Gelation by phase separation in a whey protein system: in-situ kinetics of aggregation

被引:15
作者
Renard, D
Robert, P
Garnier, C
Dufour, E
Lefebvre, J
机构
[1] INRA, Ctr Rech, Unite Phys Chim Macromol, F-44316 Nantes 3, France
[2] ENITA, Dept Qual & Econ Alimentaires, F-63370 Clermont Ferrand, Lempdes, France
关键词
beta-lactoglobulin; kinetics; gelation; phase separation;
D O I
10.1016/S0168-1656(00)00240-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The aggregation and gelation properties of beta-lactoglobulin (BLG), a globular protein from milk, was studied in aqueous ethanol solutions at room temperature. The phase state diagrams as a function of pH and ethanol concentration showed that a gel structure appeared after a period ranging from 1 min to 1 week, depending on the physico-chemical conditions. The in-situ kinetics of aggregation were followed by several methods in order to obtain a better understanding of the building of aggregates by the addition of ethanol. It was shown that the aggregation kinetics highly depended upon the pH, the process being fastest at pH 7. Viscoelasticity and infrared measurements indicated that alcohol-induced gelation would proceed via a two-step mechanism: small aggregates loosely connected between them were first built up; a real network took place in a second step. The coarse and irregular structures formed in aqueous ethanol gels revealed by confocal laser scanning microscopy could be analysed in terms of a phase separation. This observation was supported by a syneresis phenomenon visible in the final gel state. BLG in water-ethanol solution would undergo either an inhibition of the demixing by gelation or a binary phase separation accompanied by an irreversible gelation transition. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:231 / 244
页数:14
相关论文
共 55 条
[1]   Kinetic refolding of β-lactoglobulin.: Studies by synchrotron X-ray scattering, and circular dichroism, absorption and fluorescence spectroscopy [J].
Arai, M ;
Ikura, T ;
Semisotnov, GV ;
Kihara, H ;
Amemiya, Y ;
Kuwajima, K .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 275 (01) :149-162
[2]   The effect of temperature and ionic strength on the dimerisation of beta-lactoglobulin [J].
Aymard, P ;
Durand, D ;
Nicolai, T .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 1996, 19 (03) :213-221
[3]   EFFECTS OF GELATION ON SPINODAL DECOMPOSITION KINETICS IN GELATIN [J].
BANSIL, R ;
LAL, J ;
CARVALHO, BL .
POLYMER, 1992, 33 (14) :2961-2969
[4]   FACTORS AFFECTING MOLECULAR CHARACTERISTICS OF WHEY-PROTEIN GELATION [J].
BOYE, JI ;
ALLI, I ;
ISMAIL, AA ;
GIBBS, BF ;
KONISHI, Y .
INTERNATIONAL DAIRY JOURNAL, 1995, 5 (04) :337-353
[5]  
BROWN WD, 1985, J PHYS A, V18, P517
[6]   REVERSIBLE AND IRREVERSIBLE MODIFICATIONS OF BETA-LACTOGLOBULIN UPON EXPOSURE TO HEAT [J].
CAIROLI, S ;
IAMETTI, S ;
BONOMI, F .
JOURNAL OF PROTEIN CHEMISTRY, 1994, 13 (03) :347-354
[7]   STRUCTURAL AND CONFORMATIONAL-CHANGES OF BETA-LACTOGLOBULIN-B - AN INFRARED SPECTROSCOPIC STUDY OF THE EFFECT OF PH AND TEMPERATURE [J].
CASAL, HL ;
KOHLER, U ;
MANTSCH, HH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 957 (01) :11-20
[8]  
Clark AH, 1995, BIOPOLYMER MIXTURES, P37
[9]   BETA-LACTOGLOBULIN BINDING-PROPERTIES DURING ITS FOLDING CHANGES STUDIED BY FLUORESCENCE SPECTROSCOPY [J].
DUFOUR, E ;
GENOT, C ;
HAERTLE, T .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 1994, 1205 (01) :105-112
[10]   ALCOHOL-INDUCED CHANGES OF BETA-LACTOGLOBULIN RETINOL-BINDING STOICHIOMETRY [J].
DUFOUR, E ;
HAERTLE, T .
PROTEIN ENGINEERING, 1990, 4 (02) :185-190