Team:Paris Bettencourt/Project/Foot Odor

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<p class=text1>We explore the possibility of using <i>B. subtilis</i> mutants to reduce foot odor. Strains of <i>B. subtilis</i> deleted in leucine degradation pathways should produce less odor, yet fill established ecological niches on human feet and socks.</p></td>
<p class=text1>We explore the possibility of using <i>B. subtilis</i> mutants to reduce foot odor. Strains of <i>B. subtilis</i> deleted in leucine degradation pathways should produce less odor, yet fill established ecological niches on human feet and socks.</p></td>
<td><b>ACHIEVEMENTS</b></br><br>
<td><b>ACHIEVEMENTS</b></br><br>
-
<p class=text1>Demonstrated that mutant strains of <i>B. subtilis</i> produce less odor.
+
<p class=text1><li>Demonstrated that mutant strains of <i>B. subtilis</i> produce less odor.</li>
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Measured growth and viability of mutants in synthetic sweat media and on socks.
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<li>Measured growth and viability of mutants in synthetic sweat media and on socks.</li>
</p></td>
</p></td>
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<div id=part1 class=project>
<div id=part1 class=project>
<p class=text2><img id=image2 src="https://static.igem.org/mediawiki/2014/4/43/Fig1Foot.jpg"><span class=legende>
<p class=text2><img id=image2 src="https://static.igem.org/mediawiki/2014/4/43/Fig1Foot.jpg"><span class=legende>
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<br><b>Figure 1. <i>B. subtilis</i> is gram positive bacterium which is commonly found in the human foot flora, which degrades the leucine aminoacid present in the sweat to produce isovaleric acid.</b> Our strategy is to perturb the leucine degradation pathway by knocking out the vital enzymes in the pathway. The leucine dehydrogenase knock out mutants lacks the capability to produce leucine and prevents the conversion of leucine to 4-methyl 2-oxopentanoate. The isovaleryl-coA dehydrogenase α and β subunit knock mutants lacks the capability of conversion of  4-methyl 2-oxopentanoate to isovaleryl-coA. </span><br><br>
+
<br><b>Figure 1. <i>B. subtilis</i> is commonly found in the human foot flora and degrades the leucine aminoacid present in the sweat to produce isovaleric acid.</b> Our strategy is to perturb the leucine degradation pathway by knocking out the vital enzymes in the pathway. The leucine dehydrogenase knock out mutants lacks the capability to produce isovaleric acid </span><br><br>
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<img id=image3 src="https://static.igem.org/mediawiki/2014/8/8f/Isovaleric_acid_diffusion_%281%29.gif"width="
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800" height="300" > </br> <br><span class=legende><b>
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Figure 2. Diffusion model of isovaleric acid through air</b>. This animation shows the concentration of isovaleric acid diffusing through air from a foot over a time period of 0 to 1000 hours. From the graph on the left of the animation, you can see that the odor threshold is reached very early in the model, given that the concentration of isovaleric acid at the skin surface is kept at a constant concentration of 1.1*10<sup>-6</sup> M.
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<h6>Introduction</h6><br>
<h6>Introduction</h6><br>
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<p class=text2></br>
<p class=text2></br>
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<img id=image3 src="https://static.igem.org/mediawiki/2014/8/8f/Isovaleric_acid_diffusion_%281%29.gif"width="
 +
800" height="250" > </br> <br><span class=legende><b>
 +
Figure 2. Diffusion model of isovaleric acid through air</b>. This animation shows the concentration of isovaleric acid diffusing through air from a foot over a time period of 0 to 1000 hours. From the graph on the left of the animation, you can see that the odor threshold is reached very early in the model, given that the concentration of isovaleric acid at the skin surface is kept at a constant concentration of 1.1*10<sup>-6</sup> M.
<img id=image3 src="https://static.igem.org/mediawiki/2014/6/6b/Smelltestsplited333.jpg">
<img id=image3 src="https://static.igem.org/mediawiki/2014/6/6b/Smelltestsplited333.jpg">
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<br><span class=legende><b>Figure 3. B. subtilis mutants ΔBKDAα knock out and ΔBKDAβ knockout to produce less odor than the wild type. </b>The <i>B. subtilis </i> wild type and mutant strains were grown overnight in M9 minimal medium. A double blind smell test was performed. The subjects were asked to rank the tubes in the scale of 0 to 5.   
+
<br><span class=legende><b>Figure 3. B. subtilis mutants ΔBKDAα knock out and ΔBKDAβ knockout to produce less odor than the wild type. </b>The <i>B. subtilis </i> A double blind smell test was performed. The subjects were asked to rank the tubes in the scale of 0 to 5.  The data from the smell test was analyzed and the error bars plotted are designated with 95% confidence interval(n=3). Though there is variation observed between the wild type strain and the <i>bcd</i> knock out strain, it is not statistically significant. In the case of <i>bkdaα</i>  
