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Measurements and Quantification
In order to assess the efficiency and effectiveness of our yeast strains, we performed a series of quantitative measurements which would allow us to determine protein expression levels, amount of products and bi-products synthesized, and kinetic rates of the enzymes in our system. The results of these experiments also provide important initial conditions for the modeling aspect of our project, as it provides us with reliable and realistic in vivo gene expression and catalytic activity of the enzymes specific to our system. The following experiments will allow us to quantitatively determine these desired expression/synthesis in our system.
HPLC for measuring product synthesis
- Measure the amount of products (β-carotene, L-Ascorbic Acid).
- Extraction of β-carotene from yeasts*
β-carotene was extracted from yeasts for quantification. After addition of pyrogallol in methanol, cells were saponified with potassium hydroxide. The samples were incubated at 75 degrees, and beta carotene was then extracted with hexane. Samples were dried in a vacuum desiccator for future analysis.
- Spectroscopy and HPLC for measuring product synthesis:*
Measurements of product synthesis were performed by using Spectroscopy and High Performance Liquid Chromatography (HPLC) to characterize and assess the amount of β-carotene produced by our strains of yeast. HPLC allowed for the separation of β-carotene extracted from cellular extract, and based on a standard curve, //in vivo// measurements of β-carotene produced per yeast cell was determined.
Absorbance of beta carotene was measured with a UV spectrophotometer at 449nm. HPLC analysis was performed on a C18 Varian 5 micron 5x250mm column to verify the presence of beta carotene. The retention time of beta carotene 16.5 minutes.
Future plans (L-ascorbic Acid?)
- Protein Purification for enzyme assay*
In order to perform enzyme kinetics measurements for the enzymes in the β-carotene pathway, the enzymes had to be purified first. The enzymes being purified were geranylgeranyl pyrophosphate synthase, phytoene desaturase, and a bifunctional phytoene synthase and lycopene cyclase produced from the genes crtE, crtI, and crtYB, respectively. By isolating our enzymes of interest, we would greatly increase the accuracy of the kinetics experiments by eliminating overlapping background interference of absorption spectra, removing any competitive inhibitors of our enzymes, and ensuring a controlled measurement of our enzymatic rates were being measured. A procedure was designed which would allow for high amounts of product purified from extract, as well as high purity of our purification product. Using a TEV-his6X-mCherry-KAN tag, we would be able to purify our enzyme with only one high efficiency purification step (Nickel Column Purification using His-tag) and characterize product with great accuracy through the use of an mCherry (RFP) component of the tag. The following procedure is an outline of sequential experiments necessary to isolate and confirm the isolation of our enzymes.
Purify expressed protein of interest:
- Growth of yeast strains. - PCR gene of interest-TEV-his6X-linker-mCherry-KAN. Tag is on C-terminus of the protein. - Transform PCR products into yeast strains. - Microscopy to show red fluorescence. - Genomic prep from transformed cells and testing by PCR for integration of the tag at the c-terminus of the genes. - Make a cell lysate and run through a nickel column for purification. - Perform a Western Blot with DSred antibody or run a coommassie gel to assess purification (both size and quantity).
- Enzyme Assay* (Future Plans)
The set of enzyme kinetics experiments that we plan to perform for both β-carotene and L-ascorbic Acid will allow us to calculate the catalytic rates and efficiency of the enzymes in our pathways, and will allow us to optimize the system as we see fit based on environmental conditions, substrate levels, and stress created by over-stressing our pathway. Assuming Michaelis Menten kinetics for our enzymes we will be able to calculate kinetic values such as Km, kcat, and Vmax of the enzymes. In prepartion for the measurements, cellular conditions will be modeled as close as possible for this //in vitro// experiment. An //in vivo// enzyme kinetics experiment was hypothesized, but due to the complexity of our pathway, it was decided that the interference would be too great to determine our enzymes signal.
