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Tannin-immobilized cellulose was prepared by the phenolic reaction of the phenol ring of tannin with the aldehyde group of aldocellulose, where aldocellulose was prepared by the oxidization of cellulose with sodium periodate as oxidizing agent. The method of immobilized tannin is environmentally friendly due to the lack of crosslinking agent. The adsorption properties of cellulose were improved due to the introduction of tannin. The maximum adsorption capacity of the tannin-immobilized cellulose for berberine hydrochloride was 143.66 mg/g. The isothermal adsorption for berberine hydrochloride conformed to the Langmuir model well. The adsorption of tannin-immobilized cellulose for berberine hydrochloride was a weak chemical adsorption, and the adsorption process was exothermic. The adsorption equilibrium was reached within 90 min in the initial concentration 100 mg/L, and the sorption kinetics fitted well to a pseudo-first-order model. Tannin-immobilized cellulose has potential application prospect in the field of the separation and purification of alkaloids. [ABSTRACT FROM AUTHOR]

Cell surface display systems for immobilization of peptides and proteins on the surface of cells have various applications, such as vaccine generation, protein engineering, bio-conversion and bio-adsorption. Though plenty of methods have been established in terms of traditional yeast surface display systems, the development of a universal display method with high efficiency remains a challenge. Here we report an indirect yeast surface display method by anchoring Im7 proteins on the surface of P. pastoris, achieving highly efficient display of target proteins, including fluorescence proteins (sfGFP and mCherry) or enzymes (human Arginase I), with a CL7 fusion tag through the ultra-high-affinity interaction between Im7 and CL7. This indirect P. pastoris surface display approach is highly efficient and provides a robust platform for displaying biomolecules. [ABSTRACT FROM AUTHOR]