Department of Biology, McGill University, H3A 1B1, Montreal, Quebec, Canada.
Plant Cell Rep. 1990 Oct;9(6):311-5. doi: 10.1007/BF00232858.
We have assessed the capacity of cultured protoplasts from two tissue sources of several commercially-grown broccoli cultivars to regenerate plants. A procedure that employs hypocotyl protoplasts and a culture medium with a high NAA:2,4-D auxin ratio was developed. The procedure permits highly efficient formation of colonies that regenerate shoots at frequencies of 8-17% with two of the four cultivars tested. The time required for the development of plants from protoplasts was 8-11 weeks. No mtDNA rearrangements were observed among any of 17 analysed regenerants. Double-stranded RNAs were detected in mitochondrial DNA (mtDNA) preparations of some, but not all, regenerants of one of the cultivars.
我们评估了几种商业种植的西兰花品种的两种组织来源的培养原生质体再生植物的能力。开发了一种使用下胚轴原生质体和高 NAA:2,4-D 生长素比例的培养基的方法。该方法允许高度有效地形成菌落,在测试的四个品种中的两个品种中,以 8-17%的频率再生芽。从原生质体发育成植物所需的时间为 8-11 周。在分析的 17 个再生体中,没有观察到任何 mtDNA 重排。在一个品种的一些,但不是所有的再生体的线粒体 DNA(mtDNA)制剂中检测到双链 RNA。