Line 87: | Line 87: | ||
Hydrogen peroxide itself is reactive as well. The exact reaction mechanism in the cell is unknown due to its reaction speed. However, it is known that hydrogen peroxide reacts with reduced copper and/or iron ions to form hydroxyl radicals. As a weak oxidizing agent it attacks thiol groups and reduces glutathione (Liu <i>et al.</i>, 2015).</br> | Hydrogen peroxide itself is reactive as well. The exact reaction mechanism in the cell is unknown due to its reaction speed. However, it is known that hydrogen peroxide reacts with reduced copper and/or iron ions to form hydroxyl radicals. As a weak oxidizing agent it attacks thiol groups and reduces glutathione (Liu <i>et al.</i>, 2015).</br> | ||
Hydroxyl radicals are highly reactive and react with almost every molecule. Since it is highly reactive, its reaction rate is limited by diffusion. The reactivity of hydroxyl radicals derives from its high standard electrode potential (+2.3 V). Therefore, it is able to oxidize almost any molecule other than ozone (Zhang <i>et al.</i>, 2018).</br> | Hydroxyl radicals are highly reactive and react with almost every molecule. Since it is highly reactive, its reaction rate is limited by diffusion. The reactivity of hydroxyl radicals derives from its high standard electrode potential (+2.3 V). Therefore, it is able to oxidize almost any molecule other than ozone (Zhang <i>et al.</i>, 2018).</br> | ||
− | There are several origins for the different types of ROS: Superoxide anion is formed by autoxidation of distinct dehydrogenases and certain reductases, e.g. glutathione reductase. Non-enzymatic production is achieved by autoxidation of certain cellular components such as ubiquinols. Hydrogen peroxidase derives from several oxidases and the superoxide dismutase. UV radiation breaks it down into hydroxyl radicals (Mignolet-Spruyt <i>et al.</i>, 2016). Other mechanisms for the generation of hydroxyl radicals are the Fenton and/or Haber-Weiss reaction (Fagali <i>et al.</i>, 2015; Kehrer, 2000).</ | + | There are several origins for the different types of ROS: Superoxide anion is formed by autoxidation of distinct dehydrogenases and certain reductases, e.g. glutathione reductase. Non-enzymatic production is achieved by autoxidation of certain cellular components such as ubiquinols. Hydrogen peroxidase derives from several oxidases and the superoxide dismutase. UV radiation breaks it down into hydroxyl radicals (Mignolet-Spruyt <i>et al.</i>, 2016). Other mechanisms for the generation of hydroxyl radicals are the Fenton and/or Haber-Weiss reaction (Fagali <i>et al.</i>, 2015; Kehrer, 2000).</article> |
− | Haber-Weiss: | + | <table> |
− | Fenton: | + | <tr> |
− | In order to neutralize the ROS and repair the occured damage bacteria have different mechanisms they can rely on. Two types of superoxide dismutase (SOD) dismutate O<sub>2</sub><sup>-</sup> into H<sub>2</sub>O<sub>2</sub>: MnSOD and FeSOD (encoded by <i>sodA</i> and <i>sodB</i>) (Broxton & Culotta, 2016). Catalases (encoded by <i>katE</i> and <i>katG</i>) are able to disproportionate H<sub>2</sub>O<sub>2</sub> into the nontoxic components H<sub>2</sub>O and O<sub>2</sub> (Chaithawiwat <i>et al.</i>, 2016). Further detoxification is achieved by the alkyl hydroperoxide reductase Ahp (encoded by <i>ahpC</i> and <i>ahpF</i>) which scavenges various free organic hydroperoxides (Kamariah <i>et al.</i>, 2016). These genes are in <i>E. coli</i> under the control of various global regulators such as OxyR and SoxR. The regulators also promote the expression of genes involved in the repair of the damaged cell membranes, DNA and proteins and are activated by a conformational change induced by oxidative stress (Dubbs & Mongkolsuk, 2016; Seo <i>et al.</i>, 2015).</br> | + | <td> |
+ | Haber-Weiss: | ||
+ | </td> | ||
+ | <td> | ||
+ | Fe<sup>3+</sup> + •O<sub>2</sub><sup>-</sup> → Fe<sup>2+</sup> + O<sub>2</sub> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td> | ||
+ | Fenton: | ||
+ | </td> | ||
+ | <td> | ||
+ | Fe<sup>2+</sup> + H<sub>2</sub>O<sub>2</sub> → Fe<sup>3+</sup> + OH<sup>-</sup> + •OH | ||
+ | </td> | ||
+ | </tr> | ||
+ | |||
+ | </table> | ||
