Pektyny – występowanie, budowa chemiczna i właściwości

Journal Title: Wiadomości Chemiczne - Year 2014, Vol 68, Issue 7

Abstract

Pectins are important polysaccharide structure constituents of plant middle lamellae and primary cell walls ensuring their water retention performance and the pH stability [1, 11]. Due to the high gelling, stabilising and thickening properties they are widely used in the food and pharmaceutical industry [3, 9]. Commercial pectin substances are extracted from the waste material, especially citrus peels (from orange, grapefruit, lemon and lime fruit), apple pomace and sugar beet pulp. The high concentration of pectins is found also in other fruits and vegetables, mainly soy hull, mango peels and sunflower heads [3, 11, 12, 14]. The properties of pectins result mainly from their chemical structure. The pectin backbone is primarily composed of homogalacturonan (Fig. 1), which is a linear polymer consisting of α-1→4-linked d-galacturonic acid units, partially methylesterified or O-acetylated [3, 9]. Other structural elements of pectins are rhamnogalacturonan type I (Fig. 2) and type II (Fig. 3), xylogalacturonan (Fig. 5), arabinan (Fig. 6), arabinogalactan type I (Fig. 7) and type II (Fig. 8) [3, 5, 8]. The gelling property of pectins depends on the degree of methyl esterification of their carboxyl groups (DE). According to this parameter there are high ester pectins (DE > 50) and low ester pectins (DE < 50). The high ester pectins form gels in the presence of high sugar concentrations exceeding 55% and pH lower than 3.5, while in the case of low ester pectins the gelation process occurs even at low concentrations of sugar but the presence of divalent ions is required (e.g. calcium) [18, 21]. The aim of this study was a review of the available literature regarding the sources of pectins, their types, chemical structure and physicochemical properties.

Authors and Affiliations

Hanna Pińkowska, Adrianna Złocińska

Keywords

Related Articles

Wykorzystanie reakcji 1,3-dipolarnej cykloaddycji Huisgena do modyfikacji nukleozydów i ligonukleotydów

The 1,3-dipolar cycloaddition reaction between azides and terminal alkynes, known as the Huisgen reaction, constitutes a powerful tool for the synthesis of versatile molecules containing carbon – heteroatom bond. The use...

Aktywność biologiczna pochodnych 2,7-naftyrydyny

2,7-Naphthyridine is one of the six structural isomers of pyridopyridines. More than one hundred years ago, Gabriel and Colman discovered the isomer 2,7-naphthyridine, and named it “copiryne” [3]. From among of all napht...

Zastosowania biologiczne tetrazoli i ich pochodnych

Due to the wide range of applications of tetrazoles, in recent years the number of publications and patents describing the synthesis, structural and physicochemical studies of compounds that contain tetrazole fragments i...

Nitroksyl (HNO/NO-) - cząsteczka o potencjalnym znaczeniu farmakologicznym

Nitrogen compounds, as an essential component of many reactions occurring in living organisms, become the object of an extensive research. These compounds became the focus of interest after the properties of nitric oxide...

Kwasy nukleinowe jako katalizatory reakcji chemicznych

Nucleic acids, due to their specific structure, are effective and durable carriers of genetic information. They have also been used as catalysts in chemical reactions. The right-handed DNA double helix structure has beco...

Download PDF file
  • EP ID EP585261
  • DOI -
  • Views 124
  • Downloads 0

How To Cite

Hanna Pińkowska, Adrianna Złocińska (2014). Pektyny – występowanie, budowa chemiczna i właściwości. Wiadomości Chemiczne, 68(7), 683-700. https://europub.co.uk/articles/-A-585261