGE can selectively identify and oxidize cysteine residues in the sulfatase subunit(LCTPSR) at the end of the protein to form aldehyde-containing formylglycine, which can be used for enzyme immobilization. Then we immobilized CA2(L203K)-C-LCTPSR protein, and our formula for calculating the enzyme immobilized efficiency is as follows:
According to the formula, we got the efficiency of immobilized CA2(L203K)-C-LCTPSR protein is 39.09%.
2.2 Enzyme activity asssay of CA2(L203K)-C-LCTPSR protein
To further demonstrate the activity of our improved part, the enzyme activity of CA2(L203K)-C-LCTPSR (BBa_K2949013) and CA2(L203K) protein (BBa_K2547004) of CO2 capture were tested experimentally by esterase activity assay at 37℃ and 50℃.
As shown in Fig.6 and Fig.7, immobilized CA2(L203K)-C-LCTPSR protein was stable at high temperature and retained its activity, and free CA2(L203K)-C-LCTPSR protein has a higher activity than CA2(L203K) protein.
3. Application Model for detecting CO2 capture
Because the immobilized CA2(L203K)-C-LCTPSR protein have higher activity and reuse ability than immobilized CA2(L203K)-N-LCTPSR protein, so the reuse ability of the immobilized CA2(L203K)-C-LCTPSR was tested by our designed simulation model (Fig.8). Compared with the original enzyme, the immobilized enzyme still retained 54 percent activity after five times of repeated absorption experiments of CO2, as indicated in Fig.9. The result showed that the immobilized CA2(L203K)-C-LCTPSR could absorb CO2 under the simulation model and showed potential reuse ability.
In conclusion, our results demonstrated that the function of improved part has been improved with higher activity than original part, especially achieved enzyme immobilization, and the immobilized CA2(L203K)-C-LCTPSR protein showed reuse ability, which might be suitable for industrial production.