-
The data from the smell test was analyzed and the error bars plotted are designated with 95% confidence interval(n=3). Though there is variation observed between the wild type strain and the <i>bcd</i> knock out strain, it is not statistically significant. In the case of <i>bkdaα</i>  
+
knock out strain and the wild type strain there is a statistically significant variation observed. This confirms that the  
knock out strain and the wild type strain there is a statistically significant variation observed. This confirms that the  
<i>bkdaα</i> knock out strain produces less malodor compare to the wild type.</span> </br> <br>
<i>bkdaα</i> knock out strain produces less malodor compare to the wild type.</span> </br> <br>
<img id=image2 src="https://static.igem.org/mediawiki/2014/d/d6/Allfoot.jpg"><br><span class=legende>
<img id=image2 src="https://static.igem.org/mediawiki/2014/d/d6/Allfoot.jpg"><br><span class=legende>
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<b>Figure 4. The <i>B. subtilis</i> wild type and mutant strains were grown over night in M9 minimal medium supplemented with 0%, 0.1% and 0.2% leucine</b>. A double blind smell test was performed. The subjects were asked to smell the tubes and rank them in the scale of 0 to 5. The data from the smell test was analyzed and the error bars plotted are designated with 95% confidence(n=3) interval. In the wild type, <i>bcd</i> knockout and <i>bkdaα</i> knockout strains supplemented with 0%, 0.1% and 0.2% leucine, there is a statistically significant variation observed. Though there is variation observed between the 0%, 0.1% and 0.2% leucine supplemented medium in <i>bkdaβ</i> knock out strain, the difference is not statistically significant.
+
<b>Figure 4.The odor intensity is independent of the Leucine concentration for ΔBKDAβ knockout.</b>  The <i>B. subtilis</i> wild type and mutant strains were grown over night in M9 minimal medium supplemented with 0%, 0.1% and 0.2% leucine. A double blind smell test was performed. The subjects were asked to smell the tubes and rank them in the scale of 0 to 5. The data from the smell test was analyzed and the error bars plotted are designated with 95% confidence(n=3) interval.
This confirms that the leucine concentration influences the malodor production. </span> </br> <br>
This confirms that the leucine concentration influences the malodor production. </span> </br> <br>
<img id=image2 src="https://static.igem.org/mediawiki/2014/a/a2/LB_growth_curvepb.jpg"><br><span class=legende>
<img id=image2 src="https://static.igem.org/mediawiki/2014/a/a2/LB_growth_curvepb.jpg"><br><span class=legende>
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<b>Figure 5A.</b></span> </br> <br>
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<img id=image2 src="https://static.igem.org/mediawiki/2014/b/bb/SS_growth_curvef.jpg"><br><span class=legende><br><span class=legende>
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<br><b>Figure 5. Leucine degradation mutants have a growth disadvantage in synthetic sweat.</b> The B. subtilis wild type and the indicated mutant strains were grown in LB medium of synthetic sweat over 10 hours. Growth was determined by OD on a plate reader. All mutant strains showed significantly less growth, especially on sweat medium. The errors bars represent the standard error of the mean of 3 replicates.</span> </br> <br>
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<img id=image2  
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src="https://static.igem.org/mediawiki/2014/b/bb/SS_growth_curvef.jpg"><br><span class=legende><br><span class=legende>
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<br><b>Figure 5B.</b><br><b>The <i>B. subtilis</i> wild type and mutant strains were grown in LB medium for 10 hours and the growth kinetics was measured using a plate reader.</b> The growth curve represents an uneven growth pattern. This observation reflects that the mutant strain has a fitness disadvantage when compare to the wild type strain. This disadvantage is exacerbate in synthetic sweat medium. The errors bars represents the standard error of the mean.
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-
</span> </br> <br>
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<img id=image2 src="https://static.igem.org/mediawiki/2014/e/e1/Socks.jpg"
<img id=image2 src="https://static.igem.org/mediawiki/2014/e/e1/Socks.jpg"
<br><span class=legende>
<br><span class=legende>
-
<br><b>Figure 6. The <i>B. subtilis</i> wild type and mutant strains were grown in socks.</b> The overnight culture of the
+
<br><b>Figure 6. Leucine degradation mutants survive on socks.</b> Cotton socks were dipped in M9 cultures of B. subtilis wild type or the indicated mutant strains. Every day 2 cm2 of sock was cut, transferred to 5 ml of PBS, and plated on LB agar to count CFUs. Very little loss of viability was observed, even after 5 days. Error bars represent 95% confidence intervals determined from 3 replicates.</span> </br> <br>
-
 
