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Evaluation of existing guidelines for their adequacy for the molecular characterisation and environmental risk assessment of genetically modified plants obtained through synthetic biology

机译:通过合成生物学获得的分子特征和环境风险评估对现有准则的评价

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Synthetic Biology (SynBio) is an interdisciplinary field at the interface of engineering and biology aiming to develop new biological systems and impart new functions to living cells. EFSA has been asked by the European Commission to evaluate SynBio developments in agri‐food with the aim of identifying the adequacy of existing guidelines for risk assessment and determine if updated guidance is needed. The scope of this opinion covers the molecular characterisation and environmental risk assessment of such genetically modified plants obtained through SynBio, meant to be for cultivation or food and feed purposes. The previous work on SynBio by the non‐food scientific Committees (2014, 2015) was used and complemented with the output of a horizon scanning exercise, which was commissioned by the EFSA to identify the most realistic and forthcoming SynBio cases of relevance to this remit. The horizon scan did not identify other sectors/advances in addition to the six SynBio categories previously identified by the non‐food scientific committees of the European Commission. The exercise did show that plant SynBio products reaching the market in the near future (next decade) are likely to apply SynBio approaches to their development using existing genetic modification and genome editing technologies. In addition, three hypothetical SynBio case studies were selected by the working group of the Panel on Genetically Modified Organisms (GMO), to further support the scoping exercise of this Scientific Opinion. Using the selected cases, the GMO Panel concludes that the requirements of the EU regulatory framework and existing EFSA guidelines are adequate for the risk assessment of SynBio products to be developed in the next 10 years, although specific requirements may not apply to all products. The GMO Panel acknowledges that as SynBio developments evolve, a need may exist to adjust the guidelines to ensure they are adequate and sufficient.
机译:合成生物学(Synbio)是工程和生物学界面的跨学域,旨在开发新的生物系统并将新功能赋予活细胞。 EFSA已被欧洲委员会询问,以评估农业食品中的Synbio发展,目的是确定现有风险评估指南的充分性,并确定是否需要更新的指导。该意见的范围涵盖通过Synbio获得的这种遗传修饰植物的分子表征和环境风险评估,意味着用于培养或食物和饲料目的。以前的非食品科学委员会(2014年,2015年)对Synbio的工作被使用并补充了地平线扫描运动的产出,由EFSA委托,以确定最逼真的,即将与此汇款相关的综合征案件。除欧盟委员会非食品科学委员会以前确定的六个Synbio类别之外,地平线扫描还没有识别其他部门/进步。练习确实表明,在不久的将来(未来十年)中达到市场的植物Synbio产品可能会使用现有的遗传修改和基因组编辑技术应用Synbio方法。此外,基因改性生物(GMO)小组的工作组选择了三种假设的Synbio案例研究,以进一步支持这种科学意见的范围行使。使用所选案例,GMO面板的结论是,欧盟监管框架和现有EFSA指南的要求对于未来10年内开发的Synbio产品的风险评估是充足的,尽管具体要求可能不适用于所有产品。 GMO小组承认,随着Synbio的发展发展,可能存在需要调整指南,以确保它们足够且充分。
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