Difference between revisions of "Part:BBa K5034214"
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===Basic Description===
 
===Basic Description===
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This composite part includes the PPK1 gene which is initially from Citrobacter freundii and we performed codon optimization on, is expressed in the pBBR1MCS-terminator plasmid with the BBa-B0031 RBS, which is a weaker RBS compared to others. This composite part is designed to facilitate the reversible conversion between inorganic polyphosphate (PolyP) and inorganic phosphate (Pi). The PPK1 enzyme is known for its ability to synthesize PolyP from ATP and Pi and to degrade PolyP back to Pi, with a preference for the synthetic reaction, making it a versatile tool for managing phosphate metabolism in engineered systems. In a sentence, this part is activated by a weaker RBS. It can reversibly convert Poly p and Pi. This reversible process favors the generation of Poly P. For the first time, we expressed this element in a strain of Shewanella and conducted codon optimization based on Shewanella.
+
This composite part includes the <i>PPK1</i> gene which is initially from <i>Citrobacter freundii</i> and we performed codon optimization on. It is expressed in the pBBR1MCS-terminator plasmid(BBa-K5034201) with the BBa-B0031 RBS, which is a weaker RBS compared compared to others. This composite part is designed to facilitate the reversible conversion between inorganic polyphosphate (PolyP) and inorganic phosphate (Pi). The PPK1 enzyme is known for its ability to synthesize PolyP from ATP and Pi and to degrade PolyP back to Pi, with a preference for the synthetic reaction, making it a versatile tool for managing phosphate metabolism in engineered systems.  
 +
 
 +
In a sentence, this part is activated by a weaker RBS. It can reversibly convert PolyP and Pi. This reversible process favors the generation of PolyP. For the first time, we expressed this element in a strain of <i>S. oneidensis.</i> and conducted codon optimization based on <i>S. oneidensis.</i>.
 
<html>
 
<html>
 
<body>
 
<body>
 
     <div style="text-align: center;">
 
     <div style="text-align: center;">
 
         <img src="https://static.igem.wiki/teams/5034/engineering/mechanism-of-ppk1.png" style="width: 500px; height: auto;">
 
         <img src="https://static.igem.wiki/teams/5034/engineering/mechanism-of-ppk1.png" style="width: 500px; height: auto;">
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<p>Figure 1: Basic function of PPK1</p>
 
     </div>
 
     </div>
 
</body>
 
</body>
 
</html>
 
</html>
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Figure 1: Basic function of PPK1
 
  
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===Construct features===
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===Sequenece and Features===
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Promoter: Constitutive promoter for continuous expression. We use Lac promoter in our experiment.
+
  
−
RBS: Ribosome binding site for efficient translation. We use BBa-B0031 here.
+
<partinfo>BBa_K5034214 SequenceAndFeatures</partinfo>
  
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PPK1 Coding Sequence: Encodes the polyphosphate kinase 1 enzyme.
 
  
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Terminator: Efficient transcription terminator to ensure proper mRNA processing. We use rrnB T1 terminator and T7Te terminator in our experiment.
+
* Promoter: Constitutive promoter for continuous expression. We use Lac promoter in our experiment.Since our sequence does not encode the regulatory gene ''lacI'' for the repressor protein, the promoter we introduced is a constitutive promoter. This allows the subsequent genes to be continuously expressed.
 +
 
 +
* RBS: Ribosome binding site for efficient translation. We use BBa-B0031 here.
 +
 
 +
* <i>PPK1</i> Coding Sequence: Encodes the polyphosphate kinase 1 enzyme.
 +
 
 +
* Terminator: Efficient transcription terminator to ensure proper mRNA processing. We use rrnB T1 terminator and T7Te terminator in our experiment.
 +
 
 +
In this composite part, only coding sequence and RBS is included.But the translational unit is composed of components above.
  
 
The basic structure of the part is shown as follows:
 
The basic structure of the part is shown as follows:
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<body>
 
<body>
 
     <div style="text-align: center;">
 
     <div style="text-align: center;">
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         <img src="https://static.igem.wiki/teams/5034/engineering/fig9.png" style="width: 500px; height: auto;">
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         <img src="https://static.igem.wiki/teams/5034/results/new/basic-structure-of-spk3.png" style="width: 500px; height: auto;">
 +
<p>Figure 2: Basic construction of <i>PPK1</i> plasmid with BBa-B0031 RBS</p>
 
     </div>
 
     </div>
 
</body>
 
</body>
 
</html>
 
</html>
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Figure 2: Basic construction of PPK1 plasmid with BBa-B0031 RBS
 
  
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We transform the plasmids into wild-type Shewanella, express it, and perform colony PCR. The results show that PPK1 is successfully introduced into Shewanella for replication.
 
