Difference between revisions of "Part:BBa K5034212"

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PolyP + AMP --> ADP

It can reversibly convert Poly p and AMP to ADP. For the first time, we expressed this element in a strain of S. oneidensis and conducted codon optimization based on S. oneidensis. We tested the effects of the introduction of this element on electricity production and phosphorus metabolism

Basic Description

This basic part encodes the PAP gene which is initially from Acinetobacter johnsonii and we performed codon optimization on, is expressed in the PYYDT plasmid. This basic part is designed to facilitate the reversible conversion of inorganic polyphosphate (PolyP) and adenosine monophosphate (AMP) to adenosine diphosphate (ADP). The PAP enzyme plays a crucial role in phosphate and energy metabolism. PAP and PPK2 have strong poly(P) utilization activity, and the activity of PAP is 20-fold higher than that in PPK1, even though the Km values for utilization of all three enzymes are almost the same. This implies that PAP and PPK2 work mainly for poly(P) utilization in the cell. However, PAP has the same level of poly(P) synthetic activity (Km and Vmax) as PPK1, and this suggests that PAP also works for poly(P) synthesis at a significant level.

Figure 1: Basic function of PAP

Sequence and Features

Construct features

• Promoter: Constitutive promoter for continuous expression. We use tac promoter in our experiment.
• RBS: BBa_B0034
• PAP Coding Sequence: Encodes the polyphosphate:AMP phosphotransferase enzyme.
• Terminator: Efficient transcription terminator to ensure proper mRNA processing. We use T7Te terminator in our experiment.

Figure 3: PCR of target genes PCR before plasmids construction (The extra small fragment in the picture is primer dimer)

The length of the PAP gene is about 1428 base pairs, which is consistent with the results on the DNA electropherogram, proving that we have obtained the PAP gene.

Origin (Organism)

The PAP gene was sourced from Acinetobacter johnsonii.

Experimental Characterization and results

We first determined the electroproduction capacity of S. oneidensis after introduction of the SPAP enzyme (e.g. fig3)

Figure 3: Statistical data on electricity production capacity of S. oneidensis with the introduction of different hydrolases

We found that the efficiency of bacterial inhibition of electricity production did not significantly increase after SPAP introduction, and even showed a significant decrease, so it is not a good synthetic biology component to enhance the electricity production capacity of S. oneidensis

Afterwards, we also measured the phosphorus aggregation capacity of S. oneidensis(fig4) and found no significant difference from the wild type, indicating that its introduction did not promote phosphorus uptake in S. oneidensis either.

Figure 4: Statistical data on the phosphorus accumulation capacity of S. oneidensis with PAP

Tests to measure ATP levels in S. oneidensis(fig5) also showed that its introduction did not result in an increase in the metabolic strength of S. oneidensis either.

Figure 5: ATP level in S. oneidensis with the introduction of different hydrolases

In summary, the option of importing PAP is not a good one

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

Chassis and genetic

Chassis：Shewanella oneidensis MR-1.

The gene can be expressed and function properly in S. oneidensis.

Potential applications

PAP, as an enzyme class for the synthesis of ADP, plays an important role in the synthesis of intracellular high-energy phosphate compounds and is a key enzyme in the regulation of the intensity of intracellular metabolism

References

1.Itoh, H., & Shiba, T. (2004). Polyphosphate synthetic activity of polyphosphate:AMP phosphotransferase in Acinetobacter johnsonii 210A. Journal of Bacteriology, 186(15), 5178-5181.