木质素
苯丙素
单甘醇
松柏醇
细胞壁
聚合
聚合物
生物合成
单体
生物
植物
有机化学
化学
酶
作者
Yuki Tobimatsu,Fang Chen,Jin Nakashima,Luis L. Escamilla‐Treviño,Lisa A. Jackson,R. A. Dixon,John Ralph
出处
期刊:The Plant Cell
[Oxford University Press]
日期:2013-07-01
卷期号:25 (7): 2587-2600
被引量:191
标识
DOI:10.1105/tpc.113.113142
摘要
Lignins are phenylpropanoid polymers, derived from monolignols, commonly found in terrestrial plant secondary cell walls. We recently reported evidence of an unanticipated catechyl lignin homopolymer (C lignin) derived solely from caffeyl alcohol in the seed coats of several monocot and dicot plants. We previously identified plant seeds that possessed either C lignin or traditional guaiacyl/syringyl (G/S) lignins, but not both. Here, we identified several dicot plants (Euphorbiaceae and Cleomaceae) that produce C lignin together with traditional G/S lignins in their seed coats. Solution-state NMR analyses, along with an in vitro lignin polymerization study, determined that there is, however, no copolymerization detectable (i.e., that the synthesis and polymerization of caffeyl alcohol and conventional monolignols in vivo is spatially and/or temporally separated). In particular, the deposition of G and C lignins in Cleome hassleriana seed coats is developmentally regulated during seed maturation; C lignin appears successively after G lignin within the same testa layers, concurrently with apparent loss of the functionality of O-methyltransferases, which are key enzymes for the conversion of C to G lignin precursors. This study exemplifies the flexible biosynthesis of different types of lignin polymers in plants dictated by substantial, but poorly understood, control of monomer supply by the cells.
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