Difference between revisions of "Part:BBa K398005:Design"

 
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<partinfo>BBa_K398005 short</partinfo>
 
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===Design Notes===
 
===Design Notes===
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Nucleotide sequence optimized for expression in E.coli.
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Nucleotide sequence optimized for expression in E.coli. The restriction sites for XbaI, SpeI, EcoRI and PstI were removed. You can find the original sequence [http://www.ncbi.nlm.nih.gov/nuccore/AB040809.1 here]
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===Source===
 
===Source===
  
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Genbank
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Genbank: [http://www.ncbi.nlm.nih.gov/nuccore/AB040809.1 AB040809.1]
  
 
===References===
 
===References===
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Kato,T., ''et al.'' Gene Cloning of an alcohol dehydrogenase from thermophilic alkane-degrading Bacillus thermoleovorans B23, J. Biosci. Bioeng. 91 (1), 100-102 (2001).

Latest revision as of 14:50, 26 October 2010

Medium-Chain Alcohol Dehydrogenase


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Nucleotide sequence optimized for expression in E.coli. The restriction sites for XbaI, SpeI, EcoRI and PstI were removed. You can find the original sequence [http://www.ncbi.nlm.nih.gov/nuccore/AB040809.1 here]

Source

Genbank: [http://www.ncbi.nlm.nih.gov/nuccore/AB040809.1 AB040809.1]

References

Kato,T., et al. Gene Cloning of an alcohol dehydrogenase from thermophilic alkane-degrading Bacillus thermoleovorans B23, J. Biosci. Bioeng. 91 (1), 100-102 (2001).