Inclusion of tributyrin during enzymatic synthesis of cyclodextrins by β-cyclodextrin glycosyltransferase from Bacillus circulans

Supplementing tributyrin to cottonseed protein concentrate‐based diets can improve growth performance, lipid metabolism and distal intestinal immunity in hybrid grouper ( Epinephelus fuscoguttatus ♀ × Epinephelus lanceolatus ♂)

“…Tributyrin is a lipid substance produced from three molecules of butyric acid and one molecule of glycerol catalysed by sulfuric acid and is a precursor substance of butyric acid (Li et al, 2020). Compared with the traditional butyrate, tributyrin is characterized by slow release at a fixed point in the distal intestine after passing through the stomach, performs the corresponding physiological functions, and will not react with acidic gastric juice to produce harmful substances (Jin, 2018;Wu, 2019).…”

Supramolecular recognition enhanced electrochemical sensing: β-cyclodextrin and Pd nanoparticle co-decorated 3D reduced graphene oxide nanocomposite-modified glassy carbon electrode for the quantification of ractopamine

“…These obvious proton shifts of the host and guest molecules provide clear evidences for effective recognition between β-CD and RAC. 32,34…”

“…β-CD, RAC, and their aggregates were dissolved in D 2 O and NMR hydrogen spectra were recorded using an Ascend 400 MRI. The chemical displacement (Δ δ ) was calculated as follows: 34 Δ δ = δ (complex) − δ (free)…”

Preparation of phillyrin/cyclodextrin inclusion complexes and study of their physical properties, solubility enhancement, molecular docking and antioxidant activity

“…From the figure, it can be seen that the chemical shifts of the protons on the benzene ring of phillyrin such as H-5 and H-5 0 in the phillyrin/ CDs inclusion complex are shifted from d 6.933 to d 6.916 , Dd = À0.017. This indicates that there is an interaction between phillyrin and CDs, 41 but Dd r 0.02 for all inclusion complexes, which indicates that phillyrin interacts weakly with CDs. 31 Since the host and visitor molecules interact non-covalently, there may not have been a noticeable change in chemical shift.…”