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Literature summary for 4.3.1.1 extracted from

  • Tokushige, M.
    Aspartate ammonia-lyase (1985), Methods Enzymol., 113, 618-627.
    View publication on PubMed

Activating Compound

Activating Compound Comment Organism Structure
acid anhydride activates Escherichia coli
alpha-methyl-DL-aspartate activates Escherichia coli
N-hydroxysuccinimide acetate activates Escherichia coli
subtilisin BPN' activates Escherichia coli
Trypsin enzyme is activated several-fold by limited treatment Escherichia coli

Crystallization (Commentary)

Crystallization (Comment) Organism
-
Pseudomonas fluorescens

General Stability

General Stability Organism
enzyme is fairly stable in the presence of high concentrations of ammonium sulfate, potassium phosphate, and KCl Escherichia coli

Inhibitors

Inhibitors Comment Organism Structure
5,5'-dithiobis(2-nitrobenzoate)
-
Escherichia coli
aspartate beta-semialdehyde i.e. aspartic beta-semialdehyde.Inactivates as an active-site directed agent Escherichia coli
D-Aspartate competitive Escherichia coli
diethyldicarbonate reactivated by hydroxylamine Escherichia coli
EDTA partial Escherichia coli
p-hydroxymercuribenzoate
-
Escherichia coli

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
2.4
-
L-aspartate in the presence of 3 mM MgCl2, pH 9.0 Pseudomonas fluorescens

Metals/Ions

Metals/Ions Comment Organism Structure
Mg2+ activates at the alkine pH Escherichia coli
Mg2+ activates at the alkine pH Hafnia alvei
Mn2+
-
Hafnia alvei
Mn2+ activates at the alkine pH Escherichia coli

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
173000
-
sedimentation equilibrium analysis Pseudomonas fluorescens
193000
-
sedimentation equilibrium analysis Escherichia coli

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Escherichia coli enzyme synthesis is subject to catabolite repression by glucose and is suppressed under aerobic conditions ?
-
?

Organism

Organism UniProt Comment Textmining
Escherichia coli
-
-
-
Hafnia alvei
-
-
-
Pseudomonas fluorescens
-
IFO 3081
-

Purification (Commentary)

Purification (Comment) Organism
-
Escherichia coli
-
Pseudomonas fluorescens

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
68.5
-
-
Escherichia coli
229
-
-
Pseudomonas fluorescens

Storage Stability

Storage Stability Organism
2-mercaptoethanol and dithiothreitol protect enzyme against inactivation during storage Escherichia coli

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
fumarate + hydroxylamine substrates for reverse reaction Escherichia coli ?
-
?
fumarate + NH4Cl substrates for reverse reaction Escherichia coli ?
-
?
L-aspartate r Escherichia coli fumarate + NH3
-
?
L-aspartate r Pseudomonas fluorescens fumarate + NH3
-
?
L-aspartate r Hafnia alvei fumarate + NH3
-
?
L-aspartate absolutely specific Escherichia coli fumarate + NH3
-
?
L-aspartate natural substrate Escherichia coli fumarate + NH3
-
?
L-aspartate natural substrate Pseudomonas fluorescens fumarate + NH3
-
?
L-aspartate natural substrate Hafnia alvei fumarate + NH3
-
?
additional information enzyme synthesis is subject to catabolite repression by glucose and is suppressed under aerobic conditions Escherichia coli ?
-
?

Temperature Stability [°C]

Temperature Stability Minimum [°C] Temperature Stability Maximum [°C] Comment Organism
additional information
-
-
Escherichia coli

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
7.8
-
in the absence of MgCl2 Escherichia coli
8.8
-
native enzyme in the presence of MgCl2 Escherichia coli