Department of Plant Cytology and Morphology, Agricultural University, Arboretumlaan 4, NL 6703 BD, Wageningen, The Netherlands.
Plant Cell Rep. 1989 Feb;8(2):67-70. doi: 10.1007/BF00716840.
Isozyme analyses were carried out on protein extracts of non-embryogenic and embryogenic callus fromZea mays L., using polyacrylamide gel electrophoresis. We examined the isozyme patterns of glutamate dehydrogenase, peroxidase and acid phosphatase for their utility as biochemical markers of maize embryogenic callus cultures. These isozyme systems were also used to examine possible correlations between isozymes and different stages of regeneration. The zymograms of peroxidase and glutamate dehydrogenase differed for non-embryogenic and embryogenic callus. Further, some isozymes were correlated with the morphological appearance of the tissue while others seemed to be involved with the duration of the culture period. Using the same enzyme assays on fresh tissue samples we were able to test the three enzymes as cytochemical markers in embryogenic cultures. Glutamate dehydrogenase proved to be most successful to discriminate embryogenic from non-embryogenic cells.
采用聚丙烯酰胺凝胶电泳法对玉米非胚性和胚性愈伤组织的蛋白质提取物进行同工酶分析。我们研究了谷氨酸脱氢酶、过氧化物酶和酸性磷酸酶的同工酶模式,以将其作为玉米胚性愈伤组织培养的生化标记物。这些同工酶系统还用于研究同工酶与不同再生阶段之间的可能相关性。过氧化物酶和谷氨酸脱氢酶的同工酶图谱在非胚性和胚性愈伤组织之间存在差异。此外,一些同工酶与组织的形态外观相关,而另一些同工酶似乎与培养周期的长短有关。在新鲜组织样品上使用相同的酶分析,我们能够将这三种酶用作胚性培养物中的细胞化学标记物。谷氨酸脱氢酶被证明是区分胚性和非胚性细胞最成功的方法。