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− | In essence, bioethanol is no different from daily used ethanol; having the formula of C2H5OH (Zabed et al., 2014). Moreover, bioethanol has a higher octane number, evaporation enthalpy, flame speed and a wider range of flammability than the petroleum-based energy sources which increase its fuel consumption rate, making bioethanol more environmentally friendly (Zabed et al., 2014). | + | In essence, bioethanol is no different from daily used ethanol; having the formula of C2H5OH (Zabed <i>et al.</i>, 2014). Moreover, bioethanol has a higher octane number, evaporation enthalpy, flame speed and a wider range of flammability than the petroleum-based energy sources which increase its fuel consumption rate, making bioethanol more environmentally friendly (Zabed <i>et al.</i>, 2014). |
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− | Bioethanol also contains 35% oxygen which is important because of the reducing effect on particulate and nitrogen oxides emission as well as other greenhouse gases such as carbon monoxide, during combustion (Zabed et al., 2014). | + | Bioethanol also contains 35% oxygen which is important because of the reducing effect on particulate and nitrogen oxides emission as well as other greenhouse gases such as carbon monoxide, during combustion (Zabed <i>et al.</i>, 2014). |
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− | In brief, we chose bioethanol as our main focus due to its qualities of being eco-friendly, non-toxic, biodegradable, it reducing crude oil dependency from other countries and most importantly, emitting fewer greenhouse gases, thus creating less pollution (Oliveira et al., 2005; Tesfaw & Assefa, 2014; U.S. Energy Information Administration [eia], 2014; 2017; Melikoğlu & Albostan, 2011; Holzman, 2007). | + | In brief, we chose bioethanol as our main focus due to its qualities of being eco-friendly, non-toxic, biodegradable, it reducing crude oil dependency from other countries and most importantly, emitting fewer greenhouse gases, thus creating less pollution (Oliveira <i>et al.</i>, 2005; Tesfaw & Assefa, 2014; U.S. Energy Information Administration [eia], 2014; 2017; Melikoğlu & Albostan, 2011; Holzman, 2007). |
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− | Third generation biofuels are from algae cultures. Algae biofuels are common, provide a good alternative to fossil fuels and thought of as long-term energy sources (Hannon et al., 2014). However, this technology has many challenges; such as the need for strain identification and improvement, before it can compete in the fuel market (Hannon et al., 2014). | + | Third generation biofuels are from algae cultures. Algae biofuels are common, provide a good alternative to fossil fuels and thought of as long-term energy sources (Hannon <i>et al.</i>, 2014). However, this technology has many challenges; such as the need for strain identification and improvement, before it can compete in the fuel market (Hannon <i>et al.</i>, 2014). |
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− | Microalgae, on the other hand, are photosynthetic organisms that also create contrast in this market (Brennan et al., 2010). Although they can provide an enormous amount of lipids, proteins, and carbohydrates in a short period of time, they are fragile and have numerous needs; from the percentage of the nutrients in their environment to the amount of sunlight they receive (Brennan et al., 2010). Moreover, another disadvantage is that algae, in newly introduced environments, are observed to act invasively; altering ecosystems, reducing biodiversity and causing overall economic losses (Demirbas, 2010). | + | Microalgae, on the other hand, are photosynthetic organisms that also create contrast in this market (Brennan <i>et al.</i>, 2010). Although they can provide an enormous amount of lipids, proteins, and carbohydrates in a short period of time, they are fragile and have numerous needs; from the percentage of the nutrients in their environment to the amount of sunlight they receive (Brennan <i>et al.</i>, 2010). Moreover, another disadvantage is that algae, in newly introduced environments, are observed to act invasively; altering ecosystems, reducing biodiversity and causing overall economic losses (Demirbas, 2010). |
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− | The problem is that the most common pretreatment method which is dilute acid pretreatment generates byproducts such as hydroxymethylfurfural (HMF), furfural and reactive oxygen species (ROS) that inhibit microbial metabolism, severely affect redox system and cause fatal disruptions in the cell system; ultimately leading to the death of the cell (Kumar & Sharma, 2017; Höck et al., 2013; Ask et al., 2013; Jönsson & Martín, 2016; Wang et al., 2013). | + | The problem is that the most common pretreatment method which is dilute acid pretreatment generates byproducts such as hydroxymethylfurfural (HMF), furfural and reactive oxygen species (ROS) that inhibit microbial metabolism, severely affect redox system and cause fatal disruptions in the cell system; ultimately leading to the death of the cell (Kumar & Sharma, 2017; Höck <i>et al.</i>, 2013; Ask et al., 2013; Jönsson & Martín, 2016; Wang <i>et al.</i>, 2013). |
