Purification and characterization of aromatic amine dehydrogenase from Alcaligenes xylosoxidans

Kondo, T.; Kondo, E.; Maki, H.; Yasumoto, K.; Takagi, K.; Kano, K.; Ikeda, T.; Biosci. Biotechnol. Biochem. 68, 1921-1928 (2004)

Data extracted from this reference:

Inhibitors

Commentary

Organism

Structure

8-hydroxyquinoline

33% inhibition at 1 mM

Achromobacter xylosoxidans

beta-phenylethylamine

substrate inhibition at higher concentrations

Achromobacter xylosoxidans

dopamine

substrate inhibition at higher concentrations

Achromobacter xylosoxidans

EDTA

13% inhibition at 1 mM

Achromobacter xylosoxidans

histamine

weak substrate inhibition above 1 mM

Achromobacter xylosoxidans

hydrazine

complete inhibition at 0.1 mM

Achromobacter xylosoxidans

hydroxylamine

99% inhibition at 1 mM

Achromobacter xylosoxidans

iodoacetamide

28% inhibition at 1 mM

Achromobacter xylosoxidans

monoiodoacetate

15% inhibition at 1 mM

Achromobacter xylosoxidans

NaN3

30% inhibition at 1 mM

Achromobacter xylosoxidans

o-phenanthroline

17% inhibition at 1 mM

Achromobacter xylosoxidans

Semicarbazide

97% inhibition at 1 mM

Achromobacter xylosoxidans

serotonin

substrate inhibition at higher concentrations

Achromobacter xylosoxidans

tryptamine

substrate inhibition at higher concentrations

Achromobacter xylosoxidans

tyramine

substrate inhibition at higher concentrations

Achromobacter xylosoxidans

KM Value [mM]

KM Value Maximum [mM]

Substrate

Commentary

Organism

Structure

0.0018

-

beta-phenylethylamine

pH 7.5, 30°C

Achromobacter xylosoxidans

0.0069

-

tyramine

pH 7.5, 30°C

Achromobacter xylosoxidans

0.048

-

phenazine methosulfate

pH 7.5, 30°C

Achromobacter xylosoxidans

0.171

-

histamine

pH 7.5, 30°C

Achromobacter xylosoxidans

Natural Substrates

Organism

Commentary (Nat. Sub.)

Natural Products

Commentary (Nat. Pro.)

Organism (Nat. Pro.)

Reversibility

ID

beta-phenylethylamine + H2O + 2,6-dichlorophenol indophenol

Achromobacter xylosoxidans

-

phenylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

?

beta-phenylethylamine + H2O + 2,6-dichlorophenol indophenol

Achromobacter xylosoxidans IFO13495

-

phenylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

?

Reaction

Commentary

Organism

Reaction ID

ArCH2NH2 + H2O + 2 azurin = ArCHO + NH3 + 2 reduced azurin

ping-pong mechanism

Achromobacter xylosoxidans

Substrates

Commentary Substrates

Literature (Substrates)

Organism

Products

Commentary (Products)

Literature (Products)

Organism (Products)

Reversibility

Substrate Product ID

1,3-diaminopropane + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

1,3-diaminopropane + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans IFO13495

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

1,6-diaminohexane + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

1,6-diaminohexane + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans IFO13495

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

beta-phenylethylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

phenylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

beta-phenylethylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans IFO13495

phenylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

butylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

butanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

butylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans IFO13495

butanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

cadaverine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

dopamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

(3,4-dihydroxyphenyl)acetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

hexylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

hexanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

histamine + H2O + 2,6-dichlorophenol indophenol

high activity at substrate concentration 1 mM

655062

Achromobacter xylosoxidans

1H-imidazol-4-ylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

additional information

substrate specificity, overview, no activity with methylamine, dimethylamine, and trimethylamine

655062

Achromobacter xylosoxidans

?

-

-

-

-

additional information

substrate specificity, overview, no activity with methylamine, dimethylamine, and trimethylamine

655062

Achromobacter xylosoxidans IFO13495

?

