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

The novelty in this sub-project lies in the generation of a large number of B. subtilis promoters, based upon carefully considered variations to an existing promoter region. We chose the promoter region of the transcription factor SigmaA, since it is the most widely-used promoter in B. subtilis. Over 300 genes are controlled by SigA. Their promoter regions have highly conserved -10 and -35 regions, surrounded by variable sequences.

Design

Template used to create the promoter sequences:

Prefix...UpSpacer...-35...PromSpacer...-10...DownSpacer..Suffix

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 a library of promoters with different strengths.

Variance 1

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

BBPrefix...UpSpacer...N-35... PromSpacer...N-10...DownSpacer..BBSuffix

Variance 2

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

BBPrefix...UpSpacer...-35... 18N’s...-10...DownSpacer..BBSuffix

Variance 3

In the third variance we change the last two bases of minus 35 region and the first two bases of -10 region.

BBPrefix...UpSpacerNN...-35...NNPromSpacerNN...-10...NNDownSpacer..BBSuffix

Lab Work Strategies

Synthesis other strand using polymerase and a primer

Cut promoter fragments using EcoR1 and Pst1
Cut pSB1AT3 vector using EcoR1 and Pst1
Ligate the insert and the plasmid backbone, and transform E. coli DH5alpha
Subclone into Bacillus integration vector with gfp and insert at amyE

20 – 21 June 2009 - Europe workshop (London)
23 – 24 June 2009 - UK iGEM meetup (Edinburgh)
23 October Practice Presentation (Newcastle)
23 October T-shirts are ready
27 October Practice Presentation (Sunderland)
27 October Poster is ready
30 October – 2 November 2009 - Jamboree (Boston)

Team:Newcastle/Promoter Library

From 2009.igem.org