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1.
我国转基因水稻商品化应用的潜在环境生物安全问题   总被引:4,自引:1,他引:3  
转基因水稻的研发和商品化应用将为提高我国水稻的生产力提供新的机遇,并缓解我国的粮食安全问题.转基凶水稻的人规模环境释放和商品化生产可能会带来一定的环境生物安全问题,处理不好会影响转基因水稻的进一步研究和发展.通常所指的环境生物安全问题主要包括以下几个方面:(1)抗生物胁迫转基因对非靶标生物的影响及效应;(2)外源基因向非转基因作物和野生近缘种逃逸及其可能带来的生态后果;(3)转基因作物对农业生态系统、土壤微生物以及生物多样性的潜在影响;(4)抗生物胁迫转基因的长期使用导致靶标生物对转基因产生抗性等.为了安全有效和持续利用转基因生物技术及其产品,有必要对转基因水稻的环境生物安全性进行科学评价.基于风险评价的原则,本文对转基因水稻在我国商品化生产和大规模种植可能带来的环境生物安全问题进行了理性分析,希望为我国转基因水稻商品化应用的决策和生物安全评价提供科学依据.  相似文献   

2.
卢宝荣  夏辉 《生命科学》2011,(2):186-194
转基因作物的商品化生产和大规模环境释放在带来巨大利益的同时,也引起了全球对其生物安全问题的广泛关注和争议,其中转基因通过花粉介导的基因漂移逃逸到非转基因作物及其野生近缘种,进而导致的潜在环境和生态风险就是备受争议的生物安全问题之一。转基因植物的环境生物安全涉及两方面关键问题:如何科学评价转基因植物商品化种植以后带来的环境和生态影响;如何利用环境生物安全的研究成果来制定科学有效的风险监测和管理措施。对转基因逃逸及其潜在生态风险的科学评价应包括三个重要环节:(1)检测转基因的逃逸的频率;(2)检测转基因逃逸后的表达和遗传规律;(3)确定逃逸后的转基因对野生近缘种群体适合度的影响及其进化潜力,本文将围绕对转基因逃逸及其潜在环境风险的科学评价,以转基因水稻为案例来对转基因逃逸带来生态影响的研究好评价的进展进行简要介绍,并对目前依据风险评价研究成果制定的各种管理策略进行了讨论。只有提高对转基因生物环境安全研究和评价的水平,并制定有效的风险监测和管理措施,才能为我国转基因技术的发展和转基因产品的商品化应用保驾护航。  相似文献   

3.
澳大利亚是世界上重要的农产品生产国和出口国,本文对澳大利亚转基因生物安全监管从基因工程安全管理立法历程、转基因监管体系及职责、转基因日常监管与执法、转基因标识管理、生物育种新技术研究和监管等方面进行了综述。以澳大利亚转基因生物安全管理经验为启示,结合我国转基因生物安全管理的现状,提出如下建议:对我国现有转基因管理体系、法规制度体系和技术支撑体系等进行完善,严格监管执法,落实相关责任,提高公众参与度、加大信息公开力度,并尽快明确基因编辑等生物育种新技术的监管原则。  相似文献   

4.
我国转基因技术风险交流分析   总被引:3,自引:0,他引:3  
随着生物技术的迅猛发展,发展转基因产业的战略选择与公众对转基因安全疑虑的矛盾十分突出。通过转基因舆情分析,指出我国转基因风险交流存在的不足主要为风险交流工作缺乏顶层设计,信息公开程度较低,风险交流方式和内容单调,公益机构未能发挥应有作用。在此基础上,提出了加强转基因风险交流的政策建议:(1)明确转基因风险交流的目标;(2)建立转基因风险交流协调框架;(3)建立转基因信息公开平台和信息监测平台;(4)完善管理部门和公益机构的风险交流职能;(5)改革科技项目政策。  相似文献   

5.
我国农业转基因生物安全管理现状   总被引:3,自引:0,他引:3       下载免费PDF全文
转基因技术可以打破物种界限,实现作物性状的定向改造,在解决粮食增产、环境污染、节水增效,以及改进农产品质量等方面显示出巨大潜力。同时,转基因技术具有潜在的风险,转基因生物的安全性受到人们的广泛关注。本文介绍了我国农业转基因生物安全管理状况,包括法规制度体系、安全评价体系和安全监管体系,旨在让人们更好地了解我国农业转基因生物安全管理知识。  相似文献   

