Coding

Part:BBa_K3941000

Designed by: Begüm Esra Aytan   Group: iGEM21_Saint_Joseph   (2021-07-26)
Revision as of 10:48, 19 October 2021 by Boraciner (Talk | contribs)


CelAB


Summary

BBa_K3941000 is a codon-optimized (for E. coli DH5âș) version of the CelAB's catalytic region's sequence. We optimized the sequence for avoiding the codon degeneration and provide the right expression. Than we added a 6XHis at the end of the sequence. This sequence engineered to produce an endo-1, 4-β-D glucanase protein to degrade cellulose and its derivatives. ­


800px-T--Saint_Joseph--Diagram-CelAB.png

Figure 1: Codon optimized CelAB and a His-Tag


Introduction

CelAB, a homolog of CelA, produced by T. turnerae T7902, an endosymbiont of the shipworm Lyrodus pedicellatus. Substrate specificity, binding properties, and cleavage products of purified CelAB were examined to evaluate its potential multiple enzymatic activities and carbohydrate binding affinities.[1]


Design

We took the catalytic region of the original CelAB sequence to express in E.coli experiments and then codon optimized it to cloning in E. coli DH5âș bacteria. We also used E. coli BL21 to gene expression and enzyme production.

To purifying correctly our recombinant enzyme, we added a 6X His-tag at the end of our AA sequence.


Results

At first we have done a spectrophotometer absorbance analysis.


T--Saint_Joseph--Nanodrop-CelAB.png

Figure 2: Spectrophotometer results of 3 CelABs


We wanted to be sure that there were no confounding variables, so we have done an agarose gel electrophoresis.


T--Saint_Joseph--Part-Agarose.png

Figure 3: Results of gel electrophoresis under UV. A comparison of backbone and CelAB is visible.



Lastly we conducted a CMCase Activity Analysis. CelAB got an absorbance of 0,5765 and enzyme activity of 17,5 U/min. We use enzyme absorbance to calculate our enzyme activity and the activity of the CelAB wasn’t the highest of three but it was pretty good for us.


320px-T--Saint_Joseph--Standard-Glucose-Calibration-Curve.png

Figure 4: Calibration Curve for CMCase Activity Analysis

320px-T--Saint_Joseph--CelAB-absorbance-values.png

Figure 5: Graphs of CelAB's CMCase Activity Analysis



References

[1] Ekborg, Nathan & Morrill, Wendy & Burgoyne, Adam & Li, Li & Distel, Daniel. (2008). CelAB, a Multifunctional Cellulase Encoded by Teredinibacter turnerae T7902T, a Culturable Symbiont Isolated from the Wood-Boring Marine Bivalve Lyrodus pedicellatus. Applied and environmental microbiology. 73. 7785-8. 10.1128/AEM.00876-07. 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
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


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