Difference between revisions of "Part:BBa K4257000"
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<partinfo>BBa_K4257000 short</partinfo>
 
<partinfo>BBa_K4257000 short</partinfo>
  
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PPK-M is a mutant of E.coli polyphosphate kinase 1 (PPK1), which catalyzes the synthesis of polyphosphate (polyP) using cellular ATP as the substrate. Compared to native E.coli PPK1 that has an alanine and a glutamine residue in position 327 and 328, PPK-M has much more strongly charged glutamate and lysine residues. It has been documented that expression of PPK-M leads to substantially higher levels of polyP accumulation in vivo by disrupting intracellular PPK-repressing interactions, as compared to the situation found with expression of PPK1. PolyP consists of inorganic phosphate (Pi), which is essentially derived from the uptake of exogenous phosphorous by the host cell. For this reason, if enhanced uptake of exogenous phosphorous by the host cell is desired, PPK-M will be a better option. This year, our team wants to develop an engineered E.coli K12 strain that can use phosphite as a raw material to manufacture Pi, in which process intracellular polyP is the intermediate. Therefore, we picked highly active PPK-M.
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PPK-M is a mutant of E. coli polyphosphate kinase (PPK), which catalyzes the synthesis of polyphosphate (polyP) using cellular ATP as the substrate. Compared to native E. coli PPK that has an alanine and a glutamine residue in position 327 and 328, PPK-M has much more strongly charged glutamate and lysine residues. It has been documented that expression of PPK-M leads to substantially higher levels of polyP accumulation in vivo by disrupting intracellular PPK-repressing interactions, as compared to the situation found with expression of PPK (Rudat et al. 2018). PolyP consists of inorganic phosphate, which is essentially derived from the uptake of exogenous phosphorus by the host cell. For this reason, if enhanced uptake of exogenous phosphorus by the host cell is desired, PPK-M will be a better option. This year, our team wants to develop an engineered E. coli K12 strain that can use phosphite as a raw material to manufacture phosphate, in which process intracellular polyP is the intermediate. Therefore, we picked highly active PPK-M.
  
 
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1. Biomass
 
1. Biomass
  
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We first compared the biomass of two engineered E.coli K12 strains that overexpress PPK1 and PPK-M, respectively.
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We first compared the biomass of two engineered E. coli K12 strains that overexpress PPK and PPK-M, respectively.
 
[[File:CPU-Nanjing-Parts-PPK-M-1.tiff|300px|center]]
 
[[File:CPU-Nanjing-Parts-PPK-M-1.tiff|300px|center]]
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<center>Figure 1. Maximum optical density of K12/PPK-M grown in synthetic municipal wastewater compared with K12/PPK1.</center>
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<center>Figure 1. Maximum optical density of K12/PPK-M grown in synthetic municipal wastewater compared with K12/PPK.</center>
  
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As shown in Figure 1, the biomass of K12/PPK-M is almost identical to that of K12/PPK1, indicating that highly active PPK-M would not impose additional metabolic burden upon the host cell.
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As shown in Figure 1, the biomass of K12/PPK-M is almost identical to that of K12/PPK, indicating that highly active PPK-M would not impose additional metabolic burden upon the host cell.
  
  
 
2. Intracellular polyP
 
2. Intracellular polyP
  
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As expected, intracellular polyP assay showed that the amount of polyP produced by K12/PPK-M is significantly higher than that obtained by K12/PPK1 (Figure. 2).
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As expected, intracellular polyP assay showed that the amount of polyP produced by K12/PPK-M is significantly higher than that obtained by K12/PPK (Figure. 2).
 
[[File:CPU-Nanjing-Parts-PPK-M-2.png|300px|center]]
 
[[File:CPU-Nanjing-Parts-PPK-M-2.png|300px|center]]
  
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<center>Figure 2. Intracellular polyP content of K12/PPK-M compared with K12/PPK1.</center>
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<center>Figure 2. Intracellular polyP content of K12/PPK-M compared with K12/PPK.</center>
  
  
 
3. Microscopic observation
 
3. Microscopic observation
  
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Consistent with quantitative polyP assays, polyP granules observed in K12/PPK-M were significantly larger than those found in K12/PPK1 (Figure. 3).
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Consistent with quantitative polyP assays, polyP granules observed in K12/PPK-M were significantly larger than those found in K12/PPK (Figure. 3).
 
