University of Queensland, School of Biological Sciences, and ARC Centre of Excellence for Coral Reef Studies, St. Lucia 4072, Queensland, Australia.
Appl Environ Microbiol. 2011 Dec;77(24):8478-86. doi: 10.1128/AEM.05870-11. Epub 2011 Oct 14.
Coral reefs are one of the most important marine ecosystems, providing habitat for approximately a quarter of all marine organisms. Within the foundation of this ecosystem, reef-building corals form mutualistic symbioses with unicellular photosynthetic dinoflagellates of the genus Symbiodinium. Exposure to UV radiation (UVR) (280 to 400 nm) especially when combined with thermal stress has been recognized as an important abiotic factor leading to the loss of algal symbionts from coral tissue and/or a reduction in their pigment concentration and coral bleaching. UVR may damage biological macromolecules, increase the level of mutagenesis in cells, and destabilize the symbiosis between the coral host and their dinoflagellate symbionts. In nature, corals and other marine organisms are protected from harmful UVR through several important photoprotective mechanisms that include the synthesis of UV-absorbing compounds such as mycosporine-like amino acids (MAAs). MAAs are small (<400-Da), colorless, water-soluble compounds made of a cyclohexenone or cyclohexenimine chromophore that is bound to an amino acid residue or its imino alcohol. These secondary metabolites are natural biological sunscreens characterized by a maximum absorbance in the UVA and UVB ranges of 310 to 362 nm. In addition to their photoprotective role, MAAs act as antioxidants scavenging reactive oxygen species (ROS) and suppressing singlet oxygen-induced damage. It has been proposed that MAAs are synthesized during the first part of the shikimate pathway, and recently, it has been suggested that they are synthesized in the pentose phosphate pathway. The shikimate pathway is not found in animals, but in plants and microbes, it connects the metabolism of carbohydrates to the biosynthesis of aromatic compounds. However, both the complete enzymatic pathway of MAA synthesis and the extent of their regulation by environmental conditions are not known. This minireview discusses the current knowledge of MAA synthesis, illustrates the diversity of MAA functions, and opens new perspectives for future applications of MAAs in biotechnology.
珊瑚礁是最重要的海洋生态系统之一,为大约四分之一的海洋生物提供了栖息地。在这个生态系统的基础上,造礁珊瑚与单细胞光合作用的甲藻属共生体形成共生关系。暴露于紫外线辐射(UVR)(280 至 400nm),特别是当与热应激相结合时,已被认为是导致珊瑚组织中藻类共生体丧失和/或其色素浓度降低以及珊瑚白化的重要非生物因素。UVR 可能会破坏生物大分子,增加细胞中的突变水平,并使珊瑚宿主与其甲藻共生体之间的共生关系不稳定。在自然界中,珊瑚和其他海洋生物通过几种重要的光保护机制来防止有害的 UVR,包括合成紫外线吸收化合物,如菌氨酸类似物(MAAs)。MAAs 是一种小分子(<400-Da)、无色、水溶性化合物,由环己烯酮或环己烯亚胺发色团与氨基酸残基或其亚氨基醇结合而成。这些次生代谢物是天然的生物防晒霜,其最大吸收波长在 UVA 和 UVB 范围内为 310 至 362nm。除了具有光保护作用外,MAAs 还可以作为抗氧化剂,清除活性氧(ROS)并抑制单线态氧诱导的损伤。有人提出,MAAs 是在莽草酸途径的第一部分合成的,最近有人提出,它们是在戊糖磷酸途径中合成的。莽草酸途径在动物中不存在,但在植物和微生物中,它将碳水化合物的代谢与芳香族化合物的生物合成联系起来。然而,MAA 合成的完整酶途径及其受环境条件调节的程度尚不清楚。这篇小综述讨论了 MAAs 合成的最新知识,说明了 MAAs 功能的多样性,并为未来 MAAs 在生物技术中的应用开辟了新的视角。