Department of Agronomy, The University of Georgia, 30602, Athens, GA, USA.
Plant Cell Rep. 1992 Apr;11(3):122-5. doi: 10.1007/BF00232163.
A regeneration system based on repetitive somatic embryogenesis was developed for peanut (Arachis hypogaea L.). Embryogenic suspension cultures were initiated using individual somatic embryos induced from immature cotyledons cultured on a modified Murashige and Skoog medium containing 40 mg/l 2,4-D for 30 days. After transfer to a modified MS liquid medium, the somatic embryos produced masses of secondary and tertiary embryos which continued to proliferate following manual separation and subculture of the embryogenic clumps. The cultures exhibited exponential growth, and have been maintained for over one year without apparent loss of embryogenic potential. Further embryo development, germination, and conversion were achieved by placing embryo clumps onto hormone-free, solid medium. The inclusion of a desiccation period during embryo development enhanced conversion four-fold. Plants have been established in soil and appear to be phenotypically normal.
建立了一个基于体细胞胚胎重复发生的再生系统,用于花生(Arachis hypogaea L.)。将单个体细胞胚从培养在含有 40 mg/l 2,4-D 的改良 Murashige 和 Skoog 培养基上诱导的未成熟子叶中诱导出来,起始胚性悬浮培养 30 天。转移到改良 MS 液体培养基后,体细胞胚产生大量的次生和 tertiary 胚,在手动分离和胚性团块的继代培养后继续增殖。培养物表现出指数增长,并且在没有明显丧失胚胎发生潜力的情况下已经维持了一年以上。通过将胚团置于无激素的固体培养基上,进一步实现了胚胎发育、萌发和转化。在胚胎发育过程中加入干燥期可将转化率提高四倍。已在土壤中建立了植物,并且外观正常。