Lipase-catalysed acylation of starch and determination of the degree of substitution by methanolysis and GC

被引:38
作者
Alissandratos, Apostolos [1 ]
Baudendistel, Nina [2 ]
Flitsch, Sabine L. [3 ]
Hauer, Bernhard [2 ]
Halling, Peter J. [1 ]
机构
[1] Univ Strathclyde, Dept Pure & Appl Chem, WestCHEM, Glasgow G1 1XL, Lanark, Scotland
[2] BASF AG, Fine Chem & Biocatalysis Res, D-67056 Ludwigshafen, Germany
[3] Manchester Interdisciplinary Bioctr, Sch Chem, Manchester M1 7DN, Lancs, England
来源
BMC BIOTECHNOLOGY | 2010年 / 10卷
基金
英国工程与自然科学研究理事会;
关键词
ENZYMATIC MODIFICATION; REACTIVE EXTRUSION; ACETYLATION; ESTERS; ESTERIFICATION; ACETATES;
D O I
10.1186/1472-6750-10-82
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
Background: Natural polysaccharides such as starch are becoming increasingly interesting as renewable starting materials for the synthesis of biodegradable polymers using chemical or enzymatic methods. Given the complexity of polysaccharides, the analysis of reaction products is challenging. Results: Esterification of starch with fatty acids has traditionally been monitored by saponification and back-titration, but in our experience this method is unreliable. Here we report a novel GC-based method for the fast and reliable quantitative determination of esterification. The method was used to monitor the enzymatic esterification of different starches with decanoic acid, using lipase from Thermomyces lanuginosus. The reaction showed a pronounced optimal water content of 1.25 mL per g starch, where a degree of substitution (DS) of 0.018 was obtained. Incomplete gelatinization probably accounts for lower conversion with less water. Conclusions: Lipase-catalysed esterification of starch is feasible in aqueous gel systems, but attention to analytical methods is important to obtain correct DS values.
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页数:8
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