大豆愈伤组织诱导及器官发生[j]稳定。的简历。由成熟子叶和胚胎形成的金字塔。

Ebony Y. Joyner, L. S. Boykin, M. Lodhi
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引用次数: 32

摘要

大豆是世界上最重要的豆类之一。大豆植物受到多种生物和非生物因素以及病虫害的影响,降低了作物的品质和产量。为了克服这些生物和非生物的挑战,必须遵循系统的作物改良计划,以提高作物产量,其中包括使用新技术和开发具有理想品质的新品种。随着大豆基因组测序计划的完成,预期获得所需的基因序列将推进大豆改良工作。有两种常用的离体植株再生方法;体细胞胚——由未成熟的胚胎发生,由植物和种子的成熟部分器官发生。大豆离体再生取决于多种物理、生化和遗传因素。不同的基因型对再生方法的反应不同。金字塔大豆被用于几个育种和制图项目,但还没有制定出再生程序。我们项目的目标是开发大豆cv的体外再生程序。金字塔可以被基因操纵。用不同浓度的2,4- d和NAA单独或联合使用,从萌发的种子中切除子叶和胚,诱导愈伤组织。培养基中2,4- d浓度为3-21 μ M时,子叶愈伤组织诱导率为100%。愈伤组织形成后,将其转移到含BAP和Kinetin的培养基上,获得根和芽;5 μ M BAP在这方面是最有效的。发育完全的植株在不到三个月的时间里被移栽到花盆里,在7月份结出了健康的种子。
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Callus induction and organogenesis in soybean [Glycine max (L.) Merr.] cv. pyramid from mature cotyledons and embryos.
Soybean is one of the most important legumes of the world. Soybean plants are affected by several biotic and abiotic factors as well as insect pests and diseases which lower the quality and production of the crop. In order to over- come these biotic and abiotic challenges, a systematic crop improvement plan has to be followed in order to enhance crop production which involves the use of new technologies and developing new cultivars with desirable qualities. With the completion of the soybean genome sequencing project, it is anticipated that access to desirable gene sequences will advance soybean improvement efforts. Two general approaches for in vitro plant regeneration are used; somatic embryo- genesis from immature embryos and organogenesis from mature parts of the plant and seeds. In vitro regeneration in soybean depends upon several physical, biochemical and genetic factors. Different genotypes respond differently to the method of regeneration used. Pyramid soybean is used in several breeding and mapping projects but does not have a regeneration procedure worked out. The goal of our project was to develop an in vitro regeneration procedure for soybean cv. Pyramid that would be amenable to genetic manipulations. We excised cotyledons and embryos from germinating seeds and induced callus with various concentrations of 2,4-D and NAA, used alone or in combination. 2,4-D at 3-21� M concentrations in the culture media produced 100% callus induction from cotyledons. After callus formation we trans- ferred them to BAP and Kinetin containing culture media and obtained roots and shoots; 5 � M BAP was the most effec- tive for that purpose. Fully developed plants were transplanted to the pots in less than three months where they produced healthy seeds in July.
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