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wild type and mutant strains grown in synthetic sweat was diluted in sterile synthetic sweat to reach 0.1 OD. The socks
+
-
 
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were gently soaked in the diluted synthetic sweat for 15 minutes. Later the socks were allowed to air dry at room
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-
 
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temperature for 6 hrs. After the sock is completely dried 2cm<sup>2</sup> of sock was cut and transferred to 5 ml of  
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1% PBS and plated on LB agar and the colony forming unit was measured. This experiment was repeated every 24 hours. The observation reflects that the survival </span> </br> <br>
 
</p>
</p>
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Because our smell tests used human noses, we built a model to estimate the sensitivity of our instruments (Fig. 2). Using COMSOL Multiphysics, we simulated odor diffusion as a system of differential equations. Isovaleric acid can be smelled at a concentration of 80 parts per trillion (<a href="https://2014.igem.org/Team:Paris_Bettencourt/Bibliograpy">Nagata, 1993</a>). After diffusion equilibrium, this corresponds to a liquid phase concentration of 10 mg/L at a distance of 5 cm, comparable to the leucine concentration in human sweat (<a href="https://2014.igem.org/Team:Paris_Bettencourt/Bibliograpy">Callewaert <i>et al.</i>, 2014</a>). Our model confirms that human noses are able to detect isovaleric acid at physiologically relevant concentrations.</br></br>
Because our smell tests used human noses, we built a model to estimate the sensitivity of our instruments (Fig. 2). Using COMSOL Multiphysics, we simulated odor diffusion as a system of differential equations. Isovaleric acid can be smelled at a concentration of 80 parts per trillion (<a href="https://2014.igem.org/Team:Paris_Bettencourt/Bibliograpy">Nagata, 1993</a>). After diffusion equilibrium, this corresponds to a liquid phase concentration of 10 mg/L at a distance of 5 cm, comparable to the leucine concentration in human sweat (<a href="https://2014.igem.org/Team:Paris_Bettencourt/Bibliograpy">Callewaert <i>et al.</i>, 2014</a>). Our model confirms that human noses are able to detect isovaleric acid at physiologically relevant concentrations.</br></br>
We next investigated the leucine-dependence of odor production in the <i>B. subtilis</i> and mutant strains. Strains were grown in M9 minimal media supplemented with 0%, 0.1% or 0.2% leucine. All strains produced detectable odor in all conditions, indicating that <i>B. subtilis</i> produces some odorant molecules independent of the leucine pathway. Odor production in the wild-type strain was strongly leucine dependant, suggesting leucine metabolism contributes significantly to odor. The odor of the <i>BKDAβ</i> knockout strain showed no leucine dependence, consistent with the successful inactivation of an odor pathway.</br></br>
We next investigated the leucine-dependence of odor production in the <i>B. subtilis</i> and mutant strains. Strains were grown in M9 minimal media supplemented with 0%, 0.1% or 0.2% leucine. All strains produced detectable odor in all conditions, indicating that <i>B. subtilis</i> produces some odorant molecules independent of the leucine pathway. Odor production in the wild-type strain was strongly leucine dependant, suggesting leucine metabolism contributes significantly to odor. The odor of the <i>BKDAβ</i> knockout strain showed no leucine dependence, consistent with the successful inactivation of an odor pathway.</br></br>
-
If mutant <i>B. subtilis</i> are to exclude the wild type on the human foot, they must be able to grow on sweat. We found that growth of all 3 mutant strains was moderately impaired on LB media, and severely impaired on synthetic sweat, relative to wild type (Figure X).</br></br>
+
If mutant <i>B. subtilis</i> are to exclude the wild type on the human foot, they must be able to grow on sweat. We found that growth of all 3 mutant strains was moderately impaired on LB media, and severely impaired on synthetic sweat, relative to wild type (Figure 5A and 5B).</br></br>
