INRA, UMR1083 Sciences Pour l'oenologie, 2 place Viala, 34060 Montpellier Cedex 1, France.
Plant Physiol Biochem. 2013 Nov;72:1-20. doi: 10.1016/j.plaphy.2013.05.009. Epub 2013 May 28.
Land-adapted plants appeared between about 480 and 360 million years ago in the mid-Palaeozoic era, originating from charophycean green algae. The successful adaptation to land of these prototypes of amphibious plants - when they emerged from an aquatic environment onto the land - was achieved largely by massive formation of "phenolic UV light screens". In the course of evolution, plants have developed the ability to produce an enormous number of phenolic secondary metabolites, which are not required in the primary processes of growth and development but are of vital importance for their interaction with the environment, for their reproductive strategy and for their defense mechanisms. From a biosynthetic point of view, beside methylation catalyzed by O-methyltransferases, acylation and glycosylation of secondary metabolites, including phenylpropanoids and various derived phenolic compounds, are fundamental chemical modifications. Such modified metabolites have altered polarity, volatility, chemical stability in cells but also in solution, ability for interaction with other compounds (co-pigmentation) and biological activity. The control of the production of plant phenolics involves a matrix of potentially overlapping regulatory signals. These include developmental signals, such as during lignification of new growth or the production of anthocyanins during fruit and flower development, and environmental signals for protection against abiotic and biotic stresses. For some of the key compounds, such as the flavonoids, there is now an excellent understanding of the nature of those signals and how the signal transduction pathway connects through to the activation of the phenolic biosynthetic genes. Within the plant environment, different microorganisms can coexist that can establish various interactions with the host plant and that are often the basis for the synthesis of specific phenolic metabolites in response to these interactions. In the rhizosphere, increasing evidence suggests that root specific chemicals (exudates) might initiate and manipulate biological and physical interactions between roots and soil organisms. These interactions include signal traffic between roots of competing plants, roots and soil microbes, and one-way signals that relate the nature of chemical and physical soil properties to the roots. Plant phenolics can also modulate essential physiological processes such as transcriptional regulation and signal transduction. Some interesting effects of plant phenolics are also the ones associated with the growth hormone auxin. An additional role for flavonoids in functional pollen development has been observed. Finally, anthocyanins represent a class of flavonoids that provide the orange, red and blue/purple colors to many plant tissues. According to the coevolution theory, red is a signal of the status of the tree to insects that migrate to (or move among) the trees in autumn.
陆生植物出现在大约 4.8 亿至 3.6 亿年前的古生代中期,起源于绿藻门的轮藻。这些两栖植物原型成功地适应陆地生活,主要是通过大量形成“酚类紫外线屏蔽物”实现的。在进化过程中,植物产生了大量酚类次生代谢物的能力,这些次生代谢物在生长和发育的主要过程中不需要,但对它们与环境的相互作用、繁殖策略和防御机制至关重要。从生物合成的角度来看,除了 O-甲基转移酶催化的甲基化之外,包括苯丙烷类和各种衍生酚类化合物在内的次生代谢物的酰化和糖基化也是基本的化学修饰。这种修饰后的代谢物改变了极性、挥发性、细胞内以及溶液中的化学稳定性,以及与其他化合物相互作用(共色素)和生物活性的能力。植物酚类物质的产生受到潜在重叠的调控信号的控制。这些信号包括发育信号,例如在新生长的木质化过程中或在果实和花发育过程中产生花色素苷,以及对非生物和生物胁迫的保护信号。对于一些关键化合物,如类黄酮,现在对这些信号的性质以及信号转导途径如何连接到酚类生物合成基因的激活有了很好的理解。在植物环境中,不同的微生物可以共存,它们可以与宿主植物建立各种相互作用,并且通常是对这些相互作用合成特定酚类代谢物的基础。在根际中,越来越多的证据表明,根特异性化学物质(分泌物)可能启动并操纵根与土壤生物之间的生物和物理相互作用。这些相互作用包括竞争植物的根之间、根与土壤微生物之间的信号交换,以及将土壤化学和物理性质与根相关的单向信号。植物酚类物质还可以调节转录调控和信号转导等重要生理过程。植物酚类物质的一些有趣作用也与生长激素生长素有关。黄酮类化合物在功能性花粉发育中的作用也得到了观察。最后,花色苷是类黄酮的一种,为许多植物组织提供橙色、红色和蓝色/紫色。根据共同进化理论,红色是昆虫向(或在)秋季树木中迁移的树木状态的信号。