Difference between revisions of "Part:BBa K2365039"

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<partinfo>BBa_K2365039 short</partinfo>
 
<partinfo>BBa_K2365039 short</partinfo>
  
AHD1 Yeast promoter Constitutive expression  
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AHD1 Yeast promoter Constitutive expression:
 
Alcohol dehydrogenase I  promoter, full length version is very strong which can promote high expression. Truncated promoters are constitutive and have low expression. Widely exist in human and animal liver, plant and microbial cells as a key enzyme in short-chain alcohol metabolism. Glucose can promote the presence of expression, in many physiological processes play an important role.
 
Alcohol dehydrogenase I  promoter, full length version is very strong which can promote high expression. Truncated promoters are constitutive and have low expression. Widely exist in human and animal liver, plant and microbial cells as a key enzyme in short-chain alcohol metabolism. Glucose can promote the presence of expression, in many physiological processes play an important role.
  

Revision as of 07:58, 1 November 2017


ADH1 promoter

AHD1 Yeast promoter Constitutive expression: Alcohol dehydrogenase I promoter, full length version is very strong which can promote high expression. Truncated promoters are constitutive and have low expression. Widely exist in human and animal liver, plant and microbial cells as a key enzyme in short-chain alcohol metabolism. Glucose can promote the presence of expression, in many physiological processes play an important role.

Sequence and Features


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]


Improved design:

We construct the device:ADH1 promoter+GFP+CYC1 terminator.ADH1 promoter is a truncated promoter, GFP is a mutant. These is a invariable sequence upstream of GFP coding sequence.

图片1.jpg

The promoter of yeast alcohol dehydrogenase (ADH1) is widely used for the expression of heterologous genes in Saccharomyces cerevisiae. We tested the expression of GFP proteins in five transformants containing the ADH1 promoter. Our data shows that there are some differences in the fluorescence intensity of different yeast transformants with ADH1 promoter. The variation trends of promoter strengths from early-log to stationary phase varied in different transformants. Individual transformants colonies have different expression efficiency. We will test this promoter for more than three times.