Redha A, Attia T, Büter B, Saisingtong S, Stamp P, Schmid J E
Department of Botany and Microbiology, Kuwait University, PO Box 5969, Safat 13060, Kuwait, , , , , , KW.
Institute of Plant Sciences, Swiss Federal Institute of Technology (ETH) Zurich, Eschikon 33, CH-8315 Lindau, Switzerland e-mail:
Plant Cell Rep. 1998 Sep;17(12):974-979. doi: 10.1007/s002990050520.
The aim of this study was to optimize the in vitro chromosome-doubling procedure in wheat anther culture. Colchicine, at concentrations of 100-5000 mg/l, was added to the induction medium for 1-5 days. Beneficial effects were obtained with concentrations of 100 and 1000 mg/l colchicine. With time, significant reductions in embryo-like structures as well as higher doubling indices were found. Similar results were obtained with the high- and low-responding genotypes. Colchicine (100 mg/l), added 5 and 20 days after inoculation for 1 and 3 days increased the induction response, but this value was reduced when colchicine was added 10 or 15 days after inoculation. The doubling effect was similar to the control, except for a significant increase with the 3-day application 20 days after inoculation. The highest success index was reached when colchicine was added to the culture medium after 20 days.
本研究的目的是优化小麦花药培养中的体外染色体加倍程序。将浓度为100 - 5000 mg/l的秋水仙碱添加到诱导培养基中1 - 5天。秋水仙碱浓度为100和1000 mg/l时获得了有益效果。随着时间的推移,发现胚状体结构显著减少,加倍指数更高。高响应和低响应基因型都得到了类似的结果。接种后5天和20天添加100 mg/l秋水仙碱1天和3天增加了诱导反应,但接种后10天或15天添加秋水仙碱时该值降低。除接种后20天施用3天有显著增加外,加倍效果与对照相似。当在20天后将秋水仙碱添加到培养基中时,达到了最高的成功指数。