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

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         <p>To test if our pH sensitive constructs express the fluorescence proteins we cultivated the bacteria hosting the plasmids
 
         <p>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
 
             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
+
             with pH 7.0, 8.0 and 8.5 to an OD<sub>600</sub> of 0.2 using the overnight culture. After 20 and 40 minutes 1 ml of each culture where taken and adjusted
            <sub>600</sub> 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<sub>600</sub> of the three samples to standardize OD<sub>600</sub>. This was necessary growth at pH 8.0 and 8.5 was significant slower than at pH 7.0. This diluted samples
             to the lowest OD
+
             where used to measure fluorescence (extinction 490 nm, absorbance 520 nm) and again OD<sub>600</sub> with our plate reader. Three aliquots of each sample where measured (n=3), fluorescence was divided
            <sub>600</sub> of the three samples to standardize OD
+
            <sub>600</sub>. 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
+
            <sub>600</sub> with our plate reader. Three aliquots of each sample where measured (n=3), fluorescence was divided
+
 
             by OD
 
             by OD
 
             <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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         <div class="section-sub-text container">
 
         <div class="section-sub-text container">
 
             <b>Fig 1.</b> Alx controlled mNeonGreen Expression: Culture media was bufferd to pH 7, 8 and 8.5 and inoculated
 
             <b>Fig 1.</b> Alx controlled mNeonGreen Expression: Culture media was bufferd to pH 7, 8 and 8.5 and inoculated
             to an OD
+
             to an OD<sub>600</sub> of 0.2. After 20 and 40 minutes, aliquotes where taken and fluorescence (extinction 490 nm, absorbance
            <sub>600</sub> of 0.2. After 20 and 40 minutes, aliquotes where taken and fluorescence (extinction 490 nm, absorbance
+
             520 nm) and OD<sub>600</sub> were measured with the plate reader (n=3).</font>
             520 nm) and OD
+
            <sub>600</sub> were measured with the plate reader (n=3).</font>
+
 
         </div>
 
         </div>
 
     </div>
 
     </div>
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     <div class="section-text container">
 
     <div class="section-text container">
 
             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
             at ph 7, but also cultures without the mNeonGreen plasmid (data not shown) show a high basic fluorescence, leading
+
             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
 
             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
 
             8.5 after 20 and 40 minutes and fluorescence is significantly increased at pH 8 at both measuring points

Revision as of 23:03, 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 OD600 of 0.2 using the overnight culture. After 20 and 40 minutes 1 ml of each culture where taken and adjusted to the lowest OD600 of the three samples to standardize OD600. 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 OD600 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 OD600 of 0.2. After 20 and 40 minutes, aliquotes where taken and fluorescence (extinction 490 nm, absorbance 520 nm) and OD600 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