Kildgaard Sara, Subko Karolina, Phillips Emma, Goidts Violaine, de la Cruz Mercedes, Díaz Caridad, Gotfredsen Charlotte H, Andersen Birgitte, Frisvad Jens C, Nielsen Kristian F, Larsen Thomas O
DTU Bioengineering, Technical University of Denmark, Søltofts Plads 221, DK-2800 Kgs. Lyngby, Denmark.
German Cancer Research Center, Brain Tumor Translational Targets, Im Neuenheimer Feld 580, D-69120 Heidelberg, Germany.
Mar Drugs. 2017 Aug 13;15(8):253. doi: 10.3390/md15080253.
A marine-derived fungal strain was screened for new bioactive compounds based on two different approaches: (i) bio-guided approach using cytotoxicity and antimicrobial bioassays; and (ii) dereplication based approach using liquid chromatography with both diode array detection and high resolution mass spectrometry. This led to the discovery of several bioactive compound families with different biosynthetic origins, including pimarane-type diterpenoids and hybrid polyketide-non ribosomal peptide derived compounds. Prefractionation before bioassay screening proved to be a great aid in the dereplication process, since separate fractions displaying different bioactivities allowed a quick tentative identification of known antimicrobial compounds and of potential new analogues. A new pimarane-type diterpene, myrocin F, was discovered in trace amounts and displayed cytotoxicity towards various cancer cell lines. Further media optimization led to increased production followed by the purification and bioactivity screening of several new and known pimarane-type diterpenoids. A known broad-spectrum antifungal compound, ilicicolin H, was purified along with two new analogues, hydroxyl-ilicicolin H and ilicicolin I, and their antifungal activity was evaluated.
(i)使用细胞毒性和抗菌生物测定的生物导向方法;以及(ii)使用具有二极管阵列检测和高分辨率质谱的液相色谱的去重复方法。这导致发现了几个具有不同生物合成来源的生物活性化合物家族,包括海松烷型二萜类化合物和杂合聚酮-非核糖体肽衍生化合物。生物测定筛选前的预分级在去重复过程中被证明是一个很大的帮助,因为显示不同生物活性的单独级分允许快速初步鉴定已知的抗菌化合物和潜在的新类似物。痕量发现了一种新的海松烷型二萜,myrocin F,它对各种癌细胞系显示出细胞毒性。进一步的培养基优化导致产量增加,随后对几种新的和已知的海松烷型二萜进行了纯化和生物活性筛选。一种已知的广谱抗真菌化合物ilicicolin H与两种新类似物羟基-ilicicolin H和ilicicolin I一起被纯化,并评估了它们的抗真菌活性。