 
<html>
 
<html>
 
<body>
 
<body>
 
     <div style="text-align: center;">
 
     <div style="text-align: center;">
−
         <img src="https://static.igem.wiki/teams/5034/engineering/fig9.png" style="width: 500px; height: auto;">
+
         <img src="https://static.igem.wiki/teams/5034/engineering/pbbr1mcs-terminator-31-ppk1.png" style="width: 500px; height: auto;">
 +
<p>Figure 3: Construction of <i>PPK1</i> with BBa-B0031 RBS plasmid</p>
 
     </div>
 
     </div>
 
</body>
 
</body>
 
</html>
 
</html>
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Figure 3: Colony PCR indicating plasmid replication in Shewanell
 
  
−
DNA agarose gel electrophoresis results showed that we obtained the plasmid with BBa-B0031 RBS, which is approximately 2.1 kb in size.
+
DNA agarose gel electrophoresis results showed that we obtained the target gene with BBa-B0031 RBS, which is approximately 2.1 kb in size.
 
<html>
 
<html>
 
<body>
 
<body>
 
     <div style="text-align: center;">
 
     <div style="text-align: center;">
 
         <img src="https://static.igem.wiki/teams/5034/engineering/gel-ppk1.png" style="width: 500px; height: auto;">
 
         <img src="https://static.igem.wiki/teams/5034/engineering/gel-ppk1.png" style="width: 500px; height: auto;">
 +
<p>Figure 4: Agarose gel electrophoresis indicating we got the target gene with the corresponding RBS</p>
 
     </div>
 
     </div>
 
</body>
 
</body>
 
</html>
 
</html>
−
Figure 4: Agarose gel electrophoresis indicating we got the target gene with the corresponding RBS
 
  
−
We performed protein extraction for SDS-PAGE. The results showed that protein expression of the plasmid with BBa-B0031 RBS is the minimum, corresponding to the strength of RBS.
+
We transformed the plasmids into wild-type <i>S. oneidensis.</i>, expressed it, and performed colony PCR. The results showed that <i>PPK1</i> was successfully introduced into <i>S. oneidensis.</i> for replication.
 +
<html>
 +
<body>
 +
    <div style="text-align: center;">
 +
        <img src="https://static.igem.wiki/teams/5034/engineering/fig9.png" style="width: 500px; height: auto;">
 +
<p>Figure 5: Colony PCR indicating plasmid replication in <i>S. oneidensis.</i></p>
 +
    </div>
 +
</body>
 +
</html>
 +
 
 +
We performed protein extraction for SDS-PAGE. The SDS-PAGE results showed that protein expression of the plasmid with BBa-B0031 RBS is the minimum, corresponding to the strength of RBS.
 
<html>
 
<html>
 
<body>
 
<body>
 
     <div style="text-align: center;">
 
     <div style="text-align: center;">
 
         <img src="https://static.igem.wiki/teams/5034/engineering/fig10.png" style="width: 500px; height: auto;">
 
         <img src="https://static.igem.wiki/teams/5034/engineering/fig10.png" style="width: 500px; height: auto;">
 +
<p>Figure 6: SDS-PAGE results showing that the BBa-B0031 one's protein expression is the minimum, corresponding to the strength of RBS</p>
 
     </div>
 
     </div>
 
</body>
 
</body>
 
</html>
 
</html>
−
Figure 5: SDS-PAGE results showing that the BBa-B0031 one’s protein expression is the minimum, corresponding to the strength of RBS
+
 
  
 
===Origin (Organism)===
 
===Origin (Organism)===
−
The PPK1 gene was sourced from Citrobacter freundii.
+
The <i>PPK1</i> gene was sourced from <i>Citrobacter freundii</i>.
  
 
===Experimental Characterization and results===
 
===Experimental Characterization and results===
−
Alteration of protein expression intensity can regulate the metabolic networks, so we focused on RBS with varying translation strengths to facilitate the regulation of PPK1 concentration in Shewanella to develop the best ability to produce electricity and polymerize phosphorus.
+
Alteration of protein expression intensity can regulate the metabolic networks, so we focused on RBS with varying translation strengths to facilitate the regulation of PPK1 concentration in <i>S. oneidensis.</i> to develop the best ability to produce electricity and polymerize phosphorus.
−
We conduct Pi content detection to determine Pi concentration and half-cell experiment to measure the electricity production ability. We found that SPK1 with RBS BBa-B0031 has the lowest capacity for phosphorus polymerization but the highest electroproduction capability.
+
 
 +
We conducted Pi content detection to determine Pi concentration and half-cell experiment to measure the electricity production ability. We found that <i>SPK3</i> with RBS BBa-B0031 has the lowest capacity for phosphorus polymerization but the highest electroproduction capability compared to other RBS.
 
