Steroid Components of Marine-Derived Fungal Strain Penicillium levitum N33.2 and Their Biological Activities.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Chi K Hoang, Cuong H Le, Dat T Nguyen, Hang T N Tran, Chinh V Luu, Huong M Le, Ha T H Tran
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Abstract

Genus Penicillium comprising the most important and extensively studied fungi has been well-known as a rich source of secondary metabolites. Our study aimed to analyze and investigate biological activities, including in vitro anti-cancer, anti-inflammatory and anti-diabetic properties, of metabolites from a marine-derived fungus belonging to P. levitum. The chemical compounds in the culture broth of P. levitum strain N33.2 were extracted with ethyl acetate. Followingly, chemical analysis of the extract leaded to the isolation of three ergostane-type steroid components, namely cerevisterol (1), ergosterol peroxide (2), and (3β,5α,22E)-ergosta-6,8(14),22-triene-3,5-diol (3). Among these, (3) was the most potent cytotoxic against human cancer cell lines Hep-G2, A549 and MCF-7 with IC50 values of 2.89, 18.51, and 16.47 µg/mL, respectively, while the compound (1) showed no significant effect against tested cancer cells. Anti-inflammatory properties of purified compounds were evaluated based on NO-production in LPS-induced murine RAW264.7 macrophages. As a result, tested compounds performed diverse inhibitory effects on NO production by the macrophages, with the most significant inhibition rate of 81.37 ± 1.35% at 25 µg/mL by the compound (2). Interestingly, compounds (2) and (3) exhibited inhibitory activities against pancreatic lipase and α-glucosidase enzymes in vitro assays. Our study brought out new data concerning the chemical properties and biological activities of isolated steroids from a P. levitum fungus.

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海洋源真菌利维青霉N33.2甾体成分及其生物活性研究
青霉菌属是最重要和被广泛研究的真菌,它是次生代谢物的丰富来源。本研究旨在分析和研究一种海洋来源真菌P. levitum代谢物的体外抗癌、抗炎和抗糖尿病活性。采用乙酸乙酯法对levitum菌株N33.2培养液中的化学成分进行了提取。随后,对提取物进行化学分析,分离出三种麦角甾醇类类固醇成分,分别为cerevisterol(1)、麦角甾醇过氧化物(2)和(3β,5α,22E)-麦角甾醇-6,8(14)、22-triene-3,5-diol(3)。其中,(3)对人癌细胞Hep-G2、A549和MCF-7的细胞毒性最强,IC50值分别为2.89、18.51和16.47µg/mL,而化合物(1)对所测癌细胞无显著作用。通过lps诱导小鼠RAW264.7巨噬细胞no的生成来评价纯化化合物的抗炎特性。结果表明,所测试的化合物对巨噬细胞产生NO具有不同的抑制作用,在25µg/mL时,化合物的抑制率最高,为81.37±1.35%(2)。有趣的是,化合物(2)和(3)在体外实验中对胰脂肪酶和α-葡萄糖苷酶表现出抑制活性。本研究获得了从真菌中分离得到的甾体化合物的化学性质和生物活性的新数据。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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