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2025年8月15日 星期五
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莴苣叶绿体转化体系的初步建立
林春晶1,韦正乙1,1,王云鹏1,1,王月琳1,1,邢少辰2
1.
2. 吉林省农业科学院农业生物技术研究所
The Preliminary Investigation of Chloroplast Transformation in Lettuce (Lactuca sativa L.)
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摘要 作为人们广泛食用的叶用蔬菜,莴苣(Lactuca sativa L.)一直被科学家认为是一种理想的植物生物反应器平台。本研究首先以生产上常用的两个莴苣品种美国大速生(Grand Rapid)与香港玻璃生菜(Hong Kong Glass)的叶片为外植体,放置在添加不同激素成分的培养基中诱导再生小芽,在生根培养基上生根后即建立了组织培养再生体系;依据两个莴苣品种在不同培养基中的诱导再生率、出芽效率和生根率,确定表现较好的品种美国大速生作为后续叶绿体遗传转化外植体的供体。其次,根据莴苣叶绿体基因组16S-trnI-TrnA-23S区域的序列,设计特异引物,利用PCR扩增技术获得上述区域的部分片段,并作为同源重组序列插入T载体中;在同源重组序列中的Ecl136Ⅱ酶切位点处,插入带有绿色荧光蛋白基因(gfp)和aadA抗性筛选基因的化学合成表达框,构建适合莴苣叶绿体转化的特异表达载体PTLE,其中表达框内为gfp基因,壮观素酶抗性基因(aadA)具有壮观霉素和链霉素抗性。最后,利用基因枪轰击法将PTLE载体转化到莴苣叶绿体基因组中,在含有30 mg/L壮观霉素的培养基中进行两轮抗性筛选后,PCR分子检测和绿色荧光观察证明:获得的莴苣叶绿体转化植株仍处于杂合状态,还未达到完全同质化的程度。上述研究结果表明,已经初步建立了莴苣叶绿体的遗传转化体系,为进一步获得同质化纯合体和后续的植物生物反应器研究与开发提供了基础资料。
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林春晶
韦正乙
王云鹏
王月琳
邢少辰
关键词 莴苣叶绿体转化分子检测绿色荧光蛋白    
Abstract:As a popular leafy vegetable, lettuce(Lactuca sativa L.) has been considered by scientists to be an ideal platform for plant bioreactor. In the present study, 2 lettuce cultivars(Grand Rapid and Hong Kong Glass)commonly cultivated in the production were evaluated which one was feasible to be served as explants for chloroplast transformation. To do this, the tissue culture regeneration systems of both kinds of explants were developed separately in which adventitious shoot buds were induced using young leaf explants of 2 cultivars placed on induction media supplemented with different concentration of hormone and plantlets were obtained on rooting medium. The Grand Rapid cultivar was chosen to provide explants for subsequent chloroplast transformation approach because of its higher frequencies of induction, regeneration and rooting. According to the published sequence of 16S-trnI-TrnA-23S region located in lettuce chloroplast genome, the homologous recombination sequence covering most of 16S-trnI-TrnA-23S region was obtained by PCR amplification using lettuce-specific designed primers, and then inserted T vector to form an intermediate cloning vector. Chemically synthesized expression cassette harboring gfp reporter gene and aadA resistant gene were inserted to the recognizing locus of Ecl136Ⅱ restriction enzyme located in above-mentioned homologous recombination sequence so as to finally finish the construction of specific expression vector PTLE. In the expression cassette, gfp gene represents the green fluorescent protein was used as a visible marker, and aadA gene confered the resistance to spectinomycin and streptomycin by adenylylation. The PTLE vector was transferred into chloroplast genome via particle bombardment, after 2 rounds of selection on medium supplemented with spectinomycin at concentration of 30 mg/L, the surviving plants were obtained on the resistant medium. PCR amplification and green fluorescence analysis confirmed that the regenerated plants were still heteroplastomic, meaning more works of selection were needed to reach the homoplasmy. Taking together, these results suggested that the basic approach of lettuce chloroplast transformation was established and pave the road for further achieving homoplastomic plants and extending to comprehensive understanding of plant bioreactor.
Key wordsLettuce    Chloroplast transformation    Molecular detection    Green fluorescence protein
收稿日期: 2013-10-16     
通讯作者: 邢少辰   
引用本文:   
林春晶1,韦正乙1,1,王云鹏1,1,王月琳1,1,邢少辰2. 莴苣叶绿体转化体系的初步建立[J]. , 2014, 22(4): 520-528.
链接本文:  
http://journal05.magtech.org.cn/Jwk_ny/CN/     或     http://journal05.magtech.org.cn/Jwk_ny/CN/Y2014/V22/I4/520
 
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