Department of Crop Science, North Carolina State University, Box 8009, Raleigh, NC 27695, USA.
Phytochemistry. 2013 Oct;94:10-27. doi: 10.1016/j.phytochem.2013.06.002. Epub 2013 Aug 15.
Alkaloids represent an extensive group of nitrogen-containing secondary metabolites that are widely distributed throughout the plant kingdom. The pyridine alkaloids of tobacco (Nicotiana tabacum L.) have been the subject of particularly intensive investigation, driven largely due to the widespread use of tobacco products by society and the role that nicotine (16) (see Fig. 1) plays as the primary compound responsible for making the consumption of these products both pleasurable and addictive. In a typical commercial tobacco plant, nicotine (16) comprises about 90% of the total alkaloid pool, with the alkaloids nornicotine (17) (a demethylated derivative of nicotine), anatabine (15) and anabasine (5) making up most of the remainder. Advances in molecular biology have led to the characterization of the majority of the genes encoding the enzymes directly responsible the biosynthesis of nicotine (16) and nornicotine (17), while notable gaps remain within the anatabine (15) and anabasine (5) biosynthetic pathways. Several of the genes involved in the transcriptional regulation and transport of nicotine (16) have also been elucidated. Investigations of the molecular genetics of tobacco alkaloids have not only provided plant biologists with insights into the mechanisms underlying the synthesis and accumulation of this important class of plant alkaloids, they have also yielded tools and strategies for modifying the tobacco alkaloid composition in a manner that can result in changing the levels of nicotine (16) within the leaf, or reducing the levels of a potent carcinogenic tobacco-specific nitrosamine (TSNA). This review summarizes recent advances in our understanding of the molecular genetics of alkaloid biosynthesis in tobacco, and discusses the potential for applying information accrued from these studies toward efforts designed to help mitigate some of the negative health consequences associated with the use of tobacco products.
生物碱代表了一类广泛的含氮次生代谢物,广泛分布于植物界。烟草(Nicotiana tabacum L.)中的吡啶生物碱一直是特别深入研究的主题,这主要是由于社会对烟草产品的广泛使用以及尼古丁(16)(见图 1)作为主要化合物在使这些产品既令人愉悦又上瘾方面所起的作用。在典型的商业烟草植物中,尼古丁(16)约占总生物碱池的 90%,而尼古丁(16)的去甲基衍生物诺尼古丁(17)、烟碱(15)和去氢烟碱(5)构成了其余大部分。分子生物学的进步导致了编码直接负责尼古丁(16)和诺尼古丁(17)生物合成的酶的大多数基因的特征,而在烟碱(15)和去氢烟碱(5)生物合成途径中仍然存在显著的空白。涉及尼古丁(16)转录调控和运输的几个基因也已经阐明。对烟草生物碱的分子遗传学的研究不仅为植物生物学家提供了对这一重要类植物生物碱合成和积累机制的深入了解,还为改变烟草生物碱组成提供了工具和策略,从而改变叶片中尼古丁(16)的水平,或降低一种潜在的致癌烟草特异性亚硝胺(TSNA)的水平。本综述总结了我们对烟草生物碱生物合成分子遗传学理解的最新进展,并讨论了从这些研究中获得的信息应用于旨在帮助减轻与使用烟草产品相关的一些负面健康后果的努力的潜力。