Endophytic Fungi Penicillium species BCt Phytochemicals Inhibit Replication of Enzymes of Human Immuno-deficiency Virus 1 in in vitro and in silico Studies

M. Govindappa, Channabasava, Ritu Pawar, Chandrasekhar Srinivasa, C. Shivamallu, Manoj-Kumar Arthikala
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Abstract

The present investigation was aimed to know the coumarins in the methanol extract of endophytic fungi, Penicillium species BCt isolated from Calophyllum tomentosum bark tissues using qualitative and GC-MS analysis. The endophytic extract was evaluated for anti-HIV activity on three replicating enzymes in vitro and in silico. The methanol extract of Penicillium species confirmed the presence of coumarins in four qualitative methods and yielded four different types of coumarins in GC-MS. In GC-MS analysis, totally seven different phytochemicals were identified based on retention time and compared with available library data. The four coumarins are coumarin (2H-1-benzopyran-2-one), coumaric acid (3-benzofuran-carboxylic acid), hynecromone (coumarin 4), 4-hydroxy-9-(3-methyl-2-butyl) furo (3,2-g) chloronen-7-one) and other three are common phytochemicals. The HIV-1 RT (98) was strongly inhibited by the endophytic fungal extract compared to integrase (118) and protease (158) in vitro analysis. Highest inhibition of integrase was observed with coumarilic acid (-17.62) when attached to Glu-35, Asn-38, Ser-39 amino acids. The protease was inhibited strongly by hymecromone (-16.39) when attached to amino acids of Val-77, Glu-34, Pro-79, Gly-78. The inhibition of RT was observed with coumarilic acid by attaching to Ala-445, Arg-567, Asp-456, Glu-478, Ser-499, Asn-474 (-23.54) significantly. Based on above results, the endophytic fungal coumarins have the ability to inhibit the three replicating enzymes of HIV-1 significantly. The in-silico results are evidence for how coumarins inhibiting the HIV replicating proteins by binding at specific amino acids. The results will help to understand how and where phytochemicals bind to target proteins to inhibit their action and it may help to identification of drugs to treat HIV. To validate our results, the in vivo research is needed.   
内生真菌青霉菌种BCt植物化学物质抑制人类免疫缺陷病毒1酶的体外和计算机研究
本研究旨在通过定性和气相色谱-质谱分析,了解从毛毛Calophyllum tolentosum树皮组织中分离的内生真菌青霉菌BCt甲醇提取物中香豆素的含量。在体外和计算机上对三种复制酶的抗hiv活性进行了评价。甲醇提取物在4种定性方法中证实了香豆素的存在,并在GC-MS中得到了4种不同类型的香豆素。在GC-MS分析中,根据保留时间共鉴定出7种不同的植物化学物质,并与现有文库数据进行比较。这四种香豆素分别是香豆素(2 -h -1-苯并吡喃-2- 1)、香豆酸(3-苯并呋喃-羧酸)、黑素酮(香豆素4)、4-羟基-9-(3-甲基-2-丁基)呋喃(3,2-g)氯壬-7- 1)和其他三种常见的植物化学物质。在体外分析中,与整合酶(118)和蛋白酶(158)相比,内生真菌提取物对HIV-1 RT(98)有强烈的抑制作用。当香豆酸(-17.62)与Glu-35、Asn-38、Ser-39氨基酸结合时,对整合酶的抑制作用最大。当该蛋白酶与Val-77、Glu-34、Pro-79、Gly-78氨基酸结合时,被膜化素(-16.39)强烈抑制。香豆酸可与Ala-445、Arg-567、Asp-456、Glu-478、Ser-499、Asn-474(-23.54)结合,对RT有明显抑制作用。综上所述,内生真菌香豆素对HIV-1的三种复制酶具有明显的抑制作用。计算机结果证明了香豆素是如何通过结合特定的氨基酸来抑制HIV复制蛋白的。这一结果将有助于了解植物化学物质如何以及在何处与目标蛋白质结合以抑制它们的作用,并可能有助于确定治疗艾滋病毒的药物。为了验证我们的结果,需要进行体内研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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