2.3.1.183: phosphinothricin acetyltransferase
This is an abbreviated version!
For detailed information about phosphinothricin acetyltransferase, go to the full flat file.
Word Map on EC 2.3.1.183
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2.3.1.183
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pat
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herbicide
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glufosinate
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bialaphos
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viridochromogenes
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herbicide-resistant
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basta
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hygroscopicus
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aryloxyalkanoate
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herbicide-tolerant
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nopaline
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microprojectile
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biotechnology
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nptii
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glufosinate-resistant
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agriculture
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analysis
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glufosinate-ammonium
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non-gm
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bialaphos-resistant
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regenerable
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molecular biology
- 2.3.1.183
- pat
-
herbicide
- glufosinate
- bialaphos
- viridochromogenes
-
herbicide-resistant
-
basta
- hygroscopicus
-
aryloxyalkanoate
-
herbicide-tolerant
- nopaline
-
microprojectile
- biotechnology
- nptii
-
glufosinate-resistant
- agriculture
- analysis
-
glufosinate-ammonium
-
non-gm
-
bialaphos-resistant
-
regenerable
- molecular biology
Reaction
Synonyms
BAR, DR_1182, GK0593, GK2920, hpat, L-PPT N-acetyltransferase, MAT, methionine sulfone N-acetyltransferase, Pat, phosphinothricin acetyltransferase, phosphinothricin N-acetyltransferase, phosphinothricin-N-acetyltransferase, PitA, PPT acetyltransferase
ECTree
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Purification
Purification on EC 2.3.1.183 - phosphinothricin acetyltransferase
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for the purification of PAT from Pseudomonas fluorescens ammonium sulfate precipitation, a Source 15 Phenyl XK hydrophobic interaction column, and a Superdex 75 XK gel filtration column are used
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recombinant enzyme from Escherichia coli by ammonium sulfate fractionation, anion exchange, hydrophobic interaction, and hydroxylapatite chromatography, followed by gel filtration, to about 90% purity
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recombinant enzyme from Pseudomonas fluorescens to homogeneity by ammonium sulfate fractionation, hydrophobic interaction chromatography, and gel filtration
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recombinant His-tagged enzyme from Escherichia coli strain BL21(DE3) by nickel affinity chromatography, recombinant enzyme from transgenic maize and rape plants by immunoaffinity chromatography, method development, overview
simple, time-saving, inexpensive and reproducible purification method employs a single chromatography step using a reactive dye resin, Reactive brown 10-agarose. Reactive brown 10 preferentially binds the phosphinothricin acetyltransferase protein, which can then be specifically released by acetyl-CoA. Phosphinothricin acetyltransferase protein can be purified to homogeneity from cottonseed with high recovery efficiency and enzymatically active
the recombinant protein is purified by Ni2+ affinity chromatography and used for the production of polyclonal antibodies, for Western blot analysis the protein is extracted from peppers
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