Davin Laurence B, Jourdes Michaël, Patten Ann M, Kim Kye-Won, Vassão Daniel G, Lewis Norman G
Institute of Biological Chemistry, Washington State University, Pullman, WA 99164-6340, USA.
Nat Prod Rep. 2008 Dec;25(6):1015-90. doi: 10.1039/b510386j. Epub 2008 Nov 3.
This comprehensive review describes the current status and knowledge of biochemical and molecular processes involved in allyl/propenyl phenol, lignan, norlignan and lignin biosynthesis. Recent advances made over the last decade are critically discussed, and placed in context with earlier studies largely dating back to the 1950s. Beginning with the recently established formation of phenylalanine in plants, each downstream biochemical conversion is described from the perspective of the mechanistic details known to this point. Particular emphasis is placed upon proteinaceous control of monolignol-derived radical-radical coupling processes, leading to lignans and lignins, as well as apparently related processes affording the various ellagitannins and phenolic terpenoids. The evidence for non-random macromolecular lignin assembly is discussed in detail, this being in contrast to earlier notions that such processes were random. The latter assumptions have largely resulted from a lack of robust analytical procedures and rigorous quantification, as well as a lack of incisive experimental design. In addition, the often-noted severe effects of modulating lignin compositions and contents on plant vascular tissue properties (i.e. in terms of compromised biophysical properties) are described herein, as well as the severe limitations as regards recent claims of compensatory 'combinatorial chemistry' lignin formation. Much of the latter confusion has also resulted from the serious deficiencies in current lignin analytical protocols and quantification, as well as in the general lack of experimental approaches/design to probe lignin primary structure(s).
本综述全面描述了烯丙基/丙烯基苯酚、木脂素、去甲木脂素和木质素生物合成过程中涉及的生化和分子过程的现状与知识。文中批判性地讨论了过去十年取得的最新进展,并将其与主要可追溯到20世纪50年代的早期研究相结合。从植物中最近确定的苯丙氨酸形成开始,从目前已知的机制细节角度描述了每一步下游生化转化。特别强调了对源自单木质醇的自由基-自由基偶联过程的蛋白质控制,该过程会生成木脂素和木质素,以及产生各种鞣花单宁和酚类萜类化合物的明显相关过程。详细讨论了非随机大分子木质素组装的证据,这与早期认为此类过程是随机的观点形成对比。后者的假设很大程度上源于缺乏可靠的分析程序和严格的定量方法,以及缺乏精确的实验设计。此外,本文还描述了调节木质素组成和含量对植物维管组织特性(即生物物理特性受损方面)经常产生的严重影响,以及近期关于补偿性“组合化学”木质素形成的说法所存在的严重局限性。后者的许多混淆也源于当前木质素分析方案和定量方法的严重缺陷,以及普遍缺乏探究木质素一级结构的实验方法/设计。