Difference between revisions of "Part:BBa K3605001"
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Glucose hexokinase (GHK) was originated from Gluconacetobacter xylinus CGMCC 2955. Using glucose, this enzyme catalyzes the formation of glucose-6-phosphate, which is the glycolytic intermediate and the origin of substrate synthesis for Bacterial cellulose production. | Glucose hexokinase (GHK) was originated from Gluconacetobacter xylinus CGMCC 2955. Using glucose, this enzyme catalyzes the formation of glucose-6-phosphate, which is the glycolytic intermediate and the origin of substrate synthesis for Bacterial cellulose production. | ||
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+ | [[File:K3605001-1.jpg|center]] | ||
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+ | Before we clone this gene,the software SnapGene viewer was used to analyze the sequence of GHK, its feature is showed as follows: | ||
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+ | [[File:K3605001-2.jpg|center]] | ||
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+ | Glucose hexokinase (GHK) was amplified using PCR method, and inserted into the vector pSB1C3. The result was identified in figure 1. | ||
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+ | [[File:K3605001-3.jpg|center]] | ||
+ | Fig.1. The result of Glucose hexokinase (GHK) gene cloning. | ||
+ | M: Marker; 1: PCR result of GHK; 2: Digestion of pSB1C3 containing GHK. | ||
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Revision as of 13:39, 27 October 2020
Glucose hexokinase (GHK) from Gluconacetobacter xylinus
Glucose hexokinase (GHK) was originated from Gluconacetobacter xylinus CGMCC 2955. Using glucose, this enzyme catalyzes the formation of glucose-6-phosphate, which is the glycolytic intermediate and the origin of substrate synthesis for Bacterial cellulose production.
Before we clone this gene,the software SnapGene viewer was used to analyze the sequence of GHK, its feature is showed as follows:
Glucose hexokinase (GHK) was amplified using PCR method, and inserted into the vector pSB1C3. The result was identified in figure 1.
Fig.1. The result of Glucose hexokinase (GHK) gene cloning. M: Marker; 1: PCR result of GHK; 2: Digestion of pSB1C3 containing GHK.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 548
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 478