Church D L, Galston A W
Department of Biology, Yale University, New Haven, Connecticut 06511.
Plant Physiol. 1988;88(3):679-84. doi: 10.1104/pp.88.3.679.
When cultured in inductive medium containing adequate auxin and cytokinin, isolated mesophyll cells of Zinnia elegans L. cv Envy differentiate into tracheary elements with lignified secondary wall thickenings. Differentiation does not occur when cells are cultured in control medium, which has reduced levels of auxin and/or cytokinin. The activities of two enzymes involved in lignin synthesis, 4-coumarate:coenzyme A ligase and peroxidase, were examined. An induction-specific cationic isoperoxidase, visualized by low pH polyacrylamide gel electrophoresis, is detectable in soluble and wall fractions of cultured Zinnia cells long before tracheary elements visibly differentiate and is thus an early marker of differentiation. Compounds (such as antiauxins, anticytokinins, and tunicamycin) that inhibit or delay differentiation alter the expression of this isoperoxidase. 4-Coumarate:coenzyme A ligase activity increases dramatically only as cells differentiate. Together, these results suggest that the onset of lignification in differentiating Zinnia cells might be controlled by the availability of precursors synthesized by way of 4-coumarate:coenzyme A ligase. These precursors would then be polymerized into lignin in the cell wall by the induction-specific isoperoxidase.
在含有适量生长素和细胞分裂素的诱导培养基中培养时,百日草“羡慕”品种分离出的叶肉细胞会分化成具有木质化次生壁加厚的管状分子。当细胞在生长素和/或细胞分裂素水平降低的对照培养基中培养时,分化不会发生。研究了参与木质素合成的两种酶,4-香豆酸:辅酶A连接酶和过氧化物酶的活性。通过低pH聚丙烯酰胺凝胶电泳可视化的一种诱导特异性阳离子同工过氧化物酶,早在管状分子明显分化之前,就可在培养的百日草细胞的可溶性部分和细胞壁部分中检测到,因此是分化的早期标志物。抑制或延迟分化的化合物(如抗生长素、抗细胞分裂素和衣霉素)会改变这种同工过氧化物酶的表达。仅在细胞分化时,4-香豆酸:辅酶A连接酶的活性才会急剧增加。这些结果共同表明,分化的百日草细胞中木质化的开始可能受通过4-香豆酸:辅酶A连接酶合成的前体的可用性控制。然后这些前体将通过诱导特异性同工过氧化物酶在细胞壁中聚合成木质素。