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Merck

534803

Sigma-Aldrich

Amano Lipase M from Mucor javanicus

≥10,000 U/g, pH 7.0, 40 °C (Optimum pH and temperature)

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About This Item

Número de CAS:
EC Number:
MDL number:
UNSPSC Code:
12352204
NACRES:
NA.22

specific activity

≥10,000 U/g, pH 7.0, 40 °C (Optimum pH and temperature)

storage temp.

2-8°C

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-;

InChI key

QWZUIMCIEOCSJF-CHHCPSLASA-N

Application

Amano Lipase M from Mucor javanicus has been used:
  • as a component in calcium alginate beads or immobilization to study its efficiency and stability in the biocatalytic synthesis of butyl butyrate in aqueous media
  • as a component in calcium alginate beads for transmission electron microscope (TEM) imaging
  • in immobilization to study its efficiency in ester synthesis and to evaluate its catalytic behavior
  • in catalyzing Michael addition reactions of pyrimidine derivatives to disaccharide acrylates

Biochem/physiol Actions

Amano lipase M is capable of catalyzing Michael addition of pyrimidine with disaccharide acrylates in organic media.

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Biolubricant production under zero-waste Moringa oleifera Lam biorefinery approach for boosting circular economy
Barbosa MS, et al.
Industrial Crops and Products, 113542-113542 (2021)
Hong-Xia Dai et al.
Biotechnology letters, 28(18), 1503-1507 (2006-09-07)
The Michael addition of fluorouracil (0.01 mol), uracil (0.01 mol), thymine (0.01 mol) to disaccharide acrylates (0.03 mol) was carried out in pyridine (20 ml) at 50 degrees C for 72 h with lipase M from Mucor javanicus (200 mg).
Mika Henrikki Sipponen et al.
Nature communications, 9(1), 2300-2300 (2018-06-14)
Dehydration reactions proceed readily in water-filled biological cells. Development of biocatalysts that mimic such compartmentalized reactions has been cumbersome due to the lack of low-cost nanomaterials and associated technologies. Here we show that cationic lignin nanospheres function as activating anchors

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