This product is shipped at ambient temperature and may be stored at 4 °C for up to two weeks. For long term storage, -20 °C is recommended. The solution should be aliquoted prior to freezer storage. Avoid repeated freeze/thaw cycles.
SBR00022
Blasticidin S Ready Made Solution
10 mg/mL (20 mM HEPES), 0.22 μm filtered
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1 ML
131,00 $
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About This Item
Formule empirique (notation de Hill):
C17H27N8O5Cl
Poids moléculaire :
458.90
Code UNSPSC :
12352106
Nomenclature NACRES :
NA.76
Produits recommandés
Niveau de qualité
Stérilité
0.22 μm filtered
Essai
≥98% (HPLC)
Forme
liquid
Concentration
10 mg/mL (20 mM HEPES)
Couleur
colorless to faint yellow
Spectre d'activité de l'antibiotique
fungi
Mode d’action
protein synthesis | interferes
Température de stockage
−20°C
Chaîne SMILES
CN(CCC(CC(=O)NC1C=CC(OC1C(=O)O)N2C=CC(=NC2=O)N)N)C(=N)N.Cl
InChI
1S/C17H26N8O5.ClH/c1-24(16(20)21)6-4-9(18)8-12(26)22-10-2-3-13(30-14(10)15(27)28)25-7-5-11(19)23-17(25)29;/h2-3,5,7,9-10,13-14H,4,6,8,18H2,1H3,(H3,20,21)(H,22,26)(H,27,28)(H2,19,23,29);1H
Clé InChI
YQXYQOXRCNEATG-UHFFFAOYSA-N
Description générale
Blasticidin S, originally isolated from S. griseochromogenes, is a bacterial metabolite renowned for its antibacterial and fungicidal activities. This compound serves as a potent inhibitor of protein synthesis, exhibiting activity against various microorganisms, including bacteria (B. subtilis, S. lutea, E. coli, P. fluorescens, and M. tuberculosis), tumor cell lines, and nematodes.
In research, Blasticidin S has become a valuable tool, notably as a marker for strain manipulations. Recent applications involve the use of Blasticidin S as a selection agent for cells carrying plasmids conferring blasticidin resistance. The resistance is mediated by the blasticidin S deaminase genes (bsr from Bacillus cereus or BSD from Aspergillus terreus). These genes produce enzymes that catalyze the hydrolytic deamination of the cytosine moiety in blasticidin S, leading to the formation of a non-toxic deaminohydroxy derivative. This resistance mechanism is crucial in various studies involving genetic manipulations and selections in cell biology and biochemical research.
In research, Blasticidin S has become a valuable tool, notably as a marker for strain manipulations. Recent applications involve the use of Blasticidin S as a selection agent for cells carrying plasmids conferring blasticidin resistance. The resistance is mediated by the blasticidin S deaminase genes (bsr from Bacillus cereus or BSD from Aspergillus terreus). These genes produce enzymes that catalyze the hydrolytic deamination of the cytosine moiety in blasticidin S, leading to the formation of a non-toxic deaminohydroxy derivative. This resistance mechanism is crucial in various studies involving genetic manipulations and selections in cell biology and biochemical research.
Application
Blasticidin S has been:
- studies to have fungicidal properties and prevents rice blast disease.[1]
- used as a selection agent for transformed cells that contain the resistance genes bls, bsr, or bsd. Blasticidin S has been used to select HEK293-T cells with TLR-2 constructs and HEK-D5 cells.[2][3]
- used to study protein synthesis at the level of peptide bond formation.
Actions biochimiques/physiologiques
Mode of Action: It inhibits protein synthesis in bacteria and eukaryotes.[4] Blasticidin S inhibits hydrolysis of peptidyl-tRNA induced by release factors. It enhances the binding of tRNA to the large subunit of ribosomes and to an extent inhibits peptide bond formation.[4][5]
Antimicrobial Spectrum: Active against mycobacteria, several Gram-positive and Gram-negative bacteria
Antimicrobial Spectrum: Active against mycobacteria, several Gram-positive and Gram-negative bacteria
Caractéristiques et avantages
- High-quality antibiotic suitable for multiple research applications
- Ideal for Cell Biology and Biochemical research
Autres remarques
For additional information on our range of Biochemicals, please complete this form.
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 3 Oral
Code de la classe de stockage
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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Les clients ont également consulté
Suneesh Kumar Pachathundikandi et al.
PloS one, 6(5), e19614-e19614 (2011-05-17)
Helicobacter pylori is the causative agent for developing gastritis, gastric ulcer, and even gastric cancer. Virulent strains carry the cag pathogenicity island (cagPAI) encoding a type-IV secretion system (T4SS) for injecting the CagA protein. However, mechanisms of sensing this pathogen
Martha Triantafilou et al.
PloS one, 8(4), e61199-e61199 (2013-04-18)
Ureaplasma species are the most frequently isolated microorganisms inside the amniotic cavity and have been associated with spontaneous abortion, chorioamnionitis, premature rupture of the membranes (PROM), preterm labour (PL) pneumonia in neonates and bronchopulmonary dysplasia in neonates. The mechanisms by
Egor Svidritskiy et al.
Journal of molecular biology, 430(5), 591-593 (2018-01-26)
Understanding the mechanisms of inhibitors of translation termination may inform development of new antibacterials and therapeutics for premature termination diseases. We report the crystal structure of the potent termination inhibitor blasticidin S bound to the ribosomal 70S•release factor 1 (RF1)
Egor Svidritskiy et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(30), 12283-12288 (2013-07-05)
The antibiotic blasticidin S (BlaS) is a potent inhibitor of protein synthesis in bacteria and eukaryotes. We have determined a 3.4-Å crystal structure of BlaS bound to a 70S⋅tRNA ribosome complex and performed biochemical and single-molecule FRET experiments to determine
Rohini Garg et al.
Journal of immunology (Baltimore, Md. : 1950), 184(11), 5980-5987 (2010-05-05)
Vi capsular polysaccharide is a major virulence determinant of the human typhoid- causing pathogen Salmonella typhi; it is absent in nontyphoidal Salmonella serovars. We show in this study that through its specific interaction with the membrane recognition complex containing the
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