首页> 外文期刊>Journal of Agricultural and Food Chemistry >Isolation and Identification of Chlorinated Genistein from Actinoplanes sp. HBDN08 with Antioxidant and Antitumor Activities
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Isolation and Identification of Chlorinated Genistein from Actinoplanes sp. HBDN08 with Antioxidant and Antitumor Activities

机译:从Actinoplanes sp。中分离和鉴定氯化染料木黄酮。 HBDN08具有抗氧化和抗肿瘤活性

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A strain Actinoplanes sp. HBDN08 was screened by PCR-guided method using primers derived from conserved regions of halogenase genes. A new chlorinated isoflavone, 3',8-dichlorogenistein (1), along with 8-chlorogenistein (2) were isolated from the fermentation broth of Actinoplanes sp. HBDN08. Their structures were elucidated on the basis of extensive 1D and 2D NMR as well as HRESI-MS, ESI-MS, UV, and IR spectroscopic analyses. The origin of the two compounds was also investigated by high-performance liquid chromatography (HPLC) analysis. The results demonstrated that they were not biosynthesized but derived from the biotransformation of genistein by Actinoplanes sp. HBDN08. The antioxidant activities of the isolated compounds 1 and 2 were evaluated by using the lipid peroxidation assay. Their antitumor activities were calculated according to the inhibitory rate of cell proliferation against the human breast cancer cell line MDA-MB-231. The results indicated that compounds 1 (IC_(50) = 5.2 μM) and 2 (IC_(50) = 7.5 μM) showed stronger antioxidant activities than genistein (IC_(50) = 13.6 μM). In comparison with the antitumor activities of genistein, those of compounds 1 and 2 increased 7.7- and 2.6-fold, respectively. These results suggest that the PCR-guided screening strategy is a rapid method for obtaining halometabolite-producing strains. Moreover, these results reveal that chlorination has significant effects on the bioactivities of genistein. This could be important information for studying the structure-activity relationships of genistein.
机译:应变Actinoplanes sp。使用源自卤化酶基因保守区的引物,通过PCR引导的方法筛选HBDN08。从Actinoplanes sp。的发酵液中分离出一种新的氯化异黄酮3',8-dichlorogenistein(1)和8-chlorogenistein(2)。 HBDN08。在广泛的1D和2D NMR以及HRESI-MS,ESI-MS,UV和IR光谱分析的基础上阐明了它们的结构。还通过高效液相色谱(HPLC)分析研究了这两种化合物的来源。结果表明,它们不是生物合成的,而是由放线菌属物种的染料木黄酮的生物转化而得。 HBDN08。通过使用脂质过氧化测定法评价了分离的化合物1和2的抗氧化活性。根据细胞增殖对人乳腺癌细胞系MDA-MB-231的抑制率来计算其抗肿瘤活性。结果表明,化合物1(IC_(50)= 5.2μM)和2(IC_(50)= 7.5μM)显示出比染料木黄酮(IC_(50)= 13.6μM)更强的抗氧化活性。与染料木黄酮的抗肿瘤活性相比,化合物1和2的抗肿瘤活性分别增加了7.7倍和2.6倍。这些结果表明,PCR指导的筛选策略是一种获得产卤代代谢物菌株的快速方法。而且,这些结果表明氯化对金雀异黄素的生物活性具有显着影响。这对于研究染料木黄酮的构效关系可能是重要的信息。

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