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Team:TU Delft/project/hydrocarbon solubility
From 2010.igem.org
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===Proposed Method=== | ===Proposed Method=== | ||
| - | In order to overcome the mass-transfer limitations of an oil-water environment, the production of an emulsifier is proposed. The presence of an emulsifier will increase the amount of alkanes dissolved in the water phase, increasing the availably for the microorganisms. Two emulsifiers from naturally oil-degrading bacteria will be expressed in E.coli | + | In order to overcome the mass-transfer limitations of an oil-water environment, the production of an emulsifier is proposed. The presence of an emulsifier will increase the amount of alkanes dissolved in the water phase, increasing the availably for the microorganisms. Two emulsifiers from naturally oil-degrading bacteria will be expressed in E.coli DH5aplha using the BioBrick method. |
===Step 1: AlnA BioBrick Formation=== | ===Step 1: AlnA BioBrick Formation=== | ||
Revision as of 11:48, 2 August 2010
Contents |
Hydrocarbon Solubility
Aim
To create BioBricks for the production of emulsifiers AlnA and OprG. These biobricks will be implemented in Escherichia coli DH5alpha and characterized and evaluated on their emulsifying capabilities.
Proposed Method
In order to overcome the mass-transfer limitations of an oil-water environment, the production of an emulsifier is proposed. The presence of an emulsifier will increase the amount of alkanes dissolved in the water phase, increasing the availably for the microorganisms. Two emulsifiers from naturally oil-degrading bacteria will be expressed in E.coli DH5aplha using the BioBrick method.
Step 1: AlnA BioBrick Formation
Based on: Gil Walzer, Eugene Rosenberg and Eliora Z. Ron. The Acinetobacter outer membrane protein A (OmpA) is a secreted emulsifier. Environmental Microbiology 8(6): 1026–1032 (2006)
Oil-degrading strains of Acinetobacter produce a variety of high-molecular-weight biosurfactants. One of the best-studied emulsifiers is Alasan produced by Acinetobacter radioresistens (KA53). It contains three proteins of 15 kDa, 31 kDa and 45 kDa. The 45 kDa protein is associated with the major emulsifying ability and is called AlnA. AlnA is a homologue of the E. coli OmpA.
The necessary gene, AlnA, will be synthesized, and the appropriate RBS and promoter that will be used are existing BioBricks. The selection criterion for RBS and promoter for each construction will depend on the results obtained during the RBS characterization experiments.
Step 2: OprG BioBrick Formation
Based on: Gil Walzer, Eugene Rosenberg, Eliora Z. Ron. Identification of outer membrane proteins with emulsifying activity by prediction of β-barrel regions. Journal of Microbiological Methods 76:52–57 (2009)
OprG is another emulsifier, an outer membrane protein originating from Pseudomonas putida KT2440. The necessary gene, OprG, will be synthesized, and the appropriate RBS and promoter that will be used are existing BioBricks. The transformed cells will be cultivated in shake-flasks of 250ml.
Step 3: Characterization - Emulsifying activity
Strains:
- AlnA: E.coli K12/200C
- OprG: E.coli K12/201C
- Negative control: E.coli K12
In order to determine whether the emulsifiers are produced, if they are excreted or not, and how well they emulsify, a characterization procedure will be performed. This will consist of the production of the emulsifier (to be shown using SDS PAGE), and an emulsification test with cell-free supernatant, purified cell extract and purified whole cells (washed). The emulsification test will occur by creating an alkane/water bi-phase mixture and determining the absorbance before and after addition of the emulsifier, and/or by shaking the sample vigorously and measuring the height of both phases before and after.
