Plant and Animal Biotechnology Laboratory, Department of Agronomy, University of Illinois at Urbana-Champaign, 1201 West Gregory, 61801, Urbana, IL, USA.
Plant Cell Rep. 1992 Jun;11(5-6):285-9. doi: 10.1007/BF00235083.
Fourteen soybean (Glycine max L.) genotypes were evaluated for their regenerability from protoplasts using a procedure previously descibed for the cultivar Clark 63. Protoplasts were isolated from immature cotyledon tissue and were cultured in liquid or agarose gelled KP8, MS or B5 medium with different sugars. Significant differences were observed in plating efficiency, which was as high as 63% in Jack and A-2396, and as low as 38% in X-3337. Upon regular dilution with K8 medium, 1-2 mm diameter colonies were formed in 5-6 weeks with all the genotypes tested. These colonies were then transferred onto MSB (MS salts; Murashige & Skoog, 1962 + B5 organics; Gamborg et al., 1968) medium with 0.5 mg l(-1) each of 2,4-D, BA and KN and 500 mg l(-1) CH for further growth. Once the colonies had become green, compact and nodular, and were 8-10 mm in size, they were transferred to regeneration medium. Upon regular subculturing, calli of six genotypes; A-2396, Chamberlain, Heilong-26, Jack, Resnick and XP-3015 developed shoots, with the regeneration frequency being highest 27% in Jack (52 calli out of 192 produced 8-12 shoots). The regenerated shoots from different genotypes were elongated and rooted. So far, sixty three complete plants have been obtained, including twelve A-2396, nineteen Chamberlain, fifteen Jack, nine Resnick and eight XP-3015. A total of thirty five plants have been transplanted into pots in the greenhouse. Sixteen have set seeds and others are producing flowers and pods.
14 个大豆(Glycine max L.)基因型使用先前为 Clark 63 品种描述的程序从原生质体中评估其再生性。原生质体从未成熟的子叶组织中分离出来,并在液体或琼脂糖凝胶化 KP8、MS 或 B5 培养基中培养,培养基中含有不同的糖。在平板效率方面观察到显著差异,Jack 和 A-2396 的平板效率高达 63%,而 X-3337 的平板效率低至 38%。用 K8 培养基常规稀释后,所有测试的基因型在 5-6 周内形成 1-2 毫米直径的菌落。然后将这些菌落转移到 MSB(MS 盐;Murashige 和 Skoog,1962 + B5 有机物;Gamborg 等人,1968)培养基上,其中含有 0.5 mg l(-1) 的 2,4-D、BA 和 KN 以及 500 mg l(-1) 的 CH,以进一步生长。一旦菌落变绿、紧凑且呈结节状,大小为 8-10 毫米,就将它们转移到再生培养基上。在常规继代培养后,A-2396、Chamberlain、Heilong-26、Jack、Resnick 和 XP-3015 等六个基因型的愈伤组织发育出芽,其中 Jack 的再生频率最高为 27%(192 个产生的 52 个愈伤组织中产生了 8-12 个芽)。不同基因型的再生芽被伸长并生根。到目前为止,已经获得了 63 株完整的植物,其中包括 12 株 A-2396、19 株 Chamberlain、15 株 Jack、9 株 Resnick 和 8 株 XP-3015。共有 35 株植物被移植到温室中的花盆中。16 株已结种子,其余的正在开花和结荚。