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α-D-Manp-(1->2)-α-D-Manp is a disaccharide composed of two α-D-mannopyranose (α-D-Manp) units linked together through a glycosidic bond. In this specific structure, the linkage is between the C1 hydroxyl group of the first α-D-mannopyranose and the C2 hydroxyl group of the second α-D-mannopyranose. This disaccharide is an important component in various biological systems, particularly in the formation of complex carbohydrates and glycoconjugates, which play crucial roles in cell recognition, signaling, and immune responses. The α-D-Manp-(1->2)-α-D-Manp structure is also found in some plant polysaccharides and can be a target for enzymatic reactions in metabolic pathways.

50271-62-0

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50271-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50271-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,2,7 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 50271-62:
(7*5)+(6*0)+(5*2)+(4*7)+(3*1)+(2*6)+(1*2)=90
90 % 10 = 0
So 50271-62-0 is a valid CAS Registry Number.

50271-62-0Downstream Products

50271-62-0Relevant academic research and scientific papers

Large Scale Production of Recombinant α-1,2-Mannosyltransferase from E. coli for the Study of Acceptor Specificity and Use of the Recombinant Whole Cells in Synthesis

Herrmann, Guido F.,Wang, Peng,Shen, Gwo-Jenn,Garcia-Junceda, Eduardo,Khan, Shaheer H.,et al.

, p. 6356 - 6362 (1994)

We report the first large scale heterologous expression of a recombinant yeast α-1,2-mannosyltransferase in E. coli.The enzyme was isolated from 10-L and 50-L fermentations, purified and used for mannosylation reactions.The specificity of the recombinant enzyme was extensively studied by using mannose derivatives, oligosaccharides, and analogs as acceptors, and the results show that the enzyme exhibits high activities toward ManOMe and disaccharides connected by an α-1,2-mannosidic linkage.The recombinant E. coli cells were also used as a catalyst for glycosylation reaction, and mannosylation of saccharides and glycopeptides proceeded in moderate to good yields.

The extracellular polysaccharide of Pichia (Hansenula) holstii NRRLL Y-2448: The phosphorylated side chains

Parolis, Lesley A.S.,Parolis, Haralambos,Kenne, Lennart,Meldal, Morten,Bock, Klaus

, p. 77 - 87 (1998)

The exopolysaccharide produced by Pichia (Hansenula) holstii NRRL Y-2448 is composed of a phosphomannan core to which oligosaccharide diester phosphate side chains are appended. The oligosaccharides of the side chains were released as oligosaccharide phosphates and neutral oligosaccharides by mild hydrolysis with aqueous acetic acid and aqueous hydrogen fluoride, respectively. The liberated oligosaccharide phosphates were studied by NMR spectroscopy and by electrospray and fast atom bombardment mass spectrometry. The structures of the neutral oligosaccharides were determined by 1D and 2D NMR spectroscopic experiments. Further insight into the length of the side chains was obtained from a matrix assisted laser desorption ionisation-time of night mass spectrometric study of high and low molecular weight fragments obtained from partial acid hydrolysis of the native polysaccharide.

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