Department of Biotechnology, Carlsberg Research Laboratory, Carlsberg Laboratory, Gamle Carlsberg Vej 10, DK-2500, Copenhagen Valby, Denmark.
Plant Physiol. 1985 Nov;79(3):867-71. doi: 10.1104/pp.79.3.867.
Polyclonal antibodies raised against barley (1-->3,1-->4)-beta-d-glucanase, alpha-amylase and carboxypeptidase were used to detect precursor polypeptides of these hydrolytic enzymes among the in vitro translation products of mRNA isolated from the scutellum and aleurone of germinating barley. In the scutellum, mRNA encoding carboxypeptidase appeared to be relatively more abundant than that encoding alpha-amylase or (1-->3,1-->4)-beta-d-glucanase, while in the aleurone alpha-amylase and (1-->3,1-->4)-beta-d-glucanase mRNAs predominated. The apparent molecular weights of the precursors for (1-->3,1-->4)-beta-d-glucanase, alpha-amylase, and carboxypeptidase were 33,000, 44,000, and 35,000, respectively. In each case these are slightly higher (1,500-5,000) than molecular weights of the mature enzymes. Molecular weights of precursors immunoprecipitated from aleurone and scutellum mRNA translation products were identical for each enzyme.
针对大麦(1-->3,1-->4)-β-葡聚糖酶、α-淀粉酶和羧肽酶的多克隆抗体被用于检测从发芽大麦的盾片和糊粉层分离的 mRNA 的体外翻译产物中这些水解酶的前体多肽。在盾片中,编码羧肽酶的 mRNA 似乎比编码α-淀粉酶或(1-->3,1-->4)-β-葡聚糖酶的 mRNA 更为丰富,而在糊粉层中,α-淀粉酶和(1-->3,1-->4)-β-葡聚糖酶的 mRNA 占主导地位。(1-->3,1-->4)-β-葡聚糖酶、α-淀粉酶和羧肽酶前体的表观分子量分别为 33000、44000 和 35000,均略高于成熟酶的分子量(1500-5000)。从糊粉层和盾片 mRNA 翻译产物中免疫沉淀的前体的分子量对于每种酶均相同。