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Team:Bielefeld-CeBiTec/Project/CO2-fixation/GeneticalApproach
From 2014.igem.org
CO2 Fixation
Genetical approach
Introduction and motivation
Our goal is to bind carbon dioxide in organic molecules. There are many different pathways known for carbon dioxide fixation in bacteria. Most suitable for our application are the 3-hydroxypropionat bicycle and the reductive pentose phosphate cycle also called Calvin cycle. We were looking for aerobic possibilities of carbon dioxide fixation, because of the desired energy source. Electric power shuld be the only source of energy for our bacteria. Therefor an aerobic cultivation is required. The electrons should pass through the bacterial respiratory chain. Oxygen is needed as the final acceptor of electrons at the end of the respiratory chain. Finally we decided to construct a bacterial version of the calvin cycle which is well understood in plants (Referenzen). One reason was the existence of almost all essentiell enzymes in E. coli. Only enzymes for three steps are missing. The implementation of the 3-hydroxypropionate bicycle would require the heterologous expression of genes for nearly all involved enzymes. Nevertheless we developed plans for the construction of both pathways in E. coli.
Sedoheptulose-1,7-bisphosphatase
The first missing enzyme of the Calvin cycle in E. coli is the sedoheptulose-1,7-bisphosphatase (SBPase). While this enzyme is common in plants only a few bacterial versions of it are known. One bacterial SBPase was recently identified and characterized by Stolzenberger et al. in 2013. The origin of this sequence is the thermophilic Bacillus methanolicus. B. methanolicus<(/i> lives at 50°C and therefore the temperature optimum of this enzyme is also at 50°C (Stolzenberger et al., 2013). We would like to use this enzyme at 37°C in E. coli. It had not escaped our notice that this temperature difference could cause a significant reduction in activity (REFERENZ für TEmp abhängigkeit bei enzymen). To our best knowledge there are no better fitting bacterial enzymes available.
Phosphoribulokinase
The next critical step of the Calvin cycle is the phosphorylation of riublose-5-phosphate. This reaction is catalyzed by the phosphoribulokinase. E. coli lacks such an enzyme. Therefore a phosphoribulokinase encoding sequence is taken from Synechococcus elongatus. It was functionally tested before (Parikh et al., 2006).
RubisCO
The most important step is the actual carbon dioxide fixing reaction. It is catalyzed by ribulose-1,5-bisphosphate-carboxylase/oxygenase (RubisCO) in plants. We looked for a bacterial ezymes and selected two different RuBisCOs. One is an enzyme from the carboxysome of Halothiobacillus neapolitanus( Bonacchi et al. in 2011). The other one is from Synechococcus elongatus (REFERENZ?). We decided to express both in E. coli and to make a comparison between them.
The enzyme from H. neapolitanus is usually located in a special microcompartiment called "carboxysome"(Bonacchi et al. in 2011). Therefore we decided to construct a carboxysome in E. coli.
Carboxysome
The carboxysome ensures an efficient carbon fixation reaction under aerobic conditions. The concentration of carbon dioxide is slectively increased inside the carboxysome (REFERENZ + VERWEIS AUF CARBAOXYSOM). The gene cluster of the carboxysome contains many illegal restriction sites. Because of this we decided to order synthesis of some parts of the sequence to delete this recognition sites. By synthesizing we are able to optimize the codon usage for expression in E. coli.
Summary
If it is possible to enable the whole cycle in E. coli it should be able to grow with electricity and carbon dioxide. We think of feeding a pentacarbohydrate to feed the Calvin cycle if the efficiency is not high enough.
