Difference between revisions of "Part:BBa K2201009"
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Flanking sequences for the homologous recombination based deletion of codA, coding for cytosine deaminase. | Flanking sequences for the homologous recombination based deletion of codA, coding for cytosine deaminase. | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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| + | To retain the unnatural base pair formed between isoC<sup>m</sup> and isoG, the degradation of the unnatural nucleotides must be minimized. In <i>E. coli</i>, the gene <i>cod</i>A codes for the cytosine deaminase, an enzyme of the pyrimidine metabolism. The cytosine deaminase catalyzes the reaction of cytosine to uracil. Furthermore, it can catalyze the deamination of isoguanosione and isocytosine. Isoguanosine is formed during oxidative stress by reaction of the radical oxygen species (ROS) •OH with adenine. Other products from reactions of adenine with ROS include 8-oxoadenine and 6-N-hydroxyaminopurine. | ||
| + | This part provides the flanking sequences needed for a chromosomal deletion of <i>cod</i>A in <i>E. coli </i> BL21(DE3) using CRISPR/Cas9 as described in our <a href="http://2017.igem.org/Team:Bielefeld-CeBiTec/Results/unnatural_base_pair/preservation_system">wiki</a>. | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K2201009 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2201009 SequenceAndFeatures</partinfo> | ||
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| + | [[File:T--Bielefeld-CeBiTec--codA.jpeg|400px|thumb|left|<b>Figure (1): Reactions catalyzed by cytosine deaminase. </b> A) The conversion of cytosine to uracil is a normal reaction step within the pyrimidine metabolism. B) Isocytosine is also converted into uracil by the cytosine deaminase. C) Isoguanine is formed during oxidative stress. Cytosine deaminase catalyzes the reaction to the non-mutagenic xanthine. ]] | ||
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| + | <p align="justify"> | ||
| + | In E. coli, the <i>cod</i>A gene is part of the <i>cod</i>BA operon. Cytosine permease is encoded by <i>cod</i>B, while <i>cod</i>A encodes cytosine deaminase. The only way how cytosine can be metabolized is via hydrolytic deamination, a reaction that yields ammonia and uracil and is catalyzed by cytosine deaminase (Danielsen et al., 1992). | ||
| + | When isoguanosine and isocytosine are provided to the cell, they are converted to uracil in the wildtype. | ||
| + | Therefore, it is necessary to knock out or delete the codA gene to enable the stable availability of isoguanosine and isocytosine. | ||
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| + | </p> | ||
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| + | [[File:T--Bielefeld-CeBiTec--codBAoperon.jpeg|600px|thumb|center|<b>Figure (2) Arrangement of the codBA operon.</b> <i>cod</i>A is located downstream of codB and 1,3 kb in size. Both genes overlap by 11 bases. <i>cod</i>B codes for cytosine permease, while <i>cod</i>A codes for cytosine deaminase.]] | ||
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| + | <i>cod</i>A is 1281 bp in size, resulting in a protein composed of 427 amino acids after translation. The protein CodA is located in the cytosol and has an atomic mass of 47,5 kD. | ||
| + | </p> | ||
| + | </html> | ||
| + | [[File:T--Bielefeld-CeBiTec--codAstructure.jpeg|600px|thumb|center|<b>Figure 4: Crystal structure of cytosine deaminase from <i>Escherichia coli</i> complexed with zinc and phosphono-cytosine.</b>The structure was determined by X-Ray crystallography with a resolution of 1.71 Å (Hall et al., 2011).]] | ||
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Revision as of 14:10, 1 November 2017
Flanking sequences for deletion of codA
Flanking sequences for the homologous recombination based deletion of codA, coding for cytosine deaminase.
Usage and Biology
To retain the unnatural base pair formed between isoCm and isoG, the degradation of the unnatural nucleotides must be minimized. In E. coli, the gene codA codes for the cytosine deaminase, an enzyme of the pyrimidine metabolism. The cytosine deaminase catalyzes the reaction of cytosine to uracil. Furthermore, it can catalyze the deamination of isoguanosione and isocytosine. Isoguanosine is formed during oxidative stress by reaction of the radical oxygen species (ROS) •OH with adenine. Other products from reactions of adenine with ROS include 8-oxoadenine and 6-N-hydroxyaminopurine. This part provides the flanking sequences needed for a chromosomal deletion of codA in E. coli BL21(DE3) using CRISPR/Cas9 as described in our wiki. Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 580
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 580
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 580
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 580
- 1000COMPATIBLE WITH RFC[1000]
In E. coli, the codA gene is part of the codBA operon. Cytosine permease is encoded by codB, while codA encodes cytosine deaminase. The only way how cytosine can be metabolized is via hydrolytic deamination, a reaction that yields ammonia and uracil and is catalyzed by cytosine deaminase (Danielsen et al., 1992). When isoguanosine and isocytosine are provided to the cell, they are converted to uracil in the wildtype. Therefore, it is necessary to knock out or delete the codA gene to enable the stable availability of isoguanosine and isocytosine.
codA is 1281 bp in size, resulting in a protein composed of 427 amino acids after translation. The protein CodA is located in the cytosol and has an atomic mass of 47,5 kD.
