1.14.12.11: toluene dioxygenase
This is an abbreviated version!
For detailed information about toluene dioxygenase, go to the full flat file.
Word Map on EC 1.14.12.11
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1.14.12.11
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putida
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naphthalene
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trichloroethylene
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ethylbenzene
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chlorobenzene
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cis-dihydrodiols
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dihydrodiols
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cis-dihydroxylation
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dot-t1e
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ring-hydroxylating
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cis-toluene
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indene
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cis-diols
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pseudoalcaligenes
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1-indanone
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toluene-grown
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3-methylcatechol
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synthesis
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analysis
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degradation
- 1.14.12.11
- putida
- naphthalene
- trichloroethylene
- ethylbenzene
- chlorobenzene
- cis-dihydrodiols
- dihydrodiols
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cis-dihydroxylation
- dot-t1e
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ring-hydroxylating
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cis-toluene
- indene
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cis-diols
- pseudoalcaligenes
- 1-indanone
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toluene-grown
- 3-methylcatechol
- synthesis
- analysis
- degradation
Reaction
Synonyms
ISPTOD, ISPTOL, More, oxygenase, toluene 2,3-di-, oxygenaseTOL, TDO, Tod, todC1C2BA, toluene 2,3-dioxygenase
ECTree
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Application
Application on EC 1.14.12.11 - toluene dioxygenase
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analysis
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whole cell bioassay for the detection of benzene, toluene, ethyl benzene, and xylenes (BTEX)
degradation
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stable isotopes could serve as a diagnostic for detecting aerobic biodegradation of TCE by toluene oxygenases at contaminated sites. There are no significant differences in fractionation among the enzymes toluene 3-monoxygenase, toluene 4-monooxygenase, and toluene 2,3-dioxygenase for compounds trichloroethene and cis-1,2-dichloroethene
synthesis
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screening of substituted arenes containing remote chiral centers as substrates, enantiomers are indiscriminately processed to diastereomeric pairs. Some of these new metabolites are useful as synthons for morphine synthesis
synthesis
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a series of cis-dihydrodiol metabolites is obtained by bacterial biotransformation of the corresponding 1,4-disubstituted benzene substrates using Pseudomonas putida UV4, a source of toluene dioxygenase
synthesis
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Pseudomonas putida KT2442 (pSPM01) harboring TDO genes can effectively biotransform a wide-range of aromatic substrates into their cis-diols
synthesis
Escherichia coli BW25113 DELTAgldA strain harboring pBAD18-TDO system is a suitable platform for the production of the valuable compound cis-1,2-dihydrocatechol at gram scale. The DHC scaffold finds extensive application in the production of a variety of fine chemicals and bioactive compounds
synthesis
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Pseudomonas putida KT2442 (pSPM01) harboring TDO genes can effectively biotransform a wide-range of aromatic substrates into their cis-diols
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synthesis
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a series of cis-dihydrodiol metabolites is obtained by bacterial biotransformation of the corresponding 1,4-disubstituted benzene substrates using Pseudomonas putida UV4, a source of toluene dioxygenase
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