NTU@iGEM Project Introduction Methodology Team Introduction Team background Notebook Dry Lab Introduction ODEs used Modeling Constructs Parameters used Deterministic Modeling Sensitivity Analysis Stochastic Modeling Wetlab Introduction Materials and Equipment Protocols Verification of Detection & Lysis System Our New Parts Characterization Introduction Standard Promoters Characterization of pLacI-GFP pLacI-GFP images and clips Characterization of pLsrA-YFP New characterization Proposal Parameter Estimation & Correlations Acknowledgements

Contents 1 Introduction 2 Characterization of Parts 3 The FLx800™ Fluorescence Microplate Reader 4 Experiments 4.1 Characterization of Standard Biobrick via GFP Activity 4.2 Characterization of pLsrA - YFP

Introduction

The group proposed to discuss and investigate the working range of the parts and devices of our system

• The proposed variables to investigate are:
  

i) Concentration of activator

ii) Time

iii) Temperature

Characterization of Parts

We are interested in characterizing the following parts:

i) Lactose/IPTG sensitive Promoter pLac BBa_R0010

ii) Iron Sensitive Promoter pFe BBa_I716014

iii) AI2 senstive Promoter pLsrA
The characterization is carried out by ligating the desired promoter with the Green Fluorescence protein: BBa_E02040

• For the pLac BBa_R0010, it is already available in the form that we desired in the registry as BBa_J04430
• For the pLsrA promoter, the Yellow Fluorescence protein was used instead to differentiate between our two different systems.

The FLx800™ Fluorescence Microplate Reader

The FLx800™ Fluorescence Microplate Reader was available for our use courtesy of Division of Bio-engineering lab. It was purchased from BioTek and for more information about the reader, you can refer to The FLx800™ Fluorescence Microplate Reader

The FLx800™ Fluorescence Microplate Reader has a computer software KCJunior that was installed in a computer adjacent to the reader for collection and processing of data from our samples.

Experiments

Characterization of Standard Biobrick via GFP Activity

The objectives of the characterization experiment are to investigate the effects of concentration of inducer, temperature and time on the production of Green Fluorescence protein (GFP) by the Biobrick promoter part being experimented. A stronger fluorescence, as measured using NTU FLx800™ Fluorescence Microplate Reader will indicate more GFP proteins being synthesised. This also corresponds to higher promoter activity.

Top10 competent cells are transformed with plasmid carrying the following gene sequence:

The cells are cultured and upon addition of the inducer, the reaction mixtures (with both cells and inducer) are fed into the Fluorescence Microplate Reader. This machine has a inbuilt software, KCJunior, which will translate the results into excellent data suitable for analysis. The samples’ fluorescence was measured for a period of 12 hours, at the temperatures of
i) 25°C
ii) 37°C
and iii) 42°C.

The readings were than plotted to produce a 3-dimentional graph for detail analysis.

For more information please refer to Characterization of pLacI-GFP

Characterization of pLsrA - YFP

For more information please refer to Characterization of pLacI-GFP