6.
正我国转基因安全管理体制和运行机制规范、严谨,可以确保安全。一是,我国建立了一整套适合我国国情并且与国际接轨的法律法规体系,涵盖了转基因研究、试验、生产、加工、经营、进口许可以及产品强制标识等各环节。国务院颁布了《农业转基因生物安全管理条例》,农业部制定实施了《农业转基因生物安全评价管理办法》《农业转基因生物进口安全管理办法》《农业转基因生物标识管理办法》和《农业转基因生物加工审批办法》4个配套规章,国家质检总局施行  相似文献   

7.
正转基因产品的安全评价、监测和管理是否都在严格的法规和法律框架下进行?国际上以及各个国家是否都有与转基因技术及其产品评价和监管相关的法规或条文?转基因生物安全监管的国际法规国际上最具权威的与转基因生物安全监管相关的文件是《卡塔赫纳生物安全议定书》,该议定书是在《生物多样性公约》框架下的一个专门针对生物技术培育的转基因生物活体(LMO)越境转移而制定的安全议定书。该议  相似文献   

8.
转基因作物的全球大规模种植引起了全世界的广泛关注甚至争议。经过遗传改良并具有自然选择优势的转基因作物进入商品化种植,可能将带来环境生物安全的顾虑。在这些生物安全的顾虑中,转基因通过花粉介导的基因漂移向栽培作物的野生近缘种逃逸及其导致的潜在环境风险,就是世人最为关注的环境生物安全问题之一。包括中国在内的许多国家,在转基因作物进行商品化生产之前都必须对转基因逃逸及其带来的潜在环境风险进行严格评价。按照风险评价的框架,转基因向野生近缘种逃逸及其带来潜在环境风险的评价包括3个连续的步骤:1)检测转基因漂移到作物野生近缘种的频率;2)分析转基因在野生近缘种中的表达;3)确定转基因对野生近缘种群体适合度和进化潜力的影响。大量基因漂移的研究结果已表明,转基因通过基因漂移向栽培作物邻近的野生近缘种群体逃逸难以避免,而转基因也会在作物的野生近缘种群体中正常表达。因此分析和评价转基因为野生近缘种带来的适合度效应,对于转基因逃逸及其环境风险的评价至关重要。对适合度的概念及其进化意义进行介绍,并对如何利用转基因的适合度效应分析转基因逃逸的环境风险,以及对此类环境风险进行研究和评价的具体方法予以介绍。上述知识和方法的掌握将有助于人们对转基因作物环境生物安全及其评价的全面理解。  相似文献   

9.
国内新闻     
农业转基因生物安全管理条例公布施行国务院总理朱钅容基 2 0 0 1年 5月 2 3日签署第 30 4号中华人民共和国国务院令 ,公布了《农业转基因生物安全管理条例》 ,《条例》自公布之日起施行。《条例》旨在加强农业转基因生物安全管理 ,保障人体健康和动植物、微生物安全 ,保护生态环境 ,促进农业转基因生物技术研究 ,共 8章 5 6条。《条例》规定 ,国务院农业行政主管部门负责全国农业转基因生物安全的监督管理工作。国家对农业转基因生物安全实行分级管理评价制度 ,建立农业转基因生物安全评价制度 ,对农业转基因生物实行标识制度。单位和个人…  相似文献   

