Difference between revisions of "Part:BBa K3739036"

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===References===
 
===References===
 
1. https://parts.igem.org/Part:BBa_K3185005
 
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).
 
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).
  

Revision as of 17:38, 21 October 2021


J23100-B0030-Aly01-his-CBM-hutH-B0010

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_ K3739036 to construct the expression system and to express and to purify the protein. Aly01 is a signal peptide from the alginate lyase of V.natriegens, his-tag enable us to purify the linking protein, CBM can bind to cellulose and hutH is a histidine transaminase which converts histidine into urocanic acid.

Biology

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-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_ K3739036 to construct the expression system and demonstrated of the effect of secretory peptides and CBM-hutH together with BBa_ K3739071 and BBa_xxxx.

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
    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
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 679
    Illegal NgoMIV site found at 1115
    Illegal NgoMIV site found at 1850
    Illegal NgoMIV site found at 2086
    Illegal AgeI site found at 137
    Illegal AgeI site found at 425
    Illegal AgeI site found at 515
    Illegal AgeI site found at 752
    Illegal AgeI site found at 1579
    Illegal AgeI site found at 2075
  • 1000
    COMPATIBLE WITH RFC[1000]