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Team:Calgary/Project/Promoter/Bioinformatics
From 2011.igem.org
The Project
NA-Sensitive Promoters using Bioinformatics and qRT-PCR
Introduction
A recent survey (footnote: Del Rio) found that two bacterial strains LD1 and LD2 (later identified as Pseudomonas fluorescens and putida) were capable of almost completely degrading a mixture of naphthenic acids when co-cultured together.
Figure 1. Source: (Del Rio)
Figure 1 shows the percentage of remaining naphthenic acids in a solution after four weeks of bacteria culturing. Both LD1 and LD2 may be capable of some degradation on their own, but the effect of co-culturing them together is to achieve a near total degradation of all samples in the mixture.
Figure 2.
Figure 2 shows how the degradation affected the concentrations of specific naphthenic acids of varying carbon number and saturation, as measured by GC-MS. The chart on the left of figure 2 shows the initial concentrations of each of the naphthenic acids, and the chart on the right shows the concentration of the naphthenic acids after four weeks of a LD1-LD2 co-culture. Based on the decreased height and scale, the figure demonstrates that naphthenic acids were more or less indiscriminately degraded by the co-culture.
When both figure 1 and 2 are taken together, the most likely conclusion is that the genes responsible for the degradation are spread across the two species. Furthermore, there exists a collection of essential genes in this degradation pathway which are unique to one species and not present in the other. The degradation pathway has not been experimentally confirmed, but it is believed to be some sort of metabolic pathway which involves beta-oxidation (footnote: Del Rio). In any case, the promoters upstream of these essential genes would be a likely place to find a naphthenic acid promoter - and indeed, our later experiments found that they were. A weakness of the bioinformatics search was that LD1 and LD2 have not yet been sequenced, and therefore we assume similarity between them and corresponding strains that have been sequenced; this weakness complicated primer design but was not prohibitive to the project.
Abstract
Three online algorithms (DarkHorse, ProteinWorld DB, and Pseudomonas.com) were used to find target gene candidates in silico, and a fourth (MUMmer ) was used to confirm experimental hypotheses. Using the data from these sources, we were able to construct a short list of gene candidates which were then processed through a quantative Real-Time Polymerase Chain Reaction (qRT-PCR) to verify gene expression as a response to naphthenic acids. The qRT-PCR found that Enoyl CoA Hydratase, from Pseudomonas putida, was expressed as a response to naphthenic acids.
The characterization of its promoter can be found below.
DarkHorse and ProteinWorld DB Results
DarkHorse is an online database for finding phylogenetically atypical proteins in various microbial species. Generally, phylogenetic atypicality can be useful for predicting the horizontal transfer of genes; in this bioinformatics survey, this also functions to provide a list of relatively unique genes in each of the strains in Pseudomonas putida and fluorescens.
Figure 3. Source: http://darkhorse.ucsd.edu/search.shtml/.
Figure 3 shows a sample of the input used for our DarkHorse Query. The list returned by querying the database for genes in LD1 and LD2 was 258 records long. Each record contained the GI number, strain, and gene annotation for the query species and its best phylogenetic match. To sort through the data, we started by collecting data about the best match species and the gene annotations. Using the data about the species, we found that some of them had known degradation pathways and were naturally occurring in tailings. We were especially interested in such species when they donated a predicted transcription factor or metabolite.
Later on, we also found Protein World DB, a database for finding unique genes across a set of compared species. This database did not provide information on horizontal transfer, so we primarily focussed on looking for metabolites and transcription factors.
At the end of looking through these two programs, we were ready to try to verify their transcription via qRT-PCR. The genes we tested are listed below:
Quantative RT-PCR Results
Primers for the Polymerase Chain Reaction (PCR) were designed with the following guidelines in mind:
- Melting Temperature: 70-74°C (optimally 72°C)
- Primer Length: 22-24 (optimally 24)
- Product Length: 150-250 base pairs (optimally 200)
- No runs of 4 or more of the same nucleotide letter in either the forward or reverse primer.
- The primers have a GC clamp at the end (ie. end with G, C, GC, or CG)
- The last 5 nucleotides contain 3 or 4 GC's.
- GC Content between 40-60% (optimally 50%)
- All unintentional matches calculated using Primer Blast are at least 25% mismatched.
Cell cultures of LD1 and LD2 were grown in minimal media in mixtures containing either 80mg/L of naphthenic acids or Casamino acids. We used several kits from Qiagen, including RNA Protect and RNEasy, etc. 16s rRNA, a constitutively expressed conserved gene found in both LD1 and LD2, was used as a control for the experiment.
Appendix A: Pseudomonas.com Results
The genes found from a subsequent bioinformatic search on Pseudomonas.com were not used in the RT-PCR, but have been included as an appendix for the iGEM community. Pseudomonas.com is a database specializing in the annotation and collection of information related to the Pseudomonas genus, but it also has a comparative genome search tool which claims to allow the location of genes unique to one species and not the other. The list, which has not been completely processed yet, can be found here in both .xls and .xlsx format (the latter is recommended). One of the most interesting genes found on the list is annotated as glyoxalase/bleomycin resistance protein/dioxygenase, but is similar to a ring-cleaving dioxygenase also found in putida.
Appendix B: MUMmer Findings
MUMmer is an open source program which can align genomes within a matter of seconds. We used MUMmer to verify our assumption that there was a substantial degree of homology between Pseudomonas putida and fluorescens. This assumption is important, because its corollary is that there is a limited number of genes unique to either species. The fewer unique genes there are, the easier it is to find the right one.
The graph above shows the genome alignment between Pseudomonas putida and fluorescens, where the earlier is on the x-axis and the latter on the y-axis. Regions conserved between both species form a straight line going from the bottom left corner to the top right corner; the line going from the top left corner to the bottom right corner is also a conserved region between both species, except that it is backwards. Areas with a more scattered distribution indicate a more random, and therefore less homologous, aligned region between the two species.
Using RT-qPCR to Detect Upregulation of Genes in Response to NAs
The pseudomonas strains (P. putida and P. fluorescens) were exposed to NAs to see if the genes selected through the bioinformatics search were in any way upregulated when compared with ordinary levels of expression. If they were upregulated it would indicate whether or not they contained NA responsive regions and hence a possible NA responsive promoter.
After treating the cells they were then preserved by exposure to an RNA stabilizing chemical, lysed and the RNA extracted. Next the RNA was converted to cDNA using random short primers and reverse transcriptase. The cDNA was then subjected to RT-PCR with primers that would amplify select genes of interest as well as control primers that amplify 16S-RNA sequences whose levels were expected to be stable.
To date no data has been obtained from the PCRs because the primers have not been amplifying the genes. Trouble shooting and optimization are ongoing at this point to determine the best parameters for the primers to work. MAKE CHANGES HERE NEW DATA HAS BEEN OBTAINED !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
Promoter Characterization
THIS SECTION SHOULD CONTAIN CHARACTERIZATION FOR THE PROMOTER, IF IT EXISTS.
