Difference between revisions of "Part:BBa K5136230"

(Agarose gel electrophoresis (AGE))
(Reference)
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==Reference==
 
==Reference==
1.A. A. Uçkun, M. Uçkun, S. Akkurt, Efficiency of Escherichia coli Jm109 and genetical engineering strains (E. coli MT2, E. coli MT3) in cadmium removal from aqueous solutions. Environ. Technol. Innovation 24, 12 (2021).
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1. A. A. Uçkun, M. Uçkun, S. Akkurt, Efficiency of<I> Escherichia coli </I>Jm109 and genetical engineering strains (<I>E. coli</I> MT2, <I>E. coli</I> MT3) in cadmium removal from aqueous solutions.<I> Environ. Technol. Innovation</I> <b>24</b>, 12 (2021).
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 14:00, 1 October 2024


I0500-B0034-mt3-B0034-mt2a-B0015

Biology

MT3 and MT2A

The metallothioneins (MTs) are a class of low molecular weight and cysteine-rich metal binding proteins, and each one of them can bind to 6-9 heavy metal ions. The MTs are expressed as intracellular protein and are primarily responsible for metal regulation in cells of living organisms. General MTs can widely non-covalently bind divalent heavy metal ions, such as Zn2+,Ni2+, Pb2+, Hg2+, Cd2+, as well as As3+, but their effectiveness in treating Cr2O72- is not satisfactory. MT2A and MT3 are metallothioneins(MTs) found in Homo sapiens. MT2A not only has efficient adsorption capacity for ordinary metal ions, but also exhibits efficient processing capacity for Cr2O72-. And MT3 has a better adsorption effect on ordinary metal ions. (1).

Usage and Design

To absorb Cd2+ in waste water, we introduced MntA membrane protein in E. coli, which translocates external Cd2+ into the cell. To increase the strain's tolerance to Cd2+, we constructed this composite part(BBa_K5136230) to produce intracellular MT2A and MT3 in engineered bacteria, mitigating the cell damage of Cd2+.

Characterization

Agarose gel electrophoresis (AGE)

The composite part (BBa_K5136230) constructed was introduced into the backbone plasmid (pSB1C3) through standard assembly and transformed into E. coli BL21(DE3). The positive clones were selected, and colony PCR and gene sequencing were used to verify that the clones were correct. Target bands (2106 bp) can be observed at the position around 2000bp (Figure 1).



Figure 1 colony PCR of BBa_K5136230_pSB1C3 in E. coli BL21(DE3)

Reference

1. A. A. Uçkun, M. Uçkun, S. Akkurt, Efficiency of Escherichia coli Jm109 and genetical engineering strains (E. coli MT2, E. coli MT3) in cadmium removal from aqueous solutions. Environ. Technol. Innovation 24, 12 (2021).

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1205
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1144
    Illegal BamHI site found at 1239
    Illegal BamHI site found at 1472
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 979
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 961