Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, Chicago, IL 60612, USA.
Bioorg Med Chem. 2012 Oct 15;20(20):6134-43. doi: 10.1016/j.bmc.2012.08.017. Epub 2012 Aug 22.
The extract of UIC 10035, a strain obtained from a sample collected near the town of Homestead, South Florida, showed antiproliferative activity against MDA-MB-435 cells. Bioassay-guided fractionation led to the isolation of a series of cyclic lipodecapeptides, named minutissamides E-L (1-8). The planar structures were determined by analysis of HRESIMS, tandem MS, and 1D and 2D NMR data, and the stereoconfigurations were assigned by LC-MS analysis of the Marfey's derivatives after acid hydrolysis. Minutissamides E-L (1-8) exhibited antiproliferative activity against MDA-MB-435 cells with IC(50) values ranging between 1 and 10 μM. The structures of minutissamides E-L (1-8) were closely related with those of the previously reported lipopeptides, puwainaphycins A-E and minutissamides A-D, characterized by the presence of a lipophilic β-amino acid and three non-standard amino acids NMeAsn, OMeThr and Dhb (α,β-dehydro-α-aminobutyric acid). The strain UIC 10035 was designated as cf. Anabaena sp. on the basis of morphological and 16S rRNA gene sequence analyses.
从佛罗里达州霍姆斯特德附近采集的样本中获得的 UIC 10035 菌株的提取物对 MDA-MB-435 细胞显示出抗增殖活性。基于生物测定的分步分离导致了一系列环状脂肽的分离,命名为 minutissamides E-L(1-8)。通过分析 HRESIMS、串联 MS、1D 和 2D NMR 数据确定了平面结构,并通过酸水解后的 Marfey 衍生物的 LC-MS 分析确定了立体构型。Minutissamides E-L(1-8)对 MDA-MB-435 细胞表现出抗增殖活性,IC(50)值在 1 到 10 μM 之间。Minutissamides E-L(1-8)的结构与先前报道的脂肽,puwainaphycins A-E 和 minutissamides A-D 密切相关,其特征是存在亲脂性β-氨基酸和三个非标准氨基酸 NMeAsn、OMeThr 和 Dhb(α,β-脱氢-α-氨基丁酸)。根据形态学和 16S rRNA 基因序列分析,将菌株 UIC 10035 指定为 cf。鱼腥藻。