However, leucine-degradation mutant strains of <i>B. subtilis</i> showed robust survival on socks. We dipped cotton socks in dense M9 cultures of <i>ΔBCD</i>, <i>ΔBKDAα</i> knockout, <i>ΔBKDAβ</i> knockout or wild-type strains. Socks were hung to dry and sampled daily for the density of <i>B. subtilis</i> CFUs. After 5 days, we detected no significant decline in population viability. This suggests that, once introduced to socks, a metabolic mutant strain could persist and modulate odor production for an extended time.
However, leucine-degradation mutant strains of <i>B. subtilis</i> showed robust survival on socks. We dipped cotton socks in dense M9 cultures of <i>ΔBCD</i>, <i>ΔBKDAα</i> knockout, <i>ΔBKDAβ</i> knockout or wild-type strains. Socks were hung to dry and sampled daily for the density of <i>B. subtilis</i> CFUs. After 5 days, we detected no significant decline in population viability. This suggests that, once introduced to socks, a metabolic mutant strain could persist and modulate odor production for an extended time.
  </p></br></br></br>
  </p></br></br></br>
 +
</br>
<h6>Methods</h6><br>
<h6>Methods</h6><br>
<p class=text1>
<p class=text1>
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The minimal media was prepared by diluting  
The minimal media was prepared by diluting  
1 ml of 50% glucose
1 ml of 50% glucose
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1.1 ml of mgso4.3H20
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1.1 ml of MgSO4.3H20
2 ml of 1% w/v casmino acids
2 ml of 1% w/v casmino acids
2 ml of 10 mg/ml of tryptophan
2 ml of 10 mg/ml of tryptophan
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<b>Sock experiment:</b>
<b>Sock experiment:</b>
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The bacterial cell culture is diluted in synthetic sweat till it reaches 0.1 OD. The sock was soaked in the synthetic sweat and hanged till it dry. After this step 2 cm2 of sock was cut and soaked in 5 ml of 1% PBS. The tubes were stirred gently and supernatant is diluted in PBS to prepare 1X and 10X concentration of <i>B. subtilis</i>. The bacteria were then plated on LB agar.</br><br>
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The bacterial cell culture is diluted in synthetic sweat till it reaches 0.1 OD600. The sock was soaked in the synthetic sweat and hanged till it dry. After this step 2 cm2 of sock was cut and soaked in 5 ml of 1% PBS. The tubes were stirred gently and supernatant is diluted in PBS to prepare 1X and 10X concentration of <i>B. subtilis</i>. The bacteria were then plated on LB agar.</br><br>
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Thus, the diffusion coefficient of isovaleric acid was tabulated to be 1.7*10<sup>-9</sup> m<sup>2</sup> / s.<br><br></p>
Thus, the diffusion coefficient of isovaleric acid was tabulated to be 1.7*10<sup>-9</sup> m<sup>2</sup> / s.<br><br></p>
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<p class=text1><b>GC-MS analysis:</b>
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<p class=text1><b>GC-MS analysis:</b><br>
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For the GC-MS analysis, 1µl of the sample was injected into the instrument in split mode. A Rtx5MS- 30m column with 0.25-mm ID and 0.25µm df were used. The GC-MS run uses the following standardized parameters:</br>
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For the GC/MS analysis, 1µl of the sample was injected into the instrument in split mode. We used a Rtx5MS- 30m column with 0.25-mm ID and 0.25µm df. Data analysis was performed with X Caliber software. Component peaks were quantified by peak area normalized to an internal standard.<br></br></p>
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- Injection temperature: 300°C</br>
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- Interface temperature: 300°C</br>
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- Ion Source: 250°C</br>
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- Carrier Gas: Helium (flow rate of 1 ml min-1)</br></br>
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The temperature program used was 3 minutes of isothermal heating at 50⁰C followed by heating at 350⁰C for 10 minutes. Mass spectra were recorded at 2 scan sec-1 with a scanning range of 40 to 850 m/z. </br>
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X Caliber software is used to process and analyze the data from a GC-MS run. Quantify each component based on peak areas and normalization based on the internal standard.</br></p>
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</div>
</div>

