Department of Agronomy, University of Missouri, Columbia, Missouri 65211.
Plant Physiol. 1992 Jul;99(3):872-8. doi: 10.1104/pp.99.3.872.
Cessation of cell expansion has been associated with cell wall cross-linking reactions catalyzed by peroxidase. This study utilized two genotypes of tall fescue (Festuca arundinacea Schreb.) that differ in length of the leaf elongation zone to investigate the relationship between ionically bound peroxidase activity and the spatial distribution of leaf elongation. Peroxidase activity was also localized histochemically in transverse sections of the leaf blade using 3,3' -diaminobenzidine. Soluble or soluble plus ionically bound peroxidase activities were extracted from homogenized segments of the elongating leaf blade and assayed spectrophotometrically. Activity of the ionically bound fraction, expressed per milligram fresh weight or per microgram protein, increased as cells were displaced through the distal half of the elongation zone, corresponding to the region in which the elongation rate declined. In both genotypes, the initial increase in activity preceded the onset of growth deceleration by about 10 hours. In the basal region where elongation began, histochemical localization showed that peroxidase activity was found only in vascular tissues. As cells were displaced farther through the elongation zone, peroxidase activity appeared in walls of other longitudinally continuous tissues such as the epidermis and bundle sheaths. Increase in ionically bound peroxidase activity and changes in localization of peroxidase activity occurred at comparable developmental stages in the two genotypes. The results indicate that cessation of elongation followed an increase in cell wall peroxidase activity.
细胞扩张的停止与过氧化物酶催化的细胞壁交联反应有关。本研究利用两种长叶雀稗(Festuca arundinacea Schreb.)基因型,它们的叶片伸长区长度不同,来研究离子结合过氧化物酶活性与叶片伸长的空间分布之间的关系。过氧化物酶活性也使用 3,3'-二氨基联苯胺在叶片横切面上进行组织化学定位。从伸长叶片的匀浆段中提取可溶性或可溶性加离子结合过氧化物酶活性,并进行分光光度法测定。以每毫克鲜重或每微克蛋白表示的离子结合部分的活性随着细胞通过伸长区的远端一半而增加,这与伸长率下降的区域相对应。在两种基因型中,活性的初始增加先于生长减速的开始约 10 小时。在开始伸长的基部区域,组织化学定位显示过氧化物酶活性仅存在于血管组织中。随着细胞在伸长区进一步移动,过氧化物酶活性出现在其他纵向连续组织的细胞壁中,如表皮和束鞘。在两种基因型中,离子结合过氧化物酶活性的增加和过氧化物酶活性的定位变化发生在可比的发育阶段。结果表明,伸长的停止伴随着细胞壁过氧化物酶活性的增加。