Team:Hong Kong-CUHK/project-1.html

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<h2>Overview</h2>
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<h2>Introduction</h2>
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    Carbon dioxide (CO2) is notorious for its major contribution to global warming, where one of the impacts brought to the ecosystem is its excessive solvation into the ocean in carbonate form, threatening marine lifes (Baldgcchi et al., 1996). This year we would like to utilize and recharge these abundantly available CO2 by converting it to methane (CH4), an important carbon source for fuels and bio-degradable plastic production. While there are naturally existing methane-generating microorganisms, the convertion process involves multi-step metabolic reactions, not to mention that the mircoorganisms can only survive in anaerobic environment. Therefore, the difficulty of manipulating this convertion process remains high.
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    A recent research showed that a mutated form of nitrogenase from Azotobacter vinelandii, a nitrogen-fixing bacteria found in soil, has carbon fixation ability (Seefeldt et al., 2013). Yang et al. demonstrated that by introducing 70Ala and 195Gln mutations on nitrogenase alpha subunit, the nitrogenase enzyme complex reduced CO2 and CO32- to CH4 instead of converting N2 to NH3 (Yang et al., 2012). This system provided an one-step reaction to convert CO2 into CH4 and other carbon compounds directly. However, since a large electron flux, and thus energy, was wasted in producing molecular hydrogen (H2) from protons during the reaction, we utilized a soluble hydrogenase complex from Aquifex aeolicus to recycle H2 to protons. To further enhance the efficiency of carbon fixation process, we physically linked both nitrogenase and hydrogenase complexes with SH3 and PDZ ligand-domain pairs to accelerate the H2 recycling.
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Methane is a multifunctional gas that is used as fuel and an important carbon source. It is also used to make bio-degradable plastic. We aim at converting carbon dioxide and carbonate, which are excessive to the ecosystem, into methane. An engineered nitrogenase (α-70Ala, α-195Gln) in Azotobacter vinelandii has been shown to have the ability of reducing carbon dioxide and carbonate into methane and other carbon compound. However, the carbon fixation process consumes a large numbers of protons and thus decreases the reaction rate. We propose to co-express hydrogenase III from ''Aquifex aeolicus'' to speed up the carbon fixation step in A. vinelandii.</p>
Methane is a multifunctional gas that is used as fuel and an important carbon source. It is also used to make bio-degradable plastic. We aim at converting carbon dioxide and carbonate, which are excessive to the ecosystem, into methane. An engineered nitrogenase (α-70Ala, α-195Gln) in Azotobacter vinelandii has been shown to have the ability of reducing carbon dioxide and carbonate into methane and other carbon compound. However, the carbon fixation process consumes a large numbers of protons and thus decreases the reaction rate. We propose to co-express hydrogenase III from ''Aquifex aeolicus'' to speed up the carbon fixation step in A. vinelandii.</p>

Revision as of 04:11, 27 November 2014

Introduction

Carbon dioxide (CO2) is notorious for its major contribution to global warming, where one of the impacts brought to the ecosystem is its excessive solvation into the ocean in carbonate form, threatening marine lifes (Baldgcchi et al., 1996). This year we would like to utilize and recharge these abundantly available CO2 by converting it to methane (CH4), an important carbon source for fuels and bio-degradable plastic production. While there are naturally existing methane-generating microorganisms, the convertion process involves multi-step metabolic reactions, not to mention that the mircoorganisms can only survive in anaerobic environment. Therefore, the difficulty of manipulating this convertion process remains high.

A recent research showed that a mutated form of nitrogenase from Azotobacter vinelandii, a nitrogen-fixing bacteria found in soil, has carbon fixation ability (Seefeldt et al., 2013). Yang et al. demonstrated that by introducing 70Ala and 195Gln mutations on nitrogenase alpha subunit, the nitrogenase enzyme complex reduced CO2 and CO32- to CH4 instead of converting N2 to NH3 (Yang et al., 2012). This system provided an one-step reaction to convert CO2 into CH4 and other carbon compounds directly. However, since a large electron flux, and thus energy, was wasted in producing molecular hydrogen (H2) from protons during the reaction, we utilized a soluble hydrogenase complex from Aquifex aeolicus to recycle H2 to protons. To further enhance the efficiency of carbon fixation process, we physically linked both nitrogenase and hydrogenase complexes with SH3 and PDZ ligand-domain pairs to accelerate the H2 recycling.

Methane is a multifunctional gas that is used as fuel and an important carbon source. It is also used to make bio-degradable plastic. We aim at converting carbon dioxide and carbonate, which are excessive to the ecosystem, into methane. An engineered nitrogenase (α-70Ala, α-195Gln) in Azotobacter vinelandii has been shown to have the ability of reducing carbon dioxide and carbonate into methane and other carbon compound. However, the carbon fixation process consumes a large numbers of protons and thus decreases the reaction rate. We propose to co-express hydrogenase III from Aquifex aeolicus to speed up the carbon fixation step in A. vinelandii.