With the break between semesters over, the Macquarie iGEM returned to classes. For us this was the first day of iGEM 2012. We had our first meeting and discussed our project. Dr. Louise Brown and Associate Professor Rob Willows were introduced the team and we began to determine who would take on certain roles within the team.

We eagerly began our project, deciding to use the novel approach of Gibson Assembly to produce our optimised genes. We had decided to develop a gene-switch controlled by light. To do this a couple of genes would be required:

1. a bacteriophytochrome
2. Heme oxygenase

The bacteriophytochromes from Deinococcus radiodurans and Agrobacterium tumefaciens were chosen. Over the next week Matt Stclair started to develop the Gibson Blocks (gBlocks) by:

1. Acquiring the DNA sequence
2. Translating into the protein sequence
3. Using the DNA sequence, optimise codon usage for E. coli
4. Translating into protein sequence and ensuring no changes in amino acids relative to the original sequence

Our lab work began today with the preparation of liquid media, plates and buffers. The protocols we followed are located here.

We prepared the following:

• Liquid LB Media
• SOC Solution
• SOB Solution
• LB Agar Plates
• Ampicillin LB Agar Plates: 31 plates
• Chloramphenicol LB Agar Plates: 33 Plates
• Kanamyacin LB Agar Plates: 32 Plates
• TB buffer.
• TAE buffer.
• EDTA buffer.

gBlock Development

While the lab group produced the necessary materials, another team began developing the gBlocks. The gBlock team consisted of Ellaina, Matt Smith, Matt Stclair, Harry, Gazelle, Silas, Kim, and Miguel. Matt Stclair spearheaded the effort and proofread all the sequences we had developed to ensure that we had not changed the protein sequence or introduced restriction sites.

To develop our gBlocks we needed to sections of DNA that could be used as overlaps. This ment that we the end of one gBlock was identical to the start of the next. This would allow for them to assemble in the correct order. This took some careful planning as we needed to ensure that they all had a similar melting temperature within the range of ST CLAIR.

Wiki editing and Human Practice

Ryan volunteered to be the wiki chief with Erin helping out throughout the project. Ellaina ensured the key safety questions were answered, and relayed these to the rest of the team. Rob and Sarah took control of the seeking finances to get the team to Hong Kong.

In a Macquarie iGEM first, the team took a big interest in the idea of human outreach and we had a brainstorming session. Ellaina proposed that we visit a high school while Elle suggested that the Universities open day would be a great opportunity to communicate with the wider community. Ellaina took control of developing our high school visit and Elle took control of Open Day.

Over the week we finalised our gBlocks and sent them to IDT DNA for synthesis. The bacteriophytochrome genes were split into 5 gBlocks of 500 bp each (the current maximum size). Agro was able to accomodate the T7 promoter In anticipation of our gBlocks arriving next week, competent cells were prepared. The protocol followed can be seen here.

Human Practice planning went into overdrive this week. To engage the wider community, fluorescent and bioluminescent parts from the registry were selected and transformed in E. coli. Red, Green, Orange, and Cyan Florescent protein as well as Luciferase were all located and transformed in the competent cells available. More details can be seen here.

Open Day Preparation

Our open day preparation did not go as planned. Most of our transformations were unsuccessful, we believe this was because SOC was added after the heat shock. As disappointing as this was, there was one little piece of good news.

A single colony of Top 10 E. coli containing GFP insert was identified on a plate of LB agar media. LB agar and nutrient agar plates were struck using this colony. The colony was also used to inoculate 5mL of nutrient broth. Plates and stock were then incubated at 37°C overnight. Both of the streaked plates and the broth showed significant growth of E. coli colonies which could fluoresce when exposed to UV light.

Finances

We got our first news on the finances front. Unfortunately, Qantas declined to sponsor the effort of getting our team to Hong Kong. This was soon forgotten when the Macquarie University School of Medicine, Agilent and the Defence Science Institute (thanks Yagiz) all agreed to sponsor our team. Hong Kong here we come.

