Lebeau Juliana, Petit Thomas, Dufossé Laurent, Caro Yanis
Laboratoire de Chimie des Substances Naturelles et des Sciences des Aliments (LCSNSA), Université de La Réunion, 15 Avenue René Cassin, CS 92003, 97744, Saint-Denis, Réunion, France.
Département Hygiène Sécurité Environnement (HSE), IUT La Réunion, Université de La Réunion, 40 Avenue de Soweto, BP 373, 97455, Saint-Pierre, Réunion, France.
AMB Express. 2019 Nov 20;9(1):186. doi: 10.1186/s13568-019-0912-4.
Fungal naphthoquinones, like red bikaverin, are of interest due to their growing applications in designing pharmaceutical products. Though considerable work has been done on the elucidation of bikaverin biosynthesis pathway in Fusarium fujikuroi, very few reports are available regarding its bioproduction in F. oxysporum. We are hereby proposing a putative metabolic pathway for bikaverin bioproduction in a wild F. oxysporum strain by cross-linking the pigment profiles we obtained under two different fermentation conditions with literature. Naphthoquinone pigments were extracted with a pressurized liquid extraction method, and characterized by HPLC-DAD and UHPLC-HRMS. The results led to the conclusions that the F. oxysporum LCP531 strain was able to produce bikaverin and its various intermediates, e.g., pre-bikaverin, oxo-pre-bikaverin, dinor-bikaverin, me-oxo-pre-bikaverin, and nor-bikaverin, in submerged cultures in various proportions. To our knowledge, this is the first report of the isolation of these five bikaverin intermediates from F. oxysporum cultures, providing us with steady clues for confirming a bikaverin metabolic pathway as well as some of its regulatory patterns in the F. oxysporum LCP531 strain, based on the previously reported model in F. fujikuroi. Interestingly, norbikaverin accumulated along with bikaverin in mycelial cells when the strain grew on simple carbon and nitrogen sources and additional cofactors. Along bikaverin production, we were able to describe the excretion of the toxin beauvericin as main extrolite exclusively in liquid medium containing complex nitrogen and carbon sources, as well as the isolation of ergosterol derivate in mycelial extracts, which have potential for pharmaceutical uses. Therefore, culture conditions were also concluded to trigger some specific biosynthetic route favoring various metabolites of interest. Such observation is of great significance for selective production of pigments and/or prevention of occurrence of others (aka mycotoxins).
真菌萘醌类物质,如红色的比卡维林,因其在设计药品方面的应用日益广泛而备受关注。尽管在阐明藤仓镰孢菌中比卡维林生物合成途径方面已开展了大量工作,但关于尖孢镰刀菌中其生物合成的报道却非常少。在此,我们通过将在两种不同发酵条件下获得的色素谱与文献进行交叉关联,提出了一种野生尖孢镰刀菌菌株中比卡维林生物合成的推定代谢途径。采用加压液体萃取法提取萘醌类色素,并通过高效液相色谱 - 二极管阵列检测法(HPLC - DAD)和超高效液相色谱 - 高分辨质谱法(UHPLC - HRMS)对其进行表征。结果表明,尖孢镰刀菌LCP531菌株能够在深层培养中以不同比例产生比卡维林及其多种中间体,例如前比卡维林、氧代 - 前比卡维林、去甲比卡维林、甲基氧代 - 前比卡维林和降比卡维林。据我们所知,这是首次从尖孢镰刀菌培养物中分离出这五种比卡维林中间体的报道,基于先前在藤仓镰孢菌中报道的模型,为我们确认尖孢镰刀菌LCP531菌株中的比卡维林代谢途径及其一些调控模式提供了可靠线索。有趣的是,当该菌株在简单碳源、氮源和额外辅因子上生长时,降比卡维林与比卡维林一起在菌丝细胞中积累。在产生比卡维林的同时,我们能够描述毒素白僵菌素仅在含有复杂氮源和碳源的液体培养基中作为主要胞外产物的排泄情况,以及在菌丝提取物中分离出具有药用潜力的麦角甾醇衍生物。因此,还得出结论,培养条件也会触发一些特定的生物合成途径,有利于产生各种感兴趣的代谢产物。这种观察对于选择性生产色素和/或防止其他物质(即霉菌毒素)的产生具有重要意义。