Sweetpotato is an important crop for food security in many developing countries which is cultivated using vine cuttings. Studies have revealed that there are at least fifteen well characterized viruses known to infect...Sweetpotato is an important crop for food security in many developing countries which is cultivated using vine cuttings. Studies have revealed that there are at least fifteen well characterized viruses known to infect sweetpotato of which 10 are economically important that contribute to yield reduction. Planting materials use by farmers are often infected by one or more of these viruses. The aim of this study was to evaluate three different sources of planting materials of different health status for their field performance and virus presence. The sources of planting materials were in vitro generated platelets, symptomless Field materials and Farmer’s materials. Four sweetpotato varieties Apomuden, Bohye, Ligri and Dadanyuie were selected from each source of planting material. The trial was laid in a split plot design with the sources of planting material allocated to main plots and the varieties to sub-plots. The plantlets of the four varieties were planted at Botanga Irrigation Scheme in Northern region of Ghana. Viral symptom scores were taken twice, score 1 being the average from 4 - 7 weeks after planting (WAP) and score 2 being the average from 8 - 11 WAP. Nitrocellulose Membranes Enzyme Linked Immunosorbent Assay (NCM-ELISA) kits were employed for the detection of sweetpotato viruses on the field. The source of planting materials significantly influenced (P In vitro generated material showed the least symptoms of virus followed by Field materials. Apomuden and Bohye varieties recorded the highest virus score in the first and second virus symptom observational score respectively. NCM-ELISA revealed that the viruses SPFMV, SPMMV, SPMSV, SPCFV, SPCSV, and CMV were significantly present among the different sources of planting materials. In vitro, Field and Farmer materials recorded NCM-ELISA score of 0.225, 1.075 and 1.500 respectively. Apomuden variety recorded the highest virus score in the assay. Vine and root yield was higher among the in vitro generated material. Farmers should use laboratory cleaned material however, in the absence of such material they should select field material showing no symptom of virus.展开更多
The production of transgenic sweetpotato （cv.Xushu 18） plants exhibiting enhanced salt tolerance using salt overly sensitive （SOS） genes was achieved through Agrobacterium tumefaciens-mediated transformation.A.tum...The production of transgenic sweetpotato （cv.Xushu 18） plants exhibiting enhanced salt tolerance using salt overly sensitive （SOS） genes was achieved through Agrobacterium tumefaciens-mediated transformation.A.tumefaciens strain EHA105 harbors a binary vector pCAMBIA3301 with SOS genes （SOS1,SOS2 and SOS3） and bar gene.Selection culture was conducted using 0.3 mg L^-1 phosphinothricin （PPT）.A total of 40 plants were produced from the inoculated 170 cell aggregates via somatic embryogenesis.PCR analysis showed that 37 of the 40 regenerated plants were transgenic plants.The in vitro assay demonstrated that superoxide dismutase （SOD） and proline were significantly more accumulated and malonaldehyde （MDA） was significantly less accumulated in 21 transgenic plants than in control plants when they were exposed to 86 mmol L^-1 NaCl.Salt tolerance of these 21 plants was further evaluated with Hoagland solution containing 0,51,86,and 120 mmol L^-1 NaCl in the greenhouse.The results indicated that 6 of them had significantly better growth and rooting ability than the remaining 15 transgenic plants and control plants.Expression of SOS genes in the 6 salt-tolerant transgenic plants was demonstrated by RT-PCR analysis.This study provides an alternative approach for improving salt tolerance of sweetpotato.展开更多
Genetic transformation of embryogenic suspension cultures of sweetpotato cv. Lizixiang was conducted by using Agrobacterium tumefaciens strain A208SE harboring the binary vectors pROA93 with β-glucronidase(GUS)and ne...Genetic transformation of embryogenic suspension cultures of sweetpotato cv. Lizixiang was conducted by using Agrobacterium tumefaciens strain A208SE harboring the binary vectors pROA93 with β-glucronidase(GUS)and neomycin phosphotransferase(NPTⅡ)genes. The results indicated that embryogenic suspension cultures precultured for 1 - 3 d were suitable for the transformation. The optimal cocultivation time was 4 - 5 d. The optimal concentration of kanamycin was 50-75 mg L-1 for suspension culture and 100 mg L-1 for embryogenic callus proliferation and plant regeneration. The optimal concentration of carbencillin was 100 mg L-1. Transgenic plants identified with GUS assays and PCR analyses were obtained.展开更多
