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用于汞植物修复的转基因杨树的培育

Development of transgenic yellow poplar for mercury phytoremediation.

作者信息

Rugh C L, Senecoff J F, Meagher R B, Merkle S A

机构信息

Daniel B. Warnell School of Forest Resources, Department of Genetics, University of Georgia, Athens 30602, USA.

出版信息

Nat Biotechnol. 1998 Oct;16(10):925-8. doi: 10.1038/nbt1098-925.

Abstract

We examined the ability of yellow poplar (Liriodendron tulipifera) tissue cultures and plantlets to express modified mercuric reductase (merA) gene constructs. Mercury-resistant bacteria express merA to convert highly toxic, ionic mercury, Hg(II), to much less toxic, elemental mercury, Hg(O). Expression of merA in transgenic plants might provide an ecologically compatible approach for the remediation of mercury pollution. Because the alteration of the bacterial merA gene sequence is necessary for high-level expression in Arabidopsis thaliana, yellow poplar proembryogenic masses (PEMs) were transformed with three modified merA constructs via microprojectile bombardment. Each construct was synthesized to have altered flanking regions with increasing amounts of modified coding sequence. All merA constructs conferred resistance to toxic, ionic mercury in independently transformed PEM colonies. Stability of merA transgene expression increased in parallel with the extent of gene coding sequence modification. Regenerated plantlets containing the most modified merA gene (merA18) germinated and grew vigorously in media containing normally toxic levels of ionic mercury. The merA18 plantlets released elemental mercury at approximately 10 times the rate of untransformed plantlets. These results indicate that plants expressing modified merA constructs may provide a means for the phytoremediation of mercury pollution.

摘要

我们研究了黄杨(鹅掌楸)组织培养物和植株表达修饰的汞还原酶(merA)基因构建体的能力。耐汞细菌表达merA,将剧毒的离子汞Hg(II)转化为毒性小得多的元素汞Hg(0)。在转基因植物中表达merA可能为汞污染的修复提供一种生态兼容的方法。由于改变细菌merA基因序列对于在拟南芥中高水平表达是必要的,因此通过微粒轰击用三种修饰的merA构建体转化了黄杨原胚性细胞团(PEMs)。每个构建体都被合成以具有改变的侧翼区域以及增加量的修饰编码序列。所有merA构建体在独立转化的PEM菌落中赋予了对有毒离子汞的抗性。merA转基因表达的稳定性与基因编码序列修饰的程度平行增加。含有修饰程度最高的merA基因(merA18)的再生植株在含有正常毒性水平离子汞的培养基中发芽并茁壮生长。merA18植株释放元素汞的速率约为未转化植株的10倍。这些结果表明,表达修饰的merA构建体的植物可能为汞污染的植物修复提供一种手段。

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