Schachtschabel Doreen, David Anja, Menzel Klaus-Dieter, Schimek Christine, Wöstemeyer Johannes, Boland Wilhelm
Bioorganic Chemistry, Max Planck Institute for Chemical Ecology, Jena, Germany.
Chembiochem. 2008 Dec 15;9(18):3004-12. doi: 10.1002/cbic.200800477.
The fungal phylum zygomycota uses trisporic acids (TSAs), a family of apocarotenoids, during sexual reproduction to synchronize and control activity between the mycelial hyphae of opposite mating types. Separate as well as mixed cultures of Blakeslea trispora were systematically supplemented with putative, deuterium-labeled precursors downstream of beta-carotene en route to the bioactive TSAs. Analysis of the isolated metabolites allowed the reconstruction of the complete biosynthetic sequence between the first apocarotenoid, D'orenone (1), and the different series of TSAs B (8) and C (13). Both mating types produced a similar spectrum of early metabolites upstream of trisporols B (7) and C (12), while only the (+) type was able to further oxidize trisporols B (7) and C (12) to the corresponding methyltrisporoid B (5) and C (11), respectively. A novel 4-dihydrotrisporic acid B (14) that was not formed from the labeled precursors was isolated from mated strains; this compound might be derived from oxygenated beta-carotene by a parallel pathway. The ester accumulated in the culture broth of the (+) strain and was only hydrolyzed by mycelia of the (-) strain; this corresponds to a synchronization of the biosynthetic activities of both mating types.
接合菌门真菌在有性生殖过程中使用三孢酸(TSAs),这是一类脱辅基类胡萝卜素,用于同步和控制相反交配型的菌丝体之间的活性。在通往生物活性TSAs的β-胡萝卜素下游,系统地向布拉克须霉的单独培养物和混合培养物中添加假定的、氘标记的前体。对分离出的代谢产物进行分析,得以重建第一个脱辅基类胡萝卜素D'-奥雷诺酮(1)与不同系列的TSAs B(8)和C(13)之间完整的生物合成序列。两种交配型在三孢醇B(7)和C(12)上游产生的早期代谢产物谱相似,而只有(+)型能够将三孢醇B(7)和C(12)分别进一步氧化为相应的甲基三孢酸B(5)和C(11)。从交配菌株中分离出一种并非由标记前体形成的新型4-二氢三孢酸B(14);这种化合物可能通过平行途径由氧化的β-胡萝卜素衍生而来。该酯积累在(+)菌株的培养液中,仅被(-)菌株的菌丝体水解;这对应于两种交配型生物合成活性的同步。