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Merck
CN

P1236

Protease from Bacillus amyloliquefaciens

liquid, ≥0.8 U/g

Synonym(s):

Neutrase® 0.8L

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About This Item

UNSPSC Code:
12352204
EC Number:
232-752-2
NACRES:
NA.54
MDL number:
Specific activity:
≥0.8 U/g
Biological source:
Bacillus sp. (Bacillus amyloliquefaciens)
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biological source

Bacillus sp. (Bacillus amyloliquefaciens)

Quality Level

form

liquid

specific activity

≥0.8 U/g

storage temp.

2-8°C

General description

Bacterial protease produced by submerged fermentation of a selected strain of Bacillus amyloliquefaciens

Application

Protease from Bacillus amyloliquefaciens has been used for the unhairing of hides and skins. It has also been used in a study to investigate peptide bond formation using the carbamoylmethyl ester as the acyl donor.

Biochem/physiol Actions

Secretion of protease by Bacillus amyloliquefaciens can be inhibited by treatment with the fatty acid synthetase inhibitor cerulenin.

Legal Information

A product of Novozyme Corp.
Neutrase is a registered trademark of Novozymes Corp.


pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1

Storage Class

10 - Combustible liquids

wgk

WGK 1

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

常规特殊物品

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Keqin Ou et al.
Journal of agricultural and food chemistry, 58(8), 4894-4900 (2010-03-17)
Effects of enzymatic hydrolysates of whey protein concentrates (WPC) on iron absorption were studied using in vitro digestion combined with Caco-2 cell models for improved iron absorption. Neutrase- and papain-treated WPC could improve iron absorption; especially hydrolysates by Neutrase could
Cerulenin Inhibits Production of Extracellular Proteins but not Membrane Proteins in Bacillus amyloliquefaciens.
Paton, J.
Journal of General Microbiology, 118, 179-187 (1980)
Toshifumi Miyazawa et al.
Protein and peptide letters, 15(10), 1050-1054 (2008-12-17)
Bacillus amyloliquefaciens protease-catalyzed peptide bond formation was investigated using the carbamoylmethyl (Cam) ester as the acyl donor. A series of N-protected L-amino acid Cam esters were coupled with an L-amino acid amide in acetonitrile in good to excellent yields. The



Global Trade Item Number

SKUGTIN
P1236-250ML04061834354253
P1236-50ML04061834354260