4-nitrophenyl-beta-D-cellobioside

4-Nitrophenyl b-D-cellobioside Chromogenic substrate for cellulases. 4-Nitrophenyl ?-D-cellobioside is a disaccharide and an enzyme substrate. It has been used to characterize the function of endoglucanase 1 from T. harzianum, ?-glucosidase from T. xylanolyticum, and glycoside hydrolase family 3 (GH3) aryl ?-glucosidases from A. oryzae. 4-Nitrophenyl beta-D-cellobioside (p-nitrophenyl-?-D-cellobioside or PNPC) is a synthetic substrate used to measure the activity of cellobiases, enzymes that hydrolyze cellobiose to glucose monomers. PNPC is a ?-glycoside, a molecule that contains a glycosidic bond between two sugar molecules. In this case, PNPC consists of two cellobiose units connected by this bond. Physical and Chemical Properties PNPC is a yellow crystalline powder that is slightly soluble in water and ethanol. Its molecular formula is C18H21NO11, and its molecular weight is 427.35 g/mol. PNPC is stable at room temperature but decomposes at temperatures above 80?C. Synthesis and Characterization PNPC can be synthesized via several methods, including the reaction of p-nitrophenol and cellobiose in the presence of acid or catalytic amounts of an enzyme. The synthesis of PNPC can also be achieved using in vitro enzymatic synthesis. The purity and identity of PNPC can be confirmed via techniques like thin-layer chromatography (TLC), high-performance liquid chromatography (HPLC), and nuclear magnetic resonance (NMR) spectroscopy. Analytical Methods PNPC can be analyzed through enzymatic assays that monitor the rate of cellobiose hydrolysis using spectrophotometric techniques. Enzymatic assays can also be coupled with additional techniques like liquid chromatography-mass spectrometry (LC-MS) and capillary electrophoresis (CE) to obtain more detailed information about cellobiase activity. Biological Properties As a cellobiose-mimicking substrate, PNPC can be used to study the activity of cellobiases and other enzymes that hydrolyze ?-glycosides. There is limited information about the biological properties of PNPC itself, as it is primarily used as a research tool. Toxicity and Safety in Scientific Experiments PNPC is not known to be significantly toxic or hazardous when used in scientific experiments, although it may be harmful if ingested or inhaled. Researchers should take appropriate safety precautions when handling PNPC, including wearing gloves, lab coats, and eye protection. Applications in Scientific Experiments PNPC has several important applications in scientific experiments, including: ? Measuring the activity of cellobiases and related enzymes ? Studying the mechanisms and kinetics of cellobiose hydrolysis ? Developing and optimizing cellobiase assays Current State of Research PNPC has been widely used as a substrate for measuring cellobiase activity and studying the mechanisms of cellobiose hydrolysis. Recent research has focused on the development of more sensitive and specific cellobiase assays using PNPC, as well as the synthesis of modified PNPC derivatives that can be used to study other ?-glycosidases. Potential Implications in Various Fields of Research and Industry The use of PNPC and related substrates has important implications in several fields of research and industry, including: ? Bioenergy: Cellobiases are critical enzymes in the production of biofuels from lignocellulosic biomass, and PNPC can be used to develop and optimize cellobiase assays for this purpose. ? Glycoscience: ?-glycosides like PNPC are important tools for studying the structure and function of complex carbohydrates in biological systems. Limitations and Future Directions While PNPC is a valuable research tool, there are some limitations to its use. For example, PNPC is not an ideal substrate for all cellobiases and may not accurately reflect in vivo cellobiose hydrolysis. Future research directions for PNPC and related substrates may include: ? The synthesis and characterization of modified PNPC derivatives that can be used to study other ?-glycosidases ? The development of more sensitive and specific cellobiase assays for bioenergy and glycoscience applications ? The use of PNPC and related substrates to study the roles of cellobiases and ?-glycosides in biological systems beyond cellobiose hydrolysis. CAS Number 3482-57-3 Product Name 4-Nitrophenyl beta-D-cellobioside IUPAC Name (2S,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-(4-nitrophenoxy)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Molecular Formula C18H25NO13 Molecular Weight 463.4 g/mol InChI InChI=1S/C18H25NO13/c20-5-9-11(22)12(23)14(25)18(30-9)32-16-10(6-21)31-17(15(26)13(16)24)29-8-3-1-7(2-4-8)19(27)28/h1-4,9-18,20-26H,5-6H2/t9-,10-,11-,12+,13-,14-,15-,16-,17-,18+/m1/s1 InChI Key IAYJZWFYUSNIPN-KFRZSCGFSA-N SMILES C1=CC(=CC=C1[N+](=O)[O-])OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O Synonyms 4-nitrophenyl beta-cellobioside, p-nitrophenyl beta-D-cellobioside, para-nitrophenyl beta-D-cellobioside, PNPC Canonical SMILES C1=CC(=CC=C1[N+](=O)[O-])OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O Isomeric SMILES C1=CC(=CC=C1[N+](=O)[O-])O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O)O CAS No: 3482-57-3 Synonyms: PNP-cellobioside MDL No: MFCD00069845 Chemical Formula: C18H25NO13 Molecular Weight: 463.39 COA: Name : 4-Nitrophenyl beta-D-cellobioside; PNPC CAS: 3482-57-3 M.F.: C 18 H 25 NO 13 M .W.: 463.39 Items Standards Results Appearance White crystal powder Complies Solubility Easily soluble in water, insoluble in ether Complies Identification IR and HPLC Complies Appearance of solution Dissolve0.5gin 10mL water, and the solution should be clear Complies Loss weight on drying Max.0.5% 0.1% Heavy metal Max. 20ppm Complies Residue on ignition Max. 0.5% 0.1% TLC One spot One spot p-Nitrophenol Max. 20ppm Complies Any other impurity Max. 0.5% Complies Assay by HPLC Min. 98% 99.2% *Chromogenic cellobiohydralase (e.g. cellobiosidase) substrate used in histochemistry References: 1. Eckert K, Zielinski F, Lo Leggio L, Schneider E, Appl. Microbiol. Biotechnol. 2002, Vol60, Pt4, p428-436