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Related Concept Videos

Oligosaccharide Assembly01:24

Oligosaccharide Assembly

Protein glycosylation starts in the ER lumen and continues in the Golgi apparatus. Glycosyltransferases catalyze the addition of sugar molecules or glycosylation of proteins. Usually, these enzymes add sugars to the hydroxyl groups of selected serine or threonine residues to form O-linked glycans or the amino groups of asparagine residues to form N-linked glycans. Different positions on the same polypeptide chain can contain differently linked glycans.
Multiple sugar molecules that may or may...
Proteoglycans01:05

Proteoglycans

Glycans, a class of complex heterogeneous molecules, can be covalently attached to proteins to form glycosylated proteins that regulate various physiological and pathological processes. Glycosylated proteins or glycoproteins comprise N-linked and O-linked oligosaccharides. O-glycosylation is the most common type of protein glycosylation. Here, glycans attach to the oxygen atom of the hydroxyl groups of Serine or Threonine residues. O-linked glycosylation occurs later in protein processing,...
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Biosynthesis of Polysaccharides

Polysaccharides such as glycogen and starch are synthesized from nucleoside diphosphate sugars, primarily uridine diphosphate glucose (UDPG) and adenosine diphosphate glucose (ADPG). These activated glucose donors act as key intermediates in carbohydrate metabolism and biosynthesis. UDPG primarily involves glycogen synthesis in animals and many bacteria, while ADPG plays a fundamental role in starch synthesis in plants and certain bacteria.UDPG is formed when glucose-1-phosphate reacts with...
Cellulose and Pectic Polysaccharides01:15

Cellulose and Pectic Polysaccharides

Every plant cell has a cell wall that protects the cell, provides structural support, and gives the cell shape. Cellulose, the main structural component of the plant cell wall, makes up over 30% of plant matter. It is the most abundant organic compound on earth.  Cellulose is an unbranched polysaccharide composed of linear chains of glucose molecules linked by β (1→4) glycosidic bonds.
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Oral Hypoglycemic Agents: α-Glucosidase Inhibitors

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Glycosaminoglycans

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Comparative Study on the Polysaccharide Contents and Antioxidant Activities of Hippophae rhamnoides subsp. sinensis and Hippophae gyantsensis
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New acylated oligosaccharides from Pistacia integerrima.

Zia Ullah1, Rashad Mehmood, Muhammad Imran

  • 1a Department of Chemistry , University of Karachi , Karachi , 75270 , Pakistan.

Natural Product Research
|August 3, 2013
PubMed
Summary

Two novel acylated oligosaccharides, Integrisides A and B, were identified in Pistacia integerrima. Their chemical structures were determined using advanced spectroscopic methods and hydrolysis.

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Area of Science:

  • Natural Product Chemistry
  • Phytochemistry
  • Organic Chemistry

Background:

  • Pistacia integerrima is a plant species with a history of traditional medicinal use.
  • The chemical constituents of P. integerrima are not fully characterized, presenting opportunities for novel compound discovery.

Purpose of the Study:

  • To isolate and characterize new chemical entities from Pistacia integerrima.
  • To elucidate the structures of novel acylated oligosaccharides.

Main Methods:

  • Extraction of aerial parts of Pistacia integerrima using methanol.
  • Fractionation of the methanolic extract, focusing on the n-butanol-soluble sub-fraction.
  • Isolation of compounds using chromatographic techniques.
  • Structure elucidation employing spectroscopic methods (e.g., NMR, MS) and chemical hydrolysis.

Main Results:

  • Two new acylated oligosaccharides, designated Integriside A (1) and Integriside B (2), were successfully isolated.
  • The structures of Integrisides A and B were fully determined through comprehensive spectroscopic analysis and hydrolysis data.

Conclusions:

  • The study successfully identified and characterized two novel acylated oligosaccharides from Pistacia integerrima.
  • The findings contribute to the phytochemical knowledge of Pistacia integerrima and introduce new molecular structures for potential further investigation.