Part:BBa_B0015

biology	rrnBT1-T7TE
chassis	E.coli
direction	Forward
forward_efficiency	0.984[CC] 0.97[JK]
reversed_version	2146
reverse_efficiency	0.295[CC] 0.62[JK]

double terminator (B0010-B0012)

Double terminator consisting of BBa_B0010 and BBa_B0012.
This is the most commonly used terminator. It seems to be reliable.
Note, however, that Part:BBa_B0014 is a better part for forward and reverse termination.

B0010	B0012

Secondary Structure

The mfold results are annotated with the location of the subparts BBa_B0010 and BBa_B0012 and the BioBrick assembly scar.

Using primers VR/VF2 to PCR B0010 will result in excess bands.

See a full description of the problem here.

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]

Measurement

[http://openwetware.org/wiki/Cconboy:Terminator_Characterization/Results How these parts were measured]

>Internal Priming Screening Characterization of BBa_B0015: Has no possible internal priming sites between this BioBrick part and the VF2 or the VR primer.

The 2018 Hawaii iGEM team evaluated the 40 most frequently used BioBricks and ran them through an internal priming screening process that we developed using the BLAST program tool. Out of the 40 BioBricks we evaluated, 10 of them showed possible internal priming of either the VF2 or VR primers and sometime even both. The data set has a range of sequence lengths from as small as 12 bases to as large as 1,210 bases. We experienced the issue of possible internal priming during the sequence verification process of our own BBa_K2574001 BioBrick and in the cloning process to express the part as a fusion protein. BBa_K2574001 is a composite part containing a VLP forming Gag protein sequence attached to a frequently used RFP part (BBa_E1010). We conducted a PCR amplification of the Gag-RFP insert using the VF2 and VR primers on the ligation product (pSB1C3 ligated to the Gag + RFP). This amplicon would serve as template for another PCR where we would add the NcoI and BamHI restriction enzyme sites through new primers for ligation into pET14b and subsequent induced expression. Despite gel confirming a rather large, approximately 2.1 kb insert band, our sequencing results with the VR primer and BamHI RFP reverse primer gave mixed results. Both should have displayed the end of the RFP, but the VR primer revealed the end of the Gag. Analysis of the VR primer on the Gag-RFP sequence revealed several sites where the VR primer could have annealed with ~9 - 12 bp of complementarity. Internal priming of forward and reverse primers can be detrimental to an iGEM project because you can never be sure if the desired construct was correctly inserted into the BioBrick plasmid without a successful sequence verification.

Functional Parameters: Austin_UTexas

BBa_B0015 parameters

Burden Imposed by this Part:

Burden is the percent reduction in the growth rate of E. coli cells transformed with a plasmid containing this BioBrick (± values are 95% confidence limits). This BioBrick did not exhibit a burden that was significantly greater than zero (i.e., it appears to have little to no impact on growth). Therefore, users can depend on this part to remain stable for many bacterial cell divisions and in large culture volumes. Refer to any one of the BBa_K3174002 - BBa_K3174007 pages for more information on the methods, an explanation of the sources of burden, and other conclusions from a large-scale measurement project conducted by the 2019 Austin_UTexas team.

This functional parameter was added by the 2020 Austin_UTexas team.

Contribution: New documentation from Evry_Paris-Saclay 2020

BBa_B0015 is a composite terminator made by joining 2 other terminators, one derived from E. coli (BBa_B0010) and the other from the T7 phage (BBa_B0012). Unlike what one can guess from the name and origin, the E. coli terminator can terminate transcription by T7 RNA polymerase, but not the T7 TE terminator. Indeed, BBa_B0010 is the E. coli rrnB T1 terminator which was shown to be an efficient terminator for the E. coli RNA polymerase, but also for the phage SP6 and T7 RNA polymerases through two different mechanism: one involving an upstream hairpin structure and the other one a downstream sequence-specific signal [1–3]. However, the T7 TE terminator (BBa_B0012) is located at the end of the T7 DNA ligase gene which is in the early region of bacteriophage T7 genome [4]. This terminator is an efficient one for the E. coli RNA polymerase, but not for the T7 RNA polymerase [5].

References

[1] Christiansen J. The 9S RNA precursor of Escherichia coli 5S RNA has three structural domains: implications for processing. Nucleic Acids Research (1988) 16: 7457–7476.

[2] Hartvig L, Christiansen J. Intrinsic termination of T7 RNA polymerase mediated by either RNA or DNA. The EMBO journal (1996) 15: 4767–4774.

[3] Kwon YS, Kang C. Bipartite modular structure of intrinsic, RNA hairpin-independent termination signal for phage RNA polymerases. The Journal of Biological Chemistry (1999) 274: 29149–29155.

[4] Dunn JJ, Studier FW. Complete nucleotide sequence of bacteriophage T7 DNA and the locations of T7 genetic elements. Journal of Molecular Biology (1983) 166: 477–535.

[5] Dunn JJ, Studier FW. The transcription termination site at the end of the early region of bacteriophage T7 DNA. Nucleic Acids Research (1980) 8: 2119–2132.