Difference between revisions of "Part:BBa K2239014:Design"

 
 
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===Design Notes===
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===Source===
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The GDH sequence is cloned from the genome of Bacillus subtilis through PCR amplification, using the primers designed and synthesized based on its sequence.
  
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===Source===
 
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The GDH sequence is cloned from the genome of Bacillus subtilis PCR amplification, using the primers designed and synthesized based on its sequence.
 
  
 
===References===
 
===References===
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[1] Ming-Min Zheng, Ru-Feng Wang, Chun-Xiu Li, Jian-He Xu: Two-step enzymatic synthesis of ursodeoxycholic acid with a new 7β-hydroxysteroid dehydrogenase from Ruminococcus torques. Process Biochemistry, Elsevier, 2015.

Latest revision as of 00:50, 1 November 2017


GDH (glucose dehydrogenas)


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]


Source

The GDH sequence is cloned from the genome of Bacillus subtilis through PCR amplification, using the primers designed and synthesized based on its sequence.


References

[1] Ming-Min Zheng, Ru-Feng Wang, Chun-Xiu Li, Jian-He Xu: Two-step enzymatic synthesis of ursodeoxycholic acid with a new 7β-hydroxysteroid dehydrogenase from Ruminococcus torques. Process Biochemistry, Elsevier, 2015.