Latest revision as of 03:39, 18 October 2014

BACKGROUND

Isovaleric acid has a pungent smell associated with both foot odor and strong cheese. A major source of this molecule on feet is leucine degradation by Bacillus strains, including the well-known lab strain B. subtilis.

AIMS

We explore the possibility of using B. subtilis mutants to reduce foot odor. Strains of B. subtilis deleted in leucine degradation pathways should produce less odor, yet fill established ecological niches on human feet and socks.

ACHIEVEMENTS

  • Demonstrated that mutant strains of B. subtilis produce less odor.
  • Measured growth and viability of mutants in synthetic sweat media and on socks.
  • Introduction Results Methods


    Figure 1. B. subtilis is commonly found in the human foot flora and degrades the leucine aminoacid present in the sweat to produce isovaleric acid. Our strategy is to perturb the leucine degradation pathway by knocking out the vital enzymes in the pathway. The leucine dehydrogenase knock out mutants lacks the capability to produce isovaleric acid


    Introduction

    Isovaleric acid is the characteristic odorant of foot odor. It is produced primarily from leucine, found in the sweat, via the leucine degradation pathway (Fig. 1). Of the many bacterial species found on the foot, only Bacillus frequency correlates with foot odor intensity (Ara et al., 2006). We therefore chose to focus our project on the leucine degradation pathway of the model microbe B. subtilis.

    We hypothesize that a leucine degradation mutant of B. subtilis will produce less odor, yet still survive and replicate on the foot. A large population of mutants on the foot would exclude the wild-type strain and therefore attenuate odor. If the mutant strain can persist in the foot ecosystem, bacterial foot deodorants could provide a cheap alternative to traditional chemical deodorizers.




