1.14.13.154: erythromycin 12-hydroxylase
This is an abbreviated version!
For detailed information about erythromycin 12-hydroxylase, go to the full flat file.
Word Map on EC 1.14.13.154
-
1.14.13.154
-
editing
-
inosine
-
a-to-i
-
deaminases
-
deamination
-
symmetrica
-
hereditaria
-
dyschromatosis
-
rna-editing
-
rna-specific
-
adenosine-to-inosine
-
interferon-inducible
-
ifn-inducible
-
glur-b
-
site-selective
-
zalpha
-
left-handed
-
adar2-mediated
-
hypopigmented
-
dsrbds
-
recoding
-
hyperediting
-
synthesis
-
macules
-
z-dna-binding
-
genodermatosis
-
dsrna-binding
- 1.14.13.154
-
editing
- inosine
-
a-to-i
- deaminases
-
deamination
-
symmetrica
-
hereditaria
-
dyschromatosis
-
rna-editing
-
rna-specific
-
adenosine-to-inosine
-
interferon-inducible
-
ifn-inducible
-
glur-b
-
site-selective
-
zalpha
-
left-handed
-
adar2-mediated
-
hypopigmented
-
dsrbds
-
recoding
-
hyperediting
- synthesis
-
macules
-
z-dna-binding
-
genodermatosis
-
dsrna-binding
Reaction
Synonyms
CYP113A1, EryK, erythromycin C-12 hydroxylase
ECTree
Advanced search results
Application
Application on EC 1.14.13.154 - erythromycin 12-hydroxylase
Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
synthesis
systematically modulating the enzyme amounts of EryK and EryG by integrating additional eryK and eryG copies into the industrial strain Saccharopolyspora erythraea HL3168 E3 significantly enhances the process of biotransformation from erythromycin-D to erythromycin-A, nearly completely eliminates the by-products erythromycin-B and erythromycin-C, and efficiently improves erythromycin-A production and purity at the fermentation stage. In conjunction with other traditional and genetic ways to continuously evaluate the erythromycin-A production system