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通过生物弹道法将cry1ac基因导入咖啡(阿拉比卡咖啡L. cv. 卡蒂姆),不使用标记基因。

Transformation of coffee (Coffea Arabica L. cv. Catimor) with the cry1ac gene by biolistic, without the use of markers.

作者信息

De Guglielmo-Cróquer Z, Altosaar I, Zaidi M, Menéndez-Yuffá A

机构信息

Instituto de Biología Experimental, Universidad Central de Venezuela, Caracas, Venezuela.

出版信息

Braz J Biol. 2010 May;70(2):387-93. doi: 10.1590/s1519-69842010000200022.

Abstract

The transformation of coffee plantlets with the cry1ac gene of Bacillus thuringiensis was achieved by biolistic using either the whole pUBC plasmid or only the ubi-cry1ac-nos genetic cassette. The cry1ac gene was inserted into coffee plants in order to confer resistance to the leaf miner Leucoptera coffeella, an insect responsible for considerable losses in coffee crops. Bearing in mind that the genetic cassettes used for this study lack reporter genes and/or selection marker genes, the parameters for the transformation procedure by biolistic were previously standardised with a plasmid carrying the gus reporter gene. The presence of the cry1ac gene in young plantlet tissues was determined by PCR, Southern blot and reverse transcription-PCR. Our results show that the obtainment of viable coffee plantlets, transformed by bombardment with the cry1ac gene and without selection markers nor reporter genes, is feasible.

摘要

通过生物弹道法,利用完整的pUBC质粒或仅使用ubi-cry1ac-nos基因盒,实现了苏云金芽孢杆菌cry1ac基因对咖啡组培苗的转化。将cry1ac基因插入咖啡植株中,以赋予其对咖啡潜叶蛾(一种给咖啡作物造成巨大损失的昆虫)的抗性。考虑到本研究中使用的基因盒缺乏报告基因和/或选择标记基因,之前已用携带gus报告基因的质粒对生物弹道转化程序的参数进行了标准化。通过PCR、Southern杂交和逆转录PCR确定了cry1ac基因在幼组培苗组织中的存在情况。我们的结果表明,通过用cry1ac基因轰击转化且无选择标记和报告基因获得存活的咖啡组培苗是可行的。

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