Coding

Part:BBa_K3408005

Designed by: Chen Peng   Group: iGEM20_NAU-CHINA   (2020-10-03)
Revision as of 06:38, 6 October 2020 by NJAU-Chappie (Talk | contribs)


Optimized DpnI

It is an enzyme which could cut all methylated DNA so that engineering bacteria may die in a certain situation. It could be used to ensure bio-safety. Bacillus subminis has been increasingly applied in genetic engineered due to its powerful secretion capacity. As a restriction enzyme which is capable of cutting all methylated DNA, DPNI can be applied to Bacillus subtilis in the way of synthetic biology to control the environment by taking advantage of its DNA eradication.

T--NAU-CHINA--DPNI1cp.png T--NAU-CHINA--DPNI2cp.png

The histograms show the percentage of sequence codons which fall into a certain quality class. The quality value of the most frequently used codon for a given amino acid in the desired expression system is set to 100, the remaining codons are scaled accordingly (see also Sharp, P.M., Li, W.H., Nucleic Acids Res. 15 (3),1987).

T--NAU-CHINA--DPNI3cp.png T--NAU-CHINA--DPNI4cp.png

The plots show the quality of the used codon at the indicated codon position.

T--NAU-CHINA--DPNI5cp.png T--NAU-CHINA--DPNI6cp.png

The plots show the GC content in a 40 bp window centered at the indicated nucleotide position.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1322
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 210
  • 1000
    COMPATIBLE WITH RFC[1000]


[edit]
Categories
Parameters
None