10.
转基因作物的全球大规模种植引起了全世界的广泛关注甚至争议。经过遗传改良并具有自然选择优势的转基因作物进入商品化种植,可能将带来环境生物安全的顾虑。在这些生物安全的顾虑中,转基因通过花粉介导的基因漂移向栽培作物的野生近缘种逃逸及其导致的潜在环境风险,就是世人最为关注的环境生物安全问题之一。包括中国在内的许多国家,在转基因作物进行商品化生产之前都必须对转基因逃逸及其带来的潜在环境风险进行严格评价。按照风险评价的框架,转基因向野生近缘种逃逸及其带来潜在环境风险的评价包括3个连续的步骤:1)检测转基因漂移到作物野生近缘种的频率;2)分析转基因在野生近缘种中的表达;3)确定转基因对野生近缘种群体适合度和进化潜力的影响。大量基因漂移的研究结果已表明,转基因通过基因漂移向栽培作物邻近的野生近缘种群体逃逸难以避免,而转基因也会在作物的野生近缘种群体中正常表达。因此分析和评价转基因为野生近缘种带来的适合度效应,对于转基因逃逸及其环境风险的评价至关重要。对适合度的概念及其进化意义进行介绍,并对如何利用转基因的适合度效应分析转基因逃逸的环境风险,以及对此类环境风险进行研究和评价的具体方法予以介绍。上述知识和方法的掌握将有助于人们对转基因作物环境生物安全及其评价的全面理解。  相似文献   

11.
随着现代科学技术的进步与发展,转基因技术不断推广和应用,其安全性也由此备受关注。转基因舆情的发展态势体现了公众对转基因技术的接受和认知水平,因此,营造良好的舆情环境是转基因技术健康、有效发展的重要保障。通过解析国际典型转基因舆情事例、分析国际转基因舆情发展情况,指出公众对于转基因技术的认知和接受程度不断提高,国际转基因舆情呈良性发展趋势。同时,目前我国转基因舆情呈现辐射层面广、以网络阵地为主、双方主打安全旗帜、强调技术不确定性等主要特点。为保障我国转基因技术的健康可持续发展、稳步推进转基因作物产业化,通过借鉴国外舆情应对经验,对营造我国转基因舆情良性环境提出几点对策:(1)建立完善的信息公开平台;(2)加强多元化科普宣传方式;(3)加强转基因生物安全监管;(4)建立转基因舆情监测平台。  相似文献   

12.
Genetically modified organisms (GMOs) and derived food and feed products are subject to a risk analysis and regulatory approval before they can enter the market in the European Union (EU). In this risk analysis process, the role of the European Food Safety Authority (EFSA), which was created in 2002 in response to multiple food crises, is to independently assess and provide scientific advice to risk managers on any possible risks that the use of GMOs may pose to human and animal health and the environment. EFSA’s scientific advice is elaborated by its GMO Panel with the scientific support of several working groups and EFSA’s GMO Unit. This review presents EFSA’s scientific activities and highlights its achievements on the risk assessment of GMOs for the first 10 years of its existence. Since 2002, EFSA has issued 69 scientific opinions on genetically modified (GM) plant market registration applications, of which 62 for import and processing for food and feed uses, six for cultivation and one for the use of pollen (as or in food), and 19 scientific opinions on applications for marketing products made with GM microorganisms. Several guidelines for the risk assessment of GM plants, GM microorganisms and GM animals, as well as on specific issues such as post-market environmental monitoring (PMEM) were elaborated. EFSA also provided scientific advice upon request of the European Commission on safeguard clause and emergency measures invoked by EU Member States, annual PMEM reports, the potential risks of new biotechnology-based plant breeding techniques, evaluations of previously assessed GMOs in the light of new scientific publications, and the use of antibiotic resistance marker genes in GM plants. Future challenges relevant to the risk assessment of GMOs are discussed. EFSA’s risk assessments of GMO applications ensure that data are analysed and presented in a way that facilitates scientifically sound decisions that protect human and animal health and the environment.  相似文献   

13.
As the worldwide commercialization of genetically modified organisms (GMOs) increases and consumers concern the safety of GMOs, many countries and regions are issuing labeling regulations on GMOs and their products. Analytical methods and their standardization for GM ingredients in foods and feed are essential for the implementation of labeling regulations. To date, the GMO testing methods are mainly based on the inserted DNA sequences and newly produced proteins in GMOs. This paper presents an overview of GMO testing methods as well as their standardization.  相似文献   

