SRE0047

Proteinase K from Tritirachium album

Suitable for manufacturing of diagnostic kits and reagents, lyophilized powder, ≥30 units/mg protein, Molecular Biology

• Synonym(s): Endopeptidase K
• CAS Number: 39450-01-6
• EC Number: 3.4.21.64 (BRENDA, IUBMB)
• EC Number: 254-457-8
• MDL number: MFCD00132129
• UNSPSC Code: 12352204
• NACRES: NA.54

Properties

• biological source: fungus (Tritirachium album)
• Quality Level: 400
• grade: Molecular Biology
• form: lyophilized powder
• specific activity: ≥30 units/mg protein
• mol wt: 28,930 Da; 28.93 kDa
• storage condition: dry at room temperature
• technique(s): DNA extraction: suitable; RNA extraction: suitable
• impurities: ≤1 ppm DNA
• color: white
• pH: 7.5
• application(s): diagnostic assay manufacturing
• foreign activity: DNAse, Nickase and RNAse, none detected
• shipped in: wet ice
• storage temp.: −20°C

Description

General description

Proteinase K is an extracellular endopeptidase. It is synthesized by the mold Tritirachium album Limber. Proteinase K belongs to a new subfamily of the subtilisins. It is a 277 amino acid protein with a molecular weight of 28,930 Da. Active proteinase K is characterized with an unhydrolysed protein chain and autolysed polypeptide chains.[1]

Application

Proteinase K catalyzes the hydrolysis of keratin.[2]

Useful for the proteolytic inactivation of nucleases during the isolation of DNA and RNA.

Useful for the proteolytic inactivation of nucleases during the isolation of DNA and RNA.
Removes endotoxins that bind to cationic proteins such as lysozyme and ribonuclease A.
Reported useful for the isolation of hepatic, yeast, and mung bean mitochondria
Determination of enzyme localization on membranes
Treatment of paraffin embedded tissue sections to expose antigen binding sites for antibody labeling.
Digestion of proteins from brain tissue samples for prions in Transmissible Spongiform Encephalopathies (TSE) research.

Biochem/physiol Actions

Proteinase K catalyzes the hydrolysis of keratin.[3]

Proteinase K is a stable and highly reactive serine protease. Evidence from crystal and molecular structure studies indicates the enzyme belongs to the subtilisin family with an active-site catalytic triad (Asp³⁹-His⁶⁹-Ser²²⁴). It is stable in a broad range of environments: pH, buffer salts, detergents (SDS), and temperature. In the presence of 0.1-0.5% SDS, proteinase K retains activity and will digest a variety of proteins and nucleases in DNA preparations without compromising the integrity of the isolated DNA.

Other Notes

One unit will hydrolyze urea-denatured hemoglobin to produce color equivalent to 1.0 μmole of tyrosine per min at pH 7.5 at 37 °C (color by Folin-Ciocalteu reagent).

Safety Information

• pictograms: GHS08,GHS07
• signalword: Danger
• hcodes: H315,H319,H334,H335
• pcodes: P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
• Hazard Classifications: Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
• target_organs: Respiratory system
• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 1
• flash_point_f: Not applicable
• flash_point_c: Not applicable