-

-

-

-

pentylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

pentanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

phenazine methosulfate + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

propylamine + H2O + 2,6-dichlorophenol indophenol

low activity

655062

Achromobacter xylosoxidans

propanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

putrescine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

4-aminobutanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

serotonin + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

6-hydroxy-4H-indol-3-yl-acetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

spermidine + H2O + 2,6-dichlorophenol indophenol

low activity

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

spermine + H2O + 2,6-dichlorophenol indophenol

low activity

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

tryptamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

4H-indol-3-yl-acetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

tyramine + H2O + 2,6-dichlorophenol indophenol

best substrate

655062

Achromobacter xylosoxidans

4-hydroxyphenylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

Cofactor

Commentary

Organism

Structure

tryptophan tryptophylquinone

-

Achromobacter xylosoxidans

Cofactor

Commentary

Organism

Structure

tryptophan tryptophylquinone

-

Achromobacter xylosoxidans

Inhibitors

Commentary

Organism

Structure

8-hydroxyquinoline

33% inhibition at 1 mM

Achromobacter xylosoxidans

beta-phenylethylamine

substrate inhibition at higher concentrations

Achromobacter xylosoxidans

dopamine

substrate inhibition at higher concentrations

Achromobacter xylosoxidans

EDTA

13% inhibition at 1 mM

Achromobacter xylosoxidans

histamine

weak substrate inhibition above 1 mM

Achromobacter xylosoxidans

hydrazine

complete inhibition at 0.1 mM

Achromobacter xylosoxidans

hydroxylamine

99% inhibition at 1 mM

Achromobacter xylosoxidans

iodoacetamide

28% inhibition at 1 mM

Achromobacter xylosoxidans

monoiodoacetate

15% inhibition at 1 mM

Achromobacter xylosoxidans

NaN3

30% inhibition at 1 mM

Achromobacter xylosoxidans

o-phenanthroline

17% inhibition at 1 mM

Achromobacter xylosoxidans

Semicarbazide

97% inhibition at 1 mM

Achromobacter xylosoxidans

serotonin

substrate inhibition at higher concentrations

Achromobacter xylosoxidans

tryptamine

substrate inhibition at higher concentrations

Achromobacter xylosoxidans

tyramine

substrate inhibition at higher concentrations

Achromobacter xylosoxidans

KM Value [mM]

KM Value Maximum [mM]

Substrate

Commentary

Organism

Structure

0.0018

-

beta-phenylethylamine

pH 7.5, 30°C

Achromobacter xylosoxidans

0.0069

-

tyramine

pH 7.5, 30°C

Achromobacter xylosoxidans

0.048

-

phenazine methosulfate

pH 7.5, 30°C

Achromobacter xylosoxidans

0.171

-

histamine

pH 7.5, 30°C

Achromobacter xylosoxidans

Natural Substrates

Organism

Commentary (Nat. Sub.)

Natural Products

Commentary (Nat. Pro.)

Organism (Nat. Pro.)

Reversibility

ID

beta-phenylethylamine + H2O + 2,6-dichlorophenol indophenol

Achromobacter xylosoxidans

-

phenylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

?

beta-phenylethylamine + H2O + 2,6-dichlorophenol indophenol

Achromobacter xylosoxidans IFO13495

-

phenylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

?

Substrates

Commentary Substrates

Literature (Substrates)

Organism

Products

Commentary (Products)

Literature (Products)

Organism (Products)

Reversibility

ID

1,3-diaminopropane + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

1,3-diaminopropane + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans IFO13495

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

1,6-diaminohexane + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

1,6-diaminohexane + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans IFO13495

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

beta-phenylethylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

phenylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

beta-phenylethylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans IFO13495

phenylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

butylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

butanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

butylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans IFO13495

butanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

cadaverine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

dopamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

(3,4-dihydroxyphenyl)acetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

hexylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

hexanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

histamine + H2O + 2,6-dichlorophenol indophenol

high activity at substrate concentration 1 mM

655062

Achromobacter xylosoxidans

1H-imidazol-4-ylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

additional information

substrate specificity, overview, no activity with methylamine, dimethylamine, and trimethylamine

655062

Achromobacter xylosoxidans

?

