Characterisation of fractions obtained by isoamylolysis and ion-exchange chromatography of cationic waxy maize starch

被引:0
作者
Manelius, R
Maaheimo, H
Nurmi, K
Bertoft, E
机构
[1] Abo Akad Univ, Dept Biochem & Pharm, FIN-20521 Turku, Finland
[2] Univ Helsinki, VTT Biotechnol, FIN-00014 Helsinki, Finland
[3] Raisio Chem Oy, Raisio, Finland
来源
STARCH-STARKE | 2002年 / 54卷 / 02期
关键词
cationic starch; waxy maize starch; ion-exchange chromatography; isoamylolysis;
D O I
10.1002/1521-379X(200202)54:2<58::AID-STAR58>3.0.CO;2-1
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Isoamylase hydrolysates of wet- (WC) and dry-cationised (DC) waxy maize starch were fractionated by ion-exchange chromatography on CM-Sepharose into an unbound and four bound fractions. The amount of bound dextrins was higher in the WC than in the DC sample. The fractions were characterised by gel-permeation chromatography and proton-NMR spectroscopy. The unbound fraction from the WC sample consisted mainly of linear chains formed from amylopectin. The dextrins in the bound fractions contained increased amounts, from 1.2-7.9, of cationic substituents per molecule and the degree of polymerisation increased with the density of substituents. Dextrins weakly bound to CM-Sepharose had a linear structure, whereas more tightly bound fractions were mixtures of linear and branched dextrins. In the latter, the debranching was incomplete because of sterical hindrance by substituents at or close to the branch points. Most of the dextrins were partly hydrolysed by beta-amylase, but the more highly substituted fractions possessed also a population of beta-amylase resistant dextrins, suggesting substituents at the non-reducing ends.
引用
收藏
页码:58 / 65
页数:8
相关论文
共 50 条
[31]   Capillary ion-exchange chromatography with nanogram sensitivity for the analysis of monoclonal antibodies [J].
Rea, Jennifer C. ;
Freistadt, Benny S. ;
McDonald, Daniel ;
Farnan, Dell ;
Wang, Yajun Jennifer .
JOURNAL OF CHROMATOGRAPHY A, 2015, 1424 :77-85
[32]   Total plasma homocysteine as part of the routine aminogram by ion-exchange chromatography [J].
Briddon, A .
AMINO ACIDS, 1998, 15 (03) :235-239
[33]   A method for suppressing pH excursion during elution in ion-exchange chromatography [J].
Ghosh, Raja .
JOURNAL OF CHROMATOGRAPHY OPEN, 2024, 6
[34]   Predictive quantitative structure retention relationship models for ion-exchange chromatography [J].
C. B. Mazza ;
C. E. Whitehead ;
C. M. Breneman ;
S. M. Cramer .
Chromatographia, 2002, 56 :147-152
[35]   Peak intensity in ion-exchange chromatography with bulk-property detectors [J].
Watanabe, H ;
Sato, H .
ANALYTICAL SCIENCES, 1996, 12 (06) :859-867
[36]   ION-EXCHANGE AND AFFINITY-CHROMATOGRAPHY COSTS IN ALPHA-GALACTOSIDASE PURIFICATION [J].
PORTER, JE ;
LADISCH, MR .
BIOTECHNOLOGY AND BIOENGINEERING, 1992, 39 (07) :717-724
[37]   Optimization of gradient profiles in ion-exchange chromatography using computer simulation programs [J].
Drgan, Viktor ;
Kotnik, Darja ;
Novic, Marjana .
ANALYTICA CHIMICA ACTA, 2011, 705 (1-2) :315-321
[38]   Determination of Mannitol and Lactulose in Urine of Colorectal Cancer Patient by Ion-Exchange Chromatography [J].
Fu Xiao-Ling ;
Zhou Rong-Yao ;
Pan Guang-Wen .
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY, 2012, 40 (04) :608-611
[39]   Determination of acetic and formic acid in lead corrosion products by ion-exchange chromatography [J].
Edwards, R ;
Bordass, W ;
Farrell, D .
ANALYST, 1997, 122 (12) :1517-1520
[40]   Separation of butyltin and phenyltin species by ion-exchange chromatography with complexing mobile phases [J].
González-Toledo, E ;
Leal, C ;
Granados, M ;
Compaño, R ;
Prat, MD .
CHROMATOGRAPHIA, 2000, 51 (7-8) :443-449