Difference between revisions of "Part:BBa K2328059"
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arashi
 
  
 
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<partinfo>BBa_K2328059 parameters</partinfo>
 
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===Usage===
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===Usage and Biology===
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Smurfp (small ultra-red FP) is the most important part in our group. It is desirable for our in vivo imaging because with it molecule less light is scattered, absorbed, or re-emitted by endogenous biomolecules compared with cyan, green, yellow and orange FPs. Smurfp can covalently attaches a biliverdin(BV) chromophore without a lyase, and has 642/670 nm excitation - emission peaks, a large extinction coefficient and quantum yield, and photostability comparable to that of eGFP. In order to make it expressed in bifidobacterium longum, we have made this sequence optimized.
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We use Linker II and Linker A to separate smURFP from Acma.  
  
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===Biology===
 
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In order to fluoresce,Smurfp must be combined with biliverdin(BV) .We have two solutions to make in vivo imaging come true. The first one is co-expression system and the other one is surface display system.To construct the co-expression system,the gene of fluorescent protein---smurfp and the gene of the precursor of biliverdin---HO-1 should be connected to the same expression vector and then transferred to our target bacteria.The precursor of biliverdin will be transferred to biliverdin through a series of conversion ,and then fluorescent protein will combine with biliverdin directly in our target bacteria and glow in the bacteria.To construct the surface display system,the gene of fluorescent protein---smurfp and the gene of the anchoring protein should be connected to the same expression vector. After the recombinant plasmid is transferred to the target bacteria, the fluorescent protein and anchoring protein will express at the same time and become fusion protein, and then the fluorescent protein will be carried to the cell surface by anchoring protein.With the added biliverdin, fluorescent protein will combine with biliverdin and glow on the cell surface.
 
  
 
===Reference===
 
===Reference===
 
[1]Yamamoto S, Wada J, Katayama T, Jikimoto T, Nakamura M, Kinoshita S, et al. (2010) Genetically modified Bifidobacterium displaying Salmonella-antigen protects mice from lethal challenge of Salmonella Typhimurium in a murine typhoid fever model. Vaccine 28: 6684–6691.
 
[1]Yamamoto S, Wada J, Katayama T, Jikimoto T, Nakamura M, Kinoshita S, et al. (2010) Genetically modified Bifidobacterium displaying Salmonella-antigen protects mice from lethal challenge of Salmonella Typhimurium in a murine typhoid fever model. Vaccine 28: 6684–6691.
 
[2]Rodriguez EA,Tran GN , Gross LA, et al. A far-red fluorescent protein evolved from a cyanobacterial phycobiliprotein .[J].NATURE METHODS,2016:763-769
 
[2]Rodriguez EA,Tran GN , Gross LA, et al. A far-red fluorescent protein evolved from a cyanobacterial phycobiliprotein .[J].NATURE METHODS,2016:763-769

Revision as of 16:58, 26 October 2017


nonsense sequence + Linker II + Linker.a

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 165
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 50


Usage and Biology

We use Linker II and Linker A to separate smURFP from Acma.


Reference

[1]Yamamoto S, Wada J, Katayama T, Jikimoto T, Nakamura M, Kinoshita S, et al. (2010) Genetically modified Bifidobacterium displaying Salmonella-antigen protects mice from lethal challenge of Salmonella Typhimurium in a murine typhoid fever model. Vaccine 28: 6684–6691. [2]Rodriguez EA,Tran GN , Gross LA, et al. A far-red fluorescent protein evolved from a cyanobacterial phycobiliprotein .[J].NATURE METHODS,2016:763-769