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通过聚合酶链反应和限制性片段长度多态性分析测定刺槐豆胶和瓜尔豆胶。

Determination of locust bean gum and guar gum by polymerase chain reaction and restriction fragment length polymorphism analysis.

作者信息

Meyer K, Rosa C, Hischenhuber C, Meyer R

机构信息

Nestec Ltd, Nestlé Research Center, Department of Quality and Safety Assurance, Vers-chez-les-Blanc, Lausanne, Switzerland.

出版信息

J AOAC Int. 2001 Jan-Feb;84(1):89-99.

Abstract

A polymerase chain reaction (PCR) was developed to differentiate the thickening agents locust bean gum (LBG) and the cheaper guar gum in finished food products. Universal primers for amplification of the intergenic spacer region between trnL 3' (UAA) exon and trnF (GAA) gene in the chloroplast (cp) genome and subsequent restriction analysis were applied to differentiate guar gum and LBG. The presence of <5% (w/w) guar gum powder added to LBG powder was detectable. Based on data obtained from sequencing this intergenic spacer region, a second PCR method for the specific detection of guar gum DNA was also developed. This assay detected guar gum powder in LBG in amounts as low as 1% (w/w). Both methods successfully detected guar gum and/or LBG in ice cream stabilizers and in foodstuffs, such as dairy products, ice cream, dry seasoning mixes, a finished roasting sauce, and a fruit jelly product, but not in products with highly degraded DNA, such as tomato ketchup and sterilized chocolate cream. Both methods detected guar gum and LBG in ice cream and fresh cheese at levels <0.1%.

摘要

已开发出一种聚合酶链反应(PCR),用于区分成品食品中的增稠剂刺槐豆胶(LBG)和价格较低的瓜尔豆胶。应用通用引物扩增叶绿体(cp)基因组中trnL 3'(UAA)外显子和trnF(GAA)基因之间的基因间隔区,并进行后续的限制性分析,以区分瓜尔豆胶和刺槐豆胶。能够检测出添加到LBG粉末中的瓜尔豆胶粉末含量是否<5%(w/w)。基于从该基因间隔区测序获得的数据,还开发了第二种用于特异性检测瓜尔豆胶DNA的PCR方法。该检测方法能检测出LBG中低至1%(w/w)的瓜尔豆胶粉末。这两种方法均成功检测出冰淇淋稳定剂以及乳制品、冰淇淋、干调味料混合物、成品烤肉酱和果冻产品等食品中的瓜尔豆胶和/或刺槐豆胶,但无法检测出DNA高度降解的产品中的瓜尔豆胶和刺槐豆胶,如番茄酱和灭菌巧克力奶油。这两种方法检测出冰淇淋和新鲜奶酪中的瓜尔豆胶和刺槐豆胶含量均<0.1%。

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