Difference between revisions of "Part:BBa K1351021"

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Excitation peak: 584 nm Emission peak: 607 nm
 
Excitation peak: 584 nm Emission peak: 607 nm
  
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=== Usage and Biology ===
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This part was created in order to enhance the [http://2012.igem.org/Team:LMU-Munich/Bacillus_BioBricks ''Bacillus'' BioBrick Box] by adding different fluorescent proteins in order to have more reporters available in ''B. subtilis''.
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It still works very well in ''E. coli'', the rather weak coloring you see on the pictures is due to the fact, that a rather homogenous and weak ''B. subtilis'' expression vector ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K1351040 pBS0K-Pspac]) was used in ''E. coli''
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[[File:LMU14_E1010mut_microscopy.jpg|thumb|left| BBa_K1351021 in the ''B. subtilis'' expression vector [https://parts.igem.org/wiki/index.php?title=Part:BBa_K1351040 pBS0K-Pspac] in E. coli ]]
  
 
[[File:LMU14_E1010mut-Pellet.jpg|thumb|right|The left eppendorf tube contains a pink bacterial pellet of ''E. coli'' containing the BioBrick BBa_K1351021 in [https://parts.igem.org/wiki/index.php?title=Part:BBa_K1351040 pBS0K-pPspac], a ''B. subtilis'' expression vector. On the right, you can see ''E. coli'' with the empty vector]]
 
[[File:LMU14_E1010mut-Pellet.jpg|thumb|right|The left eppendorf tube contains a pink bacterial pellet of ''E. coli'' containing the BioBrick BBa_K1351021 in [https://parts.igem.org/wiki/index.php?title=Part:BBa_K1351040 pBS0K-pPspac], a ''B. subtilis'' expression vector. On the right, you can see ''E. coli'' with the empty vector]]

Revision as of 12:34, 30 October 2014

Monomeric Red Fluorescent Protein from Discosoma striata

Mutant of the Biobrick BBa_E1010 [[1]]. In order to make it compatible with the Freiburg-Standard RFC25, two AgeI-Restriction sites were deleted.

monomeric RFP: Red Fluorescent Protein.

Excitation peak: 584 nm Emission peak: 607 nm


Usage and Biology

This part was created in order to enhance the [http://2012.igem.org/Team:LMU-Munich/Bacillus_BioBricks Bacillus BioBrick Box] by adding different fluorescent proteins in order to have more reporters available in B. subtilis. It still works very well in E. coli, the rather weak coloring you see on the pictures is due to the fact, that a rather homogenous and weak B. subtilis expression vector (pBS0K-Pspac) was used in E. coli

BBa_K1351021 in the B. subtilis expression vector pBS0K-Pspac in E. coli
The left eppendorf tube contains a pink bacterial pellet of E. coli containing the BioBrick BBa_K1351021 in pBS0K-pPspac, a B. subtilis expression vector. On the right, you can see E. coli with the empty vector


This part was generated in a modified version of RFC25, where a strong Shine Dalgarno Sequence (SD) is included, and has the following prefix and suffix:

prefix with EcoRI, NotI, XbaI, SD and NgoMIV: GAATTCGCGGCCGCTTCTAGAGTAAGGAGGAGCCGGC
suffix with AgeI, SpeI, NotI and PstI: ACCGGTTAATACTAGTAGCGGCCGCTGCAG

Sites of restriction enzymes generating compatible overhangs have the same color:

EcoRI and PstI in blue, NotI in green, XbaI and SpeI in red, NgoMIV and AgeI in orange. Shine-Dalgarno sequence and stop codons are underlined.

This part is used in the 2014 LMU-Munich iGEM project [http://2014.igem.org/Team:LMU-Munich BaKillus].


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
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]