Kotani Akari, Ozaki Taro, Takino Junya, Mochizuki Susumu, Akimitsu Kazuya, Minami Atsushi, Oikawa Hideaki
Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo, Japan.
International Institute of Rare Sugar Research and Education and Faculty of Agriculture, Kagawa University, Kagawa, Japan.
Biosci Biotechnol Biochem. 2022 Feb 24;86(3):287-293. doi: 10.1093/bbb/zbab214.
Previously, we succeeded to produce the core structure of the host-selective ACR toxin (1) on brown leaf spot on rough lemon when the polyketide synthase ACRTS2 gene was heterologously expressed in Aspergillus oryzae (AO). To confirm the production of 1 in AO, the detection limit and suppressing decarboxylation were improved, and these efforts led us to conclude the direct production of 1 instead of its decarboxylation product. During this examination, minor ACR-toxin-related metabolites were found. Their structure determination enabled us to propose a decarboxylation mechanism and a novel branching route forming byproducts from the coupling of the dihydropyrone moiety of 1 with the acetaldehyde and kojic acid abundant in AO. The involvement of putative cyclase ACRTS3 in the chain release of linear polyketide was excluded by the coexpression analysis of ACRTS2 and ACRTS3. Taken together, we concluded that the production of 1 in AO is solely responsible for ACRTS2.
此前,当聚酮合酶ACRTS2基因在米曲霉(AO)中异源表达时,我们成功在粗柠檬的褐斑上产生了宿主选择性ACR毒素(1)的核心结构。为了确认AO中1的产生,提高了检测限并抑制了脱羧反应,这些努力使我们得出结论,直接产生的是1而非其脱羧产物。在此检测过程中,发现了与ACR毒素相关的次要代谢产物。它们的结构测定使我们能够提出一种脱羧机制以及一种由1的二氢吡喃部分与AO中丰富的乙醛和曲酸偶联形成副产物的新分支途径。通过ACRTS2和ACRTS3的共表达分析排除了推定的环化酶ACRTS3参与线性聚酮链释放的可能性。综上所述,我们得出结论,AO中1的产生完全由ACRTS2负责。