TY - JOUR
T1 - Development of a genetic transformation method for seabuckthorn ( Hippophae rhamnoides L.).
AU - Sriskandarajah, Sridevy
AU - Clapham, David
AU - Lundquist, Per-Olof
PY - 2014
Y1 - 2014
N2 - Seabuckthorn (Hippophae rhamnoides L.) is a dioecious plant with berries containing highamounts of several bioactive compounds with nutritional and medicinal traits. It is also planted tocontrol soil erosion. A genetic transformation procedure will facilitate studies of the control ofplant development and interactions with symbionts and pathogens, and will provide a tool forplant breeding. Here, we present a particle bombardment method for transforming seabuckthorn.The early stages of induced adventitious shoots from roots were chosen as a novel target tissue forthe transformation procedure. The root system was bombarded with gold particles coated withplasmid pRT99gus containing genes for plant kanamycin resistance and for β-glucuronidase expression,and shoots were regenerated under kanamycin selection. PCR analysis of the regeneratedtransformed lines confirmed the presence of a 603 bp gus (uidA) gene fragment and a 1.5 kbfragment from the 35S promoter in three shoots from independent transformation events.
AB - Seabuckthorn (Hippophae rhamnoides L.) is a dioecious plant with berries containing highamounts of several bioactive compounds with nutritional and medicinal traits. It is also planted tocontrol soil erosion. A genetic transformation procedure will facilitate studies of the control ofplant development and interactions with symbionts and pathogens, and will provide a tool forplant breeding. Here, we present a particle bombardment method for transforming seabuckthorn.The early stages of induced adventitious shoots from roots were chosen as a novel target tissue forthe transformation procedure. The root system was bombarded with gold particles coated withplasmid pRT99gus containing genes for plant kanamycin resistance and for β-glucuronidase expression,and shoots were regenerated under kanamycin selection. PCR analysis of the regeneratedtransformed lines confirmed the presence of a 603 bp gus (uidA) gene fragment and a 1.5 kbfragment from the 35S promoter in three shoots from independent transformation events.
UR - https://res.slu.se/id/publ/66853
UR - http://www.scirp.org/journal/PaperInformation.aspx?PaperID=43556#.VTT8PGZ4wqY
U2 - 10.4236/ajps.2014.55067
DO - 10.4236/ajps.2014.55067
M3 - Journal article
SN - 2158-2742
VL - 5
SP - 528
EP - 534
JO - American Journal of Plant Sciences
JF - American Journal of Plant Sciences
IS - 5
ER -