4.7 Article

Broad specificity immunoassay for detection of Bacillus thuringiensis Cry toxins through engineering of a single chain variable fragment with mutagenesis and screening

期刊

出版社

ELSEVIER
DOI: 10.1016/j.ijbiomac.2017.09.058

关键词

Saturation mutagenesis; Cry protein; Generic specificity

资金

  1. National Natural Science Foundation of China [31401784, 31371778, 31401813]
  2. China Postdoctoral Science Foundation [2014M561604]
  3. Jiangsu Postdoctoral Science Foundation [1401015A]
  4. Natural Science Foundation of Jiangsu Province [BK20140744]
  5. Fundamental Research Funds for the Jiangsu Academy of Agricultural Sciences [ZX (15) 4052]

向作者/读者索取更多资源

The cultivation of genetically modified crops (GMCs) has greatly increased worldwide. Given the fact that over 10 Bacillus thuringiensis Cry toxins have been applied in GMCs, there is a need to develop an efficient and economically affordable detection method that simultaneously screen such compounds with similar structures in crops and foodstuff. Here we described an approach using a site-directed mutagenesis that enhances the generic specificity of single chain variable fragment (scFv). After three rounds of panning against mixed antigen (Cry1Ab, Cry1Ac, Cry1B, Cry1C and Cry1F) from the constructed mutagenesis library, one mutant showed greater ability to bind to a range of Cry toxins. The phage mutant, named D9, was cloned into pET26b expression vector, and then induced and purified. The mutant D9 was used to develop an indirect competitive immunoassay that sucessfully recognizes five targeted Cry1 toxins with a working range from 0.20 to 2.22 mu g mL(-1). The recoveries of five Cry toxins from spiked rice samples ranged from 86.67% to 96.67%, with a coefficient of variation less than 8%. The results suggest that the immunoassay based on a scFv is a promising approach for detection of Cry toxins with a broad specificity. (C) 2017 Published by Elsevier B.V.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据