Difference between revisions of "Part:BBa K3866033"

 
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<partinfo>BBa_K3866033 short</partinfo>
 
<partinfo>BBa_K3866033 short</partinfo>
  
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Bglx <bbpart>BBa_K523002</bbpart> under control of a constitutive promoter <bbpart>BBa_K3505012</bbpart>.
  
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[[File:T--Thessaly--composite.bglX.png|700px|thumb|none|<i><b>Fig.1:</b> ΒglX  under control of a constitutive promoter. </i>]]
  
  
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===Usage and Biology===
 
===Usage and Biology===
  
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<p>Τhis part consists of AndersonJ23115 promoter <bbpart>BBa_K3505012</bbpart>, bglx <bbpart>BBa_K523002</bbpart> and Double Terminator <bbpart>BBa_K3505017</bbpart>. By this way, as AndersonJ23115 is a strong constitutive promoter, bglx is constitutively expressed. The product protein is expected to be in the periplasm.
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<span class='h3bb'>Sequence and Features</span>
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===Design Notes===
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Τhe coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in alpha1R vector <bbpart>BBa_K3505008</bbpart>and has overhangs compatible for GoldenBraid cloning.
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===Experimental Use and Experience===
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[[Image:T--Thessaly--No_carbon.png|600px|thumb|none|<I><b>Figure 4.</b>  Growth (OD600) of E. coli MC1061 cells transformed with N20-BglX (N20), native-peptide BglX (SP) or an empty vector (EMPTY), in a minimal M9 medium without a carbon source (-)</i>]]
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[[Image:T--Thessaly--CELLOBIOSE.png|600px|thumb|none|<I><b>Figure 5.</b>Growth (OD600) of E. coli MC1061 cells transformed with N20-BglX (N20), native-peptide BglX (SP) or an empty vector (EMPTY), in a minimal M9 medium with Cellobiose as a carbon source (CB).</i>]]
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[[Image:T--Thessaly--BOTH(1).png|600px|thumb|none|<I><b>Figure 6.</b> Growth (OD600) of E. coli MC1061 cells transformed with N20-BglX (N20), native-peptide BglX (SP) or an empty vector (EMPTY), in a minimal M9 medium with Glucose and Cellobiose as a carbon source (2). </i>]]
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[[Image:T--Thessaly--glucose.png|600px|thumb|none|<I><b>Figure 7.</b> Growth (OD600) of E. coli MC1061 cells transformed with N20-BglX (N20), native-peptide BglX (SP) or an empty vector (EMPTY), in a minimal M9 medium with Glucose as a carbon source (GL).</i>]]
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===Conclusion===
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N20-bglX bacteria grow more and faster than the SP-bglX and EMPTY bacteria in a 24-hour time-frame and with cellobiose as the only carbon resource. The engineered enzyme provides an advantage in situations where cellobiose is the only abundant carbon source. Also, N20-bglX bacteria reach an exponential-like phase much quicker than the native peptide or the empty vector control bacteria, which means quicker valorization cellobiose and update of glucose by the cell.
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===Sequence and Features===
 
<partinfo>BBa_K3866033 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K3866033 SequenceAndFeatures</partinfo>
  
  
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===Functional Parameters===
 
 
<partinfo>BBa_K3866033 parameters</partinfo>
 
<partinfo>BBa_K3866033 parameters</partinfo>
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===Source===
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Synthesized by IDT.

Latest revision as of 11:49, 15 October 2021


pAndersonJ23115:RBS-bglX-terminator

Bglx BBa_K523002 under control of a constitutive promoter BBa_K3505012.

Fig.1: ΒglX under control of a constitutive promoter.


Usage and Biology

Τhis part consists of AndersonJ23115 promoter BBa_K3505012, bglx BBa_K523002 and Double Terminator BBa_K3505017. By this way, as AndersonJ23115 is a strong constitutive promoter, bglx is constitutively expressed. The product protein is expected to be in the periplasm.

Design Notes

Τhe coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in alpha1R vector BBa_K3505008and has overhangs compatible for GoldenBraid cloning.


Experimental Use and Experience

Figure 4. Growth (OD600) of E. coli MC1061 cells transformed with N20-BglX (N20), native-peptide BglX (SP) or an empty vector (EMPTY), in a minimal M9 medium without a carbon source (-)
Figure 5.Growth (OD600) of E. coli MC1061 cells transformed with N20-BglX (N20), native-peptide BglX (SP) or an empty vector (EMPTY), in a minimal M9 medium with Cellobiose as a carbon source (CB).
Figure 6. Growth (OD600) of E. coli MC1061 cells transformed with N20-BglX (N20), native-peptide BglX (SP) or an empty vector (EMPTY), in a minimal M9 medium with Glucose and Cellobiose as a carbon source (2).
Figure 7. Growth (OD600) of E. coli MC1061 cells transformed with N20-BglX (N20), native-peptide BglX (SP) or an empty vector (EMPTY), in a minimal M9 medium with Glucose as a carbon source (GL).

Conclusion

N20-bglX bacteria grow more and faster than the SP-bglX and EMPTY bacteria in a 24-hour time-frame and with cellobiose as the only carbon resource. The engineered enzyme provides an advantage in situations where cellobiose is the only abundant carbon source. Also, N20-bglX bacteria reach an exponential-like phase much quicker than the native peptide or the empty vector control bacteria, which means quicker valorization cellobiose and update of glucose by the cell.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 11
    Illegal NheI site found at 34
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 62
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1721
    Illegal AgeI site found at 1943
    Illegal AgeI site found at 2132
  • 1000
    COMPATIBLE WITH RFC[1000]


Source

Synthesized by IDT.