    Figure 2. Diffusion model of isovaleric acid through air. This animation shows the concentration of isovaleric acid diffusing through air from a foot over a time period of 0 to 1000 hours. From the graph on the left of the animation, you can see that the odor threshold is reached very early in the model, given that the concentration of isovaleric acid at the skin surface is kept at a constant concentration of 1.1*10-6 M.
    Figure 3. B. subtilis mutants ΔBKDAα knock out and ΔBKDAβ knockout to produce less odor than the wild type. The B. subtilis A double blind smell test was performed. The subjects were asked to rank the tubes in the scale of 0 to 5. The data from the smell test was analyzed and the error bars plotted are designated with 95% confidence interval(n=3). Though there is variation observed between the wild type strain and the bcd knock out strain, it is not statistically significant. In the case of bkdaα knock out strain and the wild type strain there is a statistically significant variation observed. This confirms that the bkdaα knock out strain produces less malodor compare to the wild type.


    Figure 4.The odor intensity is independent of the Leucine concentration for ΔBKDAβ knockout. The B. subtilis wild type and mutant strains were grown over night in M9 minimal medium supplemented with 0%, 0.1% and 0.2% leucine. A double blind smell test was performed. The subjects were asked to smell the tubes and rank them in the scale of 0 to 5. The data from the smell test was analyzed and the error bars plotted are designated with 95% confidence(n=3) interval. This confirms that the leucine concentration influences the malodor production.





    Figure 5. Leucine degradation mutants have a growth disadvantage in synthetic sweat. The B. subtilis wild type and the indicated mutant strains were grown in LB medium of synthetic sweat over 10 hours. Growth was determined by OD on a plate reader. All mutant strains showed significantly less growth, especially on sweat medium. The errors bars represent the standard error of the mean of 3 replicates.



    Figure 6. Leucine degradation mutants survive on socks. Cotton socks were dipped in M9 cultures of B. subtilis wild type or the indicated mutant strains. Every day 2 cm2 of sock was cut, transferred to 5 ml of PBS, and plated on LB agar to count CFUs. Very little loss of viability was observed, even after 5 days. Error bars represent 95% confidence intervals determined from 3 replicates.


    Results

    We found B. subtilis mutants ΔBKDAα knock out and ΔBKDAβ knockout to produce less odor than the wild type. We obtained 3 deletion strains from the Bacillus Genetic Stock Center (BGSC): ΔBCD, ΔBKDAα knockout and ΔBKDAβ knockout. Each of these mutants blocks the metabolic pathway connecting leucine to Isovaleryl-CoA. Double-blind smell tests with human smellers revealed that cultures of ΔBKDAα knockout and ΔBKDAβ knockout had significantly less intense odor than wild type. No significant difference was detected for the ΔBCD strain (Fig. 3).

    Because our smell tests used human noses, we built a model to estimate the sensitivity of our instruments (Fig. 2). Using COMSOL Multiphysics, we simulated odor diffusion as a system of differential equations. Isovaleric acid can be smelled at a concentration of 80 parts per trillion (Nagata, 1993). After diffusion equilibrium, this corresponds to a liquid phase concentration of 10 mg/L at a distance of 5 cm, comparable to the leucine concentration in human sweat (Callewaert et al., 2014). Our model confirms that human noses are able to detect isovaleric acid at physiologically relevant concentrations.

    We next investigated the leucine-dependence of odor production in the B. subtilis and mutant strains. Strains were grown in M9 minimal media supplemented with 0%, 0.1% or 0.2% leucine. All strains produced detectable odor in all conditions, indicating that B. subtilis produces some odorant molecules independent of the leucine pathway. Odor production in the wild-type strain was strongly leucine dependant, suggesting leucine metabolism contributes significantly to odor. The odor of the BKDAβ knockout strain showed no leucine dependence, consistent with the successful inactivation of an odor pathway.

    If mutant B. subtilis are to exclude the wild type on the human foot, they must be able to grow on sweat. We found that growth of all 3 mutant strains was moderately impaired on LB media, and severely impaired on synthetic sweat, relative to wild type (Figure 5A and 5B).

    However, leucine-degradation mutant strains of B. subtilis showed robust survival on socks. We dipped cotton socks in dense M9 cultures of ΔBCD, ΔBKDAα knockout, ΔBKDAβ knockout or wild-type strains. Socks were hung to dry and sampled daily for the density of B. subtilis CFUs. After 5 days, we detected no significant decline in population viability. This suggests that, once introduced to socks, a metabolic mutant strain could persist and modulate odor production for an extended time.





