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Merck

62298

Lipase from Mucor miehei

powder, slightly brown, ~1 U/mg

Synonym(s):

Triacylglycerol acylhydrolase, Triacylglycerol lipase

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100 MG

1 010,00 kr

1 010,00 kr


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About This Item

CAS Number:
UNSPSC Code:
12352204
NACRES:
NA.54
EC Number:
232-619-9
EC Number:
MDL number:

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Product Name

Lipase from Mucor miehei, powder, slightly brown, ~1 U/mg

InChI key

QWZUIMCIEOCSJF-CHHCPSLASA-N

InChI

1S/C11H9N3O2.Na/c15-8-4-5-9(10(16)7-8)13-14-11-3-1-2-6-12-11;/h1-7,16H,(H,12,14);/q;+1/b13-9-;

form

powder

specific activity

~1 U/mg

color

slightly brown

storage temp.

2-8°C

Quality Level

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Show Differences

1 of 4

This Item
L9031L890680612
specific activity

~1 U/mg

specific activity

≥4,000 units/mg solid (using olive oil)

specific activity

≥300 units/mg solid (using olive oil)

specific activity

≥30 U/mg

form

powder

form

lyophilized powder

form

lyophilized powder

form

powder

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

color

slightly brown

color

-

color

-

color

light brown

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

-

Application

Lipases are used industrially for the resolution of chiral compounds and the transesterification production of biodiesel.

Biochem/physiol Actions

Mucor miehei lipase hydrolizes triglycerides and catalyzes the synthesis of esters from glycerol and long-chain fatty acids in vitro. Tri-, di-, and monoglycerides are hydrolyzed (in decreasing order of rate).
Tri-, di-, and monoglycerides are hydrolyzed (in decreasing order of rate).

Other Notes

1 U corresponds to the amount of enzyme which liberates 1 μmol oleic acid per minute at pH 8.0 and 40 °C (triolein, Cat. No. 62314 as substrate)
Characterization[1][2]; In the synthesis of fatty hydroxamic acids[3]; Esterification[4]

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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B. Huge-Jensen et al.
Journal of the American Oil Chemists' Society, 65, 905-905 (1988)
B. Huge-Jensen et al.
Lipids, 22, 559-559 (1987)
F. Servat et al.
Journal of the American Oil Chemists' Society, 67, 646-646 (1990)
P.A.S.S. Marques et al.
Journal of Chemical Technology and Biotechnology, 55, 25-25 (1992)
P L Okorokov et al.
Fiziologiia cheloveka, 38(6), 105-112 (2013-02-12)
Food behavior disorderes (high fat diet) and systematic strong drinks use could be the most important causes of excess intake of intestinal endotoxin (ET) in circulation (endotoxin aggression development) and induction of inflammation. In this work we investigated antiendotoxin immunity

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