Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
Science. 2010 Sep 24;329(5999):1653-6. doi: 10.1126/science.1193637. Epub 2010 Sep 2.
Ultraviolet UV-A and UV-B radiation is harmful to living systems, causing damage to biological macromolecules. An important strategy for dealing with UV exposure is the biosynthesis of small-molecule sunscreens. Among such metabolites, the mycosporine and mycosporine-like amino acids (MAAs) are remarkable for their wide phylogenetic distribution and their unique chemical structures. Here, we report the identification of a MAA biosynthetic gene cluster in a cyanobacterium and the discovery of analogous pathways in other sequenced organisms. We have expressed the cluster in a heterologous bacterial host and characterized all four biosynthetic enzymes in vitro. In addition to clarifying the origin of the MAAs, these efforts have revealed two unprecedented enzymatic strategies for imine formation.
紫外线(UV-A 和 UV-B)辐射对生命系统有害,会破坏生物大分子。应对紫外线照射的一个重要策略是合成小分子防晒剂。在这些代谢产物中,真菌嘧啶和真菌嘧啶类氨基酸(MAAs)因其广泛的系统发育分布和独特的化学结构而引人注目。在这里,我们报告了在一种蓝细菌中发现 MAA 生物合成基因簇,并在其他测序的生物体中发现了类似的途径。我们在异源细菌宿主中表达了该基因簇,并在体外对所有四种生物合成酶进行了表征。除了阐明 MAAs 的起源外,这些努力还揭示了两种用于亚胺形成的前所未有的酶促策略。