Difference between revisions of "Part:BBa K3332047"

Revision as of 23:26, 27 October 2020

J23100-RBS-INPNC-iNAP-terminator

The iNAP is fused at N-terminal with INPNC anchoring protein. We use K880005 to construct the expression system and anchor iNAP on the surface of E.coli.

Biology

GRHPR, a glyoxylate reductase from human liver, can reduce glyoxylic acid when NADPH is used as cofactor. GRHPR converts glyoxylic acid while consuming NADPH. NADPH is a suitable target compound that can be detected by the signal of fluorescence or OD₃₄₀.^[1]

Fig 1. GRHPR mechanism.

Usage

By codon optimization and adding a 6His-tag, the sequence suitable for expression in E. coli was constructed, and we hoped that it could reduce glyoxylic acid in E. coli to get fluorescence signal in the next processes we design.

The coding sequence of target gene was inserted into an expression vectors with BBa_K880005(BBa_J23100 & BBa_B0034) to obtain BBa_K3332056. We transformed the constructed plasmid into E. coli BL21 (DE3) to verify its successful heterologous expression.

Fig 2. Gene circuit of GRHPR.

Characterization

1. Identification

After receiving the synthesized DNA, restriction digestion was done to certify that the plasmid was correct, and the experimental results were shown in figure 3.

Fig 3. DNA gel electrophoresis of restriction digest products of GRHPR-His-pSB1C3 (Xbal I & Pst I sites)

2. Purification and Proof of the expression

We used J23100 promoter to highly express GRHPR-Histag in E. coli in our composite part BBa_K3332056. Then, we used GE AKTA Prime Plus FPLC System to get purified GRHPR protein. We found an apparent protein peak in AKTA FPLC System and correct purified protein.

Then, our target bands are observed through SDS-PAGE and the result is shown in figure4.

Fig 4. SDS-PAGE of purification products of GRHPR-Histag-pSB1C3

3. Ability of consuming NADPH

We mixed glyoxylic acid solution, NADPH solution and purified GRHPR protein dissolved in Tris-HCl(pH=7.5). Then, we immediately measured OD₃₄₀ changes of our samples. And when NADPH is consumed, OD₃₄₀ declines.

The experimental result is shown on Figure 5. We can see the OD₃₄₀ of samples adding GRHPR decrease very quickly while the OD₃₄₀ of control stay almost the same.

Fig 5.' Enzyme activity of GRHPR.

4. Kinetic parameter determination

We successfully got OD₃₄₀-Time curves of GRHPR in the presence of NADPH concentration and OD₃₄₀-Time curves of GRHPR in the presence of glyoxylic acid concentration. Then we calculated relevant enzyme activity and drew 1/V-1/[NADPH] and 1/V-1/[glyoxylic acid] curves, from which we can obtain relevant Km and Vmax.

The result is shown in figure 6 and figure 7.

Fig 6. 1/V-1/[NADPH] curve of purified GRHPR reacting with NADPH and glyoxylic acid

Fig 7. 1/V-1/[glyoxylic acid] curve of purified GRHPR reacting with NADPH and glyoxylic acid

References

1. ↑ Rumsby G, Cregeen D P. Identification and expression of a cDNA for human hydroxypyruvate/glyoxylate reductase[J]. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1999, 1446(3): 383-388.

Sequence and Features