-

-

-

-

additional information

substrate specificity, overview, no activity with methylamine, dimethylamine, and trimethylamine

655062

Achromobacter xylosoxidans IFO13495

?

-

-

-

-

pentylamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

pentanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

phenazine methosulfate + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

propylamine + H2O + 2,6-dichlorophenol indophenol

low activity

655062

Achromobacter xylosoxidans

propanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

putrescine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

4-aminobutanal + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

serotonin + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

6-hydroxy-4H-indol-3-yl-acetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

spermidine + H2O + 2,6-dichlorophenol indophenol

low activity

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

spermine + H2O + 2,6-dichlorophenol indophenol

low activity

655062

Achromobacter xylosoxidans

? + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

tryptamine + H2O + 2,6-dichlorophenol indophenol

-

655062

Achromobacter xylosoxidans

4H-indol-3-yl-acetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

tyramine + H2O + 2,6-dichlorophenol indophenol

best substrate

655062

Achromobacter xylosoxidans

4-hydroxyphenylacetaldehyde + NH3 + reduced 2,6-dichlorophenol indophenol

-

-

-

?

No.

1st author

Pub Med

title

organims

journal

volume

pages

year

Activating Compound

Application

Cloned(Commentary)

Crystallization (Commentary)

Engineering

General Stability

Inhibitors

KM Value [mM]

Localization

Metals/Ions

Molecular Weight [Da]

Natural Substrates/ Products (Substrates)

Organic Solvent Stability

Organism

Oxidation Stability

Posttranslational Modification

Purification (Commentary)

Reaction

Renatured (Commentary)

Source Tissue

Specific Activity [micromol/min/mg]

Storage Stability

Substrates and Products (Substrate)

Subunits

Synonyms

Temperature Optimum [°C]

Temperature Range [°C]

Temperature Stability [°C]

Turnover Number [1/s]

pH Optimum

pH Range

pH Stability

Cofactor

Ki Value [mM]

pI Value

IC50 Value

Activating Compound (protein specific)

Application (protein specific)

Cloned(Commentary) (protein specific)

Cofactor (protein specific)

Crystallization (Commentary) (protein specific)

Engineering (protein specific)

General Stability (protein specific)

IC50 Value (protein specific)

Inhibitors (protein specific)

Ki Value [mM] (protein specific)

KM Value [mM] (protein specific)

Localization (protein specific)

Metals/Ions (protein specific)

Molecular Weight [Da] (protein specific)

Natural Substrates/ Products (Substrates) (protein specific)

Organic Solvent Stability (protein specific)

Oxidation Stability (protein specific)

Posttranslational Modification (protein specific)

Purification (Commentary) (protein specific)

Renatured (Commentary) (protein specific)

Source Tissue (protein specific)

Specific Activity [micromol/min/mg] (protein specific)

Storage Stability (protein specific)

Substrates and Products (Substrate) (protein specific)

Subunits (protein specific)

Temperature Optimum [°C] (protein specific)

Temperature Range [°C] (protein specific)

Temperature Stability [°C] (protein specific)

Turnover Number [1/s] (protein specific)

pH Optimum (protein specific)

pH Range (protein specific)

pH Stability (protein specific)

pI Value (protein specific)

Expression

General Information

General Information (protein specific)

Expression (protein specific)

KCat/KM [mM/s]

KCat/KM [mM/s] (protein specific)

685206

Hothi

Catalysis by the isolated tryp ...

Alcaligenes faecalis, Alcaligenes faecalis IFO 14479

Biochemistry

47

183-194

2008

-

-

-

-

-

-

1

-

-

-

-

-

-

10

-

-

1

-

-

1

-

-

8

-

2

-

-

-

-

-

-

-

1

-

-

-

-

-

-

1

-

-

-

-

1

-

-

-

-

-

-

-

-

-

1

-

1

-

-

8

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

685188

Hothi

Isotope effects reveal that pa ...

