Difference between revisions of "Part:BBa K1033914"

(Characterisation)
(Characterisation)
Line 42: Line 42:
 
<gallery mode=packed-hover>
 
<gallery mode=packed-hover>
 
File:K1033914 lime culture.jpg|Liquid culture of ''E. coli'' expressing amajLime
 
File:K1033914 lime culture.jpg|Liquid culture of ''E. coli'' expressing amajLime
<!-- pfad für lime zell pellet|Cell pellet after centrifugation--->
+
File:K1033914 lime pellet.jpg|Cell pellet after centrifugation
 
File:K1033914 lime lys.jpg|Cleared cell lysate  
 
File:K1033914 lime lys.jpg|Cleared cell lysate  
 
</gallery>
 
</gallery>

Revision as of 13:08, 14 October 2019

amajLime, yellow-green chromoprotein (incl RBS & J23110)

This chromoprotein from the coral Anemonia majano, amajLime (also known as amajCFP or amFP486), naturally exhibits strong color when expressed. The protein has an absorption maximum at 458 nm giving it a yellow-green color visible to the naked eye. Compared to many other chromoproteins, such as amilCP (BBa_K592009), amilGFP (BBa_K592010), spisPink (BBa_K1033932), asPink (BBa_K1033933) and aeBlue (BBa_K864401), the color development is slower. The color is readily observed in both LB or on agar plates after 24-48 hours of incubation. The protein amajLime has significant sequence homologies with proteins in the GFP family.

Characterisation

Team: Humboldt_Berlin 2019


ExPASy ProtParam Results:


Number of amino acids: 228

Molecular weight: 25185.49 Da

Theoretical pI: 7.27

Total number of negatively charged residues (Asp + Glu): 22

Total number of positively charged residues (Arg + Lys): 22


Extinction coefficients:

Ext. coefficient 26150 M-1 cm-1

Abs 0.1% (=1 g/l) 1.038, assuming all pairs of Cys residues form cystines

Ext. coefficient 25900 M-1 cm-1

Abs 0.1% (=1 g/l) 1.028, assuming all Cys residues are reduced

Instability index: The instability index (II) is computed to be 27.07. This classifies the protein as stable.

Aliphatic index: 51.71

Grand average of hydropathicity (GRAVY): -0.379


In order to measure absorbance and fluorescence spectra of amajLime we transformed the construct (consisting of J23110 Promotor, B0034 RBS and amajLime coding sequence) into competent E. coli. After cultivation and we lysed the harvested cells according to this protocol.

The fluorescence and absorbance spectra was measured for 24 samples of 150 µl lysate in 96-well plate on TECAN Plate Reader Infinite 200 Pro. In figure 1 you can see the relative absorbance and emission spectra including the respective standard deviation.



Figure 1. amajLime absorbance and fluorescence spectra

References

[http://www.nature.com/nbt/journal/v17/n10/full/nbt1099_969.html] Matz, Mikhail V., et al. "Fluorescent proteins from nonbioluminescent Anthozoa species." Nature biotechnology 17.10 (1999): 969-973.

[http://www.pnas.org/content/102/36/12712.short] Henderson, J. Nathan, and S. James Remington. "Crystal structures and mutational analysis of amFP486, a cyan fluorescent protein from Anemonia majano." Proceedings of the National Academy of Sciences of the United States of America 102.36 (2005): 12712-12717.

[http://www.ncbi.nlm.nih.gov/pubmed/18648549] Alieva, N. O., et al. 2008. Diversity and evolution of coral fluorescent proteins. PLoS One 3:e2680.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]