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Merck

D7876

Diamine Oxidase from porcine kidney

≥0.05 unit/mg solid

Sinónimos:

Amine:oxygen oxidoreductase (deaminating) (pyridoxal-containing)

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Número CAS:
Número CE:
UNSPSC Code:
12352204
EC Number:
232-613-6
NACRES:
NA.54
MDL number:
Specific activity:
≥0.05 unit/mg solid
Biological source:
Porcine kidney

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biological source

Porcine kidney

Quality Level

form

solid

specific activity

≥0.05 unit/mg solid

mol wt

170 kDa

solubility

100 mM sodium phosphate buffer, pH 7.2: soluble 10 mg/mL

foreign activity

monoamine oxidase (benzylamine substrate) ≤1%

storage temp.

−20°C

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Este artículo
A5222A2580L6007
specific activity

≥0.05 unit/mg solid

specific activity

≥1.5 units/mg solid

specific activity

≥10 units/mg protein (Bradford)

specific activity

≥12 units/mg protein (biuret)

biological source

Porcine kidney

biological source

-

biological source

-

biological source

Porcine kidney

form

solid

form

powder

form

lyophilized powder

form

lyophilized powder

solubility

100 mM sodium phosphate buffer, pH 7.2: soluble 10 mg/mL

solubility

-

solubility

-

solubility

-

mol wt

170 kDa

mol wt

-

mol wt

-

mol wt

320 kDa

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

General description

Diamine oxidase from porcine kidney is a homodimer consisting of two equal subunits with a molecular weight of 87 kDa each. Each subunit contains one molecule of pyridoxal phosphate and one atom of copper. The molecular mass of the enzyme is found to be 170 kDa.[1] The enzyme is a glycoprotein containing 5% hexose, 3.3% glucosamine, 2.6% N-acetylglucosamine, and 0.25% N-acetylneuraminic acid. The enzyme exhibits a high affinity for concanavalin A.[2] Optimum pH with cadverine and histamine as substrates is found to be 6.3-7.4.

Application

Diamine oxidase from porcine kidney has been used in a study to investigate a luminescence-based test for determining ornithine decarboxylase activity. Diamine oxidase from porcine kidney has also been used in a study to investigate N-linked oligosaccharide structures in diamine oxidase.
Diamine Oxidase from porcine kidney has been used in the construction of histamine biosensor.

Biochem/physiol Actions

Diamine Oxidase catalyzes the oxidation of monoamines, diamines, and histamine to aldehydes, ammonia, and hydrogen peroxide. The enzyme is classified as a copper amine oxidase and it is a key enzyme in nitrogen metabolism. Diamine oxidase is inhibited by diethyldithiocarbamate, phenylhydrazine, semicarbazide, cyanide, isonicotinic acid hydrazide.

Other Notes

One unit will oxidize 1.0 μmole of putrescine per hr at pH 7.2 at 37 °C.

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Diamine oxidase and catalase are expressed in the same cells but are present in different subcellular compartments in porcine kidney.
H G Schwelberger et al.
Inflammation research : official journal of the European Histamine Research Society ... [et al.], 48 Suppl 1, S81-S82 (1999-06-01)
A Rinaldi et al.
Preparative biochemistry, 12(1), 11-28 (1982-01-01)
Several methods for the isolation of apparently homogeneous pig kidney diamine oxidase have been reported in recent years (1-7), but these procedures allow to obtain only little amounts of material making very difficult the study of the molecular properties of
Y Huang et al.
Carbohydrate research, 323(1-4), 111-125 (2000-04-27)
Structures of the N-linked glycans released from porcine kidney diamine oxidase (DAO) were characterized utilizing various analytical techniques, including matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI/TOF-MS), high-performance capillary electrophoresis (HPCE), and high-pH anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD). The
A PRELIMINARY INVESTIGATION ON A HISTAMINE BIOSENSOR CONSTRUCTED FROM DIAMINE OXIDASE IMMOBILISED ONTO AN OXYGEN PROBE
The Enzymes (1970)
HISTAMINE BIOSENSOR: A REVIEW
NorazlinaOthman F, et al.
The Malaysian Journal of Analytical Sciences (2006)

Protocolos

To standardize a procedure for the enzymatic assay of Diamine Oxidase.

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