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  • 116981-90-9 , 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside
116981-90-9 , 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside

116981-90-9 , 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside

Cas:116981-90-9 ,
4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside
C28H35F3O18 / 716.56
MFCD31726176

4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside

4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside is a chromogenic substrate that can be used for the staining of bacteria. The substrate is also used in food testing to detect the presence of pathogens, such as Listeria monocytogenes and Salmonella enterica. It has been shown to be an excellent ligand for use with flow cytometry. 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside has been used in diagnostics to test for fluorescence due to its fluorogenic properties.

Definition and Background:

4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside is a fluorogenic substrate commonly used in the field of carbohydrate chemistry. It is a synthetic analog of cellulose oligosaccharides that incorporates a fluorescent reporter that allows for the sensitive and specific measurement of cellulase activity. This compound is used extensively in scientific research to study the enzymatic degradation of cellulose, a primary component of plant cell walls, by cellulase enzymes.

Physical and Chemical Properties:

4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside is a white to light yellow powder with a molecular weight of 569.51 g/mol. It has a melting point range of 224-226°C and is soluble in dimethyl sulfoxide (DMSO), acetonitrile, and other organic solvents. The chemical structure of 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside is shown in Figure 1.

Synthesis and Characterization:

4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside is synthesized through a multi-step process that involves the protection and deprotection of various functional groups on the cellulose backbone. The final step involves the reaction of 4-methylumbelliferone with the protected cellulose oligosaccharide to produce the desired fluorogenic substrate. The purity and identity of 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside are determined through a combination of physical and chemical characterization techniques, including NMR spectroscopy and high-performance liquid chromatography (HPLC).

Analytical Methods:

The enzymatic activity of cellulases on 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside can be measured through the detection of fluorescent 4-methylumbelliferone produced by the hydrolysis of the substrate. This can be detected using spectrofluorometry, which allows for the precise measurement of cellulase activity over time. Additionally, the purity and identity of 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside can be determined using spectroscopic and chromatographic techniques, as mentioned above.

Biological Properties:

4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside has been shown to be an effective substrate for the measurement of cellulase activity in both bacterial and fungal systems. This compound has been used in a variety of experimental settings, including the screening of cellulase-producing microorganisms and the characterization of recombinant cellulase enzymes. Due to its specificity and sensitivity, 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside is a useful tool for the study of cellulase biology and the optimization of cellulase-based processes.

Toxicity and Safety in Scientific Experiments:

While 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside has not been extensively studied for its toxicity, it is recommended that proper precautions be taken when handling this compound. This includes the use of appropriate personal protective equipment, such as gloves and goggles, and the disposal of all waste material according to local regulations. Additionally, it is important to ensure that 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside is used only in accordance with recommended protocols and that appropriate training is provided to all personnel involved in its use.

Applications in Scientific Experiments:

The use of 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside has a wide range of applications in the field of carbohydrate chemistry. In addition to its use in the study of cellulase activity, this compound has been used in the analysis of other glycosidases, such as xylanases and beta-glucosidases. It has also been used in the development of diagnostic tests for bacterial and viral pathogens that utilize glycoside hydrolases.

Current State of Research:

Research into the use of 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside continues to expand, with new applications and uses being developed. Recent studies have focused on the use of this substrate in the study of cellulase gene expression, the optimization of cellulase production, and the development of new cellulase-based bioprocessing platforms.

Potential Implications in Various Fields of Research and Industry:

The use of 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside has significant implications in a variety of fields, including biotechnology, biofuels, and environmental science. Its ability to measure cellulase activity with high sensitivity and specificity makes it a valuable tool for the optimization of cellulase-based processes, including the production of biofuels and the conversion of plant biomass into high-value products. Additionally, the development of new diagnostic tests based on this substrate could have significant medical and public health implications.

Limitations and Future Directions:

While 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside has been extensively studied for its use in the characterization of cellulase activity, there are several limitations to its application. One limitation is the potential for false positives, where other enzymes may hydrolyze the substrate in addition to cellulases. Another limitation is the specificity of this substrate to b-D-cellotrioside, which limits its applicability to the study of other glycosidases. To address these limitations, researchers are currently working on the development of new fluorogenic substrates with enhanced specificity and broader applicability.

Future directions for research into 4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside include the development of new high-throughput screening methods for cellulase-producing microorganisms, the development of new cellulase-based bioprocessing platforms for the conversion of plant biomass into high-value products, and the synthesis of new fluorogenic substrates for the measurement of other glycosidases. Additionally, the continued study of the biological and toxicological properties of this compound will be important for the safe and effective use of this substrate in future research and industry applications.

CAS Number116981-90-9
Product Name4-(Trifluoromethyl)umbelliferyl-b-D-cellotrioside
IUPAC Name7-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-(trifluoromethyl)chromen-2-one
Molecular FormulaC28H35F3O18
Molecular Weight716.6 g/mol
InChIInChI=1S/C28H35F3O18/c29-28(30,31)10-4-15(35)44-11-3-8(1-2-9(10)11)43-25-21(41)18(38)23(13(6-33)46-25)49-27-22(42)19(39)24(14(7-34)47-27)48-26-20(40)17(37)16(36)12(5-32)45-26/h1-4,12-14,16-27,32-34,36-42H,5-7H2/t12-,13-,14-,16-,17+,18-,19-,20-,21-,22-,23-,24-,25-,26+,27+/m1/s1
InChI KeyCSEGIKFULSNPJZ-KHEBRHQFSA-N
SMILESC1=CC2=C(C=C1OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)OC(=O)C=C2C(F)(F)F
Canonical SMILESC1=CC2=C(C=C1OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)OC(=O)C=C2C(F)(F)F
Isomeric SMILESC1=CC2=C(C=C1O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)O)O)O)O)OC(=O)C=C2C(F)(F)F


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