Chagas Fernanda Oliveira, Caraballo-Rodríguez Andrés Mauricio, Dorrestein Pieter C, Pupo Mônica Tallarico
Departamento de Ciências Farmacêuticas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo , Avenida do Café, s/n, Ribeirão Preto, SP 14040-903, Brazil.
Collaborative Mass Spectrometry Innovation Center, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego , 9500 Gilman Drive, La Jolla, California 92093-0751, United States.
J Nat Prod. 2017 May 26;80(5):1302-1309. doi: 10.1021/acs.jnatprod.6b00870. Epub 2017 Apr 4.
During an investigation of the chemistry of the endophytic actinobacterium Streptomyces albospinus RLe7, which was isolated from the roots of the Brazilian medicinal plant Lychnophora ericoides, three new natural products, (2R*,4S*)-2-((1'S*)-hydroxy-4'-methylpentyl)-4-(hydroxymethyl)butanolide (1), (3R*,4S*,5R*,6S*)-tetrahydro-4-hydroxy-3,5,6-trimethyl-2-pyranone (2), and 1-O-(phenylacetyl)glycerol (3), together with known secondary metabolites (S)-4-benzyl-3-oxo-3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazine-6-carbaldehyde (4), (S)-4-isobutyl-3-oxo-3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazine-6-carbaldehyde (5), and the diketopiperazines cyclo(l-Tyr-l-Pro) (6) and cyclo(l-Val-l-Pro) (7), were isolated. The role of isolated natural products in the interaction between S. albospinus RLe7 and the fungus Coniochaeta sp. FLe4, an endophyte from the same plant, was investigated. None of these isolated actinobacterial compounds were able to inhibit the fungus or induce the fungal red pigmentation observed when both endophytes interact. Further investigation using mass spectrometry approaches enabled identifying the well-known antifungal compound amphotericin B (9) as a microbial metabolite of S. albospinus RLe7. Finally, compound 9 was demonstrated as at least one of the agents responsible for both the antifungal activity and induction of red-pigmented fungal phenotype.
在对从巴西药用植物毛丝花(Lychnophora ericoides)根部分离得到的内生放线菌白色链霉菌RLe7的化学性质进行研究期间,分离出了三种新的天然产物,即(2R*,4S*)-2-((1'S*)-羟基-4'-甲基戊基)-4-(羟甲基)丁内酯(1)、(3R*,4S*,5R*,6S*)-四氢-4-羟基-3,5,6-三甲基-2-吡喃酮(2)和1-O-(苯乙酰基)甘油(3),以及已知的次生代谢产物(S)-4-苄基-3-氧代-3,4-二氢-1H-吡咯并[2,1-c][1,4]恶嗪-6-甲醛(4)、(S)-4-异丁基-3-氧代-3,4-二氢-1H-吡咯并[2,1-c][1,4]恶嗪-6-甲醛(5),还有二酮哌嗪环(L-酪氨酸-L-脯氨酸)(6)和环(L-缬氨酸-L-脯氨酸)(7)。研究了分离出的天然产物在白色链霉菌RLe7与同一种植物的内生真菌锥毛壳菌(Coniochaeta sp.)FLe4相互作用中的作用。这些分离出的放线菌化合物均不能抑制该真菌,也不能诱导两种内生菌相互作用时观察到的真菌红色色素沉着。使用质谱方法进行的进一步研究能够鉴定出著名的抗真菌化合物两性霉素B(9)是白色链霉菌RLe7的一种微生物代谢产物。最后,化合物9被证明是至少一种负责抗真菌活性和诱导真菌红色色素表型的物质。