+ | <article>In order to neutralize the ROS and repair the occured damage bacteria have different mechanisms they can rely on. Two types of superoxide dismutase (SOD) dismutate O<sub>2</sub><sup>-</sup> into H<sub>2</sub>O<sub>2</sub>: MnSOD and FeSOD (encoded by <i>sodA</i> and <i>sodB</i>) (Broxton & Culotta, 2016). Catalases (encoded by <i>katE</i> and <i>katG</i>) are able to disproportionate H<sub>2</sub>O<sub>2</sub> into the nontoxic components H<sub>2</sub>O and O<sub>2</sub> (Chaithawiwat <i>et al.</i>, 2016). Further detoxification is achieved by the alkyl hydroperoxide reductase Ahp (encoded by <i>ahpC</i> and <i>ahpF</i>) which scavenges various free organic hydroperoxides (Kamariah <i>et al.</i>, 2016). These genes are in <i>E. coli</i> under the control of various global regulators such as OxyR and SoxR. The regulators also promote the expression of genes involved in the repair of the damaged cell membranes, DNA and proteins and are activated by a conformational change induced by oxidative stress (Dubbs & Mongkolsuk, 2016; Seo <i>et al.</i>, 2015).</br> | ||
In order to increase the cell’s resistance to oxidative stress a sophisticated approach is needed. An overexpression of the oxidative stress dependent regulators SoxR and OxyR should improve the cell’s ability to cope with an elevated number of ROS. Various combinations of the defense mechanisms are tested in order to determine the ideal defense against oxidative stress in order to maximize the longevity in presence of heavy metals. Agents like phytochelatin which are rich in cysteine and/or histidine residues are meant to bind free metal ions to lower the potential for Fenton and/or Haber-Weiss reactions. | In order to increase the cell’s resistance to oxidative stress a sophisticated approach is needed. An overexpression of the oxidative stress dependent regulators SoxR and OxyR should improve the cell’s ability to cope with an elevated number of ROS. Various combinations of the defense mechanisms are tested in order to determine the ideal defense against oxidative stress in order to maximize the longevity in presence of heavy metals. Agents like phytochelatin which are rich in cysteine and/or histidine residues are meant to bind free metal ions to lower the potential for Fenton and/or Haber-Weiss reactions. | ||
</article> | </article> |
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.bubble.x1, .bubble.x2, .bubble.x8, .bubble.x9, .bubble.x10{ display:none; }
}
@media only screen and (max-width: 1200px) {
.bubble.x1, .bubble.x2, .bubble.x7, .bubble.x8, .bubble.x9, .bubble.x10{ display:none; } }
.timer_box{
border: white; border-style: solid; padding-bottom: 125px; padding-left: 10px; padding_top:10px; marging-bottom: 100px;
}
- gold {
float: left; font-size: 50px; margin-top: 10px; width: 50%; color:white;
text-align: center;
}
- gold_text {
float: left; font-size: 20px; margin-top: 0px; width: 50%; color:white;
text-align: center; }
- silver {
float: left; text-align: center; font-size: 50px; margin-top: 10px; width: 50%; color:white;
}
- silver_text {
float: left; text-align: center; font-size: 20px; margin-top: 0px; width: 50%; color:white;
}
.img_text{ text-align:center; position:absolute; }
- home_imgs {
margin-top:100px; width:60%;
}
@media only screen and (max-width: 1300px) {
- home_imgs{
width:70%;
}
- silver{
font-size: 30px;
}
- gold{
font-size: 30px;
}
- silver_text{
font-size: 20px;
}
- gold_text{
font-size: 20px; }
}
@media only screen and (max-width: 900px) {
.timer_box{
border: white; border-style: solid; padding-bottom: 100px; padding-left: 10px; padding_top:10px; marging-bottom: 100px;
}
- home_imgs{
margin-top:50px; width:90%; }
- silver{
font-size: 20px;
}
- gold{
font-size: 20px;
}
- silver_text{
font-size: 15px;
}
- gold_text{
font-size: 15px; }
}
@media only screen and (max-width: 600px) {
.timer_box{
border: white; border-style: solid; padding-bottom: 100px; padding-left: 10px; padding_top:10px; marging-bottom: 100px;
}
- home_imgs{
margin-top:15px; width:100%; }
- silver{
font-size: 15px;
}
- gold{
font-size: 15px;
}
- silver_text{
font-size: 10px;
}
- gold_text{
font-size: 10px; }
}
@media only screen and (max-width: 400px) {
.timer_box{
border: white; border-style: solid; padding-bottom: 50px; padding-left: 10px; padding_top:10px; marging-bottom: 100px;
}
- home_imgs{
margin-top:5px; width:100%; }
- silver{
font-size: 10px;
}
- gold{
font-size: 10px;
}
- silver_text{
font-size: 5px;
}
- gold_text{
font-size: 5px; }
}
Gold
Silver
Copper
Iron
Reactive oxygen species
Haber-Weiss: | Fe3+ + •O2- → Fe2+ + O2 |
Fenton: | Fe2+ + H2O2 → Fe3+ + OH- + •OH |