Kotake T, Nakagawa N, Takeda K, Sakurai N
Department of Environmental Studies, Faculty of Integrated Arts & Sciences, Hiroshima University, Higashi-Hiroshima, 739-8521 Japan.
Plant Cell Physiol. 2000 Nov;41(11):1272-8. doi: 10.1093/pcp/pcd056.
When auxin stimulates rapid cell elongation growth of cereal coleoptiles, it causes a degradation of 1,3:1,4-beta-glucan in hemicellulosic polysaccharides. We examined gene expressions of endo-1,3:1,4-beta-glucanase (EI) and exo-beta-glucanase (ExoII), of which optimum pH are about 5, and molecular distribution of hemicellulosic polysaccharides in barley (Hordeum vulgare L.) coleoptile segments treated with or without IAA. IAA (10(-5) M) stimulated the gene expression of EI, while it did not affect that of ExoII. IAA induced gene expression of EI after 4 h and increased wall-bound glucanase activity after 8 h. The molecular weight distribution of hemicellulosic polysaccharides from coleoptile cell walls was shifted to lower molecular weight region by 2 h of IAA treatment. Fusicoccin (10(-6) M) mimicked IAA-induced elongation growth and the decrease in molecular weight of hemicellulosic 1,3:1,4-beta-glucan of coleoptiles in the first 4 h, but it did not promote elongation growth thereafter. These facts suggest that acidification of barley cell walls by IAA action enhances pre-existing cell wall-bound glucanase activity in the early first phase of IAA-induced growth and the late second phase involves the gene expression of EI by IAA.
当生长素刺激谷类作物胚芽鞘细胞快速伸长生长时,它会导致半纤维素多糖中的1,3:1,4-β-葡聚糖降解。我们检测了内切-1,3:1,4-β-葡聚糖酶(EI)和外切-β-葡聚糖酶(ExoII)的基因表达,其最适pH约为5,以及在有或无吲哚乙酸(IAA)处理的大麦(Hordeum vulgare L.)胚芽鞘切段中半纤维素多糖的分子分布。IAA(10⁻⁵ M)刺激了EI的基因表达,而对ExoII的基因表达没有影响。IAA在4小时后诱导EI的基因表达,并在8小时后增加细胞壁结合的葡聚糖酶活性。IAA处理2小时后,胚芽鞘细胞壁半纤维素多糖的分子量分布向较低分子量区域转移。壳梭孢菌素(10⁻⁶ M)在前4小时模拟了IAA诱导的伸长生长以及胚芽鞘半纤维素1,3:1,4-β-葡聚糖分子量的降低,但此后并未促进伸长生长。这些事实表明,IAA作用使大麦细胞壁酸化,在IAA诱导生长的早期第一阶段增强了预先存在的细胞壁结合葡聚糖酶活性,而在后期第二阶段涉及IAA诱导的EI基因表达。