首页|木薯淀粉分支酶SBEⅠ反义基因遗传转化木薯的研究

木薯淀粉分支酶SBEⅠ反义基因遗传转化木薯的研究

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旨在获得转淀粉分支酶反义SBEⅠ基因的‘华南木薯8号’转基因植株,为利用转基因技术改良木薯淀粉品质打下基础.在建立了木薯从胚状体子叶到完整植株的再生体系的基础上,用块根特异表达启动子Sporamin驱动的木薯淀粉分支酶SBEⅠ反义基因,通过农杆菌介导法对‘华南木薯8号’进行遗传转化.共接种‘华南木薯8号’子叶517块,获得7株生长良好的转化再生植株,转化再生频率达到1.35%.经PCR检测,其中5株转化再生植株扩增出目的条带,初步证实木薯淀粉分支酶SBEⅠ反义基因已整合进了‘华南木薯8号’基因组中.通过农杆菌介导法可以将淀粉分支酶SBEⅠ反义基因导入到‘华南木薯8号’基因组中,获得了5株转基因植株.
Genetic Transformation of Cassava with Its SBE Ⅰ Antisense Gene
This study aimed to gain transgenic 'SC-8' cassava with the transformation of starch branching enzyme (SBE I) antisense gene, and provide basis for using transgenic technology in the improvement of cassava starch quality. Based on the cassava regeneration system which could take the embryoid cotyledon to complete plants, the SBE I antisense gene was transformed by Agrobacterium-mediated transformation and the tuber-specific promoter Sporamin was used. 517 'SC-8' cassava cotyledons were inoculated which resulted in 7 well grown regenerated plants with a transformation rate of 1.35%. By PCR analysis, the SBE I antisense gene products were amplified in 5 regenerated plants which could provide evidence for the combination of SBE I antisense gene in cassava genome. The SBE I antisense gene can be successfully transformed to 'SC-8' cassava by the Agrobacterium-mediaied transformation method. 5 transgenic 'SC-8' cassava plants were obtained.

cassavastarch branching enzymeantisense genegenetic transformation

郭运玲、孔华、尹奇、左娇、黄启星、贺立卡、郭安平

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中国热带农业科学院热带生物技术研究所/农业部热带作物生物学与遗传资源利用重点实验室,海口571101

木薯 淀粉分支酶 反义基因 遗传转化

国家自然科学基金现代农业产业技术体系项目国家重点基础研究发展规划(973计划)

30960204nycytx-172010CB126605

2013

中国农学通报
中国农学会

中国农学通报

CSTPCDCSCD
影响因子:0.891
ISSN:1000-6850
年,卷(期):2013.29(9)
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