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− | The byproducts furfural and HMF act as thiol-reactive electrophiles and as a result, cellular glutathione levels get depleted in their presence, leading to the accumulation of reactive oxygen species (Kim et al., 2013). | + | The byproducts furfural and HMF act as thiol-reactive electrophiles and as a result, cellular glutathione levels get depleted in their presence, leading to the accumulation of reactive oxygen species (Kim <i>et al.</i>, 2013). |
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− | When furfural, another byproduct is present in the field, its reduction mechanism by NADPH-dependent oxidoreductases goes active (Zheng, 2013). In this mechanism, the expression of oxidoreductases that are NADPH-dependent, such as YqhD, are shown to inhibit the growth and fermentation in E.coli by competing with biosynthesis for NADPH (Zheng, 2013). The native conversion of NADH to NADPH in E. coli is already insufficient to revitalize the NADPH pool during fermentation, so the actions shouldn’t be interfering with NADPH metabolism as it leads to reduced cell mass followed by cell death (Wang et al., 2011). | + | When furfural, another byproduct is present in the field, its reduction mechanism by NADPH-dependent oxidoreductases goes active (Zheng, 2013). In this mechanism, the expression of oxidoreductases that are NADPH-dependent, such as YqhD, are shown to inhibit the growth and fermentation in E.coli by competing with biosynthesis for NADPH (Zheng, 2013). The native conversion of NADH to NADPH in <i>E. coli</i> is already insufficient to revitalize the NADPH pool during fermentation, so the actions shouldn’t be interfering with NADPH metabolism as it leads to reduced cell mass followed by cell death (Wang <i>et al.</i>, 2011). |
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− | Thus, the overexpression of plasmid-based NADH-dependent propanediol oxidoreductase (FucO) gene will reduce the need for oxidoreductases that are NADPH dependent, and convert furfural to furfuryl alcohol without interfering with the biosynthesis of NADPH (Wang et al., 2011). | + | Thus, the overexpression of plasmid-based NADH-dependent propanediol oxidoreductase (FucO) gene will reduce the need for oxidoreductases that are NADPH dependent, and convert furfural to furfuryl alcohol without interfering with the biosynthesis of NADPH (Wang <i>et al.</i>, 2011). |
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− | In normal circumstances, both the detoxification of ROS and the conversion of HMF & furfural result in a more oxidized intracellular environment; by interfering with the NADPH metabolism thus deteriorating the antioxidant defense system of the cell, decreasing its mass and ultimately resulting in death. With these considered, we have come to the conclusion that the solution to this problem was in the dual overexpression of GSH and FucO (Ask et al., 2013). | + | In normal circumstances, both the detoxification of ROS and the conversion of HMF & furfural result in a more oxidized intracellular environment; by interfering with the NADPH metabolism thus deteriorating the antioxidant defense system of the cell, decreasing its mass and ultimately resulting in death. With these considered, we have come to the conclusion that the solution to this problem was in the dual overexpression of GSH and FucO (Ask <i>et al.</i>, 2013). |
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− | So, we have come to the conclusion that the simultaneous overexpression of GSH and FucO would increase cellular growth rates, lifespan and ethanol yield in E. coli ethanologenic strain KO11 since GSH is the master antioxidant in living organisms coping with ROS; and FucO is the gene that converts HMF & furfural to non-toxic alcohols without interfering with the NADPH metabolism (Ask et al., 2013; Höck et al., 2013; Wang et al., 2011). | + | So, we have come to the conclusion that the simultaneous overexpression of GSH and FucO would increase cellular growth rates, lifespan and ethanol yield in <i>E. coli</i> ethanologenic strain KO11 since GSH is the master antioxidant in living organisms coping with ROS; and FucO is the gene that converts HMF & furfural to non-toxic alcohols without interfering with the NADPH metabolism (Ask <i>et al.</i>, 2013; Höck <i>et al.</i>, 2013; Wang <i>et al.</i>, 2011). |
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Revision as of 00:40, 16 October 2018