2.6.1.82: putrescine-2-oxoglutarate transaminase
This is an abbreviated version!
For detailed information about putrescine-2-oxoglutarate transaminase, go to the full flat file.
Word Map on EC 2.6.1.82
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2.6.1.82
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cadaverine
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synthesis
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l-lysine
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gamma-aminobutyric
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gamma-aminobutyraldehyde
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agmatine
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transamination
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glutamicum
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volumetric
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corynebacterium
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5-aminovalerate
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pyrroline
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putida
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adaptor
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aminotransferases
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synchrotron
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l-arginine
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clpap
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n-degron
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catabolite
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klebsiella
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l-ornithine
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polyamide
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semialdehyde
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diamines
- 2.6.1.82
- cadaverine
- synthesis
- l-lysine
-
gamma-aminobutyric
- gamma-aminobutyraldehyde
- agmatine
-
transamination
- glutamicum
-
volumetric
-
corynebacterium
- 5-aminovalerate
-
pyrroline
- putida
- adaptor
- aminotransferases
-
synchrotron
- l-arginine
- clpap
-
n-degron
-
catabolite
-
klebsiella
- l-ornithine
- polyamide
- semialdehyde
-
diamines
Reaction
Synonyms
FG99_07980, KES24511, PatA, PATase, Pp-SpuC, putrescine aminotransferase, putrescine transaminase, putrescine-alpha-ketoglutarate transaminase, putrescine:2-oxoglutarate aminotransferase, SpuC, YgjG, YjgG
ECTree
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Application
Application on EC 2.6.1.82 - putrescine-2-oxoglutarate transaminase
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synthesis
a route for the production of GABA via putrescine in Corynebacterium glutamicum. A putrescine-producing recombinant Corynebacterium glutamicum strain is converted into a GABA producing strain by heterologous expression of putrescine transaminase PatA and gamma-aminobutyraldehyde dehydrogenase PatD genes from Escherichia coli. The resultant strain produces 5.3 g per l of GABA. GABA production is improved further by adjusting the concentration of nitrogen in the culture medium, by avoiding the formation of the by-product N-acetylputrescine and by deletion of the genes for GABA catabolism and GABA re-uptake. GABA accumulation by this strain is increased by 5% to 8.0 g per l, and the volumetric productivity is increased to 0.31 g per l and h
synthesis
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enzyme prefers diaminoalkanes as substrates and thereby generates cyclic imines from the omega-amino aldehyde intermediates. The addition of a mild chemical reducing agent rapidly reduces the imine intermediate in situ to furnish a range of N-heterocycle products
synthesis
enzyme prefers diaminoalkanes as substrates and thereby generates cyclic imines from the omega-amino aldehyde intermediates. The addition of a mild chemical reducing agent rapidly reduces the imine intermediate in situ to furnish a range of N-heterocycle products
synthesis
enzyme prefers diaminoalkanes as substrates and thereby generates cyclic imines from the omega-amino aldehyde intermediates. The addition of a mild chemical reducing agent rapidly reduces the imine intermediate in situ to furnish a range of N-heterocycle products
synthesis
putrescine transaminase Pp-SpuC application in the transamination of a comprehensive range of ketones/aldehydes for the production of a variety of benzylamine derivatives. Applications of enzyme Pp-SpuC as a biocatalyst with broad substrate tolerance
synthesis
Pseudomonas putida NBRC 14161
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putrescine transaminase Pp-SpuC application in the transamination of a comprehensive range of ketones/aldehydes for the production of a variety of benzylamine derivatives. Applications of enzyme Pp-SpuC as a biocatalyst with broad substrate tolerance
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synthesis
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enzyme prefers diaminoalkanes as substrates and thereby generates cyclic imines from the omega-amino aldehyde intermediates. The addition of a mild chemical reducing agent rapidly reduces the imine intermediate in situ to furnish a range of N-heterocycle products
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