Alcaligenes faecalis, Alcaligenes faecalis IFO 14479

Biochemistry

46

9250-9259

2007

-

-

-

1

-

-

-

-

-

-

-

-

-

9

-

-

1

-

-

1

-

-

4

1

2

-

-

-

-

-

-

-

1

-

-

-

-

-

-

1

1

-

-

-

-

-

-

-

-

-

-

-

-

-

1

-

1

-

-

4

1

-

-

-

-

-

-

-

-

-

-

-

-

-

-

687589

Roujeinikova

New insights into the reductiv ...

Alcaligenes faecalis, Alcaligenes faecalis IFO 14479

J. Biol. Chem.

282

23766-23777

2007

-

-

-

-

-

-

-

-

-

-

2

-

-

9

-

-

1

-

-

-

-

-

8

1

2

-

-

-

-

-

-

-

1

-

-

-

-

-

-

1

-

-

-

-

-

-

-

-

-

2

-

-

-

-

1

-

-

-

-

8

1

-

-

-

-

-

-

-

-

-

-

-

-

-

-

672092

Sukumar

Crystal structure of an electr ...

Alcaligenes faecalis

Biochemistry

45

13500-13510

2006

-

-

-

1

-

-

-

-

-

-

-

-

-

3

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

1

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

673559

Hothi

Tryptophan tryptophylquinone c ...

Alcaligenes faecalis

FEBS J.

273

430

2006

-

-

-

-

-

-

-

3

-

-

-

-

-

1

-

-

1

1

-

-

1

-

2

-

-

-

-

-

2

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

3

-

-

-

-

-

-

-

1

-

-

1

-

2

-

-

-

-

2

-

-

-

-

-

-

-

-

-

-

674733

Roujeinikova

Atomic level insight into the ...

Alcaligenes faecalis

J. Biol. Chem.

281

40264-40272

2006

-

-

-

1

-

-

-

-

-

-

-

-

-

2

-

-

-

1

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

1

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

677123

Massgrau

Atomic description of an enzym ...

Alcaligenes faecalis

Science

312

237-241

2006

-

-

-

-

-

-

-

-

-

-

-

-

-

1

-

-

-

1

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

655062

Kondo

Purification and characterizat ...

Achromobacter xylosoxidans, Achromobacter xylosoxidans IFO13495

Biosci. Biotechnol. Biochem.

68

1921-1928

2004

-

-

-

-

-

-

15

4

-

-

3

2

-

3

-

-

1

1

-

1

1

1

23

1

2

1

1

3

-

1

-

1

1

-

-

-

-

-

-

1

-

-

-

-

15

-

4

-

-

3

2

-

-

-

1

-

1

1

1

23

1

1

1

3

-

1

-

1

-

-

-

-

-

-

-

396596

Chistoserdov

Cloning, sequencing and mutage ...

Achromobacter xylosoxidans, Alcaligenes faecalis

Microbiology

147

2195-2202

2001

-

-

-

-

-

-

-

-

1

-

2

-

-

5

-

-

-

-

-

-

2

-

1

1

2

-

-

-

-

-

-

-

-

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1

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2

-

-

-

-

-

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-

2

-

1

1

-

-

-

-

-

-

-

-

-

-

-

-

-

-

396595

Hyun

Gated and ungated electron tra ...

Alcaligenes faecalis, Alcaligenes faecalis IFO 14479

J. Biol. Chem.

274

29081-29086

1999

-

-

-

-

-

-

-

-

-

-

-

2

-

10

-

-

-

-

-

-

-

-

4

-

-

-

-

-

-

-

-

-

1

-

-

-

-

-

-

1

-

-

-

-

-

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-

-

-

-

2

-

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-

-

-

-

-

4

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

715340

Zhu

Localization of periplasmic re ...

Alcaligenes faecalis

J. Bacteriol.

181

6540-6542

1999

-

-

-

1

-

-

-

-

1

-

-

-

-

3

-

-

-

-

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-

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-

-

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-

-

-

-

-

-

-

-

-

-

-

-

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-

1

-

-

-

-

-

-

1

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

714515

Adachi

-

Characterization of quinohemop ...

