Shirgurkar Mrudul V, Naik Vaishali B, von Arnold Sara, Nadgauda Rajani S, Clapham David
Tissue Culture Pilot Plant, National Chemical Laboratory, Dr. Homi Bhabha Road, Pashan, Pune 411008, India.
Plant Cell Rep. 2006 Mar;25(2):112-6. doi: 10.1007/s00299-005-0033-1. Epub 2006 Jan 6.
Turmeric (Curcuma longa L.) is an important spice crop plant that is sterile and cannot be improved by conventional breeding. An efficient method for stable transformation for turmeric, C. longa L., was developed using particle bombardment. Callus cultures initiated from shoots were bombarded with gold particles coated with plasmid pAHC25 containing the bar and gusA genes each driven by the maize ubiquitin promoter. Transformants were selected on medium containing glufosinate. Transgenic lines were established on selection medium from 50% of the bombarded calluses. Transgenic shoots regenerated from these were multiplied and stably transformed plantlets were produced. Polymerase chain reaction (PCR) and histochemical GUS assay confirmed the stable transformation. Transformed plantlets were resistant to glufosinate.
姜黄(Curcuma longa L.)是一种重要的香料作物,它是不育的,无法通过传统育种方法改良。利用粒子轰击技术,开发了一种用于姜黄(Curcuma longa L.)稳定转化的有效方法。从芽诱导产生的愈伤组织培养物用包被有质粒pAHC25的金颗粒进行轰击,该质粒含有分别由玉米泛素启动子驱动的bar基因和gusA基因。在含有草铵膦的培养基上筛选转化体。从50% 的轰击愈伤组织中在选择培养基上建立了转基因株系。从这些株系再生的转基因芽进行增殖,从而获得稳定转化的植株。聚合酶链反应(PCR)和组织化学GUS分析证实了稳定转化。转化植株对草铵膦具有抗性。