Difference between revisions of "Part:BBa K629001"
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<partinfo>BBa_K629001 short</partinfo> | <partinfo>BBa_K629001 short</partinfo> | ||
| − | The recA gene of Escherichia coli is involved in genetic recombination, in postreplication repair, and in a number of other cellular functions such as mutagenesis, phage induction, and cell division. RecA protein is related to SOS system-- DNA repair, which is activated by recA promoter. The active level of recA promoter is fluctuates from low basal levels to very high levels after treatments that damage DNA or stall DNA replication. In our project, recA promoter is used to detect single-chain DNA which result from ionizing radiation, x-ray, ultraviolet radiation and some kinds of drug. According to the charater, ionizing radiation can activate recA promoter and raise the level of gene expression which under recA promoter's regulation. | + | |
| + | == Background == | ||
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| + | The ''recA'' gene of ''Escherichia coli'' is involved in genetic recombination, in postreplication repair, and in a number of other cellular functions such as mutagenesis, phage induction, and cell division. RecA protein is related to SOS system-- DNA repair, which is activated by recA promoter. The active level of recA promoter is fluctuates from low basal levels to very high levels after treatments that damage DNA or stall DNA replication. In our project, recA promoter is used to detect single-chain DNA which result from ionizing radiation, x-ray, ultraviolet radiation and some kinds of drug. According to the charater, ionizing radiation can activate recA promoter and raise the level of gene expression which under recA promoter's regulation. | ||
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| + | == Two exchangable ways to start ''recAp'' == | ||
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| + | Because of the special pathway in start of recAp, which is small pieces of break DNA can lead to the SOS system, there has been several ways to start this promoter from research and our try. In this case, the range of usage of this promoter could be spread. | ||
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| + | 1. UV light | ||
| + | This way is based on the basic theroy of start of ''recAp'', which means that when UV light damage DNA into some small pieces, ''recAp'' would be started. | ||
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| + | What a pity in this method is that the parameters cannot be determined for the unstable data. | ||
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| + | 2. Nalidixic Acid | ||
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| + | Nalidixic acid selectively and reversibly blocks DNA replication in susceptible bacteria. Nalidixic acid and related antibiotics inhibit a subunit of DNA gyrase and induce formation of relaxation complex analogue. It also inhibits the nicking dosing activity on the subunit of DNA gyrase that releases the positive binding stress on the supercoiled DNA. Nalidixic acid is effective against both gram-positive and gram-negative bacteria. In lower concentrations, it acts in a bacteriostatic manner; that is, it inhibits growth and reproduction. In higher concentrations, it is bactericidal, meaning that it kills bacteria instead of merely inhibiting their growth. | ||
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| + | All in all, nalidixic acid inhibits DNA gyrase, blocking DNA replication and leading to degradation of DNA. As a result, it could be an optimal alternative for nuclear radiation. As a result, it has ability to start ''recAp''. | ||
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Revision as of 02:04, 6 October 2011
recAp, could be started with exposure to irradiation, UV, nalidixic acid
Background
The recA gene of Escherichia coli is involved in genetic recombination, in postreplication repair, and in a number of other cellular functions such as mutagenesis, phage induction, and cell division. RecA protein is related to SOS system-- DNA repair, which is activated by recA promoter. The active level of recA promoter is fluctuates from low basal levels to very high levels after treatments that damage DNA or stall DNA replication. In our project, recA promoter is used to detect single-chain DNA which result from ionizing radiation, x-ray, ultraviolet radiation and some kinds of drug. According to the charater, ionizing radiation can activate recA promoter and raise the level of gene expression which under recA promoter's regulation.
Two exchangable ways to start recAp
Because of the special pathway in start of recAp, which is small pieces of break DNA can lead to the SOS system, there has been several ways to start this promoter from research and our try. In this case, the range of usage of this promoter could be spread.
1. UV light This way is based on the basic theroy of start of recAp, which means that when UV light damage DNA into some small pieces, recAp would be started.
What a pity in this method is that the parameters cannot be determined for the unstable data.
2. Nalidixic Acid
Nalidixic acid selectively and reversibly blocks DNA replication in susceptible bacteria. Nalidixic acid and related antibiotics inhibit a subunit of DNA gyrase and induce formation of relaxation complex analogue. It also inhibits the nicking dosing activity on the subunit of DNA gyrase that releases the positive binding stress on the supercoiled DNA. Nalidixic acid is effective against both gram-positive and gram-negative bacteria. In lower concentrations, it acts in a bacteriostatic manner; that is, it inhibits growth and reproduction. In higher concentrations, it is bactericidal, meaning that it kills bacteria instead of merely inhibiting their growth.
All in all, nalidixic acid inhibits DNA gyrase, blocking DNA replication and leading to degradation of DNA. As a result, it could be an optimal alternative for nuclear radiation. As a result, it has ability to start recAp.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]