[[File:CPU-Nanjing-Parts-PPK-M-3.png|300px|center]]
 
[[File:CPU-Nanjing-Parts-PPK-M-3.png|300px|center]]
  
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<center>Figure 3. Light microscopy images of Albert stained cells. Intracellular polyP granules appear blue-purple, whereas cells appear blue-green. Scale bar, 2 μm.</center>
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<center>Figure 3. Light microscopy images of toluidine blue stained cells. Intracellular polyP granules appear blue-purple, whereas cells appear blue-green. Scale bar, 2 μm.</center>
  
 
===References===
 
===References===
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Rudat, A. K., et al. (2018). "Mutations in Escherichia coli polyphosphate kinase that lead to dramatically increased in vivo polyphosphate levels." 200(6): e00697-00617.
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Rudat, A.K., Pokhrel, A., Green, T.J. and Gray, M. (2018) Mutations in Escherichia coli polyphosphate kinase that lead to dramatically increased in vivo polyphosphate levels. Journal of Bacteriology 200(6), e00697-00617.
  
  

Revision as of 16:04, 26 September 2022

PPK-M

PPK-M is a mutant of E. coli polyphosphate kinase (PPK), which catalyzes the synthesis of polyphosphate (polyP) using cellular ATP as the substrate. Compared to native E. coli PPK that has an alanine and a glutamine residue in position 327 and 328, PPK-M has much more strongly charged glutamate and lysine residues. It has been documented that expression of PPK-M leads to substantially higher levels of polyP accumulation in vivo by disrupting intracellular PPK-repressing interactions, as compared to the situation found with expression of PPK (Rudat et al. 2018). PolyP consists of inorganic phosphate, which is essentially derived from the uptake of exogenous phosphorus by the host cell. For this reason, if enhanced uptake of exogenous phosphorus by the host cell is desired, PPK-M will be a better option. This year, our team wants to develop an engineered E. coli K12 strain that can use phosphite as a raw material to manufacture phosphate, in which process intracellular polyP is the intermediate. Therefore, we picked highly active PPK-M.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Unknown
  • 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]


Data:CPU-Nanjing 2022 TEAM

The yield of our final product is positively correlated with the amount of intracellular polyP and the cell biomass.


1. Biomass

We first compared the biomass of two engineered E. coli K12 strains that overexpress PPK and PPK-M, respectively.

CPU-Nanjing-Parts-PPK-M-1.tiff
Figure 1. Maximum optical density of K12/PPK-M grown in synthetic municipal wastewater compared with K12/PPK.

As shown in Figure 1, the biomass of K12/PPK-M is almost identical to that of K12/PPK, indicating that highly active PPK-M would not impose additional metabolic burden upon the host cell.


2. Intracellular polyP

As expected, intracellular polyP assay showed that the amount of polyP produced by K12/PPK-M is significantly higher than that obtained by K12/PPK (Figure. 2).

CPU-Nanjing-Parts-PPK-M-2.png
Figure 2. Intracellular polyP content of K12/PPK-M compared with K12/PPK.


3. Microscopic observation

Consistent with quantitative polyP assays, polyP granules observed in K12/PPK-M were significantly larger than those found in K12/PPK (Figure. 3).

CPU-Nanjing-Parts-PPK-M-3.png
Figure 3. Light microscopy images of toluidine blue stained cells. Intracellular polyP granules appear blue-purple, whereas cells appear blue-green. Scale bar, 2 μm.

References

Rudat, A.K., Pokhrel, A., Green, T.J. and Gray, M. (2018) Mutations in Escherichia coli polyphosphate kinase that lead to dramatically increased in vivo polyphosphate levels. Journal of Bacteriology 200(6), e00697-00617.