Difference between revisions of "Team:NAWI Graz/Results"

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             <sub>600</sub> and average of the three aliquots where taken to obtain the data shown in Figure 3.</p>
 
             <sub>600</sub> and average of the three aliquots where taken to obtain the data shown in Figure 3.</p>
 
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             <b>Fig 1.</b> Alx controlled mNeonGreen Expression: Culture media was bufferd to pH 7, 8 and 8.5 and inoculated
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            <sub>600</sub> of 0.2. After 20 and 40 minutes, aliquotes where taken and fluorescence (extinction 490 nm, absorbance
                <b>Fig 1. Alx controlled mNeonGreen Expression: </b>Culture media was bufferd to pH 7, 8 and 8.5 and inoculated
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            520 nm) and OD
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            <sub>600</sub> were measured with the plate reader (n=3).</font>
                <sub>600</sub> of 0.2. After 20 and 40 minutes, aliquotes where taken and fluorescence (extinction 490 nm, absorbance
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                520 nm) and OD
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                <sub>600</sub> were measured with the plate reader (n=3).</font>
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             As shown in figure 1. Expression of mNeonGreen is increased at pH 8 and 8.5 compared to standard pH 7. Cultures
 
             As shown in figure 1. Expression of mNeonGreen is increased at pH 8 and 8.5 compared to standard pH 7. Cultures

Revision as of 21:52, 31 October 2017

RESULTS

pH-Sensing

To test if our pH sensitive constructs express the fluorescence proteins we cultivated the bacteria hosting the plasmids in LPM with pH 7 overnight. For expression control for our alx-mNeonGreen construct, we inoculated 20 ml LPM with pH 7.0, 8.0 and 8.5 to an OD 600 of 0.2 using the overnight culture. After 20 and 40 minutes 1 ml of each culture where taken and adjusted to the lowest OD 600 of the three samples to standardize OD 600. This was necessary growth at pH 8.0 and 8.5 was significant slower than at pH 7.0. This diluted samples where used to measure fluorescence (extinction 490 nm, absorbance 520 nm) and again OD 600 with our plate reader. Three aliquots of each sample where measured (n=3), fluorescence was divided by OD 600 and average of the three aliquots where taken to obtain the data shown in Figure 3.

[Diagramm_alx.xlsx]
Fig 1. Alx controlled mNeonGreen Expression: Culture media was bufferd to pH 7, 8 and 8.5 and inoculated to an OD 600 of 0.2. After 20 and 40 minutes, aliquotes where taken and fluorescence (extinction 490 nm, absorbance 520 nm) and OD 600 were measured with the plate reader (n=3).
As shown in figure 1. Expression of mNeonGreen is increased at pH 8 and 8.5 compared to standard pH 7. Cultures at ph 7, but also cultures without the mNeonGreen plasmid (data not shown) show a high basic fluorescence, leading to the conclusion that the cells naturally show emission at 520 nm. Still, fluorescence is increased twofold at pH 8.5 after 20 and 40 minutes and fluorescence is significantly increased at pH 8 at both measuring points