Team:Penn State/ButanolProject
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<h2 style="color: green" ID="Back"> Background</h2> | <h2 style="color: green" ID="Back"> Background</h2> | ||
<p> | <p> | ||
- | ... | + | Our work focuses on the ATP dependent pathway described by the University of |
+ | California. The image below gives an outline of the pathway used. Refer to the red line. | ||
+ | <img src="http://www.pnas.org/content/109/16/6018/F1.large.jpg"/> | ||
+ | |||
</p> | </p> | ||
<p> | <p> | ||
- | + | http://www.pnas.org/content/109/16/6018/F1.large.jpg | |
+ | </p> | ||
+ | <p> | ||
+ | We designed three constructs based on the pathways for the synthesis of butanol and | ||
+ | PHB. The first of the three (Castor) is the same for both pathways and brings the reaction to the | ||
+ | intermediate 3-(R)-hydroxybutyryl-CoA. After that the reaction can proceed as shown above or | ||
+ | with the enzyme Polyhydroxyalkanoate synthase or PhaC the intermediate can be used to make | ||
+ | PHB. Castor can be ligated together with either of the other two constructs to create a useful | ||
+ | pathway for one of our products. | ||
</p> | </p> | ||
<h2 style="color: green" ID="Meth"> Method </h2> | <h2 style="color: green" ID="Meth"> Method </h2> | ||
<p> | <p> | ||
- | ... | + | The amino acid sequences used for the enzymes were converted back into nucleotide |
+ | sequences and then optimized for use in plants, or more specifically Physcomitrella patens. The | ||
+ | sequences were then optimized into ~500 base pair gBlocks | ||
+ | final constructs were then built using Gibson Assembly or CBAR. Then the constructs were | ||
+ | ligated into our vectors; which were Ti-plasmids. | ||
+ | TM which were synthesized. The | ||
+ | </p> | ||
+ | <p> | ||
+ | The entire pathway was broken into two distinct pieces, each of which gives us | ||
+ | one of our two final desired products. The first half of both constructs brings us to 3-(R)- | ||
+ | hydroxybutyryl-CoA and is referred to as Castor. This can then be converted into either butanol | ||
+ | or PHB depending on the following enzyme(s) in the pathway. The first construct consists of the | ||
+ | preliminary pathway and an additional four enzymes in a construct referred to as Pollux which | ||
+ | converts 3-(R)-hydroxybutyryl-CoA into butanol. The other is a single enzyme after the first | ||
+ | half that gives us PHB. The construct containing the single enzyme is named after the enzyme: | ||
+ | PhaC. | ||
</p> | </p> | ||
+ | |||
<h2 style="color: green" ID="Result"> Results</h2> | <h2 style="color: green" ID="Result"> Results</h2> | ||
<p> | <p> |
Revision as of 19:08, 8 August 2013
Butanol in Plants Project
The butanol project’s goal is to synthetically produce the enzymes that make up the University of California’s cyanobacteria pathway to produce n-butanol within physcomitrella. Thereby making a plant directly produce n-butanol, an industrially relevant compound that can serve as a more efficient biofuel than ethanol. The project took on another goal when it was realized that an intermediary compound in the pathway could be used to produce (R)-Polyhydroxybutyrate, a biodegradable plastic.
Introduction
Butanol is a four carbon alcohol with several different industrial uses such as the creation of polymers and pharmaceuticals. However, its most notable use is as a fuel for internal combustion engines. Butanol is fairly non-polar due to its longer hydrocarbon chain, and is more similar to gasoline than other small alcohols such as ethanol. The fact that it is similar in function to gasoline means that butanol can be used in automobiles without any changes. This is significant because butanol can be synthesized from biomass. Organisms such as cyanobacteria, diatoms, and the bacterium Clostridium acetobutylicum have already been shown to produce butanol using various methods.
Our other potential product is polyhydroxybutyrate or PHB. PHB is a polymer in the polyesters class that has many uses similar to other plastics of the same variety. The reason this one is an interesting option is the fact that it is nontoxic and biodegradable. This fact makes PHB an excellent choice for potential use in the medical industry as well as others. Biosynthesis of the polymer is currently achieved using microorganisms. Our goal was to extend the production capabilities to plants; specifically Physcomitrella patens.
Background
Our work focuses on the ATP dependent pathway described by the University of California. The image below gives an outline of the pathway used. Refer to the red line.
http://www.pnas.org/content/109/16/6018/F1.large.jpg
We designed three constructs based on the pathways for the synthesis of butanol and PHB. The first of the three (Castor) is the same for both pathways and brings the reaction to the intermediate 3-(R)-hydroxybutyryl-CoA. After that the reaction can proceed as shown above or with the enzyme Polyhydroxyalkanoate synthase or PhaC the intermediate can be used to make PHB. Castor can be ligated together with either of the other two constructs to create a useful pathway for one of our products.
Method
The amino acid sequences used for the enzymes were converted back into nucleotide sequences and then optimized for use in plants, or more specifically Physcomitrella patens. The sequences were then optimized into ~500 base pair gBlocks final constructs were then built using Gibson Assembly or CBAR. Then the constructs were ligated into our vectors; which were Ti-plasmids. TM which were synthesized. The
The entire pathway was broken into two distinct pieces, each of which gives us one of our two final desired products. The first half of both constructs brings us to 3-(R)- hydroxybutyryl-CoA and is referred to as Castor. This can then be converted into either butanol or PHB depending on the following enzyme(s) in the pathway. The first construct consists of the preliminary pathway and an additional four enzymes in a construct referred to as Pollux which converts 3-(R)-hydroxybutyryl-CoA into butanol. The other is a single enzyme after the first half that gives us PHB. The construct containing the single enzyme is named after the enzyme: PhaC.
Results
...
Discussion
...
Further Study
...
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