Vemanna Ramu S, Vennapusa Amaranatha Reddy, Easwaran Murugesh, Chandrashekar Babitha K, Rao Hanumantha, Ghanti Kirankumar, Sudhakar Chinta, Mysore Kirankumar S, Makarla Udayakumar
Department of Crop Physiology, University of Agricultural Sciences, GKVK, Bangalore, India.
Plant Biology Division, The Samuel Roberts Noble Foundation, Ardmore, OK, USA.
Plant Biotechnol J. 2017 Jul;15(7):794-804. doi: 10.1111/pbi.12632. Epub 2017 May 11.
In recent years, concerns about the use of glyphosate-resistant crops have increased because of glyphosate residual levels in plants and development of herbicide-resistant weeds. In spite of identifying glyphosate-detoxifying genes from microorganisms, the plant mechanism to detoxify glyphosate has not been studied. We characterized an aldo-keto reductase gene from Pseudomonas (PsAKR1) and rice (OsAKR1) and showed, by docking studies, both PsAKR1 and OsAKR1 can efficiently bind to glyphosate. Silencing AKR1 homologues in rice and Nicotiana benthamiana or mutation of AKR1 in yeast and Arabidopsis showed increased sensitivity to glyphosate. External application of AKR proteins rescued glyphosate-mediated cucumber seedling growth inhibition. Regeneration of tobacco transgenic lines expressing PsAKR1 or OsAKRI on glyphosate suggests that AKR can be used as selectable marker to develop transgenic crops. PsAKR1- or OsAKRI-expressing tobacco and rice transgenic plants showed improved tolerance to glyphosate with reduced accumulation of shikimic acid without affecting the normal photosynthetic rates. These results suggested that AKR1 when overexpressed detoxifies glyphosate in planta.
近年来,由于植物中草甘膦残留水平以及抗除草剂杂草的出现,人们对抗草甘膦作物的使用愈发关注。尽管已从微生物中鉴定出草甘膦解毒基因,但植物对草甘膦进行解毒的机制尚未得到研究。我们对来自假单胞菌(PsAKR1)和水稻(OsAKR1)的一种醛酮还原酶基因进行了表征,并通过对接研究表明,PsAKR1和OsAKR1均能有效结合草甘膦。在水稻和本氏烟草中沉默AKR1同源基因,或在酵母和拟南芥中使AKR1发生突变,均显示出对草甘膦的敏感性增加。外源施用AKR蛋白可挽救草甘膦介导的黄瓜幼苗生长抑制。在草甘膦上再生表达PsAKR1或OsAKRI的烟草转基因株系表明,AKR可作为选择标记来培育转基因作物。表达PsAKR1或OsAKRI的烟草和水稻转基因植物对草甘膦的耐受性提高,莽草酸积累减少,且不影响正常光合速率。这些结果表明,AKR1过表达时可在植物体内对草甘膦进行解毒。