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Team:Korea U Seoul/Project
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| + | To sense heavy metals, we select promoters which are expressed in the presence of heavy metals. These promoters encode proteins maintaing cell conditions resistant to heavy metals. ParsR is promoter to arsenic and PzntA is for zinc. | ||
| + | Low concentrations can have devastating effects, interfering with processes in the cell. Because of the similarity to phosphate, sometimes arsenate is mistaken for phosphate, which is how it is introduced into living organisms, including E. coli, by the phosphate uptake system. Other molecules such as As(III) can also be introduced into the cells by various membrane transporters. Cells have effective defenses to deal with elevated levels of arsenic variants, which are under the control of metal sensitive promoters. The transcription is mostly regulated by proteins binding to, or releasing from the promoter site, like ArsR. | ||
| + | ArsR negatively controls the expression of the genes involved in arsenical and antimonite metals resistance, whose expression is induced in the presence of these metals. | ||
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| + | In case of cadmium, there is no promoters encoding resistant to cadium directly. So we select Promoter yodA. | ||
| + | At low cadmium concentrations, cells are able to adapt and resume growth after a period of stasis. Promoter yodA is only transiently activated during cadmium-induced growth inhibition. Aryl acylamidase is an enzyme that acts on the amide bond between aryl- and acyl groups. The most typical reaction is the hydrolysis of an anilide, producing a carboxylate and aniline, which is also reversible. Acetaminophen(Tyrenol) is an aryl acyl compound having amide bond is hydrolyzed by the enzyme and produce acetate and p-aminophenol. Because p-Aminophenol have red-purple color, aryl acylamidase gene will apply to reporter gene. | ||
| + | Since aryl acylamidase gene(mAAA, BBa_K400628) is not registered to iGEM, we registered this gene. | ||
='''measurement'''= | ='''measurement'''= | ||
Revision as of 11:21, 27 October 2010
Contents |
abstract
Toxic heavy metals such as arsenic, zinc, and cadmium in water are very harmful. Detecting these heavy metals is an important task. So we designed a heavy-metal-detecting E. coli. In order to design the system, we employed two fluorescence proteins (GFP, RFP) and aryl acylamidase as signal reporters. The aryl acylamidase converts a colorless acetaminophen(Tylenol TM) to a brown color substrate. Since the detecting E. coli has three heavy metal promoters, if more than two heavy metals coexist in a solution, the E. coli emit mixed fluorescence, so we simultaneously detect metals. Our goal is to synthetic modules put these three genes for different heavy metals in a row in E. coli and then utilized in the form of a lyophilized powder, which can be stored in a drug capsule to make it portable so that analysis of water is easily processed. We call it a "Capsule Cop".
Introduction
design
To sense heavy metals, we select promoters which are expressed in the presence of heavy metals. These promoters encode proteins maintaing cell conditions resistant to heavy metals. ParsR is promoter to arsenic and PzntA is for zinc. Low concentrations can have devastating effects, interfering with processes in the cell. Because of the similarity to phosphate, sometimes arsenate is mistaken for phosphate, which is how it is introduced into living organisms, including E. coli, by the phosphate uptake system. Other molecules such as As(III) can also be introduced into the cells by various membrane transporters. Cells have effective defenses to deal with elevated levels of arsenic variants, which are under the control of metal sensitive promoters. The transcription is mostly regulated by proteins binding to, or releasing from the promoter site, like ArsR. ArsR negatively controls the expression of the genes involved in arsenical and antimonite metals resistance, whose expression is induced in the presence of these metals.
In case of cadmium, there is no promoters encoding resistant to cadium directly. So we select Promoter yodA. At low cadmium concentrations, cells are able to adapt and resume growth after a period of stasis. Promoter yodA is only transiently activated during cadmium-induced growth inhibition. Aryl acylamidase is an enzyme that acts on the amide bond between aryl- and acyl groups. The most typical reaction is the hydrolysis of an anilide, producing a carboxylate and aniline, which is also reversible. Acetaminophen(Tyrenol) is an aryl acyl compound having amide bond is hydrolyzed by the enzyme and produce acetate and p-aminophenol. Because p-Aminophenol have red-purple color, aryl acylamidase gene will apply to reporter gene. Since aryl acylamidase gene(mAAA, BBa_K400628) is not registered to iGEM, we registered this gene.
measurement
Result
Discussion
Freeze dry
| The process of freeze-drying(lyophilization) involves the removal of water vapour by vacuum
sublimation from the frozen state. Freeze-drying has been widely used for many years as one of the preferred method for long-term preservation. Freeze-drying is particularly suitable for collections which supply cultures on demand because of its broad applicability, economy of storage space and ease of distribution. Freeze-drying is the most technologically complex of the preservation methods in use. It is labour intensive and requires the highest level of technical skill. The method is suitable for many types of microorganisms including most bacteria, yeast, sporing-fungi and some viruses, algae and protozoa. |
| One of the major advantages of freeze-drying is that the ampoules are particularly suitable as a means of distributing cultures because the viability and intengrity of the ampoules the airmail services. |
| A disadvantage of freeze-drying is the relativelt high capital cost of commercial equipment. However, the principle of freeze-drying is quite simple and for small scale operations a laboratory freeze-dryer can be manufactures readily by any competent workshop. All that is a vacuum pump, a moisture trap, an evacuation chamber and a drying manifold. |
