Difference between revisions of "Part:BBa K2934000"
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− | Glucose Oxidase gene is coding for the Glucose Oxidase (GOx) enzyme, which catalyzes the oxidation of glucose to D-glucono-lacton and release of hydrogen peroxide. The enzyme origin is from A. niger and is optimized for B. subtilis. | + | Glucose Oxidase gene is coding for the Glucose Oxidase (GOx) enzyme, which catalyzes the oxidation of glucose to D-glucono-lacton and release of hydrogen peroxide. The sequence includes histag (6xHis), connected with seven amino acids linker protein at the N terminal of the protein. The enzyme origin is from A. niger and is optimized for B. subtilis. |
===Usage and Biology=== | ===Usage and Biology=== |
Revision as of 09:33, 11 October 2019
Glucose Oxidase-Histag A. niger optimized for B. subtilis
Glucose Oxidase gene is coding for the Glucose Oxidase (GOx) enzyme, which catalyzes the oxidation of glucose to D-glucono-lacton and release of hydrogen peroxide. The sequence includes histag (6xHis), connected with seven amino acids linker protein at the N terminal of the protein. The enzyme origin is from A. niger and is optimized for B. subtilis.
Usage and Biology
Glucose oxidase (GOx) catalyzes the oxidation of glucose to using molecular oxygen to create hydrogen peroxide and D-glucono lactone. GOx requires the cofactor flavin adenine dinucleotide (FAD) that acts as an electron acceptor in a redox reaction. It is reduced to FADH2, then it is oxidized by molecular oxygen, which is then reduced to hydrogen peroxide [1].
References
[1] Frederick KR, Tung J, Richard S. Emerick F, Chamberlain SH, Vasavada A, Steven R, Chakraborty S, Schopter LM, Schopter LM, Massey V. 1990. Glucose Oxidase from Aspergillus niger. J Biol Chem 265:3793–3802.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 30
Illegal BsaI site found at 361
Illegal BsaI.rc site found at 307
Illegal BsaI.rc site found at 1132