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New Researches in Biotechnology - Facultatea de Biotehnologii ...

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Proceed<strong>in</strong>g of the 4 rd International Symposium“NEW RESEARCH IN BIOTECHNOLOGY” USAMV Bucharest, Romania, 2011THERAPEUTIC EFFECT OF MONASCUS METABOLITESNicoleta Radu 13 , Sidira Marianthi 2 , Mariana Fer<strong>de</strong>s 3 , Mariana Voicescu 41 U.S.A.M.V. Cluj Napoca, Bioeng<strong>in</strong>eer<strong>in</strong>g and <strong>Biotechnology</strong> Department. Correspond<strong>in</strong>g author: Nicoleta Radu,e-mail: nicolbiotec@yahoo.com, phone number: 0730. 728.6942 Department of Molecular Biology & Genetics, Democritus University of Thrace, Alexandroupolis Greece3 Politehnica University of Bucharest, Bioeng<strong>in</strong>eer<strong>in</strong>g and <strong>Biotechnology</strong> Department4 Romanian Aca<strong>de</strong>my,Institute of Physical Chemistry IC Murgulescu, Dept of Supramolecular ChemistryAbstract. Many reports <strong>in</strong>dicate the therapeutic effects for red yeast rice [1-3]. From this po<strong>in</strong>t ofview, experiments performed on cell l<strong>in</strong>e type Hep2 and WiDr <strong>in</strong>dicated an <strong>in</strong>hibitory effect on cancercells. Another study performed on mur<strong>in</strong> cell type RAW 264.7 stimulated with LPS reveal the<strong>in</strong>hibition of nitrogen oxi<strong>de</strong> production <strong>in</strong> comparison with quercet<strong>in</strong> used as witness. Theseproperties is due to presence of some compounds like monakar<strong>in</strong> A-F, monacol<strong>in</strong> K, dimerumic acid,monascopyrid<strong>in</strong>e C-D, xanthomonas<strong>in</strong> A-B, monascumic acid, which exists <strong>in</strong> metabolites producedof Monascus and the presence of ascorbic acid and polifenols. Our study performed with alcoholicred yeast rice extracts <strong>in</strong> the presence of 1% of collagen, reveals a powerful antioxidant effect, <strong>in</strong>which the quench<strong>in</strong>g ratio is 95% <strong>in</strong> comparison with lum<strong>in</strong>ol, used as witness. Studies performed <strong>in</strong>vivo, regard<strong>in</strong>g cicatrisation effect on mouse with the same sample (alcoholic extract of red yeast riceand 1 % collagen) <strong>in</strong>dicate a potential cicatrisation effect, probably due to presence of glucosam<strong>in</strong>ecompound which acts as cicatrisation factor.Keywords: Monascus metabolite, therapeutic effect1481. INTRODUCTIONThe pigments from Monascus metabolites, named red Monascus or Monascus, represent amixture of lypophylic azaphylone. These mixtures conta<strong>in</strong> yellow pigments (ankaflav<strong>in</strong> andmonasc<strong>in</strong>), their oxidised compounds respectively orange pigments (monascorubr<strong>in</strong>e andrubropunctat<strong>in</strong>e) and correspond<strong>in</strong>g compounds with N (red pigment) rubropunctam<strong>in</strong>eand monascorubram<strong>in</strong>e, which <strong>de</strong>rived from isochromene (figure 1) [1-4]. The polyketidiccha<strong>in</strong>s of azaphylones was asambled from acetic acid (which represent the startercompound) and 5 molecules of malonic acid (units of cha<strong>in</strong> extension) [5-8].The chromophores from hexaketidic compounds were obta<strong>in</strong>ed via monascusone A. Theexternal cha<strong>in</strong>s of this compounds constitute a closed system of gama lactons obta<strong>in</strong>edwith con<strong>de</strong>nsation of 2-oxohexanoic acid with 2 –octooctanoic acid <strong>de</strong>rived from fattyacids. The Nitrogen analogues of azaphylones were obta<strong>in</strong>ed by their reaction witham<strong>in</strong>oacids.Another type of compounds produced of Monascus sp. (named monascot<strong>in</strong>ates) wasi<strong>de</strong>ntified from ethyl acetate extracts of Monascus pilosus BCRC 38093 metabolites. Thesecompounds have the structure presented <strong>in</strong> figure 2 and reveals the follow<strong>in</strong>g spectralcharacteristics:Monasnicot<strong>in</strong>ate A (1). Yellow oil. UV λ max (MeOH): 253, 280, 330 nm. IR ν max(near): 1668, 1712 cm -1 (C=0). ESI-MS: 380 ([M+Na] 4 ). HR-ESI-MS: 380,1837 ([M+Na] + ,C 2i H 27 NaN0 + 4 ; calc. 380,18353).

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