Date published: 2026-5-24

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p-Nitrophenyl β-D-Cellotetraoside (CAS 129411-62-7)

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Application:
p-Nitrophenyl β-D-Cellotetraoside is a probe for cellulase processing activity
CAS Number:
129411-62-7
Molecular Weight:
787.7
Molecular Formula:
C30H45NO23
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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p-Nitrophenyl β-D-Cellotetraoside is a synthetic glycoside used extensively in the field of enzymology to study the activity and specificity of cellulases, enzymes that degrade cellulose. This compound consists of a p-nitrophenyl group linked to a β-D-cellotetraose, a cellulose oligomer, which serves as a substrate mimic for cellulases involved in the breakdown of cellulosic materials. The p-nitrophenyl group functions as a chromophoric reporter, releasing p-nitrophenol upon enzymatic cleavage. The release of this molecule can be quantitatively measured by its absorbance at 405 nm, providing a straightforward method for monitoring enzyme kinetics and activity. This feature makes p-Nitrophenyl β-D-Cellotetraoside particularly valuable for assaying cellulase activity in various research contexts, including studies aimed at understanding the enzymatic breakdown of biomass and the optimization of industrial processes such as biofuel production. Research utilizing this compound helps to explain the mechanisms by which cellulases recognize and cleave their cellulose substrates, contributing to advancements in biotechnology and environmental science. By understanding the specifics of enzyme-substrate interactions, scientists can engineer more efficient enzymes for the conversion of cellulose into fermentable sugars, enhancing the sustainability and efficiency of biofuel production processes. This chemical thus plays a crucial role in fundamental research aimed at improving the utilization of renewable resources.


p-Nitrophenyl β-D-Cellotetraoside (CAS 129411-62-7) References

  1. Isolation and analysis of two cellulase cDNAs from Orpinomyces joyonii.  |  Qiu, X., et al. 2000. Gene. 245: 119-26. PMID: 10713452
  2. Biochemical characterization and mechanism of action of a thermostable beta-glucosidase purified from Thermoascus aurantiacus.  |  Parry, NJ., et al. 2001. Biochem J. 353: 117-127. PMID: 11115405
  3. A novel alkaline endoglucanase from an alkaliphilic Bacillus isolate: enzymatic properties, and nucleotide and deduced amino acid sequences.  |  Endo, K., et al. 2001. Appl Microbiol Biotechnol. 57: 109-16. PMID: 11693906
  4. A newly described cellulosomal cellobiohydrolase, CelO, from Clostridium thermocellum: investigation of the exo-mode of hydrolysis, and binding capacity to crystalline cellulose.  |  Zverlov, VV., et al. 2002. Microbiology (Reading). 148: 247-255. PMID: 11782517
  5. Enzymatic properties, crystallization, and deduced amino acid sequence of an alkaline endoglucanase from Bacillus circulans.  |  Hakamada, Y., et al. 2002. Biochim Biophys Acta. 1570: 174-80. PMID: 12020807
  6. Molecular cloning and characterization of a cellulase gene from a symbiotic protist of the lower termite, Coptotermes formosanus.  |  Inoue, T., et al. 2005. Gene. 349: 67-75. PMID: 15777663
  7. Transcellobiosylation Reactions Catalyzed by Different Exoglucanase Components of a Trichoderma viride Cellulase in Aqueous Organic Solvent  |  Hayashi, Y., Kitayaki, M., Takezaki, K., Ikeuchi, H., & Kunugi, S. 2003. Biocatalysis and Biotransformation. 21(1): 25-31.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

p-Nitrophenyl β-D-Cellotetraoside, 1 mg

sc-222113
1 mg
$265.00