Gibson Assembly Preparation

Design of the G Blocks continued. The fragments were designed with melting temperatures NEED TO ASK STCLAIR. However, IDT had significant synthesising them due to GC rich regions. Unfortunately for the MQ iGEM team, IDT is based in the USA and our lab sessions do not coincide with business hours. The G Block saga continued for a couple of weeks with new GC rich regions that affected synthesis identified with each modification made.

G Block Update

The team received the best news of the iGEM experience so far. Our G Blocks finally had no GC rich regions that inhibited synthesis. With the G Blocks arriving in the next week, we prepared for the assembly and took the opportunity to spend more time planning our two aspects of human practice.

Checking Competency

The efficiency of the competent cells produced was determined by transforming with the fluorescent constructs being used for the open day activities.

Outreach Planning

The two outreach teams prepared the presentations for next week. The school outreach team would be travelling up to Green Point Christian College on Tuesday next week to talk to their Year 12 HSC Biology class about ethics in synthetic biology.

The open day team developed more powerpoint presentations and posters for the activities planned. As part of this planning we drew pictures of different Australian icons with Green Fluorescent and Red Fluorescent proteins. The protocol we followed can be seen here here.

Our G Blocks finally arrived, after a long period of time getting the GC content down. Unfortunately for us, they arrived late on Friday afternoon, so the Gibson Assembly would need to wait to till the following Tuesday. Problems encountered from August 11th - August 26th included high GC content in the sequences to be synthesised, in particular, the Deinococcus fragments. These sequences had to be codon optimized and accepted by IDT before synthesis began.

The human outreach school team consisting of Ellaina, Ryan, Daniel and Matt Smith all visited Green Point Christian College to talk about the ethics and concerns surrounding synthetic biology. We received wonderful feedback and had a great discussion of what we were doing in our project. The students also had a few ideas for synthetic constructs that could be used in future iGEM teams.

The students completed surveys so we could gauge the change in their perspective of synthetic biology before and after our seminar. The results of our surveys can be seen here here.

The activities for open day were finalised and all of our prosters were prepared. We decided to try to communicate to a younger audience by using a Lego theme. All of our posters can be seen by clicking on the heading above

In anticipation of the Gibson assembly we prepared more competent cells. Harry, Matt St Clair, Silas and Kim performed our first Gibson Assembly reaction for each gene we prepared with different linearised vector (Parts PSB-1C3, PSB-1K3, PSB-1A3 from the registry). The synthesised genes were transformed in the competent cells prepared. For a more detailed analysis of the

Matt looked at the transformed cells we cultured the previous day (04/09/12). Two small colonies of the transformed Deinococcus bacteriophytochome without the T7 promoter were grown on kanamycin. The positive control was successful, so we could infer that the reactions were proceeding as expected. The positive control was also cultured on XGal and incubated overnight.

The Deinococcus fragment was cultured in 2 tubes of LB broth (2 mL) containing kanamycin. The transformations performed on the previous day were done again with a slightly different method. We choose to redo the transformations as the efficiency was relatively low. The transformations were re-innoculated onto fresh plates and incubated over night.

We continued on from the Gibson assembly and transformations we performed. Daniel did a plasmid prep using a QIAprep Spin Miniprep Kit by Qiagen, for two colonies from the Deinococcus bacteriophytochrome. The plasmid preparation protocol can be seen here.

Plasmid Preparation and Nanodrop Results

Plasmid Preparation was continued from Thursday, by Daniel and Harry, using the QIAprep Spin Miniprep Kit by Qiagen. A total of 7 colony cultures were used as the remaining did not grow. Successful cultures included 6 colonies from 1C and 1 colony from 3K. The DNA concentration was then determined for each sample by NanoDrop, with EB buffer from the Miniprep Kit used as a blank. The concentration of the plasmid extracted was determined using a NanoDrop and the results can be seen here.

Sequencing Results

The team received excellent news from the sequences performed on Friday. We had produced our first gene that is suitable for a biobrick! We had successfully produced the T7 promoter containing Heme Oxygenase. We then took this plasmid and inserted into BL21 E. coli to overproduce the protein and allow us to characterise the gene.