<html>
 
<html>
 
<body>
 
<body>
 
     <div style="text-align: center;">
 
     <div style="text-align: center;">
 
         <img src="https://static.igem.wiki/teams/5034/engineering/fig12.png" style="width: 500px; height: auto;">
 
         <img src="https://static.igem.wiki/teams/5034/engineering/fig12.png" style="width: 500px; height: auto;">
 +
<p>Figure 7: Electricity production capacity of <i>S. oneidensis.</i> after the introduction of <i>PPK1</i> with different RBS</p>
 
     </div>
 
     </div>
 
</body>
 
</body>
 
</html>
 
</html>
−
Figure 5: Electricity production capacity of Shewanella after the introduction of PPK1 with different RBS
 
 
<html>
 
<html>
 
<body>
 
<body>
 
     <div style="text-align: center;">
 
     <div style="text-align: center;">
 
         <img src="https://static.igem.wiki/teams/5034/engineering/fig11.png" style="width: 500px; height: auto;">
 
         <img src="https://static.igem.wiki/teams/5034/engineering/fig11.png" style="width: 500px; height: auto;">
 +
<p>Figure 8: Phosphorus accumulation capacity of <i>S. oneidensis.</i> after the introduction of <i>PPK1</i> with different RBS</p>
 
     </div>
 
     </div>
 
</body>
 
</body>
 
</html>
 
</html>
−
Figure 6: Phosphorus accumulation capacity of Shewanella after the introduction of PPK1 with different RBS
+
This is the end of our one cycle, and through this successful cycle, we have achieved an improvement in phosphorus accumulation ability while maintaining almost unchanged electricity production capacity of <i>S.oneidensis</i>.
  
−
Details of all experiments can be found in the <html><body><a href="https://2024.igem.wiki/nanjing-china/experiments">Experiments section on the Wiki.</a></body></html>
+
Experimental manipulation：
  
−
==Chassis and genetic==
+
<html><a href="https://2024.igem.wiki/nanjing-china/experiments#s16">Electricity production:</a>Using half-cell reaction(electrochemistry) We use half-cell experiment to measure the electricity production ability.</html>
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Chassis：Shewanella onediensis MR-1
+
  
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The gene can be expressed and function properly in Shewanella.
+
<html><a href="https://2024.igem.wiki/nanjing-china/experiments#s11">Capacity to absorb phosphorus:</a>Conducting molybdate assays to determine Pi concentration.</html>
  
−
==Potential applications==
+
Details of all experiments can be found in the <html><body><a href="https://2024.igem.wiki/nanjing-china/experiments">Experiments section on the Wiki.</a></body></html>
−
The PPK1 gene (polyphosphate kinase 1) has potential applications in:
+
  
−
Industrial Microbial Engineering: Enhances the production of biofuels, amino acids, or antibiotics by boosting polyphosphate synthesis in microorganisms.
+
===Chassis and genetic===
 +
Chassis：<i>Shewanella onediensis</i> MR-1
  
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Environmental Bioremediation: Assists in the accumulation of heavy metals or radioactive substances for pollution control.
+
This part can be expressed and function properly in <i>S. oneidensis.</i>.
  
−
===References===
+
===Potential applications===
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1.Itoh, H., & Shiba, T. (2004). Polyphosphate synthetic activity of polyphosphate:AMP phosphotransferase in Acinetobacter johnsonii 210A. Journal of Bacteriology, 186(15), 5178-5181.
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The <i>PPK1</i> gene (polyphosphate kinase 1) has potential applications in:
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<!-- Add more about the biology of this part here
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===Usage and Biology===
+
  
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<!-- -->
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It can enhance the production of some phosphorus-related substances production  by boosting polyphosphate synthesis in microorganisms and create greater economic value
−
<span class='h3bb'>Sequence and Features</span>
+
−
<partinfo>BBa_K5034214 SequenceAndFeatures</partinfo>
+
  
 +
It can manage phosphate levels in contaminated environments.
  
−
<!-- Uncomment this to enable Functional Parameter display
+
It can enhance the performance of bioelectrochemical systems for electricity generation in providing a renewable and sustainable source of electricity, reducing reliance on fossil fuels and contributing to cleaner energy production.
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===Functional Parameters===
+
 
−
<partinfo>BBa_K5034214 parameters</partinfo>
+
===References===
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<!-- -->
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<i>Wang X , Wang X , Hui K , et al. Highly Effective Polyphosphate Synthesis, Phosphate Removal and Concentration Using Engineered Environmental Bacteria Based on a Simple Solo Medium-copy Plasmid Strategy[J]. Environmental Science & Technology, 2017:acs.est.7b04532.</i>

Latest revision as of 08:19, 2 October 2024


PolyP <->Pi

Basic Description

This composite part includes the PPK1 gene which is initially from Citrobacter freundii and we performed codon optimization on. It is expressed in the pBBR1MCS-terminator plasmid(BBa-K5034201) with the BBa-B0031 RBS, which is a weaker RBS compared compared to others. This composite part is designed to facilitate the reversible conversion between inorganic polyphosphate (PolyP) and inorganic phosphate (Pi). The PPK1 enzyme is known for its ability to synthesize PolyP from ATP and Pi and to degrade PolyP back to Pi, with a preference for the synthetic reaction, making it a versatile tool for managing phosphate metabolism in engineered systems.