文摘Sweetpotato is an important crop for food security in many developing countries which is cultivated using vine cuttings. Studies have revealed that there are at least fifteen well characterized viruses known to infect sweetpotato of which 10 are economically important that contribute to yield reduction. Planting materials use by farmers are often infected by one or more of these viruses. The aim of this study was to evaluate three different sources of planting materials of different health status for their field performance and virus presence. The sources of planting materials were in vitro generated platelets, symptomless Field materials and Farmer’s materials. Four sweetpotato varieties Apomuden, Bohye, Ligri and Dadanyuie were selected from each source of planting material. The trial was laid in a split plot design with the sources of planting material allocated to main plots and the varieties to sub-plots. The plantlets of the four varieties were planted at Botanga Irrigation Scheme in Northern region of Ghana. Viral symptom scores were taken twice, score 1 being the average from 4 - 7 weeks after planting (WAP) and score 2 being the average from 8 - 11 WAP. Nitrocellulose Membranes Enzyme Linked Immunosorbent Assay (NCM-ELISA) kits were employed for the detection of sweetpotato viruses on the field. The source of planting materials significantly influenced (P In vitro generated material showed the least symptoms of virus followed by Field materials. Apomuden and Bohye varieties recorded the highest virus score in the first and second virus symptom observational score respectively. NCM-ELISA revealed that the viruses SPFMV, SPMMV, SPMSV, SPCFV, SPCSV, and CMV were significantly present among the different sources of planting materials. In vitro, Field and Farmer materials recorded NCM-ELISA score of 0.225, 1.075 and 1.500 respectively. Apomuden variety recorded the highest virus score in the assay. Vine and root yield was higher among the in vitro generated material. Farmers should use laboratory cleaned material however, in the absence of such material they should select field material showing no symptom of virus.
基金supported by China Agriculture Research System(Sweetpotato)the National High-Tech R&D Program of China(2009AA10Z102)the National Transgenic Plants Project of China(2009ZX08009-064B)
文摘The production of transgenic sweetpotato （cv.Xushu 18） plants exhibiting enhanced salt tolerance using salt overly sensitive （SOS） genes was achieved through Agrobacterium tumefaciens-mediated transformation.A.tumefaciens strain EHA105 harbors a binary vector pCAMBIA3301 with SOS genes （SOS1,SOS2 and SOS3） and bar gene.Selection culture was conducted using 0.3 mg L^-1 phosphinothricin （PPT）.A total of 40 plants were produced from the inoculated 170 cell aggregates via somatic embryogenesis.PCR analysis showed that 37 of the 40 regenerated plants were transgenic plants.The in vitro assay demonstrated that superoxide dismutase （SOD） and proline were significantly more accumulated and malonaldehyde （MDA） was significantly less accumulated in 21 transgenic plants than in control plants when they were exposed to 86 mmol L^-1 NaCl.Salt tolerance of these 21 plants was further evaluated with Hoagland solution containing 0,51,86,and 120 mmol L^-1 NaCl in the greenhouse.The results indicated that 6 of them had significantly better growth and rooting ability than the remaining 15 transgenic plants and control plants.Expression of SOS genes in the 6 salt-tolerant transgenic plants was demonstrated by RT-PCR analysis.This study provides an alternative approach for improving salt tolerance of sweetpotato.
基金supported by the National Natural Science Foundation of China(30170587)the National High Tech R&D Program,China(863 Program,2002AA241031,2001AA241181)the Teaching and Research Award Program for Outstanding Young Teachers in Higher Education Institutions of Ministry of Education,China.
文摘Genetic transformation of embryogenic suspension cultures of sweetpotato cv. Lizixiang was conducted by using Agrobacterium tumefaciens strain A208SE harboring the binary vectors pROA93 with β-glucronidase(GUS)and neomycin phosphotransferase(NPTⅡ)genes. The results indicated that embryogenic suspension cultures precultured for 1 - 3 d were suitable for the transformation. The optimal cocultivation time was 4 - 5 d. The optimal concentration of kanamycin was 50-75 mg L-1 for suspension culture and 100 mg L-1 for embryogenic callus proliferation and plant regeneration. The optimal concentration of carbencillin was 100 mg L-1. Transgenic plants identified with GUS assays and PCR analyses were obtained.
