Difference between revisions of "Part:BBa K3332011"

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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 OD<sub>340</sub>.<ref>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.</ref>
 
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 OD<sub>340</sub>.<ref>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.</ref>
 
  
 
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         <img src="https://2020.igem.org/wiki/images/8/82/T--XMU-China--XMU-China_2020-GRHPR%E9%94%9A%E5%AE%9A.png" width="90%" style="float:center">
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         <img src="https://2020.igem.org/wiki/images/8/82/T--XMU-China--XMU-China_2020-GRHPR%E9%94%9A%E5%AE%9A.png" width="40%" style="float:center">
 
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:Fig 1. GRHPR mechanism
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:'''Fig 1.''' GRHPR mechanism.
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===Usage===
 
===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.
 
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.
  
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     <figure>
 
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         <img src="https://2020.igem.org/wiki/images/2/2e/T--XMU-China--XMU-China_2020-J23100_B0034_grhpr-his-tag_B0015.png" width="90%" style="float:center">
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         <img src="https://2020.igem.org/wiki/images/2/2e/T--XMU-China--XMU-China_2020-J23100_B0034_grhpr-his-tag_B0015.png" height="150" style="float:center">
 
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:Fig 2. Gene circuit of GRHPR
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 +
:'''Fig 2.''' Gene circuit of GRHPR.
 +
 
  
 
===Characterization===
 
===Characterization===
  
 
'''1. Identification'''
 
'''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.
 
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.
 +
 
<html>
 
<html>
 
     <figure>
 
     <figure>
         <img src="https://2020.igem.org/wiki/images/e/e8/T--XMU-China--07181.png" width="90%" style="float:center">
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         <img src="https://2020.igem.org/wiki/images/e/e8/T--XMU-China--07181.png" width="65%" style="float:center">
 
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Fig 3.DNA gel electrophoresis of restriction digest products of GRHPR-His-pSB1C3 (''Xbal'' I & ''Pst'' I sites)
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 +
:'''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'''
 
'''2.  Purification and Proof of the expression'''
 +
 
We used J23100 promoter to highly express GRHPR-Histag in ''E. coli'' in our composite part <partinfo>BBa_K3332056</partinfo>. 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.  
 
We used J23100 promoter to highly express GRHPR-Histag in ''E. coli'' in our composite part <partinfo>BBa_K3332056</partinfo>. 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.
 
Then, our target bands are observed through SDS-PAGE and the result is shown in figure4.
 +
 
<html>
 
<html>
 
     <figure>
 
     <figure>
         <img src="https://2020.igem.org/wiki/images/b/b1/T--XMU-China--XMU-China_2020-GRHPR_and_GOX.png" width="90%" style="float:center">
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         <img src="https://2020.igem.org/wiki/images/b/b1/T--XMU-China--XMU-China_2020-GRHPR_and_GOX.png" width="80%" style="float:center">
 
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:Fig 4. SDS-PAGE of purification products of GRHPR-Histag-pSB1C3
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:'''Fig 4.''' SDS-PAGE of purification products of GRHPR-Histag-pSB1C3
  
 
'''3. Ability of consuming NADPH'''  
 
'''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 OD<sub>340</sub> changes of our samples. And when NADPH is consumed, OD<sub>340</sub> declines.
 
We mixed glyoxylic acid solution, NADPH solution and purified GRHPR protein dissolved in Tris-HCl(pH=7.5). Then, we immediately measured OD<sub>340</sub> changes of our samples. And when NADPH is consumed, OD<sub>340</sub> declines.
 +
 
The experimental result is shown on Figure 5. We can see the OD<sub>340</sub> of samples adding GRHPR decrease very quickly while the OD<sub>340</sub> of control stay almost the same.
 
The experimental result is shown on Figure 5. We can see the OD<sub>340</sub> of samples adding GRHPR decrease very quickly while the OD<sub>340</sub> of control stay almost the same.
 +
 
<html>
 
<html>
 
     <figure>
 
     <figure>
         <img src="https://2020.igem.org/wiki/images/d/d4/T--XMU-China--XMU-China_2020-GRHPR酶活.png" width="90%" style="float:center">
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         <img src="https://2020.igem.org/wiki/images/d/d4/T--XMU-China--XMU-China_2020-GRHPR酶活.png" width="45%" style="float:center">
 
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     </figure>
 
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:Fig 5. Enzyme activity of GRHPR
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:'''Fig 5.'''' Enzyme activity of GRHPR.
  
 
'''4. Kinetic parameter determination'''
 
'''4. Kinetic parameter determination'''
 +
 
We successfully got OD<sub>340</sub>-Time curves of GRHPR in the presence of NADPH concentration and OD<sub>340</sub>-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.
 
We successfully got OD<sub>340</sub>-Time curves of GRHPR in the presence of NADPH concentration and OD<sub>340</sub>-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.
 
The result is shown in figure 6 and figure 7.
 +
 
<html>
 
<html>
 
     <figure>
 
     <figure>
         <img src="https://2020.igem.org/wiki/images/4/4c/T--XMU-China--XMU-China_2020-GRHPR_动力学参数1-NADPH底物.png" width="90%" style="float:center">
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         <img src="https://2020.igem.org/wiki/images/4/4c/T--XMU-China--XMU-China_2020-GRHPR_动力学参数1-NADPH底物.png" width="50%" style="float:center">
 
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     </figure>
 
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:'''Fig 6.''' 1/V-1/[NADPH] curve of purified GRHPR reacting with NADPH and glyoxylic acid
:Fig 6. 1/V-1/[NADPH] curve of purified GRHPR reacting with NADPH and glyoxylic acid
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<html>
 
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     <figure>
 
     <figure>
         <img src="https://2020.igem.org/wiki/images/3/3d/T--XMU-China--XMU-China_2020-GRHPR动力学参数-2-glyoxycolic_底物.png"width="90%" style="float:center">
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         <img src="https://2020.igem.org/wiki/images/3/3d/T--XMU-China--XMU-China_2020-GRHPR动力学参数-2-glyoxycolic_底物.png"width="50%" style="float:center">
 
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</html>
:Fig 7. 1/V-1/[glyoxylic acid] curve of purified GRHPR reacting with NADPH and glyoxylic acid
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:'''Fig 7.''' 1/V-1/[glyoxylic acid] curve of purified GRHPR reacting with NADPH and glyoxylic acid
  
  

Revision as of 13:33, 27 October 2020


GRHPR-his-tag

The enzyme efficiently catalyzes the reaction of reducing glyoxalic acid and consuming NADPH. His-tag was added to purify the protein. We use K880005 to construct the expression system and to express and to purify the protein.


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


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 547
  • 1000
    COMPATIBLE WITH RFC[1000]