In a sentence, this part is activated by a weaker RBS. It can reversibly convert PolyP and Pi. This reversible process favors the generation of PolyP. For the first time, we expressed this element in a strain of S. oneidensis. and conducted codon optimization based on S. oneidensis..

Figure 1: Basic function of PPK1

Sequenece 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
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


  • Promoter: Constitutive promoter for continuous expression. We use Lac promoter in our experiment.Since our sequence does not encode the regulatory gene lacI for the repressor protein, the promoter we introduced is a constitutive promoter. This allows the subsequent genes to be continuously expressed.
  • RBS: Ribosome binding site for efficient translation. We use BBa-B0031 here.
  • PPK1 Coding Sequence: Encodes the polyphosphate kinase 1 enzyme.
  • Terminator: Efficient transcription terminator to ensure proper mRNA processing. We use rrnB T1 terminator and T7Te terminator in our experiment.

In this composite part, only coding sequence and RBS is included.But the translational unit is composed of components above.

The basic structure of the part is shown as follows:

Figure 2: Basic construction of PPK1 plasmid with BBa-B0031 RBS

Figure 3: Construction of PPK1 with BBa-B0031 RBS plasmid

DNA agarose gel electrophoresis results showed that we obtained the target gene with BBa-B0031 RBS, which is approximately 2.1 kb in size.

Figure 4: Agarose gel electrophoresis indicating we got the target gene with the corresponding RBS

We transformed the plasmids into wild-type S. oneidensis., expressed it, and performed colony PCR. The results showed that PPK1 was successfully introduced into S. oneidensis. for replication.

Figure 5: Colony PCR indicating plasmid replication in S. oneidensis.

We performed protein extraction for SDS-PAGE. The SDS-PAGE results showed that protein expression of the plasmid with BBa-B0031 RBS is the minimum, corresponding to the strength of RBS.

Figure 6: SDS-PAGE results showing that the BBa-B0031 one's protein expression is the minimum, corresponding to the strength of RBS


Origin (Organism)

The PPK1 gene was sourced from Citrobacter freundii.

Experimental Characterization and results

Alteration of protein expression intensity can regulate the metabolic networks, so we focused on RBS with varying translation strengths to facilitate the regulation of PPK1 concentration in S. oneidensis. to develop the best ability to produce electricity and polymerize phosphorus.

We conducted Pi content detection to determine Pi concentration and half-cell experiment to measure the electricity production ability. We found that SPK3 with RBS BBa-B0031 has the lowest capacity for phosphorus polymerization but the highest electroproduction capability compared to other RBS.

Figure 7: Electricity production capacity of S. oneidensis. after the introduction of PPK1 with different RBS

Figure 8: Phosphorus accumulation capacity of S. oneidensis. after the introduction of PPK1 with different RBS

This is the end of our one cycle, and through this successful cycle, we have achieved an improvement in phosphorus accumulation ability while maintaining almost unchanged electricity production capacity of S.oneidensis.

Experimental manipulation：

Electricity production:Using half-cell reaction(electrochemistry) We use half-cell experiment to measure the electricity production ability.

Capacity to absorb phosphorus:Conducting molybdate assays to determine Pi concentration.

Details of all experiments can be found in the Experiments section on the Wiki.

Chassis and genetic

Chassis：Shewanella onediensis MR-1

This part can be expressed and function properly in S. oneidensis..

Potential applications

The PPK1 gene (polyphosphate kinase 1) has potential applications in:

It can enhance the production of some phosphorus-related substances production by boosting polyphosphate synthesis in microorganisms and create greater economic value

It can manage phosphate levels in contaminated environments.

It can enhance the performance of bioelectrochemical systems for electricity generation in providing a renewable and sustainable source of electricity, reducing reliance on fossil fuels and contributing to cleaner energy production.

References

Wang X , Wang X , Hui K , et al. Highly Effective Polyphosphate Synthesis, Phosphate Removal and Concentration Using Engineered Environmental Bacteria Based on a Simple Solo Medium-copy Plasmid Strategy[J]. Environmental Science & Technology, 2017:acs.est.7b04532.