Pleurotus ostreatus lectin (POL) is derived from the fruiting body of edible oyster mushrooms and belongs to Fungal Lectin. It is a dimer of molecular weight 80 kDa consisting of two polypeptide chains and disulfide bonds. Each domain of POL contains carbohydrate binding sites since calcium. Notably, POL specifically recognizes galactose residues and is tightly associated with galactosidase activity. The binding effect of POL and carbohydrates is closely related to its 3D structure. Therefore, CD BioGlyco provides a series of services, such as POL extraction, separation, and identification, to accelerate the client's project progress in lectin research.
All the oyster mushrooms are harvested at the mushroom hothouse to ensure freshness. Each step is performed at 4°C. The fruiting bodies are homogenized with water and extracted with stirring. The suspension is centrifuged and the supernatant, as well as sediment, are gathered in isolation. The supernatant lyophilized powder is dissolved in a buffer. Then purified using an agarose gel column. During the washout process, collect tube by tube. All fractions are freeze-dried and reconstituted, followed by the addition of solid ammonium sulfate and centrifugation to collect the precipitate. Redissolve in distilled water and dialyze. The target components are collected after a secondary purification using an affinity chromatography column. The fractions are dialyzed with distilled water and lyophilized to obtain high-purity POL.
The development of its functionality and application characteristics requires a thorough analysis of the POL. For purified POL, we provide precise analysis services to clients. Our professional team has a wealth of proven experience, so feel free to leave your samples in our hands!
Fig.1 Schematic diagram of POL analysis services. (CD BioGlyco)
Paper Title: Structure and properties of the oyster mushroom (Pleurotus ostreatus) lectin (POL)
Journal: Glycobiology
IF: 5.594
Published: 2020
Results: Detection of 14 species of mushrooms showed the strongest food intake inhibitory activity. It was a single band of 40 kDa as shown by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) but had a natural molecular weight of 80 kDa and the surface POL was a dimer. Matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF-MS) treatment confirmed the cation dependence of POL, and all cations such as calcium, manganese, and zinc had a role in their recovery activity.
Fig.2 Stereoscopic view of the hydrogen bonding network in a complex. (Perduca, et al., 2020)
CD BioGlyco provides Lectin Production Services and reliable data supported by a team of specialists. We emphasize the quality of natural products, and all extraction and separation services are carried out under strict conditions. Please feel free to contact us.
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