    Methods

    Synthetic sweat: The chemical constituents present in the human sweat were analyzed with the aid of gas chromatography and mass spectroscopy. Synthetic sweat was prepared by diluting the exact concentration of all the amino acids and salts found in human sweat, the pH of the synthetic sweat was adjusted to 6.5 with the aid of a pH meter. The synthetic sweat was then autoclaved and stored at 4°C to avoid bacterial contamination.

    M9 minimal media: The minimal media was prepared by diluting 1 ml of 50% glucose 1.1 ml of MgSO4.3H20 2 ml of 1% w/v casmino acids 2 ml of 10 mg/ml of tryptophan in 100 ml of distilled water The media is then filter sterilized under a laminar air flow cabinet.

    Strain: The leucine dehydrogenase, isovaleryl coA alpha subunit and isovaleryl coA beta subunit. The knockout strains were obtained from Bacillus Genetic Stock Centre, where the knockout library of the B. subtilis was generated by replacing each gene with the erythromycin cassette. The mutant strains are trp- so they require supplementation of tryptophan in the growth media. The knockout strains were validated with the PCR reaction.

    Growth curve: The growth kinetics of the wild type and the mutant strains of B. subtilis were studied with the aid of micro plate reader to have insights about the fitness advantage and disadvantage within the mutant and wild type strain.

    Smell test: The presence of isovaleric acid in the bacterial culture was sensed with double blind smell test, where neither the subject nor the experimenter is aware of the tube labels. In order to optimize this smell test we grew the B. subtilis in odorless M9 minimal media. The media was supplemented with 0.1% of leucine to study the influence of leucine in production of foot odor.

    Sock experiment: The bacterial cell culture is diluted in synthetic sweat till it reaches 0.1 OD600. The sock was soaked in the synthetic sweat and hanged till it dry. After this step 2 cm2 of sock was cut and soaked in 5 ml of 1% PBS. The tubes were stirred gently and supernatant is diluted in PBS to prepare 1X and 10X concentration of B. subtilis. The bacteria were then plated on LB agar.

    Diffusion model of isovaleric acid: The model is based on a 2D axisymmetric geometry, with the air modeled as the space 5 cm around the skin surface. Here, the skin surface is kept at a constant concentration, C0 = 1.1E-6 M. This value refers to the approximate amount of isovaleric acid in sweat (Harvey, 2010). The diffusivity of isovaleric acid through the air was calculated using the Chapman-Enskog theory of gas diffusivity given by the following equation:
    D = [1.858*10-3* T-3/2*√(1/M1+1/M2)] / [p * s122 * w)]

    - D is the diffusivity of the isovaleric acid.
    - T is the room temperature (298 K).
    - p is the air pressure (1 atm).
    - M1 is the mass of the isovaleric acid (102.13 g/mol).
    - M2 is the mass of the air (29 g/mol).
    - s12 is the average collision diameter, which is around 340 Angstroms for gas molecules in air.
    - w is the dimensionless temperature-dependent collision integral,
    usually on the order of 1.

    Thus, the diffusion coefficient of isovaleric acid was tabulated to be 1.7*10-9 m2 / s.

    GC-MS analysis:
    For the GC/MS analysis, 1µl of the sample was injected into the instrument in split mode. We used a Rtx5MS- 30m column with 0.25-mm ID and 0.25µm df. Data analysis was performed with X Caliber software. Component peaks were quantified by peak area normalized to an internal standard.

    Centre for Research and Interdisciplinarity (CRI)
    Faculty of Medicine Cochin Port-Royal, South wing, 2nd floor
    Paris Descartes University
    24, rue du Faubourg Saint Jacques
    75014 Paris, France
    +33 1 44 41 25 22/25
    paris-bettencourt-igem@googlegroups.com
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