Pseudomonas putida, Pseudomonas putida IFO 15366

Biosci. Biotechnol. Biochem.

62

469-478

1998

-

-

-

1

-

-

4

-

-

-

4

-

-

2

-

-

-

-

-

-

1

-

6

1

2

-

-

-

-

-

-

-

1

-

-

-

-

-

-

1

1

-

-

-

4

-

-

-

-

4

-

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-

-

-

-

1

-

6

1

-

-

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-

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-

-

-

-

-

-

-

-

-

396593

Hyun

Electron transfer reactions be ...

Alcaligenes faecalis, Alcaligenes faecalis IFO 14479

Biochemistry

34

12249-12254

1995

-

-

-

-

-

-

-

2

-

-

-

2

-

10

-

-

-

-

-

-

-

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6

-

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-

-

2

-

-

-

1

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1

-

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2

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2

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-

-

-

6

-

-

-

-

2

-

-

-

-

-

-

-

-

-

-

396594

Hyun

Unusually large isotope effect ...

Alcaligenes faecalis, Alcaligenes faecalis IFO 14479

Biochim. Biophys. Acta

1251

198-200

1995

-

-

-

-

-

-

-

2

-

-

-

-

-

9

-

-

-

-

-

-

-

-

2

-

-

-

-

-

2

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

2

-

-

-

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-

-

2

-

-

-

-

2

-

-

-

-

-

-

-

-

-

-

715426

Edwards

Spectroscopic evidence for a c ...

Alcaligenes faecalis

J. Biol. Chem.

270

4293-4298

1995

-

-

-

1

-

-

-

-

-

-

-

-

-

4

-

-

-

-

-

-

-

-

1

-

1

-

-

-

-

-

-

-

1

-

-

-

-

-

-

1

1

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

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-

-

1

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

396592

Govindaraj

Aromatic amine dehydrogenase, ...

Alcaligenes faecalis, Alcaligenes faecalis IFO 14479

J. Bacteriol.

176

2922-2929

1994

-

-

-

-

-

1

8

3

-

-

4

-

-

9

-

-

1

-

-

-

2

-

6

1

-

-

-

1

-

-

-

-

1

3

-

-

-

-

-

1

-

-

1

-

8

3

3

-

-

4

-

-

-

-

1

-

-

2

-

6

1

-

-

1

-

-

-

-

-

-

-

-

-

-

-

288289

Cuskey

Initial catabolism of aromatic ...

Pseudomonas aeruginosa

J. Bacteriol.

169

2398-2404

1987

-

-

1

-

-

-

-

-

1

-

-

1

-

3

-

-

-

-

-

-

-

-

3

-

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-

-

-

-

-

-

-

-

-

-

-

-

-

1

-

-

-

-

-

-

-

-

1

-

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1

-

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-

3

-

-

-

-

-

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-

-

-

-

-

-

-

-

396589

Nozaki

Aromatic amine dehydrogenase f ...

Alcaligenes faecalis, Alcaligenes faecalis IFO 14479

Methods Enzymol.

142

650-655

1987

-

-

-

1

-

-

3

-

-

-

3

-

-

10

-

-

1

-

-

-

1

-

10

1

-

1

-

-

-

-

-

-

1

-

-

-

-

-

-

1

1

-

-

-

3

-

-

-

-

3

-

-

-

-

1

-

-

1

-

10

1

1

-

-

-

-

-

-

-

-

-

-

-

-

-

396591

Iwaki

Crystallization and properties ...

Pseudomonas sp.

Arch. Biochem. Biophys.

220

253-262

1983

-

-

-

1

-

-

6

4

-

2

3

-

-

5

-

-

1

-

-

-

1

-

10

1

-

-

-

-

-

2

1

-

-

-

-

-

-

-

-

-

1

-

-

-

6

-

4

-

2

3

-

-

-

-

1

-

-

1

-

10

1

-

-

-

-

2

1

-

-

-

-

-

-

-

-