Composite

Part:BBa_K3739106

Designed by: Shichen Geng   Group: iGEM21_XMU-China   (2021-09-30)
Revision as of 13:24, 10 October 2021 by Oliviatong (Talk | contribs) (main body except characterization)


K525998(T7-RBS)-Aly01-his-CBM-hutH-B0010

Aly01 here represents a signal peptide used to secrect the fusion protein outside the cell, his-tag enable us to purify the linking protein. The fusion protein CBM-hutH works on the surface of single cell Phaeocystis. globosa and the enzyme catalyzes the reaction of converting histidine to form toxic urocanic acid. His-tag is added to purify the protein. We use BBa_K3739106 to construct the expression system and to express and to purify the protein.


Biology

Aly01

Aly01 is alginate lyase from 'Vibrio natriegens' SK42.001, which is secreted out and able to digest alginate to unsaturated alginate oligosaccharide. Its signal peptide (named Aly01 in our parts), which is fused with heterogenous protein, is performed well in E. coli. It is implied that the heterogenous protein fused with Aly01 signal peptide may be also secreted efficiently.

CBM

Cellulose enzymes have two domains, and the one that helps bind to cellulose is called cellulose binding module (CBM), and therefore it helps our fusion protein bind to cellulose-rich cell wall. Here we choose the CBM of CenA from 'Cellulomonas fimi', which has been successfully expressed in 'Escherichia coli'.

hutH

The HutH comes from 'Pseudomonas putida'. Under natural conditions, many microorganisms can use the histidine ammonia-lyase (HutH) to change L-histidine into urocanic acid. HutH catalyzes the first step in the degradation of histidine, and the product urocanic acid is further metabolized to glutamate. This enzyme could be found in the liver of vertebrates and in bacteria such as 'Escherichia coli', 'Salmonella' and 'Pseudomonas'. It is specific for L-histidine and can be inhibited by D-histidine or imidazole. The active center of the enzyme is thought to be dehydroalanine.

Usage

In order to easily purify HutH, we added a his-tag (6*His) at the C-terminal. We ligased the strong promoter (BBa_J23100) and the parts (RBS-Aly01-his-CBM-hutH-Terminator) on the expression vector pET-28a (+) by standard assembly. Then the ligation mixture was transformed into 'E. coli' DH5α, and the correct recombinant one was confirmed by kanamycin, colony PCR and sequencing. Here, we used BBa_K3739106 to construct the expression system and demonstrated of the effect of secretory peptides and CBM-hutH together with BBa_K3739109 and BBa_xxxx.

Characterization

References

1.https://parts.igem.org/Part:BBa_K3185005
2.Meng, Q. et al. Characterization and enhanced extracellular overexpression of a new salt-activated alginate lyase. Journal of the science of food and agriculture 101, 5154-5162, doi:10.1002/jsfa.11161 (2021).


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
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 653
    Illegal NgoMIV site found at 1089
    Illegal NgoMIV site found at 1824
    Illegal NgoMIV site found at 2060
    Illegal AgeI site found at 111
    Illegal AgeI site found at 399
    Illegal AgeI site found at 489
    Illegal AgeI site found at 726
    Illegal AgeI site found at 1553
    Illegal AgeI site found at 2049
  • 1000
    COMPATIBLE WITH RFC[1000]


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Categories
Parameters
None