Quantitative determination of bound water in wheat starch by time domain NMR spectroscopy

被引:95
作者
Le Botlan, D
Rugraff, Y
Martin, C
Colonna, P
机构
[1] Univ Nantes, Fac Sci, Lab Anal Isotop & Electrochim Metab, CNRS,UPRESA 06006, F-44322 Nantes, France
[2] INRA, Biochim & Technol Glucides Lab, F-44316 Nantes, France
关键词
wheat starch; bound water; NMR;
D O I
10.1016/S0008-6215(98)00068-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Above a water content of about 0.42 g per g of dry starch (DS), the Carr-Purcell-Meiboom-Gill (CPMG) relaxation-curve analysis of wheat starch-water suspensions shows two components. The intensity of the short component (T(2) approximate to 1.5 ms) corresponding to 'bound' water increases over the full hydration range studied from 0.55 to 0.9 g of water per g of DS. Assuming an intermediate exchange rate between 'weakly bound' and 'bound' water at 20 degrees C, a constant 'bound' water content of 0.170 +/- 0.008 g of water per g of DS has been obtained. The existence of a two-site exchange process has been argued to validate this amount of 'bound' water. This result takes into account the fact that about 7% of the starch gives a 'liquid-like' signal. A complete treatment of the FID signal (solid and liquid parts) allowed us to determine the signal in arbitrary units per atom g of hydrogen present in the samples. Thus, we have been able to transpose the signal obtained by a relaxation curves analysis (in arbitrary units), to grams of water. This 'bound' water, determined through NMR CPMG sequence, would correspond to a bilayer of water. The concept of 'potentially free' water has been introduced to explain the lack of noticeable 'weakly bound' water by a CPMG sequence in the range of 0.17-0.42 g water content. The NMR data are discussed in relation to similar measurements made on sorption curves and in relation to plasticization. Overall, the concept of several populations of water molecules presenting different mobilities is reinforced. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:29 / 36
页数:8
相关论文
共 38 条
[11]  
DINOLA A, 1983, J FOOD TECHNOL, V18, P125
[12]  
FRENCH D, 1981, STARCH CHEM TECHNOLO, P183
[13]   PROTON NUCLEAR-MAGNETIC-RESONANCE RELAXATION RATES IN AQUEOUS-SOLUTIONS OF AMINO-ACIDS [J].
GRUCKER, D ;
STEIBEL, J ;
MAUSS, Y ;
DUMITRESCO, B ;
ARMSPACH, JP ;
CHAMBRON, J .
MOLECULAR PHYSICS, 1990, 70 (05) :903-919
[14]   THE DOUBLE-HELICAL NATURE OF THE CRYSTALLINE PART OF A-STARCH [J].
IMBERTY, A ;
CHANZY, H ;
PEREZ, S ;
BULEON, A ;
TRAN, V .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 201 (02) :365-378
[15]   O-17 NUCLEAR-MAGNETIC-RESONANCE STUDIES OF WATER MOBILITY DURING BREAD STALING [J].
KIMSHIN, MS ;
MARI, F ;
RAO, PA ;
STENGLE, TR ;
CHINACHOTI, P .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1991, 39 (11) :1915-1920
[16]   WATER ORGANIZATION AND MOLECULAR MOBILITY IN MAIZE STARCH INVESTIGATED BY 2-DIMENSIONAL SOLID-STATE NMR [J].
KULIK, AS ;
DECOSTA, JRC ;
HAVERKAMP, J .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1994, 42 (12) :2803-2807
[17]   LOW-FIELD NUCLEAR-MAGNETIC-RESONANCE RELAXATION STUDY OF STORED OR PROCESSED COD [J].
LAMBELET, P ;
RENEVEY, F ;
KAABI, C ;
RAEMY, A .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1995, 43 (06) :1462-1466
[18]   LOW RESOLUTION NMR-SPECTROSCOPY - A TOOL TO STUDY PROTEIN DENATURATION .1. APPLICATION TO DIAMAGNETIC WHEY PROTEINS [J].
LAMBELET, P ;
BERROCAL, R ;
DUCRET, F .
JOURNAL OF DAIRY RESEARCH, 1989, 56 (02) :211-222
[19]   PULSED LOW-RESOLUTION NMR INVESTIGATIONS OF PROTEIN SOLS AND GELS [J].
LAMBELET, P ;
BERROCAL, R ;
DESARZENS, C ;
FROEHLICHER, I ;
DUCRET, F .
JOURNAL OF FOOD SCIENCE, 1988, 53 (03) :943-&
[20]   180 degrees pulse imperfection effects on fitting of relaxation curves obtained by low field NMR spectroscopy [J].
LeBotlan, D ;
Rugraff, Y ;
Ouguerram, L .
SPECTROSCOPY LETTERS, 1996, 29 (06) :1091-1102