A rapid analytical method using loop-mediated isothermal amplification (LAMP): visual detection of cry1Ab gene in genetically modified maize seeds and food products.
IF 2.5 4区 生物学Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Monika Singh, Shiwani, Kushaldeep Kaur, Divyaditya Awasthi, Amit Kumar Singh
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引用次数: 0
Abstract
Insect resistance is a predominant trait in the globally approved genetically modified (GM) crops. The cry1Ab transgene is featured in over 25% of globally approved insect resistant GM events including both single as well as stacked trait events. GM maize notably contributes for 87% among the approved GM events with cry1Ab gene. GM detection of cry1Ab gene in maize seeds and food products is important for authentication purpose in the countries where GM maize events with cry1Ab gene such as Bt11, Bt176, MON810 are approved, and for surveillance of unauthorized occurrence of such events in the countries where these are not approved. Cost-efficient and rapid GM detection methods are essential for decentralized monitoring for unauthorized GM events across agricultural fields, border inspections, and food supply chains, and for regulatory compliance enabling quick decision-making. A rapid GM detection method employing loop-mediated isothermal amplification (LAMP) was developed for visual analysis of cry1Ab gene in GM maize. The developed assay showed acceptable specificity, which could reliably detect as low as 0.005% of cry1Ab within 60 min. Practical applicability of this assay was also verified for GM detection in maize containing products. The developed method offers a convenient, rapid and cost-effective tool for checking the cry1Ab gene either for regulatory purpose in the countries where the GM crops with cry1Ab gene are restricted or for confirmatory purpose for the samples with cry1Ab gene whenever required.
期刊介绍:
Biotechnology Letters is the world’s leading rapid-publication primary journal dedicated to biotechnology as a whole – that is to topics relating to actual or potential applications of biological reactions affected by microbial, plant or animal cells and biocatalysts derived from them.
All relevant aspects of molecular biology, genetics and cell biochemistry, of process and reactor design, of pre- and post-treatment steps, and of manufacturing or service operations are therefore included.
Contributions from industrial and academic laboratories are equally welcome. We also welcome contributions covering biotechnological aspects of regenerative medicine and biomaterials and also cancer biotechnology. Criteria for the acceptance of papers relate to our aim of publishing useful and informative results that will be of value to other workers in related fields.
The emphasis is very much on novelty and immediacy in order to justify rapid publication of authors’ results. It should be noted, however, that we do not normally publish papers (but this is not absolute) that deal with unidentified consortia of microorganisms (e.g. as in activated sludge) as these results may not be easily reproducible in other laboratories.
Papers describing the isolation and identification of microorganisms are not regarded as appropriate but such information can be appended as supporting information to a paper. Papers dealing with simple process development are usually considered to lack sufficient novelty or interest to warrant publication.