SAE0092
Mutanolisina from Streptomyces globisporus ATCC 21553
free of DNA contaminants, suitable for Microbiome research, lyophilized powder, ≥4000 units/mg protein (biuret)
Sinónimos:
Mutanolysin
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About This Item
Productos recomendados
biological source
Streptomyces sp. (Streptomyces globisporus ATCC 21553)
form
lyophilized powder
specific activity
≥4000 units/mg protein (biuret)
mol wt
23 kDa
~18.5 kDa
feature
DNA free
concentration
≥40% protein
technique(s)
nucleic acid detection: suitable
suitability
suitable for cell lysis
application(s)
life science and biopharma
shipped in
wet ice
storage temp.
−20°C
Categorías relacionadas
Application
Proporciona una lisis celular suave para el aislamiento de biomoléculas y ARN fácilmente degradables de bacterias. Se ha utilizado en la formación de esferoplastos para el aislamiento del ADN.
Purified Mutanolysin SAE0092 undergoes strict quality control testing to ensure the absence of detectable levels of contaminating DNA using 35 cycles PCR amplification of 16S and 18S rDNA using universal primer sets.
Mutanolysin is a muralytic enzyme, suitable for usage in isolation of nucleic acids, from Gram-positive bacteria (e.g. Listeria, Lactobacillus, Lactococcus),(8) and also from other bacteria that are difficult to lyse with lysozyme only.
Mutanolysin is a muralytic enzyme, suitable for usage in isolation of nucleic acids, from Gram-positive bacteria (e.g. Listeria, Lactobacillus, Lactococcus),(8) and also from other bacteria that are difficult to lyse with lysozyme only.
Biochem/physiol Actions
La mutanolisina es una N-acetilmuramidasa. Al igual que la lisozima, es una enzima muralítica que rompe el enlace β-N-acetilmuramil-(1→4)-N-acetilglucosamina del polímero de la pared celular bacteriana peptidoglucano-polisacárido. Sus restos carboxi terminales están implicadas en el reconocimiento y la unión de polímeros de pared celular únicos. Mutanolisina lisa Listeria y otras bacterias grampositivas como Lactobacillus y Lactococcus.
Features and Benefits
Suitable for difficult-to-lyse samples.
Microbial DNA free, minimizing DNA contamination from reagents in workflow.
Suitable for the isolation of nucleic acids from Gram-positive bacteria, including Listeria, Lactobacillus, and Lactococcus.
Microbial DNA free, minimizing DNA contamination from reagents in workflow.
Suitable for the isolation of nucleic acids from Gram-positive bacteria, including Listeria, Lactobacillus, and Lactococcus.
Unit Definition
One unit will produce a ΔA600 of 0.01 per minute at pH 6.0 at 37 °C in a 1 mL volume using a suspension of Streptococcus faecalis cell wall as substrate.
Physical form
Lyophilized powder containing Ficoll® and sodium succinate buffer salts
Legal Information
Ficoll is a registered trademark of Cytiva
signalword
Danger
hcodes
pcodes
Hazard Classifications
Resp. Sens. 1
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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Stacey M Broomall et al.
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Effective microbial forensic analysis of materials used in a potential biological attack requires robust methods of morphological and genetic characterization of the attack materials in order to enable the attribution of the materials to potential sources and to exclude other
G B Calandra et al.
Infection and immunity, 28(3), 1033-1037 (1980-06-01)
Group B streptococci, refractory to previously tested muralysins under physiological conditions, were successfully converted to protoplasts by use of a recently describede N-acetyl muramidase, mutanolysin, derived from a streptomycete. Purified enzyme was effective, but crude preparations, although degrading cell walls
K Yokogawa et al.
Antimicrobial agents and chemotherapy, 6(2), 156-165 (1974-08-01)
Mutanolysin partially purified from the culture filtrate of Streptomyces globisporus 1829 consists of two main lytic enzymes with an isoelectric point near pH 8.5 and 10, respectively, and proteolytic enzyme is associated with the latter lytic enzyme. Mutanolysin exhibited maximal
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