Difference between revisions of "CH391L/S13/Metabolic Engineering and Thermophiles"
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Revision as of 09:56, 15 April 2013
Metabolic Engineering is the changing and optimization of metabolic pathways in an organism for the increased production of a chemical product. This can include the addition of enzymatic steps catalyzed from enzymes encoded by exogenous genes. With economically viable feedstocks metabolic engineering has become a relevant process by which companies can create sustainable chemicals and pharmaceuticals.
Metabolic engineering was first done by chemical mutagenesis of organisms and screening for organisms with increased production of the desired metabolite. Eventually, with increased knowledge of metabolic pathways and genetic engineering techniques in the 1990s the constraints on a metabolic pathway and production of a desired metabolite could be more easily relieved. Modern techniques combine genetic engineering, systems biology, and directed evolution to improve yields in metabolic engineering. A particularly valuable systems biology technique called flux balance analysis, which is "a mathematical method for simulating metabolism in genome scale reconstructions of metabolic networks," has been particularly useful (Example). Bernhard Palsson, an innovator in systems biology, co-founded a metabolic engineering company based on on flux balance analysis  (software link)
Examples of Metabolic Engineering
Government and Metabolic Engineering
The U.S. Department of Energy (DOE) through the Bioenergy Technologies Office is heavily involved in research and funding of metabolic engineering projects for biofuels and bioproducts . Their website is a good reference for the basics of the field .
Organisms on earth are found to live between temperatures of −15°C to 122°C. Thermophiles are a type of extremophile that like to live in high temperature. Thermophiles are broken down into two groups "obligate' thermophiles (require high temperatures for growth) and faculative thermophiles (can live at high or low temperatures). Thermophiles are best known in biology as the source for the enzymes used in PCR, these orgasnims were isolated in hot springs and deep sea hydrothermal vents.
Terms for organisms based on their temperature preference
- Psychrophile grow down to −15°C to +10°C
- Mesophile grow typically between 20 and 45 °C
- Thermophile grow between 45 and 122 °C
- Hyperthermophile optimal temperatures are above 80°C
Use of thermophiles in metabolic Engineering
Thermophiles have distinct advantages and disadvantages in large scale production of biomolecules. Using thermophiles for enzymatic reactions are typically better than their mesophile counterparts because performing enzymatic reactions at high temperatures allows higher substrate concentrations, fewer risks of microbial contaminations, and often higher reaction rates. In addition, many Hyperthermophiles use exotic metabolic pathways not seen in typical mesophiles, such as using sulfur instead of oxygen in cellular respiration. The downsides to working with such organisms include: harder to culture, difficult genetic transformations, lack of selectable markers, different G/C content, smaller amount of studied "parts" to choose from, and a general smaller amount of knowledge about the organisms. The majority of research in metabollic engineering of thermophiles has been on cellulosic ethanol production.
Example model thermophilic organisms
- Sulfolobus solfataricus
- Thermus aquaticus
- Pyrococcus furiosus
- Thermosynechococcus elongatus
- Geobacillus stearothermophilus
Examples of thermophiles in metabolic Engineering
Metabolic Engineering of Thermophilic Bacillus licheniformis for Chiral Pure D-2,3-Butanediol Production
2,3-Butanediol is a potential fuel and a platform chemical. Organisms that natively produce the chemical are pathogenic and can only form the product with fermentations at 37°C. To transform the organism they had to use a protoplast fusion method. They were able to utilize xylose as a feedstock at 50°C to create product. This will be helpful to utilize lignocellulose substrates as higher temperatures are helpful in degradation.
Metabolic engineering of a thermophilic bacterium to produce ethanol at high yield
In this paper the authors used Thermoanaerobacterium saccharolyticum and made knockouts in the genes for acetate kinase, phosphate acetyltransferase, and L-lactate dehydrogenase. Their strain was able to produce high yields of ethanol as the only measurable fermentation byproduct. Cellulase, an enzyme added exogenously for the breakdown of cellulose, was reduced 2.5 fold when compared to the process in Saccharomyces cerevisiae at 37°C. The organism was transformed by selection on Erythromycin. They mention that these hemicellulolytic thermophilies along with Cellulolytic thermophiles like Clostridium thermocellum can be used for the entire process of cellulosic ethanol production .
Exploiting microbial hyperthermophilicity to produce an industrial chemical, using hydrogen and carbon dioxide
In this paper the authors discuss using hydrogen gas to reduce carbon dioxide directly into products as opposed to using organic feedstocks. They transformed Pyrococcus furiosus with five genes from Metallosphaera sedula of the carbon fixation cycle. With hydrogen gas and carbon dioxide they were able to produce 3-hydroxypropionic acid (a DOE top target chemical).
Notable tools and resources for metabolic engineering
- KEGG pathways - Wiring diagrams of molecular interactions, reactions, and relations
- Cell Designer - modeling tool of biochemical networks
Team Alberta 2012 (http://2011.igem.org/Team:Alberta) focused on making Neurospora crassa, which naturally breaks down cellulose. They were able to up-regulatie fatty acid synthesis and inhibit beta-oxidation. This created a fatty acid overproducer. Achievements page(http://2011.igem.org/Team:Alberta/Achievements/Overview).
Also, some team in texas metabollically engineered E. coli to grow on caffeine by introducing the N-demethylation pathway from Pseudomonas putida CBB5. (http://2012.igem.org/Team:Austin_Texas/Caffeinated_coli)