Department of Bio-organic Chemistry, State University of Utrecht, 3522 AD Utrecht (The Netherlands).
Plant Physiol. 1983 Oct;73(2):262-7. doi: 10.1104/pp.73.2.262.
Lipoxygenases 1 and 2 were localized in etiolated germinating soybean seeds (Glycine max [L.]. Merr. var. Williams) by an indirect immunofluorescence staining technique. Sections of paraffin-embedded seedlings were stained with affinity-purified antibodies directed against lipoxygenase 1 or 2. The specificity of the immunofluorescence technique was examined by use of nonimmune serum or immunoglobulin G preparations after total adsorption with the appropriate lipoxygenase coupled to Sepharose 4B.After immunofluorescence staining with antilipoxygenase 1 or 2 IgG storage tissues of cotyledons fluoresce strongly the first days of germination. After 3 days, the abaxial hypodermis, the epidermis, and the vascular bundle sheaths show fluorescence, especially after incubation with antilipoxygenase 2 IgG. Fluorescence in cortex and pith of the hypocotyl migrates to the vascular cylinder during germination. In primary leaves, all tissues show fluorescence after 1 day of germination. In storage tissues of cotyledons, cytoplasm around the protein bodies fluoresces, whereas in other tissues protein bodies or other large cell organelles fluoresce.It is reasonable to suggest that lipoxygenase exerts its function in cells at the time that rigorous changes in metabolism take place, namely at the start of mobilization of reserves in storage tissues and start of biosynthesis of chloroplastids in several tissues.
脂氧合酶 1 和 2 被定位于避光发芽的大豆种子(Glycine max [L.]. Merr. var. Williams)中,通过间接免疫荧光染色技术。用针对脂氧合酶 1 或 2 的亲和纯化抗体对石蜡包埋的幼苗切片进行染色。通过用适当的脂氧合酶与 Sepharose 4B 偶联物完全吸附后,使用非免疫血清或免疫球蛋白 G 制剂来检查免疫荧光技术的特异性。在用抗脂氧合酶 1 或 2 IgG 进行免疫荧光染色后,子叶的贮藏组织在发芽的最初几天强烈荧光。3 天后,下表皮、表皮和维管束鞘显示荧光,特别是在用抗脂氧合酶 2 IgG 孵育后。在萌发过程中,下胚轴的皮层和髓质中的荧光迁移到维管束中。在初生叶中,所有组织在发芽后 1 天均显示荧光。在子叶的贮藏组织中,蛋白体周围的细胞质发出荧光,而在其他组织中,蛋白体或其他大细胞器官发出荧光。可以合理地假设脂氧合酶在代谢发生严格变化时在细胞中发挥作用,即在贮藏组织中储备动员和几个组织中叶绿体生物合成开始时。