Dissolving Lignin in Water through Enzymatic Sulfation with Aryl Sulfotransferase
| Autor: | Gadi Rothenberg, Ron Wever, Aloysius F. Hartog, Pepijn Prinsen, Anand Narani |
|---|---|
| Přispěvatelé: | Faculty of Science, Biocatalysis (HIMS, FNWI), HCSC+ (HIMS, FNWI) |
| Jazyk: | angličtina |
| Rok vydání: | 2017 |
| Předmět: |
Magnetic Resonance Spectroscopy
General Chemical Engineering Organosolv macromolecular substances 010402 general chemistry 01 natural sciences Lignin complex mixtures chemistry.chemical_compound Sulfation Environmental Chemistry Phenol Organic chemistry General Materials Science Solubility Aryl sulfotransferase 010405 organic chemistry fungi technology industry and agriculture Water food and beverages Arylsulfotransferase 0104 chemical sciences General Energy chemistry Reagent Spectrophotometry Ultraviolet Kraft paper |
| Zdroj: | ChemSusChem, 10(10), 2267-2273. Wiley-VCH Verlag |
| ISSN: | 1864-5631 |
| DOI: | 10.1002/cssc.201700376 |
| Popis: | We introduce the concept of using site-specific sulfation of various lignins for increasing their aqueous solubility and thereby their processability. Using p-nitrophenylsulfate as a sulfate source and an aryl sulfotransferase enzyme as catalyst, lignins are easily sulfated at ambient conditions. We demonstrate the specific sulfation of phenolic hydroxyl groups on five different lignins: Indulin AT (Kraft softwood), Protobind 1000 (mixed wheat straw/Sarkanda grass soda) and three organosolv lignins. The reaction proceeds smoothly and the increase in solubility is visible to the naked eye. We then examine the reaction kinetics, and show that these are easily monitored qualitatively and quantitatively using UV/Vis spectroscopy. The UV/Vis results are validated with P-31 NMR spectroscopy of the lignin phenol groups after derivatization with phosphorylation reagent II. In general, the results are more significant with organosolv lignins, as Kraft and soda lignins are produced from aqueous lignocellulose extraction processes. |
| Databáze: | OpenAIRE |
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