Forest Biology Division, The Institute of Paper Chemistry, 54912, Appleton, WI, USA.
Plant Cell Rep. 1987 Feb;6(1):35-8. doi: 10.1007/BF00269734.
A method for quantitative determination of the level of somatic embryogenesis in Norway spruce embryogenic callus is described. Embryogenic callus was dispersed in liquid by agitation and plated in a thin layer of medium containing 0.6% low melting point agarose. The number of embedded somatic embryos per mg of callus ranged from 0.2 to 1.5 among 11 embryogenic callus lines surveyed. Each callus line was derived from an individual immature embryo explant. Further development occurred as somatic embryos grew out of the agarose layer. This method was useful for identifying highly embryogenic callus lines among phenotypically similar lines, and should be useful for quantitatively determining the effect of medium and growth regulator modifications on somatic embryo density and developmental capacity.
描述了一种定量测定挪威云杉胚性愈伤组织体胚发生水平的方法。通过搅拌将胚性愈伤组织分散在液体中,并在含有 0.6%低熔点琼脂糖的薄层培养基中培养。在所调查的 11 条胚性愈伤组织系中,每毫克愈伤组织中包埋的体细胞胚数从 0.2 到 1.5 不等。每个愈伤组织系都来自于一个单独的未成熟胚胎外植体。随着体细胞胚从琼脂糖层中生长出来,进一步发育。该方法可用于在表型相似的系中鉴定高胚性愈伤组织系,并且应该有助于定量确定培养基和生长调节剂修改对体细胞胚密度和发育能力的影响。