Diverse polyketides and alkaloids from Penicillium sp. KHMM: structural elucidation, biological and molecular docking studies

被引:6
|
作者
Hamed, Abdelaaty [2 ,3 ]
Ismail, Mohamed [2 ,4 ]
El-Metwally, Mohammad M. [5 ]
Frese, Marcel [2 ]
Ibrahim, Tarek M. A. [3 ]
El-Haddad, Atef F. [3 ]
Sewald, Norbert [2 ]
Shaaban, Mohamed [1 ,2 ]
机构
[1] Natl Res Ctr, Chem Nat Cpds Dept, Pharmaceut & Drug Ind Res Div, El Behoos St 33, Dokki 12622, Egypt
[2] Bielefeld Univ, Dept Chem, Organ & Bioorgan Chem, Univ Str 25, D-33501 Bielefeld, Germany
[3] Al Azhar Univ, Fac Sci, Chem Dept, Nasr City Cairo 11884, Egypt
[4] Helwan Univ, Fac Sci, Microbiol Dept, Helwan Cairo, Egypt
[5] Damanhour Univ, Fac Sci, Bot & Microbiol Dept, Damanhour, Egypt
关键词
alpha; beta tubulins; biological properties; mol-docking; Penicillium sp; polyketide-alkaloides; FUNGUS; QUINOLINONE; METABOLITES; CYCLOPENIN; INHIBITORS; CELL;
D O I
10.1515/znc-2018-0145
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As a continuation of our earlier research concerning the investigation of microbial bioactive secondary metabolites from the terrestrial Penicillium sp.KH Link 1809 isolate KHMM, the fungus was re-cultivated on a large scale to explore its bioactive compounds intensively. Fifteen compounds, including seven alkaloids (1-7), one sesquiterpene (8), an acetylenic system (9), two sterols, and sphengolipid, were identified. Their structures were established on the bases of extensive one- and two-dimensional nuclear magnetic resonance and mass measurements, and by comparison with literature data. The antimicrobial activity of the fungal extract and the corresponding compounds were studied using a panel of pathogenic microorganisms, and their in vitro cytotoxicity against the human cervix carcinoma cell line (KB-3-1) was reported as well. The molecular docking of the isolated compounds showed promising affinities for the alkaloidal compounds 4 6 towards alpha,beta tubulins.
引用
收藏
页码:131 / 137
页数:7
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