Madhulika Singh, Pooja Asthana, Manoj K. Rai, Uma Jaiswal
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引用次数: 0
摘要
本研究介绍了一种通过体细胞胚胎发生从细胞悬浮培养物中进行植物再生的方法,该方法适用于一种具有重要商业和药用价值的树种--无患子(Sapindus trifoliatus)。在含有 5.0 mg l-1 2, 4-D 和 0.01 mg l-1 Kin 的琼脂固体 MS 培养基上,从叶盘诱导胼胝体。将叶片衍生的易碎胼胝体置于不含 PGR、含 3% 蔗糖的全强度 MS 液体培养基中,建立胚胎细胞悬浮培养。细胞悬浮培养的生长受 MS 矿物溶液和 L-谷氨酰胺浓度的显著影响。将悬浮液培养在半固体的 MS 培养基上会形成球状结构。这些胚胎球状结构在半固体 MS 培养基上分化成次生球状结构或体细胞胚胎。在培养基中添加 200 mg l-1 L-谷氨酰胺可促进球状结构和不同阶段的体细胞胚(从球状胚到子叶胚)的分化。相对高浓度(5%)的蔗糖或 ABA(0.01 毫克/升)可促进体细胞胚的成熟。在含 2% 蔗糖的半强度 MS 培养基上,体细胞胚发芽率和小植株转化率最高(约 90%)。植株在土壤中硬化和成活率达到 90%。
Somatic embryogenesis and plant regeneration from suspension cultures of Sapindus trifoliatus
A procedure for plant regeneration from cell suspension cultures through somatic embryogenesis is described for Sapindus trifoliatus, a commercially and medicinally important tree. Callus was induced from leaf disc on agar-solidified MS medium with 5.0 mg l−1 2, 4-D and 0.01 mg l−1 Kin. Embryogenic cell suspension cultures were established by placing leaf-derived friable calli in PGR-free full-strength MS liquid medium with 3% sucrose. The growth of cell suspension culture was significantly affected by the strength of the MS mineral solution and L-glutamine. Plating of the suspension on semisolid MS medium resulted in the formation of globular structures. These embryogenic globular structures differentiated into secondary globular structures or somatic embryos on a semisolid MS medium. The differentiation of globular structures and different stages of somatic embryos (from globular to cotyledonary) was enhanced by the addition of 200 mg l−1 L-glutamine in the medium. Sucrose at relatively high concentrations (5%) or ABA (0.01 mg l−1) promoted somatic embryo maturation. The highest percentage (about 90%) of germination of somatic embryo and plantlet conversion was achieved on a half-strength MS medium containing 2% sucrose. The plants were hardened and established in soil with a 90% survival rate
期刊介绍:
This journal highlights the myriad breakthrough technologies and discoveries in plant biology and biotechnology. Plant Cell, Tissue and Organ Culture (PCTOC: Journal of Plant Biotechnology) details high-throughput analysis of gene function and expression, gene silencing and overexpression analyses, RNAi, siRNA, and miRNA studies, and much more. It examines the transcriptional and/or translational events involved in gene regulation as well as those molecular controls involved in morphogenesis of plant cells and tissues.
The journal also covers practical and applied plant biotechnology, including regeneration, organogenesis and somatic embryogenesis, gene transfer, gene flow, secondary metabolites, metabolic engineering, and impact of transgene(s) dissemination into managed and unmanaged plant systems.