Pectin depolymerase [Pectic enzymes] activities associated with cell walls from Cicer arietinum L. epicotyl

The hydrolytic activity of the proteins extracted with 3 M LiCl from chick-pea (Cicer arietinum) cell walls to pectic fractions extracted with 50 mM trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid (CDTA) and 50 mM sodium carbonate was studied. The pectic fractions contained acidic...

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Published inPlant and cell physiology Vol. 38; no. 11; pp. 1259 - 1263
Main Authors Sevillano, J.M. (Universidad de Leon (Spain)), Zarra, I, Acebes, J.L
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 1997
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Abstract The hydrolytic activity of the proteins extracted with 3 M LiCl from chick-pea (Cicer arietinum) cell walls to pectic fractions extracted with 50 mM trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid (CDTA) and 50 mM sodium carbonate was studied. The pectic fractions contained acidic polysaccharides with high molecular mass (higher than 5 x 10(3) kDa), mainly composed of uronic acids, galactose, arabinose and rhamnose. The extracted proteins depolymerized the pectic polysaccharides and also a commercial preparation of polygalacturonic acid from citrus, detected by a decrease in their viscosity and a shift of their molecular mass distribution. The extract was able to depolymerize a uronic acid-rich component in all the cases, although in different extent. Also, with regard to the CDTA-soluble pectins, a degradation of polyuronide and a shift of the molecular mass distribution of arabinogalactan was observed
AbstractList The hydrolytic activity of the proteins extracted with 3 M LiCl from chick-pea (Cicer arietinum) cell walls to pectic fractions extracted with 50 mM trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid (CDTA) and 50 mM sodium carbonate was studied. The pectic fractions contained acidic polysaccharides with high molecular mass (higher than 5 x 10(3) kDa), mainly composed of uronic acids, galactose, arabinose and rhamnose. The extracted proteins depolymerized the pectic polysaccharides and also a commercial preparation of polygalacturonic acid from citrus, detected by a decrease in their viscosity and a shift of their molecular mass distribution. The extract was able to depolymerize a uronic acid-rich component in all the cases, although in different extent. Also, with regard to the CDTA-soluble pectins, a degradation of polyuronide and a shift of the molecular mass distribution of arabinogalactan was observed
The hydrolytic activity of the proteins extracted with 3 M LiCl from chick-pea (Cicer arietinum) cell walls to pec-tic fractions extracted with 50 mM trans-l,2-diaminocy-clohexane-N,N,N,N,-tetraacetic acid (CDTA) and 50 mM sodium carbonate was studied. The pectic fractions contained acidic polysaccharides with high molecular mass (higher than 5 × 103 kDa), mainly composed of uronic acids, galac-tose, arabinose and rhamnose. The extracted proteins depo-lymerized the pectic polysaccharides and also a commercial preparation of polygalacturonic acid from citrus, detected by a decrease in their viscosity and a shift of their molecular mass distribution. The extract was able to depolymerize a uronic acid-rich component in all the cases, although in different extent. Also, with regard to the CDTA-soluble pectins, a degradation of polyuronide and a shift of the molecular mass distribution of arabinogalactan was observed.
The hydrolytic activity of the proteins extracted with 3 M LiCl from chick-pea (Cicer arietinum) cell walls to pectic fractions extracted with 50 mM trans-1,2-diaminocyclohexane-N,N,N,N-tetraacetic acid (CDTA) and 50 mM sodium carbonate was studied. The pectic fractions contained acidic polysaccharides with high molecular mass (higher than 5 x 10(3) kDa), mainly composed of uronic acids, galactose, arabinose and rhamnose. The extracted proteins depolymerized the pectic polysaccharides and also a commercial preparation of polygalacturonic acid from citrus, detected by a decrease in their viscosity and a shift of their molecular mass distribution. The extract was able to depolymerize a uronic acid-rich component in all the cases, although in different extent. Also, with regard to the CDTA-soluble pectins, a degradation of polyuronide and a shift of the molecular mass distribution of arabinogalactan was observed.
Author Zarra, I
Acebes, J.L
Sevillano, J.M. (Universidad de Leon (Spain))
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Issue 11
Keywords Enzyme
Pectin
Polygalacturonase
Cell wall
Hydrolysis
Leguminosae
Enzymatic activity
Cicer arietinum
Dicotyledones
Glycosidases
Angiospermae
Hydrolases
Isolation
Spermatophyta
O-Glycosidases
Polysaccharide
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Snippet The hydrolytic activity of the proteins extracted with 3 M LiCl from chick-pea (Cicer arietinum) cell walls to pectic fractions extracted with 50 mM...
The hydrolytic activity of the proteins extracted with 3 M LiCl from chick-pea (Cicer arietinum) cell walls to pec-tic fractions extracted with 50 mM...
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StartPage 1259
SubjectTerms Arabinogalactan
arabinose
Biological and medical sciences
Cell wall
cell wall components
CELL WALLS
CICER ARIETINUM
enzyme activity
Enzymes
epicotyls
Fundamental and applied biological sciences. Psychology
galactans
galactose
GLICOSIDASAS
GLYCOSIDASE
GLYCOSIDASES
hydrolysis
Metabolism
PARED CELULAR
PAROI CELLULAIRE
Pectin
Pectin-depolymerase
PECTINAS
PECTINE
PECTINS
Plant physiology and development
polygalacturonase
polymerization
Polyuronide
polyuronides
protein composition
rhamnose
uronic acids
Title Pectin depolymerase [Pectic enzymes] activities associated with cell walls from Cicer arietinum L. epicotyl
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