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测定转 Bt 基因玉米 MON810 田间试验最后 9 年生长季采集的土壤中的杀虫 Cry1Ab 蛋白。

Determination of insecticidal Cry1Ab protein in soil collected in the final growing seasons of a nine-year field trial of Bt-maize MON810.

机构信息

Bavarian State Research Center for Agriculture, Institute for Crop Science and Plant Breeding, Am Gereuth 8, 85354, Freising, Germany.

出版信息

Transgenic Res. 2012 Feb;21(1):77-88. doi: 10.1007/s11248-011-9509-7. Epub 2011 Apr 16.

DOI:10.1007/s11248-011-9509-7
PMID:21499757
Abstract

Cultivation of genetically modified maize (Bt-maize; event MON810) producing recombinant δ-endotoxin Cry1Ab, leads to introduction of the insecticidal toxin into soil by way of root exudates and plant residues. This study investigated the fate of Cry1Ab in soil under long-term Bt-maize cultivation in an experimental field trial performed over nine growing seasons on four South German field sites cultivated with MON810 and its near isogenic non Bt-maize variety. Cry1Ab protein was quantified in soil (<2 mm size) using an in-house validated ELISA method. The assay was validated according to the criteria specified in European Commission Decision 2002/657/EC. The assay enabled quantification of Cry1Ab protein at a decision limit (CCα) of 2.0 ng Cry1Ab protein g(-1) soil with analytical recovery in the range 49.1-88.9%, which was strongly correlated with clay content. Cry1Ab protein was only detected on one field site at concentrations higher than the CCα, with 2.91 and 2.57 ng Cry1Ab protein g(-1) soil in top and lower soil samples collected 6 weeks after the eighth growing season. Cry1Ab protein was never detected in soil sampled in the spring before the next farming season at any of the four experimental sites. No experimental evidence for accumulation or persistence of Cry1Ab protein in different soils under long-term Bt-maize cultivation can be drawn from this field study.

摘要

转Bt 基因玉米(MON810 事件)产生重组 δ-内毒素 Cry1Ab,通过根系分泌物和植物残体将杀虫毒素引入土壤。本研究在德国南部四个田间试验点进行了长达九年的田间试验,调查了长期种植 Bt 玉米(MON810)及其近等基因非 Bt 玉米品种时 Cry1Ab 在土壤中的命运。采用内部验证的 ELISA 方法定量分析土壤中<2mm 粒径的 Cry1Ab 蛋白。该检测方法符合欧洲委员会 2002/657/EC 号决定规定的标准进行验证。该检测方法可在 2.0ngCry1Ab 蛋白 g(-1)土壤的决策限(CCα)下定量 Cry1Ab 蛋白,分析回收率在 49.1-88.9%之间,与粘粒含量密切相关。在第八个生长季后 6 周采集的表层和下层土壤样品中,仅在一个田间试验点检测到高于 CCα 的 Cry1Ab 蛋白浓度,分别为 2.91 和 2.57ngCry1Ab 蛋白 g(-1)土壤。在四个试验点的任何一个试验点,在下一个农季之前的春季都从未检测到 Cry1Ab 蛋白。本田间研究未发现长期种植 Bt 玉米时 Cry1Ab 蛋白在不同土壤中积累或持续存在的实验证据。

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本文引用的文献

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Degradation of Cry1Ab protein from genetically modified maize (MON810) in relation to total dietary feed proteins in dairy cow digestion.与奶牛消化日粮中总饲料蛋白相关的转基因玉米(MON810)Cry1Ab 蛋白的降解。
Transgenic Res. 2010 Aug;19(4):683-9. doi: 10.1007/s11248-009-9339-z. Epub 2009 Nov 4.
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Sensitive and highly specific quantitative real-time PCR and ELISA for recording a potential transfer of novel DNA and Cry1Ab protein from feed into bovine milk.用于记录新型DNA和Cry1Ab蛋白从饲料潜在转移至牛乳中的灵敏且高度特异的定量实时聚合酶链反应和酶联免疫吸附测定。
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Phage-Mediated Competitive Chemiluminescent Immunoassay for Detecting Cry1Ab Toxin by Using an Anti-Idiotypic Camel Nanobody.利用抗独特型骆驼纳米抗体的噬菌体介导竞争性化学发光免疫分析法检测Cry1Ab毒素
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Effects of long-term cultivation of transgenic Bt rice (Kefeng-6) on soil microbial functioning and C cycling.转 Bt 基因抗虫水稻(克丰 6 号)长期种植对土壤微生物功能和 C 循环的影响。
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Microbial Utilization of Free and Clay-Bound Insecticidal Toxins from Bacillus thuringiensis and Their Retention of Insecticidal Activity after Incubation with Microbes.苏云金芽孢杆菌游离态和结合态杀虫毒素的微生物利用及其与微生物共孵育后杀虫活性的保留。
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Insecticidal Activity of the Toxins from Bacillus thuringiensis subspecies kurstaki and tenebrionis Adsorbed and Bound on Pure and Soil Clays.苏云金芽孢杆菌亚种 kurstaki 和 tenebrionis 的毒素在纯土和土壤粘土上的吸附和结合的杀虫活性。
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Cry1Ab protein from Bt transgenic rice does not residue in rhizosphere soil.来自Bt转基因水稻的Cry1Ab蛋白不会残留在根际土壤中。
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