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Contents 1 Construction of plasmids 1.1 pSB1C3_IntK 1.1.1 sfGFP with LVA tag for describing circadian behaviour 1.1.2 Luciferase(s) 1.2 pSB1A3_IntC (From 2010 Utah's iGEM team) 1.3 pSB1C3_IntS 1.3.1 Substrate production under Pcaa3 1.3.2 Substrate production under PsigE 2 Synechocystis 2.1 Standardizing growth conditions 2.2 Transforming Synechocystis PCC 6803 2.3 Reestreaking 2.4 Confirming DNA 2.5 Conclusions 3 Revealing phenotypes 3.1 Microscopy 3.2 Luminometer readings 3.3 Conclusions

Construction of plasmids

pSB1C3_IntK

Our first attempts to build the construct ([BBa_K743004]) through Gibson Assemly were unsuccessful due to problems involving high compexity of the reaction, however we were able to Biobrick the recombination sites ([| Part:BBa_K743000] and | Part:BBa_K743001). Afterwards we decided to build a simple backbone first before continuing with more complex assemblies.

Through standard assembly we managed to build K743006 which led us to continue assembling our constructs through simpler Gibson Assemblies.

sfGFP with LVA tag for describing circadian behaviour

To describe the circadian behaviour of the promoter we built a fast-degrading reporter consisting of sfGPF I746916 with a LVA degradation tag in the C-terminal end of the protein. This construct will serve as a real-time reporter of promoter activity, you may find more information about the half-life of proteins with the LVA tag | here. The construct has been verified by digestion and corroborated by sequencing.

Luciferase(s)

In short time we were able to build our final constructs for the luciferase using 2 different versions of it available in the registry (| From Photorhabdus luminiscent, BBa_K743014 and | from Vibrio fisherii, BBa_K743015) under an endogenous Synechocystis's promoter (transaldolase Reference???). All constructs and parts have been verified by digestion and corroborated by sequencing.

pSB1A3_IntC (From 2010 Utah's iGEM team)

We decided to use this plasmid to place the LuxCDEG part of the Lux operon in this plasmid, however after various attempts to transform Synechocystis without success we reconsidered (see below SOMEWHERE!!! [[]]) due to problems regarding the design of this plasmid backbone. After analyzing the sequence of the vector (CODE HERE) we blasted the sequences of the recombination sites and we found out that position of the sequences of each recombination site are swapped, leaving the backbone part of the plasmid to be integrated into the genome. Furthermore, the recombination sites are separated by aproximately 2.2 kilobases, knocking out 4 genes.

pSB1C3_IntS

After we reconsidered about using pSB1A3_IntC we designed a new plasmid backbone to place the LuxCDEG (substrate regeneration part of the Lux operon) under the Synechocystis's promoters we choose through our modelling (LINK HERE). We have obtained the plasmid backbone including all parts through Gibson Assembly and the plasmid has validated through digestion and was corroborated through sequencing.

Substrate production under Pcaa3

We have amplified all parts for the Gibson Assembly of the final construct under the Pcaa3 promoter (which has also been Biobricked with code | K743002 and we will make the assembly today (9/25/12).

Substrate production under PsigE

We are re-amplifying the LuxCD part (to obtain higher concentrations of the insert) and we will try the assembly today (9/25/12).

Synechocystis

Standardizing growth conditions

While we managed to acquire an inoculum of Synechocystis PCC 6803, no conditions were set for working with Synechocystis PCC 6803 in our faculty. We proceeded to standardize our own growth conditions by building a custom made cyanobacterial incubator based on growth conditions described in the literature (References?)
Here we show our growth curve for Synechocystis PCC 6803 using the conditions set in our DIY) shaking incubator (40uE/s²/m²), 90 RPM, 30°C.

Methods for the growth curve characterization of Synechocystis PCC 6803 over here.

Transforming Synechocystis PCC 6803

Reestreaking

Confirming DNA

Conclusions

Revealing phenotypes

Microscopy

Luminometer readings

Conclusions