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携带二酰基甘油乙酰转移酶(EaDAcT)基因的[具体对象]的可行再生及农杆菌介导转化

Feasible regeneration and agro bacterium-mediated transformation of with diacylglycerol acetyltransferase (EaDAcT) gene.

作者信息

Naeem Ijaz, Munir Iqbal, Durrett Timothy P, Iqbal Aqib, Aulakh Karanbir S, Ahmad Mian Afaq, Khan Hayat, Khan Imtiaz Ali, Hussain Firasat, Shuaib Muhammad, Shah Asad Ali, Muhammad Ikram, Bahadur Saraj, Begim Khaist, Hussain Fida

机构信息

Institute of Biotechnology Genetic Engineering, The University of Agriculture, Peshawar, Khyber Pakhtunkhwa 25130, Pakistan.

Department of Biotechnology, University of Swabi, Khyber Pakhtunkhwa 23561, Pakistan.

出版信息

Saudi J Biol Sci. 2020 May;27(5):1324-1332. doi: 10.1016/j.sjbs.2019.12.036. Epub 2020 Jan 8.

Abstract

In the present study an effort has been made to optimize the regeneration protocol for -mediated transformation of because of its importance as oilseed crops. The highest callus induction frequency of 87% was observed on MS (Murashige and Skoog, 1962) medium supplemented with 4 µM 6-benzyladenine (BA) after four weeks of culture period. Subculturing of organogenic calli in MS media with a similar hormonal composition resulted in shoot organogenesis after six weeks of culture cultivation. The highest shoot induction frequency (92%) was recorded on MS medium containing 4 µM BA in combination with 1 µM of α-naphthalene acetic acid (NAA). Further, well-developed roots were formed in MS media augmented with 6 µM of Indole acetic acid (IAA) in combination with 1 µM Kinetin (Kn). Cotyledon explants were exploited for the successful transformation of . A binary vector comprised of the diacylglycerol acetyltransferase (DAcT) gene under the transcriptional control of a glycinin promoter and with a basta selection marker was introduced into strain GV3101 via electroporation. DAcT gene is responsible for unusual triacylglycerol's production where the sn-3 position is esterified with acetate instead of the long-chain fatty acid found in the triacylglycerol's. The highest regeneration frequency (100%) of transgenic shoots was observed on MS medium supplemented with 4 µM BA plus 1 µM NAA in the presence of 25 mg l basta and 160 mg l timintin. The efficiency of stable transformation was found to be approximately 7% in the transgenic plants. Moreover, the transformed regenerated shoots were confirmed by PCR analysis using DAcT gene-specific primers.

摘要

在本研究中,由于其作为油料作物的重要性,已努力优化介导的转化再生方案。培养四周后,在添加4 μM 6-苄基腺嘌呤(BA)的MS(Murashige和Skoog,1962)培养基上观察到最高愈伤组织诱导频率为87%。将器官发生愈伤组织在具有相似激素组成的MS培养基中继代培养,培养六周后诱导出芽器官。在含有4 μM BA和1 μM α-萘乙酸(NAA)的MS培养基上记录到最高芽诱导频率(92%)。此外,在添加6 μM吲哚乙酸(IAA)和1 μM激动素(Kn)的MS培养基中形成了发育良好的根。利用子叶外植体成功转化。将由大豆球蛋白启动子转录控制且带有巴斯塔选择标记的二酰甘油乙酰转移酶(DAcT)基因组成的二元载体通过电穿孔导入菌株GV3101。DAcT基因负责异常三酰甘油的产生,其中sn-3位用乙酸酯酯化,而不是三酰甘油中发现的长链脂肪酸。在添加4 μM BA加1 μM NAA、25 mg l巴斯塔和160 mg l替卡西林的MS培养基上观察到转基因芽的最高再生频率(100%)。发现转基因植物中稳定转化效率约为7%。此外,使用DAcT基因特异性引物通过PCR分析确认了转化的再生芽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e24c/7182792/56d25a4374e5/gr1.jpg

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