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Merck

34046

Supelco

Lysozyme from chicken egg white

VETRANAL®, analytical standard

Synonim(y):

Mucopeptide N-acetylmuramoylhydrolase, Muramidase

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About This Item

Numer CAS:
Numer EC enzymu:
Numer WE:
Numer MDL:
Kod UNSPSC:
41116107
NACRES:
NA.24

klasa czystości

analytical standard

Poziom jakości

linia produktu

VETRANAL®

aktywność właściwa

8000-120000 U/mg

okres trwałości

limited shelf life, expiry date on the label

masa cząsteczkowa

single-chain 14.3 kDa
Mr ~14000

klasy chemiczne analitów

amino acids, peptides, proteins

metody

HPLC: suitable

Zastosowanie

food and beverages

format

neat

temp. przechowywania

2-8°C

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Opis ogólny

Lysozyme from chicken egg white, is a protein that can show broad spectrum of antibacterial activity against gram positive and gram negative bacteria. Its antimicrobial activity can be enhanced by pretreatment of the target microbial cells with chelating agents like ethylenediaminetetraacetic acid (EDTA).
Lysozyme from chicken egg white, is a protein that can show broad spectrum of antibacterial activity against gram positive and gram negative bacteria. Its antimicrobial activity can be enhanced by pretreatment of the target microbial cells with chelating agents like ethylenediaminetetraacetic acid (EDTA).

Zastosowanie

Lysozyme from chicken egg white may be used as an analytical reference standard for the determination of the analyte in:
  • Hard and pasta filata cheeses using reversed-phase high performance liquid chromatography with diode array and fluorimetric detection [(RP-HPLC-DAD) and (RP-HPLC-FLD)].
  • Food samples using high-performance liquid chromatography (HPLC) and enzyme-linked immunosorbent assay (ELISA).

Enzyme breaks down the cell walls of bacteria; used to prepare spheroplasts.

Działania biochem./fizjol.

Lysozyme hydrolyzes β(1→4) linkages between N-acetylmuramic acid and N-acetyl-D-glucosamine residues in peptidoglycan and between N-acetyl-D-glucosamine residues in chitodextrin. Gram-positive cells are quite susceptible to this hydrolysis as their cell walls have a high proportion of peptidoglycan. Gram-negative bacteria are less susceptible due to the presence of an outer membrane and a lower proportion of peptidoglycan. However, these cells may be hydrolyzed in the presence of EDTA that chelates metal ions in the outer bacterial membrane.

The enzyme is active over a broad pH range (6.0 to 9.0). At pH 6.2, maximal activity is observed over a wider range of ionic strengths (0.02 to 0.100 M) than at pH 9.2 (0.01 to 0.06 M).

Definicja jednostki

1 unit corresponds to the amount of enzyme which decreases the absorbance at 450 nm by 0.001 per minute at pH 7.0 and 25 deg C.

Informacje prawne

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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Piktogramy

Health hazard

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Zwroty wskazujące środki ostrożności

Klasyfikacja zagrożeń

Resp. Sens. 1

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

Eyeshields, Gloves, type N95 (US)


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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Development of an RP-HPLC method for the simultaneous determination of benzoic acid, sorbic acid, natamycin and lysozyme in hard and pasta filata cheeses.
Guarino C, et al.
Food Chemistry, 127(3), 1294-1299 (2011)
"Identification and isolation of a bactericidal domain in chicken egg white lysozyme"
Pellegrini.A, et al
Journal of Applied Microbiology, 82(03), 372-378 (1997)
"Antimicrobial peptides released by enzymatic hydrolysis of hen egg white lysozyme"
Mine Y, et al.
Journal of Agricultural and Food Chemistry, 52(05), 1088-1094 (2004)
Identification and isolation of a bactericidal domain in chicken egg white lysozyme
Pellegrini.A, et al.
Journal of Applied Microbiology, 82, 372-378 (1997)
Detection of hen?s egg white lysozyme in food: Comparison between a sensitive HPLC and a commercial ELISA method.
Kerkaert B, et al.
Food Chemistry, 120(2), 580-584 (2010)

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