Difference between revisions of "Part:BBa K4361017"

 
Line 3: Line 3:
 
<partinfo>BBa_K4361017 short</partinfo>
 
<partinfo>BBa_K4361017 short</partinfo>
  
Similar to BBa_K4361016, but inserting an additional "gcgggtcagcgggtc" before the second IR1.
+
BlcR is a transcription factor originating from the bacterium <i>Agrobacterium tumefaciens</i> ([[Part:BBa_K4361100]]). In a homodimer state it contains a single DNA-binding domain that specifically binds one of two DNA sequences. Both sequences are so-called inverted repeat pairs (IRs), short DNA sequences whose ends are reverse complements of each other. For the Blc operator, these sequences are 'ACTCTAATgATTCAAGT' (IR1) and 'ATTAGttgaactCTAAT' (IR2), as further explained in [[Part:BBa_K4361001]]. <br>
 
+
This part has been designed to test whether or not multiple separate BlcR tetramers can form on a single DNA molecule. To create this part, a second IR1-tca-IR2 set has been added after the 3' end of the original IR2 in the wildtype sequence, spaced by a 15 nt linker (gcgggtcagcgggtc). The BlcR-binding domain of this part thus consists of IR1-tca-IR2-gcgggtcagcgggtc-IR1-tca-IR2. The distance between the IR sets is assumed to be sufficient to prevent the two potential BlcR tetramers from sterically hindering each other, as well as placing them on opposite sides of the DNA molecule due to being spaced 15 nt apart.
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 08:56, 10 October 2022


BlcR-binding oligo, 106 bp, IR1+IR2 + 15 bp linker + IR1+IR2

BlcR is a transcription factor originating from the bacterium Agrobacterium tumefaciens (Part:BBa_K4361100). In a homodimer state it contains a single DNA-binding domain that specifically binds one of two DNA sequences. Both sequences are so-called inverted repeat pairs (IRs), short DNA sequences whose ends are reverse complements of each other. For the Blc operator, these sequences are 'ACTCTAATgATTCAAGT' (IR1) and 'ATTAGttgaactCTAAT' (IR2), as further explained in Part:BBa_K4361001.
This part has been designed to test whether or not multiple separate BlcR tetramers can form on a single DNA molecule. To create this part, a second IR1-tca-IR2 set has been added after the 3' end of the original IR2 in the wildtype sequence, spaced by a 15 nt linker (gcgggtcagcgggtc). The BlcR-binding domain of this part thus consists of IR1-tca-IR2-gcgggtcagcgggtc-IR1-tca-IR2. The distance between the IR sets is assumed to be sufficient to prevent the two potential BlcR tetramers from sterically hindering each other, as well as placing them on opposite sides of the DNA molecule due to being spaced 15 nt apart.

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]