2.1.1.117: (S)-scoulerine 9-O-methyltransferase
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For detailed information about (S)-scoulerine 9-O-methyltransferase, go to the full flat file.
Word Map on EC 2.1.1.117
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2.1.1.117
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benzylisoquinoline
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coptis
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s-scoulerine
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japonica
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poppy
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californica
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eschscholzia
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s-tetrahydrocolumbamine
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n-methylated
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regio-specific
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papaveraceae
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n-methyltransferase
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norreticuline
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methylenedioxy
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isoquinoline
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benzophenanthridine
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opium
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virus-induced
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sanguinarine
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7-o-methylated
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allocryptopine
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noscapine
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medicine
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analysis
- 2.1.1.117
-
benzylisoquinoline
- coptis
-
s-scoulerine
- japonica
- poppy
- californica
-
eschscholzia
-
s-tetrahydrocolumbamine
-
n-methylated
-
regio-specific
- papaveraceae
- n-methyltransferase
- norreticuline
-
methylenedioxy
- isoquinoline
-
benzophenanthridine
-
opium
-
virus-induced
- sanguinarine
-
7-o-methylated
- allocryptopine
- noscapine
- medicine
- analysis
Reaction
Synonyms
(S)-Adenosyl-L-methionine:(S)-scoularine 9-O-methyltransferase, (S)-scoulerine 9-O-methyltransferase, Methyltransferase, (S)-scoularine 9-, Methyltransferase, (S)-scoularine 9- (Coptis japonica clone pCJSMT), scoulerine 9-O-methyltransferase, scoulerine 9-OMT, scoulerine-9-O-methyltransferase, scoulerine/reticuline O-methyltransferase, SMT, SOMT, SOMT1
ECTree
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Application
Application on EC 2.1.1.117 - (S)-scoulerine 9-O-methyltransferase
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analysis
transient RNA silencing of scoulerine 9-O-methyltransferase expression by double stranded RNA in Coptis japonica protoplasts. Utility of gene silencing based on in vitro synthesized dsRNA to study function and behavior of endogenous enzymes
medicine
a Saccharomyces cerevisiae strain is engineered to express seven heterologous enzymes (Papaper somniferum norcoclaurine 6-O-methyltransferase (Ps6OMT), Papaver somniferum 3'-hydroxy-N-methylcoclaurine 4'-O-methyltransferase 2 (Ps4'OMT), Papapver somniferum coclaurine N-methyltransferase (PsCNMT), Papaver somniferum berberine bridge enzyme (PsBBE), Thalictrum flavum scoulerine 9-O-methyltransferase (TfS9OMT), Thalictrum flavum canadine synthase (TfCAS), and Arabidopsis thaliana cytochrome P450 reductase 1 (CPR)), resulting in protoberberine alkaloid production from a simple benzylisoquinoline alkaloid precursor. A number of strategies are implemented to improve flux through the pathway, including enzyme variant screening, genetic copy number variation, and culture optimization. This leads to an over 70-fold increase in canadine titer up to 1.8 mg/l. Increased canadine titers enable extension of the pathway to produce berberine, a major constituent of several traditional medicines in a microbial host. This strain is viable at pilot scale