Difference between revisions of "Part:BBa K3496005"
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| − | + | [[File:T--BIT-China--images-name.jpg|550px|thumb|center|Figure 1. Flavonoid 3'-hydroxylase converts the substrate naringenin to eriodictyol. ]] | |
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===Usage and Biology=== | ===Usage and Biology=== | ||
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F3‘H is widely available from different plants, including Glycine max, Pilosella officinarum, Vitis vinifera, Plectranthus scutellarioides, Matthiola incana, Fragaria vesca. This part is derived from Fragaria vesca, with rather high enzymatic activity. | F3‘H is widely available from different plants, including Glycine max, Pilosella officinarum, Vitis vinifera, Plectranthus scutellarioides, Matthiola incana, Fragaria vesca. This part is derived from Fragaria vesca, with rather high enzymatic activity. | ||
| + | ===Reference=== | ||
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| + | Baba, S. A., & Ashraf, N. (2019). Functional characterization of flavonoid 3′-hydroxylase, CsF3′H, from Crocus sativus L: Insights into substrate specificity and role in abiotic stress. Archives of Biochemistry and Biophysics, 667, 70–78. doi:10.1016/j.abb.2019.04.012 | ||
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Latest revision as of 16:03, 27 October 2020
Flavonoid 3'-hydroxylase
Flavonoid 3'-hydroxylase from Fragaria vesca Flavonoid 3′-hydroxylase is the last enzyme during the eriodictyol metabolic pathway which converts the substrate naringenin to the final product.
Usage and Biology
Flavonoids are the class of plant secondary metabolites with C6-C3-C6 basic carbon skeleton famous for its high-value effects, such as, improving the body's anti-oxidation capacity and immunity.
The detailed skeletal structure flavonoids is a 2-phenylbenzopyranone where two phenyl groups (commonly named A- and B-ring) are banded with the C ring (three‑carbon bridge cyclized with oxygen) . According to the hydroxylation pattern of B-ring, flavonoids can be divided into three subclasses including B-ring 4’-hydroxylated, 3’,4’-dihydroxylated, and 3′,4’,5’-trihydroxylated flavonoids.
Eriodictyol, as a natural edible flavonoid, is mainly derived from lemon fruits. It has a hydroxyl group on the B ring and higher anti-oxidation activity. Both F3’H and F3’5’H can help format the 3’,4’-dihydroxylated Eriodictyol.
F3’H belongs to the Cytochrome P450 proteins (P450s), a huge group of heme-containing mixed oxidases catalyzing NADPH- or NADH-dependent oxygenation reactions. P450 exists in almost all cultures from microbes to Vertebrata. In life process, the P450 family is responsible for endogenous metabolism, the activity and degradation of exogenous compounds.
In the last step of eriodictyol metabolic pathway when P450 enzyme F3‘H hydroxylated naringenin to obtain the final product eriodictyol, it is supposed to happen in eukaryotic organisms instead of a prokaryotic cell which is unable to provide the membrane structure required for post-modification of the enzyme.
Resource
F3‘H is widely available from different plants, including Glycine max, Pilosella officinarum, Vitis vinifera, Plectranthus scutellarioides, Matthiola incana, Fragaria vesca. This part is derived from Fragaria vesca, with rather high enzymatic activity.
Reference
Baba, S. A., & Ashraf, N. (2019). Functional characterization of flavonoid 3′-hydroxylase, CsF3′H, from Crocus sativus L: Insights into substrate specificity and role in abiotic stress. Archives of Biochemistry and Biophysics, 667, 70–78. doi:10.1016/j.abb.2019.04.012
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 972
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 1199
Illegal XhoI site found at 1228 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1202