Gibson Assembly Round 2

Unfortunately none of the bacteriophytochrome Gibson reactions were successful, so these were repeated by Ryan, Kim, Silas and Matt. Unlike the first assembly, for the second round of Gibson assembly we decided to assmble into 3 different vectors for each reaction. That is, each bacteriophytochrome genes were assembled into one of three different vectors, each containing antibiotic resistance for kanamycin, chloramphenicol and ampicillin. In total 9 Gibson reactions were performed which are summarised below and details of this procedure can be seen here

The previous Gibson reaction used heat transformations, we wanted to determine whether electroporation yielded greater efficiency. Therefore we performed transformations using both of these techniques to determine which is the better method.

Using the standard procedures, more kanamycin and chloramphenicol plates were prepared.

The transformations from the previous day were examined and colonies were counted. Growth was slow so they were left till the afternoon to be counted. The counts can be seen here. It was determined that electroporation was a significantly more efficient transformation procedure than heat shock. This can be seen easily in the graph below,

Blue bars signify electroporation counts and red (yes they are there) signify heat shock counts.

Ryan inoculated cultures of the transformations in the morning so Andrew and Daniel could complete the plasmid prep in the afternoon. The concentrations of the plasmids obtained can be seen here. All of the plasmids were sent for sequencing to determine if the assembly had proceeded as expected.

With our midsemester break beginning and no other classes we could commit more time to the project. With the deadline fast approaching and the sequencing data returning tomorrow, we took the opportunity to digest all of our plasmids and prepare them for ligations. We were able to characterise the biobricks we had produced by inspecting the digestion pattern on the gel. The digest we performed are summarised below,

The Biobricks we had produced were characterised by running on a gel following the restriction digest.

1. There are relatively equal intensities of the two bands present. At approximately 750 bp is the heme oxygenase insert and at 2000 bp is the vector backbone.
2. In these lanes, there was less material loaded and thus the two bands present are poorly resolved. The Deinococcus phytochrome insert and the backbone are approximately the same size (2000 bp) as expected. The digestion may have been incomplete and thus there is a presence of circular and supercoiled plasmid, phytochrome insert and cut backbone.

1. No digest occurred and does not have the expected bands
2. Another incomplete digestion occurred and the enzymes used were the same as in the Deinococcus digestion with X + P and again, may not be reliable.
3. The lanes with expected bands are shown in the 1st and 3rd lanes of this Agro T7 treatment.
4. Linearized backbones

The heme oxygenase BioBrick was characterised by incubating in the presence of ALA and IPTG. Old colonies of transformed BL21 were used. As our BioBrick was under control of the T7 promoter, the enzyme would need to be induced using IPTG. The heme pathway was also stimulated using d-aminolevulinic acid (ALA). We incubated overnight with a 1 mM final concentrations of ALA and IPTG.

The sequencing results finally returned for our second round of Gibson Assembly (the bacteriophytochromes). The first look is very promising, Our Blast searches suggested that there were no significant mutations with the protein sequences identical. With this news we began to assemble the switch.

Using the digests we performed yesterday, we ligated our Heme Oxygenase and Bacteriophytochrome BioBricks and those from vectors not applicable to being a BioBrick. Ellaina performed the ligation using a standard procedure which is listed here.

Plates from the transformations of Top 10 cells with the ligation products were inspected. No colonies from the 2K-4K ligations grew. 9 colonies from the 1C-3C and single colony from 1C-5C colonies had grown. These colonies were used to inoculate into LB Kanamycin and left overnight for growth.

Rob and Matt spun down the BL21 colonies that had been transformed with plasmids containing the T7-HO genes (1C) and had been growing overnight after inducing with IPTG in the presence of ALA. 2 of the cultures were not induced but still had ALA added. These cultures had varying levels of green pigment visible in the pellet after being spun down. One culture was subjected to an additional 10ul of 100mM ALA and left to grow in the refrigerator. This culture will be left to grow for a further 48-72 hours to assess if there is any increase in pigmentation. Pellets from the remaining treatments are in the -18 freezer and will be used to run SDS-PAGE.

The liquid cultures used for the earlier minipreps were used to streak agar plates and these are now in the incubator. The cultures were then transferred into glycerol stocks and frozen.

******************************** add Andrew's work + Nano Drop results

This is a trial. I do not know if this is going to work or not!