14.
自1996年全球转基因作物大规模商业化生产以来,转基因作物种植面积以年均10%左右的速度迅速增长,2013年种植面积已达1.75亿hm2。其在解决全球粮食问题、环境保护、提升粮食营养质量和品质、制药以及推动经济可持续发展方面展现了重要作用。但是,随着转基因商业化生产的深入,转基因技术的潜在风险性引起了社会以及国际上更广泛的关注。事实上,在转基因技术出现之初,科学家们就开始关注其安全性问题。相关国际组织(FAO、WHO、CAC、OECD等)经过数次研究制订了一系列与转基因食品安全性有关的评价原则、指南与措施等。随着转基因技术的发展,这些安全评价策略也在不断完善。我国目前已经基本建立了转基因食品的安全评价和管理体系。转基因食品在进入市场前要经过十分全面以及系统的安全性评价,包括营养学、毒理学、过敏性等方面,从而保障转基因食品的安全性。  相似文献   

15.
16.
Detection of nonauthorized genetically modified organisms (GMOs) has always presented an analytical challenge because the complete sequence data needed to detect them are generally unavailable although sequence similarity to known GMOs can be expected. A new approach, differential quantitative polymerase chain reaction (PCR), for detection of nonauthorized GMOs is presented here. This method is based on the presence of several common elements (e.g., promoter, genes of interest) in different GMOs. A statistical model was developed to study the difference between the number of molecules of such a common sequence and the number of molecules identifying the approved GMO (as determined by border-fragment-based PCR) and the donor organism of the common sequence. When this difference differs statistically from zero, the presence of a nonauthorized GMO can be inferred. The interest and scope of such an approach were tested on a case study of different proportions of genetically modified maize events, with the P35S promoter as the Cauliflower Mosaic Virus common sequence. The presence of a nonauthorized GMO was successfully detected in the mixtures analyzed and in the presence of (donor organism of P35S promoter). This method could be easily transposed to other common GMO sequences and other species and is applicable to other detection areas such as microbiology.  相似文献   

17.
The safety of genetically modified organisms (GMOs) has attracted much attention recently. Polymerase chain reaction (PCR) amplification is a common method used in the identification of GMOs. However, a major disadvantage of PCR is the potential amplification of non-target DNA, causing false-positive identification. Thus, there remains a need for a simple, reliable and ultrasensitive method to identify and quantify GMO in crops. This report is to introduce a magnetic bead-based PCR-free method for rapid detection of GMOs using dual-color fluorescence cross-correlation spectroscopy (FCCS). The cauliflower mosaic virus 35S (CaMV35S) promoter commonly used in transgenic products was targeted. CaMV35S target was captured by a biotin-labeled nucleic acid probe and then purified using streptavidin-coated magnetic beads through biotin-streptavidin linkage. The purified target DNA fragment was hybridized with two nucleic acid probes labeled respectively by Rhodamine Green and Cy5 dyes. Finally, FCCS was used to detect and quantify the target DNA fragment through simultaneously detecting the fluorescence emissions from the two dyes. In our study, GMOs in genetically engineered soybeans and tomatoes were detected, using the magnetic bead-based PCR-free FCCS method. A detection limit of 50 pM GMOs target was achieved and PCR-free detection of GMOs from 5 µg genomic DNA with magnetic capture technology was accomplished. Also, the accuracy of GMO determination by the FCCS method is verified by spectrophotometry at 260 nm using PCR amplified target DNA fragment from GM tomato. The new method is rapid and effective as demonstrated in our experiments and can be easily extended to high-throughput and automatic screening format. We believe that the new magnetic bead-assisted FCCS detection technique will be a useful tool for PCR-free GMOs identification and other specific nucleic acids.  相似文献   

18.
Genetically modified organisms (GMOs) and their behavior in the environment are complex and can only be assessed if the different components are distinguished. This article examines, how by EU law the real causation processes from the GMO release to various endpoints are dissected, individually analysed and then again viewed in their entirety. In addition, the articles includes, how the intellectual process of assessment is divided into the steps of tiered generation, shared submission and structured evaluation of relevant knowledge. The framework proposed for such an examination allows to identify strengths and weaknesses of GMO risk assessment in the EU.  相似文献   

19.
GMDD: a database of GMO detection methods   总被引:1,自引:0,他引:1  

Background  

Since more than one hundred events of genetically modified organisms (GMOs) have been developed and approved for commercialization in global area, the GMO analysis methods are essential for the enforcement of GMO labelling regulations. Protein and nucleic acid-based detection techniques have been developed and utilized for GMOs identification and quantification. However, the information for harmonization and standardization of GMO analysis methods at global level is needed.  相似文献   

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