Team:Newcastle/Promoter Library

From 2009.igem.org

(Difference between revisions)
(Variance 2)
(Design)
Line 40: Line 40:
# BBPrefix...UpSpacerNN...-35...NNPromSpacerNN...-10...NNDownSpacer..BBSuffix
# BBPrefix...UpSpacerNN...-35...NNPromSpacerNN...-10...NNDownSpacer..BBSuffix
# BBPrefix...UpSpacer...-35... 18N’s...-10...DownSpacer..BBSuffix
# BBPrefix...UpSpacer...-35... 18N’s...-10...DownSpacer..BBSuffix
 +
====Variance 1 ====
====Variance 1 ====
Line 47: Line 48:
[[Image:Team_Newcastle_iGEM_Promoter_Library4.png|500px]]
[[Image:Team_Newcastle_iGEM_Promoter_Library4.png|500px]]
 +
====Variance 2 ====
====Variance 2 ====
Line 52: Line 54:
[[Image:Team_Newcastle_iGEM_Promoter_Library5.png|500px]]
[[Image:Team_Newcastle_iGEM_Promoter_Library5.png|500px]]
 +
 +
[[Image:Team_Newcastle_iGEM_Promoter_Library7.png|500px]]
 +
====Variance 3 ====
====Variance 3 ====

Revision as of 21:12, 21 October 2009


Promoter Library

Introduction

In order to effectively model genetic circuits, databases of parts with known characteristics are essential. Without such databases, computationally designed circuits may not be feasible to implement in vivo. Unfortunately, parameters such as promoter strength, RBS affinity, transcription, translation and decay rates are hard to find in the literature, and those which do exist are rarely measured under standardised conditions.

Several efforts to produce parts libraries are currently underway.As part of our contribution to synthetic biology, we decided to create a promoter library for B. subtilis.

Novelty in this sub-project

A library of promoters with different strengths would be very useful for engineering biological devices. Promoters' strength can be compared with their PoPS values. However measuring the PoPS is not a trivial process. We can instead meausure their strengths relatively.

Design

Template used to create the promoter sequences: Prefix...UpSpacer...-35...PromSpacer...-10...DownSpacer..Suffix

Team Newcastle iGEM Promoter Library1.png

Team Newcastle iGEM Promoter Library2.png


  • BBPrefix - StandardBioBrickPrefix EcoR1 and Xba1 - gaattcgcggccgcttctagag
  • UpSpacer - attta - consensus sigA 5 bases 5'
  • -35 - TTGACA
  • PromSpacer - length 17 - consensus ttttatttaaattatga
  • -10 - TATAAT
  • DownSpacer (from ackA)- ggaaaag
  • BBSuffix - Standard BioBrick suffix Spe1 and Pst1 - tactagtagcggccgctgcag

Variances

We designed three variances to create library of promoters with different strengths.

  1. Degenerating -35 and -10 sequences.
 BBPrefix...UpSpacer...N-35... PromSpacer...N-10...DownSpacer..BBSuffix
  1. BBPrefix...UpSpacerNN...-35...NNPromSpacerNN...-10...NNDownSpacer..BBSuffix
  2. BBPrefix...UpSpacer...-35... 18N’s...-10...DownSpacer..BBSuffix


Variance 1

In this variance we only degenerate -35 and -10 sequences.

Team Newcastle iGEM Promoter Library3.png

Team Newcastle iGEM Promoter Library4.png


Variance 2

In the second variance we use N's for the promoter sequence between -35 and -10 regions

Team Newcastle iGEM Promoter Library5.png

Team Newcastle iGEM Promoter Library7.png


Variance 3

Team Newcastle iGEM Promoter Library6.png

Lab Work Strategies

Other Presentations and Diagrams




News

Events

Social Net

  • Newcastle iGEM Twitter
  • [http://www.facebook.com/home.php#/group.php?gid=131709337641 Newcastle on Facebook]
  • [http://www.youtube.com/user/newcastle2009igem Newcastle Youtube Channel]