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Measurement

In any scientific project there is a continuous cycle of making hypotheses, setting up experiments, measuring and evaluating the results. In this process the next set of hypotheses and experiments can therefore only be as good as the measurement techniques employed. Hence, high performing scientific measuring instruments have become the most costly investment many labs around the world choose to make. Fortunately the University of Groningen has an arsenal of excellent measuring equipment available spread around multiple buildings in the city that we were able to get access to.
Once impactful decisions have to be made based upon laboratory results, accurate measurement techniques become of immeasurable value. Nobody likes false positive or false negative results. Giving up on a promising line of experiments because of a mistake during measurement without ever knowing what could have been possible must be amongst the worst nightmares of the modern scientist. The Groningen iGEM team 2018 is happy to be free of such doubts because of the state of the art RP-HPLC UV-DAD, GC-MS, GC-FID, Nanodrop, Plate Reader machines, and many more that have provided us with reliable data to make the best decisions on how to proceed with our project and to get the best results towards our proof of concept. On this page we will highlight how some of these methods work, how we modified them and where their results come into our project.

What to measure? Styrene!

To prove our concept of a styrene producing, cellulolytic S. cerevisiae strain the detection of styrene is an essential part. For the identification and quantification of styrene, a variety of approaches that utilize different chemical characteristics of styrene are known. The purification procedure for styrene for measurement is different from the one for harvesting from a fermenter because the styrene only has to be detected and quantified, not purified for polymerization. To detect something in a mixture one has to find a signal that is both specific and sensitive for the compound of interest. This means that the generated signal cannot be created by something else that is present in the mixture at the point of measurement while the signal has to already be caused by small quantities of the analyte. Interesting physical and chemical properties of styrene that could be used to discriminate it from other compounds in the mixture include its UV activity at 245 nm, its high log P of 2,7, the high enthalpy in the reduced C-C and C-H bonds and last but not least its affinity to aromatic receptors in the human nose.

Which methods and detectors should we use?

To capitalize on styrene’s high log P, mainly chromatographic methods come to mind. These methods can identify styrene based upon its preference for a stationary phase over a mobile phase which leads to a difference in retention time. The signal for styrene detection can subsequently be generated in many ways, including UV absorbance measurement at 245 nm, measurement of an entire UV spectrum or even by burning the analyte as it comes off the column to detect forming carbonium ions.

How does chromatography work?

In chromatography, a liquid or gaseous mobile phase is lead over a stationary phase over a certain distance in a column. At the beginning of the column, a constant flow of new mobile phase is supplied. There is also a side for the injection of the sample for measurement. At the end of the column, a variety of signal generating and measuring devices can be installed that measure what comes off the column over time. Analytes that interact strongly with the stationary phase will reach the end of the column later. This so called retention behaviour is characteristic of the analytes physical chemical properties and reproducible under identical circumstances. Chromatographic techniques can be optimized in plenty of parameters: choice of stationary phase, choice of mobile phase, choice of signal generation, flow speed, temperature and usage of a gradient mobile phase. In a gradient mobile phase two or more solvents are employed whose composition changes over time. This allows for even better separation of peaks over time. To ensure reproducible measurements in chromatography, the machines have to be purged with fresh mobile phase after every run. To protect the column from contamination that might alter the retention behaviour of analytes, samples have to be freed of all enzymes, most cellular macromolecules and the lipid bilayer. The sample preparation for chromatography samples from living cells therefore commonly involves steps such as cell lysis, centrifugation, liquid-liquid extraction and filtration.

How did we employ RP-HPLC to detect styrene?

A Reverse Phase High Performance Liquid Chromatography (RP-HPLC) method was evaluated for styrene identification by injection of styrene in ethyl acetate, measuring the retention time and recording a UV spectrum using a Diode Array Detector. Reverse Phase describes a chromatography method in which the stationary phase is apolar while the mobile phase is polar. The stationary phase of choice was a C18 column. The first mobile phase evaluated was a gradient system of water 100 % to 0 % and acetonitrile 0 % to 100 %. This was tested in a 60 minute run to determine at which percentage of acetonitrile the styrene would elute. As styrene eluted as late as 80 % acetonitrile it was decided to switch to a gradient mobile phase with water 100 % to 0 % and methanol 0 % to 100 %. In this case, styrene eluted at 50 % methanol. As nothing significant eluted at a low methanol percentage it was decided to validate and settle on a 60 minute run with a water 70 % to 0 % and methanol 30 % to 100 % gradient mobile phase. With this method, styrene eluted at 17,5 minutes.