Coding

Part:BBa_K3408005

Designed by: Chen Peng   Group: iGEM20_NAU-CHINA   (2020-10-03)
Revision as of 07:37, 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<i/></b> 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 <b><i>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